Register
Medicines reference
Active substance

Moxidectin

Macrocyclic lactone (milbemycin). Registered in Georgia: 39 veterinary products. Forms: chewable tablet, scored tablet, spot-on, tablet.

Dose and use

Doses

Each dose comes with its source. Check the label of the product you use.

Active substance Moxidectin
Before use

Safety information

Known Contraindications

  • Critical
    Do not use in cases of hypersensitivity to the active substances or to any of the excipients.
    Sources: VMD SPC · VMD
  • Critical (Dog)
    Do not use in puppies under 7 weeks of age. The safe use... has not been established in puppies and dogs less than 7 weeks of age or less than 3 lbs. body weight.
    Sources: VMD SPC · VMD · FDA
  • Critical (Cat)
    Do not use in kittens under 9 weeks of age. Do not use on cats less than 9 weeks of age or less than 2 lbs. body weight.
    Sources: VMD SPC · VMD · FDA
  • Warning
    The safety of the veterinary medicinal product has not been established during pregnancy and lactation in the target species.... The use is not recommended during pregnancy and lactation. Fertility: Do not use in breeding animals. The safety... has not been established in breeding, pregnant, or lactating
    Sources: VMD SPC · VMD · FDA
  • Warning
    The use is not recommended during pregnancy and lactation.
    Sources: VMD SPC · VMD · FDA
  • Warning (Dog)
    special care should be taken with Collie or Old English Sheep dogs and related breeds or crossbreeds... in particular, oral uptake by Collie or Old English Sheep dogs and related breeds or crossbreeds should be prevented. Dogs with this mutation may develop signs of severe avermectin toxicity if they ingest this product. The most common breeds associated with this mutation include Collies and Collie crosses.
    Sources: VMD SPC · VMD · FDA
  • Warning (Dog)
    Do not use in dogs classified as Class 4 for heartworm disease has not been evaluated in heartworm-positive dogs with Class 4 heartworm disease
    Sources: VMD SPC · VMD · FDA
  • Warning (Cat)
    use of the veterinary medicinal product on cats or ferrets which have adult heartworms may cause serious adverse effects, including death No adverse reactions were associated with the topical application... to experimentally heartworm-infected cats.
    Sources: VMD SPC · VMD · FDA
  • Warning (Cat)
    Do not use on sick, debilitated, or underweight cats Several otherwise healthy, thin geriatric cats experienced prolonged lethargy and sleepiness after using this drug.
    Sources: VMD SPC · VMD · FDA
  • Caution (Dog)
    Use with caution in sick, debilitated, or underweight animals.
    Sources: VMD SPC · VMD · FDA
  • Known Breed Sensitivities
    Collie, Collie (unspecified), Collie - Scottish Rough, Collie - Scottish Smooth, Sheepdog - Old English
    special care should be taken with Collie or Old English Sheep dogs and related breeds or crossbreeds... oral uptake... should be prevented.
Latin name
Moxidectin
Georgian name
მოქსიდექტინი
Authorisation status
Authorised veterinary medicine
An authorised veterinary medicine containing this substance exists. Whether a particular use is on-label depends on the species and the indication - see each dose rule.
Registered in Georgia
39 of 39 forms
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026
All forms and registration39

Registration in Georgia and abroad: the register, number, validity and source are behind (i).

Advantage Multi 40 mg/4 mg, Spot-on

imidacloprid 40 mg + moxidectin 4 mg, spot-on solution for cats up to 4 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Cat
8.5/10
Very good
vetman assessment

Advantage Multi

40 mg/4 mg, imidacloprid 40 mg + moxidectin 4 mg, spot-on solution for cats up to 4 kg
Assessed clinical scopeCat · Full labelled species-specific scope for susceptible flea, mite, louse, gastrointestinal or cardiopulmonary nematode targets, including applicable heartworm prevention · On the skin
Care settingMonthly or indication-specific single-pipette spot-on treatment after exact species, weight, parasite, heartworm and macrocyclic-lactone risk assessment
vetman score 8.5/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 348-11 · Verified on 15 Oct 2026

A mature, broadly effective topical endectocide supported by FDA and the equivalent EU Advocate dossier; use the exact Georgian kilogram presentation rather than importing US pound-band assumptions.

Regulatory and scientific credibility9.0/10

The exact presentation is registered in Georgia and FDA-authorised under the same brand; its Georgian kilogram bands correspond to the EU Advocate line rather than the differently bounded US pound bands, which must not be interchanged.

Clinical efficacy9.0/10

A mature regulatory dossier and controlled laboratory and field programmes support the combination across its broad species-specific flea, mite, nematode and heartworm roles; exact target and repeat schedule remain indication-dependent.

Safety and tolerability7.5/10

The safety profile is extensively characterised, but the concentrated canine formulation can seriously harm cats; young, underweight, sick or debilitated patients, heartworm-positive animals, oral exposure, MDR1-sensitive dogs and concurrent macrocyclic lactones require strict precautions.

Clinical practicality8.5/10

A premeasured monthly pipette is practical and covers several parasite groups, but exact species/concentration selection, direct skin application, drying, licking prevention and indication-specific retreatment intervals are essential.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Use only the exact species, concentration and weight-band pipette. The canine 2.5% moxidectin formulation must never be used on cats, and EU/Georgian kilogram bands must not be replaced with US pound-band assumptions.
  • Do not combine with another antiparasitic macrocyclic lactone unless the exact label and a documented veterinarian-led benefit-risk decision support it.
  • Apply the complete pipette directly to exposed skin, prevent oral exposure and licking, keep animals apart until dry, and follow the indication-specific bathing and repeat-treatment interval.
  • Do not use below nine weeks of age. A cat below 1 kg, or a sick, debilitated or underweight cat, requires the strictest applicable label and a veterinarian-led benefit-risk decision.
  • Establish heartworm status and exact indication before use: applicable EU and FDA labels differ on heartworm-positive cats, and adult infection may carry severe risk.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Elanco · United States
Manufacturer (register)
KVP Pharma + Veterinar Produkte GmbH, Germany
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1253, 19 Oct 2026.
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: ადვანტეიჯ მულტი® კანზე დასაწვეთებელი ხსნარი ≤ 4კგ-მდე წონის კატებისთვის
№ 348-11
Verified on: 15 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-251, 141-254
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Advantage Multi 80 mg/8 mg, Spot-on

imidacloprid 80 mg + moxidectin 8 mg, spot-on solution for cats 4-8 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Cat
8.5/10
Very good
vetman assessment

Advantage Multi

80 mg/8 mg, imidacloprid 80 mg + moxidectin 8 mg, spot-on solution for cats 4-8 kg
Assessed clinical scopeCat · Full labelled species-specific scope for susceptible flea, mite, louse, gastrointestinal or cardiopulmonary nematode targets, including applicable heartworm prevention · On the skin
Care settingMonthly or indication-specific single-pipette spot-on treatment after exact species, weight, parasite, heartworm and macrocyclic-lactone risk assessment
vetman score 8.5/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 345-11 · Verified on 15 Oct 2026

A mature, broadly effective topical endectocide supported by FDA and the equivalent EU Advocate dossier; use the exact Georgian kilogram presentation rather than importing US pound-band assumptions.

Regulatory and scientific credibility9.0/10

The exact presentation is registered in Georgia and FDA-authorised under the same brand; its Georgian kilogram bands correspond to the EU Advocate line rather than the differently bounded US pound bands, which must not be interchanged.

Clinical efficacy9.0/10

A mature regulatory dossier and controlled laboratory and field programmes support the combination across its broad species-specific flea, mite, nematode and heartworm roles; exact target and repeat schedule remain indication-dependent.

Safety and tolerability7.5/10

The safety profile is extensively characterised, but the concentrated canine formulation can seriously harm cats; young, underweight, sick or debilitated patients, heartworm-positive animals, oral exposure, MDR1-sensitive dogs and concurrent macrocyclic lactones require strict precautions.

Clinical practicality8.5/10

A premeasured monthly pipette is practical and covers several parasite groups, but exact species/concentration selection, direct skin application, drying, licking prevention and indication-specific retreatment intervals are essential.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Use only the exact species, concentration and weight-band pipette. The canine 2.5% moxidectin formulation must never be used on cats, and EU/Georgian kilogram bands must not be replaced with US pound-band assumptions.
  • Do not combine with another antiparasitic macrocyclic lactone unless the exact label and a documented veterinarian-led benefit-risk decision support it.
  • Apply the complete pipette directly to exposed skin, prevent oral exposure and licking, keep animals apart until dry, and follow the indication-specific bathing and repeat-treatment interval.
  • Do not use below nine weeks of age. A cat below 1 kg, or a sick, debilitated or underweight cat, requires the strictest applicable label and a veterinarian-led benefit-risk decision.
  • Establish heartworm status and exact indication before use: applicable EU and FDA labels differ on heartworm-positive cats, and adult infection may carry severe risk.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Elanco · United States
Manufacturer (register)
KVP Pharma + Veterinar Produkte GmbH, Germany
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1250, 19 Oct 2026.
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: ადვანტეიჯ მულტი® კანზე დასაწვეთებელი ხსნარი > 4კგ-დან 8კგ-მდე წონის კატებისთვის
№ 345-11
Verified on: 15 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-251, 141-254
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Advantage Multi 100 mg/25 mg, Spot-on

imidacloprid 100 mg + moxidectin 25 mg, spot-on solution for dogs 4-10 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
8.5/10
Very good
vetman assessment

Advantage Multi

100 mg/25 mg, imidacloprid 100 mg + moxidectin 25 mg, spot-on solution for dogs 4-10 kg
Assessed clinical scopeDog · Full labelled species-specific scope for susceptible flea, mite, louse, gastrointestinal or cardiopulmonary nematode targets, including applicable heartworm prevention · On the skin
Care settingMonthly or indication-specific single-pipette spot-on treatment after exact species, weight, parasite, heartworm and macrocyclic-lactone risk assessment
vetman score 8.5/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 347-11 · Verified on 15 Oct 2026

A mature, broadly effective topical endectocide supported by FDA and the equivalent EU Advocate dossier; use the exact Georgian kilogram presentation rather than importing US pound-band assumptions.

Regulatory and scientific credibility9.0/10

The exact presentation is registered in Georgia and FDA-authorised under the same brand; its Georgian kilogram bands correspond to the EU Advocate line rather than the differently bounded US pound bands, which must not be interchanged.

Clinical efficacy9.0/10

A mature regulatory dossier and controlled laboratory and field programmes support the combination across its broad species-specific flea, mite, nematode and heartworm roles; exact target and repeat schedule remain indication-dependent.

Safety and tolerability7.5/10

The safety profile is extensively characterised, but the concentrated canine formulation can seriously harm cats; young, underweight, sick or debilitated patients, heartworm-positive animals, oral exposure, MDR1-sensitive dogs and concurrent macrocyclic lactones require strict precautions.

Clinical practicality8.5/10

A premeasured monthly pipette is practical and covers several parasite groups, but exact species/concentration selection, direct skin application, drying, licking prevention and indication-specific retreatment intervals are essential.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Use only the exact species, concentration and weight-band pipette. The canine 2.5% moxidectin formulation must never be used on cats, and EU/Georgian kilogram bands must not be replaced with US pound-band assumptions.
  • Do not combine with another antiparasitic macrocyclic lactone unless the exact label and a documented veterinarian-led benefit-risk decision support it.
  • Apply the complete pipette directly to exposed skin, prevent oral exposure and licking, keep animals apart until dry, and follow the indication-specific bathing and repeat-treatment interval.
  • Do not use below seven weeks of age; animals below 1 kg, or sick, debilitated or underweight dogs, require the exact label and an explicit benefit-risk decision.
  • Before heartworm use, establish infection status and clinical class. Class 4 disease is contraindicated or unevaluated by the applicable labels; microfilariae treatment and MDR1-sensitive breeds require strict observation for neurologic or acute reactions.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Elanco · United States
Manufacturer (register)
KVP Pharma + Veterinar Produkte GmbH, Germany
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1252, 19 Oct 2026.
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: ადვანტეიჯ მულტი® კანზე დასაწვეთებელი ხსნარი > 4კგ-დან 10კგ-მდე წონის ძაღლებისთვის
№ 347-11
Verified on: 15 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-251, 141-254
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Advantage Multi 250 mg/62.5 mg, Spot-on

imidacloprid 250 mg + moxidectin 62.5 mg, spot-on solution for dogs 10-25 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
8.5/10
Very good
vetman assessment

Advantage Multi

250 mg/62.5 mg, imidacloprid 250 mg + moxidectin 62.5 mg, spot-on solution for dogs 10-25 kg
Assessed clinical scopeDog · Full labelled species-specific scope for susceptible flea, mite, louse, gastrointestinal or cardiopulmonary nematode targets, including applicable heartworm prevention · On the skin
Care settingMonthly or indication-specific single-pipette spot-on treatment after exact species, weight, parasite, heartworm and macrocyclic-lactone risk assessment
vetman score 8.5/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 346-11 · Verified on 15 Oct 2026

A mature, broadly effective topical endectocide supported by FDA and the equivalent EU Advocate dossier; use the exact Georgian kilogram presentation rather than importing US pound-band assumptions.

Regulatory and scientific credibility9.0/10

The exact presentation is registered in Georgia and FDA-authorised under the same brand; its Georgian kilogram bands correspond to the EU Advocate line rather than the differently bounded US pound bands, which must not be interchanged.

Clinical efficacy9.0/10

A mature regulatory dossier and controlled laboratory and field programmes support the combination across its broad species-specific flea, mite, nematode and heartworm roles; exact target and repeat schedule remain indication-dependent.

Safety and tolerability7.5/10

The safety profile is extensively characterised, but the concentrated canine formulation can seriously harm cats; young, underweight, sick or debilitated patients, heartworm-positive animals, oral exposure, MDR1-sensitive dogs and concurrent macrocyclic lactones require strict precautions.

Clinical practicality8.5/10

A premeasured monthly pipette is practical and covers several parasite groups, but exact species/concentration selection, direct skin application, drying, licking prevention and indication-specific retreatment intervals are essential.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Use only the exact species, concentration and weight-band pipette. The canine 2.5% moxidectin formulation must never be used on cats, and EU/Georgian kilogram bands must not be replaced with US pound-band assumptions.
  • Do not combine with another antiparasitic macrocyclic lactone unless the exact label and a documented veterinarian-led benefit-risk decision support it.
  • Apply the complete pipette directly to exposed skin, prevent oral exposure and licking, keep animals apart until dry, and follow the indication-specific bathing and repeat-treatment interval.
  • Do not use below seven weeks of age; animals below 1 kg, or sick, debilitated or underweight dogs, require the exact label and an explicit benefit-risk decision.
  • Before heartworm use, establish infection status and clinical class. Class 4 disease is contraindicated or unevaluated by the applicable labels; microfilariae treatment and MDR1-sensitive breeds require strict observation for neurologic or acute reactions.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Imidacloprid250 mg Moxidectin62.5 mg
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Elanco · United States
Manufacturer (register)
KVP Pharma + Veterinar Produkte GmbH, Germany
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1251, 19 Oct 2026.
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: ადვანტეიჯ მულტი® კანზე დასაწვეთებელი ხსნარი > 10კგ-დან 25კგ-მდე წონის ძაღლებისთვის
№ 346-11
Verified on: 15 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-251, 141-254
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Advantage Multi 400 mg/100 mg, Spot-on

imidacloprid 400 mg + moxidectin 100 mg, spot-on solution for dogs 25-40 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
8.5/10
Very good
vetman assessment

Advantage Multi

400 mg/100 mg, imidacloprid 400 mg + moxidectin 100 mg, spot-on solution for dogs 25-40 kg
Assessed clinical scopeDog · Full labelled species-specific scope for susceptible flea, mite, louse, gastrointestinal or cardiopulmonary nematode targets, including applicable heartworm prevention · On the skin
Care settingMonthly or indication-specific single-pipette spot-on treatment after exact species, weight, parasite, heartworm and macrocyclic-lactone risk assessment
vetman score 8.5/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 349-11 · Verified on 15 Oct 2026

A mature, broadly effective topical endectocide supported by FDA and the equivalent EU Advocate dossier; use the exact Georgian kilogram presentation rather than importing US pound-band assumptions.

Regulatory and scientific credibility9.0/10

The exact presentation is registered in Georgia and FDA-authorised under the same brand; its Georgian kilogram bands correspond to the EU Advocate line rather than the differently bounded US pound bands, which must not be interchanged.

Clinical efficacy9.0/10

A mature regulatory dossier and controlled laboratory and field programmes support the combination across its broad species-specific flea, mite, nematode and heartworm roles; exact target and repeat schedule remain indication-dependent.

Safety and tolerability7.5/10

The safety profile is extensively characterised, but the concentrated canine formulation can seriously harm cats; young, underweight, sick or debilitated patients, heartworm-positive animals, oral exposure, MDR1-sensitive dogs and concurrent macrocyclic lactones require strict precautions.

Clinical practicality8.5/10

A premeasured monthly pipette is practical and covers several parasite groups, but exact species/concentration selection, direct skin application, drying, licking prevention and indication-specific retreatment intervals are essential.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Use only the exact species, concentration and weight-band pipette. The canine 2.5% moxidectin formulation must never be used on cats, and EU/Georgian kilogram bands must not be replaced with US pound-band assumptions.
  • Do not combine with another antiparasitic macrocyclic lactone unless the exact label and a documented veterinarian-led benefit-risk decision support it.
  • Apply the complete pipette directly to exposed skin, prevent oral exposure and licking, keep animals apart until dry, and follow the indication-specific bathing and repeat-treatment interval.
  • Do not use below seven weeks of age; animals below 1 kg, or sick, debilitated or underweight dogs, require the exact label and an explicit benefit-risk decision.
  • Before heartworm use, establish infection status and clinical class. Class 4 disease is contraindicated or unevaluated by the applicable labels; microfilariae treatment and MDR1-sensitive breeds require strict observation for neurologic or acute reactions.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Imidacloprid400 mg Moxidectin100 mg
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Elanco · United States
Manufacturer (register)
KVP Pharma + Veterinar Produkte GmbH, Germany
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1254, 19 Oct 2026.
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: ადვანტეიჯ მულტი® კანზე დასაწვეთებელი ხსნარი > 25კგ-დან 40კგ-მდე წონის ძაღლებისთვის
№ 349-11
Verified on: 15 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-251, 141-254
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Advocate 40 mg/4 mg, Spot-on

imidacloprid 40 mg + moxidectin 4 mg, spot-on solution for cats up to 4 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Cat
8.6/10
Very good
vetman assessment

Advocate

40 mg/4 mg, imidacloprid 40 mg + moxidectin 4 mg, spot-on solution for cats up to 4 kg
Assessed clinical scopeCat · Full labelled species-specific scope for susceptible flea, mite, louse, gastrointestinal or cardiopulmonary nematode targets, including applicable heartworm prevention · On the skin
Care settingMonthly or indication-specific single-pipette spot-on treatment after exact species, weight, parasite, heartworm and macrocyclic-lactone risk assessment
vetman score 8.6/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 20-11 · Verified on 15 Oct 2026

A mature, broadly effective topical endectocide with strong regulatory and clinical support; its wide label does not remove the need for exact species, concentration and heartworm-risk selection.

Regulatory and scientific credibility9.5/10

The exact presentation is registered in Georgia and belongs to the mature centrally authorised EU Advocate line, with matching current UK and FDA counterpart documentation.

Clinical efficacy9.0/10

A mature regulatory dossier and controlled laboratory and field programmes support the combination across its broad species-specific flea, mite, nematode and heartworm roles; exact target and repeat schedule remain indication-dependent.

Safety and tolerability7.5/10

The safety profile is extensively characterised, but the concentrated canine formulation can seriously harm cats; young, underweight, sick or debilitated patients, heartworm-positive animals, oral exposure, MDR1-sensitive dogs and concurrent macrocyclic lactones require strict precautions.

Clinical practicality8.5/10

A premeasured monthly pipette is practical and covers several parasite groups, but exact species/concentration selection, direct skin application, drying, licking prevention and indication-specific retreatment intervals are essential.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Use only the exact species, concentration and weight-band pipette. The canine 2.5% moxidectin formulation must never be used on cats, and EU/Georgian kilogram bands must not be replaced with US pound-band assumptions.
  • Do not combine with another antiparasitic macrocyclic lactone unless the exact label and a documented veterinarian-led benefit-risk decision support it.
  • Apply the complete pipette directly to exposed skin, prevent oral exposure and licking, keep animals apart until dry, and follow the indication-specific bathing and repeat-treatment interval.
  • Do not use below nine weeks of age. A cat below 1 kg, or a sick, debilitated or underweight cat, requires the strictest applicable label and a veterinarian-led benefit-risk decision.
  • Establish heartworm status and exact indication before use: applicable EU and FDA labels differ on heartworm-positive cats, and adult infection may carry severe risk.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Elanco · United States
Manufacturer (register)
KVP Pharma + Veterinär Produkte GmbH, Germany
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 59, 19 Oct 2026.
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: ადვოკატი 4კგ–მდე კატებისათვის
№ 20-11
Verified on: 15 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-251, 141-254
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Advocate 80 mg/8 mg, Spot-on

imidacloprid 80 mg + moxidectin 8 mg, spot-on solution for cats 4-8 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Cat
8.5/10
Very good
vetman assessment

Advocate

80 mg/8 mg, imidacloprid 80 mg + moxidectin 8 mg, spot-on solution for cats 4-8 kg
Assessed clinical scopeCat · Full labelled species-specific scope for susceptible flea, mite, louse, gastrointestinal or cardiopulmonary nematode targets, including applicable heartworm prevention · On the skin
Care settingMonthly or indication-specific single-pipette spot-on treatment after exact species, weight, parasite, heartworm and macrocyclic-lactone risk assessment
vetman score 8.5/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 34-11 · Verified on 15 Oct 2026

A mature, broadly effective topical endectocide with strong regulatory and clinical support; its wide label does not remove the need for exact species, concentration and heartworm-risk selection.

Regulatory and scientific credibility9.0/10

The exact 80/8 mg presentation is mature and currently authorised in Europe, but the historical Georgian register row names Advocate while listing imidacloprid alone, so the local composition record is internally incomplete.

Clinical efficacy9.0/10

A mature regulatory dossier and controlled laboratory and field programmes support the combination across its broad species-specific flea, mite, nematode and heartworm roles; exact target and repeat schedule remain indication-dependent.

Safety and tolerability7.5/10

The safety profile is extensively characterised, but the concentrated canine formulation can seriously harm cats; young, underweight, sick or debilitated patients, heartworm-positive animals, oral exposure, MDR1-sensitive dogs and concurrent macrocyclic lactones require strict precautions.

Clinical practicality8.5/10

A premeasured monthly pipette is practical and covers several parasite groups, but exact species/concentration selection, direct skin application, drying, licking prevention and indication-specific retreatment intervals are essential.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Use only the exact species, concentration and weight-band pipette. The canine 2.5% moxidectin formulation must never be used on cats, and EU/Georgian kilogram bands must not be replaced with US pound-band assumptions.
  • Do not combine with another antiparasitic macrocyclic lactone unless the exact label and a documented veterinarian-led benefit-risk decision support it.
  • Apply the complete pipette directly to exposed skin, prevent oral exposure and licking, keep animals apart until dry, and follow the indication-specific bathing and repeat-treatment interval.
  • Do not use below nine weeks of age. A cat below 1 kg, or a sick, debilitated or underweight cat, requires the strictest applicable label and a veterinarian-led benefit-risk decision.
  • Establish heartworm status and exact indication before use: applicable EU and FDA labels differ on heartworm-positive cats, and adult infection may carry severe risk.
  • The Georgian historical row for Advocate 80/8 mg names Advocate but lists imidacloprid alone; verify the physical pack contains both imidacloprid 80 mg and moxidectin 8 mg before use.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Elanco · United States
Registration
Georgia Yes, veterinary
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-251, 141-254
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Advocate 400 mg/100 mg, Spot-on

imidacloprid 400 mg + moxidectin 100 mg, spot-on solution for dogs 25-40 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
8.6/10
Very good
vetman assessment

Advocate

400 mg/100 mg, imidacloprid 400 mg + moxidectin 100 mg, spot-on solution for dogs 25-40 kg
Assessed clinical scopeDog · Full labelled species-specific scope for susceptible flea, mite, louse, gastrointestinal or cardiopulmonary nematode targets, including applicable heartworm prevention · On the skin
Care settingMonthly or indication-specific single-pipette spot-on treatment after exact species, weight, parasite, heartworm and macrocyclic-lactone risk assessment
vetman score 8.6/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 19-11 · Verified on 15 Oct 2026

A mature, broadly effective topical endectocide with strong regulatory and clinical support; its wide label does not remove the need for exact species, concentration and heartworm-risk selection.

Regulatory and scientific credibility9.5/10

The exact presentation is registered in Georgia and belongs to the mature centrally authorised EU Advocate line, with matching current UK and FDA counterpart documentation.

Clinical efficacy9.0/10

A mature regulatory dossier and controlled laboratory and field programmes support the combination across its broad species-specific flea, mite, nematode and heartworm roles; exact target and repeat schedule remain indication-dependent.

Safety and tolerability7.5/10

The safety profile is extensively characterised, but the concentrated canine formulation can seriously harm cats; young, underweight, sick or debilitated patients, heartworm-positive animals, oral exposure, MDR1-sensitive dogs and concurrent macrocyclic lactones require strict precautions.

Clinical practicality8.5/10

A premeasured monthly pipette is practical and covers several parasite groups, but exact species/concentration selection, direct skin application, drying, licking prevention and indication-specific retreatment intervals are essential.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Use only the exact species, concentration and weight-band pipette. The canine 2.5% moxidectin formulation must never be used on cats, and EU/Georgian kilogram bands must not be replaced with US pound-band assumptions.
  • Do not combine with another antiparasitic macrocyclic lactone unless the exact label and a documented veterinarian-led benefit-risk decision support it.
  • Apply the complete pipette directly to exposed skin, prevent oral exposure and licking, keep animals apart until dry, and follow the indication-specific bathing and repeat-treatment interval.
  • Do not use below seven weeks of age; animals below 1 kg, or sick, debilitated or underweight dogs, require the exact label and an explicit benefit-risk decision.
  • Before heartworm use, establish infection status and clinical class. Class 4 disease is contraindicated or unevaluated by the applicable labels; microfilariae treatment and MDR1-sensitive breeds require strict observation for neurologic or acute reactions.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Imidacloprid400 mg Moxidectin100 mg
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Elanco · United States
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: ადვოკატი 25-40 კგ ძაღლებისათვის
№ 19-11
Verified on: 15 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-251, 141-254
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Bravecto Plus 112.5 mg/5.6 mg, Spot-on

fluralaner 112.5 mg + moxidectin 5.6 mg, spot-on solution for cats 1.2-2.8 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Cat
8.6/10
Very good
vetman assessment

Bravecto Plus

112.5 mg/5.6 mg, fluralaner 112.5 mg + moxidectin 5.6 mg, spot-on solution for cats 1.2-2.8 kg
Assessed clinical scopeCat · Full labelled feline scope when flea or tick treatment and at least one additional parasite indication are required concurrently: fleas, ticks, ear mites, gastrointestinal nematodes, heartworm and lungworm prevention · On the skin
Care settingVeterinary-selected integrated feline parasite control after risk assessment and exact weighing
vetman score 8.6/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 373-11 · Verified on 15 Oct 2026

A strong long-interval integrated parasite product for cats when its fixed multi-parasite scope matches the patient; avoid using the combination when only a single target needs treatment.

Regulatory and scientific credibility9.5/10

The exact feline range is centrally authorised in the EU with current combined official product information and strong indication-specific trials; Georgian registration is shown separately per presentation.

Clinical efficacy9.0/10

Randomised field and controlled studies show high, sustained efficacy across fleas, ticks and labelled nematodes, including lungworm prevention; the fixed combination is appropriate only when ectoparasite control and another labelled parasite target are needed together.

Safety and tolerability7.0/10

Generally well tolerated, but transient skin, gastrointestinal and rare neurologic reactions are recognised; young or underweight cats, reproduction, adult heartworm assessment and P-glycoprotein inhibitor combinations require specific precautions.

Clinical practicality9.0/10

One whole weight-banded pipette gives broad long-interval coverage, but direct skin placement, prevention of grooming, indication-specific retreatment and pre-treatment parasite-risk assessment are essential.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Use only when treatment against ticks or fleas and at least one other labelled parasite is indicated concurrently; this fixed combination is not justified for a single target alone.
  • Do not use in hypersensitivity; treatment is not recommended below 9 weeks or 1.2 kg, in breeding males, during pregnancy or lactation.
  • In heartworm-risk areas, assess for adult Dirofilaria infection before prevention; the product does not treat adult heartworms.
  • Review concurrent P-glycoprotein inhibitors such as ciclosporin, ketoconazole, spinosad or verapamil and use only after benefit-risk assessment.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Fluralaner112.5 mg Moxidectin5.6 mg
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
MSD Animal Health · United States
Manufacturer (register)
Intervet Productions SA, France
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1588, 19 Oct 2026.
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: ბრავექტო™ პლუს 112.5მგ/5.6მგ გარეგანი გამოყენების ხსნარი პატარა ზომის კატებისთვის (1.2-2.8კგ)
№ 373-11
Verified on: 15 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-518
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Bravecto Plus 250 mg/12.5 mg, Spot-on

fluralaner 250 mg + moxidectin 12.5 mg, spot-on solution for cats >2.8-6.25 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Cat
8.6/10
Very good
vetman assessment

Bravecto Plus

250 mg/12.5 mg, fluralaner 250 mg + moxidectin 12.5 mg, spot-on solution for cats >2.8-6.25 kg
Assessed clinical scopeCat · Full labelled feline scope when flea or tick treatment and at least one additional parasite indication are required concurrently: fleas, ticks, ear mites, gastrointestinal nematodes, heartworm and lungworm prevention · On the skin
Care settingVeterinary-selected integrated feline parasite control after risk assessment and exact weighing
vetman score 8.6/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 375-11 · Verified on 21 Oct 2026

A strong long-interval integrated parasite product for cats when its fixed multi-parasite scope matches the patient; avoid using the combination when only a single target needs treatment.

Regulatory and scientific credibility9.5/10

The exact feline range is centrally authorised in the EU with current combined official product information and strong indication-specific trials; Georgian registration is shown separately per presentation.

Clinical efficacy9.0/10

Randomised field and controlled studies show high, sustained efficacy across fleas, ticks and labelled nematodes, including lungworm prevention; the fixed combination is appropriate only when ectoparasite control and another labelled parasite target are needed together.

Safety and tolerability7.0/10

Generally well tolerated, but transient skin, gastrointestinal and rare neurologic reactions are recognised; young or underweight cats, reproduction, adult heartworm assessment and P-glycoprotein inhibitor combinations require specific precautions.

Clinical practicality9.0/10

One whole weight-banded pipette gives broad long-interval coverage, but direct skin placement, prevention of grooming, indication-specific retreatment and pre-treatment parasite-risk assessment are essential.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Use only when treatment against ticks or fleas and at least one other labelled parasite is indicated concurrently; this fixed combination is not justified for a single target alone.
  • Do not use in hypersensitivity; treatment is not recommended below 9 weeks or 1.2 kg, in breeding males, during pregnancy or lactation.
  • In heartworm-risk areas, assess for adult Dirofilaria infection before prevention; the product does not treat adult heartworms.
  • Review concurrent P-glycoprotein inhibitors such as ciclosporin, ketoconazole, spinosad or verapamil and use only after benefit-risk assessment.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Fluralaner250 mg Moxidectin12.5 mg
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Manufacturer (register)
Intervet Productions SA, France
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1590, 19 Oct 2026.
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: ბრავექტო™ პლუსი 250 მგ/12.5 მგ გარეგანი გამოყენების ხსნარი საშუალო ზომის კატებისთვის (>2.8-6.25 კგ)
№ 375-11
Verified on: 21 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-518
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Bravecto Plus 500 mg/25 mg, Spot-on

fluralaner 500 mg + moxidectin 25 mg, spot-on solution for cats >6.25-12.5 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Cat
8.6/10
Very good
vetman assessment

Bravecto Plus

500 mg/25 mg, fluralaner 500 mg + moxidectin 25 mg, spot-on solution for cats >6.25-12.5 kg
Assessed clinical scopeCat · Full labelled feline scope when flea or tick treatment and at least one additional parasite indication are required concurrently: fleas, ticks, ear mites, gastrointestinal nematodes, heartworm and lungworm prevention · On the skin
Care settingVeterinary-selected integrated feline parasite control after risk assessment and exact weighing
vetman score 8.6/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 374-11 · Verified on 15 Oct 2026

A strong long-interval integrated parasite product for cats when its fixed multi-parasite scope matches the patient; avoid using the combination when only a single target needs treatment.

Regulatory and scientific credibility9.5/10

The exact feline range is centrally authorised in the EU with current combined official product information and strong indication-specific trials; Georgian registration is shown separately per presentation.

Clinical efficacy9.0/10

Randomised field and controlled studies show high, sustained efficacy across fleas, ticks and labelled nematodes, including lungworm prevention; the fixed combination is appropriate only when ectoparasite control and another labelled parasite target are needed together.

Safety and tolerability7.0/10

Generally well tolerated, but transient skin, gastrointestinal and rare neurologic reactions are recognised; young or underweight cats, reproduction, adult heartworm assessment and P-glycoprotein inhibitor combinations require specific precautions.

Clinical practicality9.0/10

One whole weight-banded pipette gives broad long-interval coverage, but direct skin placement, prevention of grooming, indication-specific retreatment and pre-treatment parasite-risk assessment are essential.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Use only when treatment against ticks or fleas and at least one other labelled parasite is indicated concurrently; this fixed combination is not justified for a single target alone.
  • Do not use in hypersensitivity; treatment is not recommended below 9 weeks or 1.2 kg, in breeding males, during pregnancy or lactation.
  • In heartworm-risk areas, assess for adult Dirofilaria infection before prevention; the product does not treat adult heartworms.
  • Review concurrent P-glycoprotein inhibitors such as ciclosporin, ketoconazole, spinosad or verapamil and use only after benefit-risk assessment.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Fluralaner500 mg Moxidectin25 mg
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
MSD Animal Health · United States
Manufacturer (register)
Intervet Productions SA, France
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1589, 19 Oct 2026.
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: ბრავექტო™ პლუს 500მგ/25მგ გარეგანი გამოყენების ხსნარი დიდი ზომის კატებისთვის (>6.25-12.5კგ)
№ 374-11
Verified on: 15 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-518
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Inspector Quadro C 0.4 ml, Spot-on

spot-on solution for dogs 1-4 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
7.0/10
Situational / acceptable
vetman assessment

Inspector Quadro C

0.4 ml, spot-on solution for dogs 1-4 kg
Assessed clinical scopeDog · Labelled canine topical scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention · On the skin
Care settingVeterinary-selected home application to dry intact skin after parasite and heartworm assessment, with diagnosis-specific follow-up
vetman score 7.0/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 000151 · Verified on 21 Oct 2026

Registered exact canine spot-on supported by a public SPC and small exact-product studies. Do not treat every broad combination claim as equally proven; use the exact dog weight band after parasite and heartworm assessment.

Regulatory and scientific credibility7.5/10

Exact strengths have current Georgian registrations and an indefinite Bulgarian authorization with a public product-specific SPC confirming composition, dog-only use and weight bands.

Clinical efficacy7.0/10

An exact-product report found high activity against several natural infestations, but groups were small, control detail limited and an author was affiliated with the producer. The broad label has moderate, not definitive, clinical support.

Safety and tolerability6.5/10

A small exact-product study found no measured abnormalities at up to five times the label dose, but cannot exclude uncommon harms. Licking, overdose, reproduction, age or illness, other antiparasitics, ear integrity and environmental exposure need safeguards.

Clinical practicality7.0/10

A whole weight-banded pipette simplifies routine dosing. Direct-to-skin placement, prevention of licking, keeping dry and separation until dry add practical burden.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with hypersensitivity, infectious disease or debilitation, on wet or damaged skin, or outside the exact labelled species, age and weight band.
  • Do not combine with another antiparasitic unless a veterinarian has checked ingredients, intervals and cumulative toxicity.
  • During pregnancy or lactation and below 1 kg, use only after an individual veterinary benefit-risk assessment.
  • For ear-directed use, confirm tympanic-membrane integrity; with a perforated eardrum the product must not enter the ear canal.
  • Prevent licking and monitor for local irritation, depression, hypersalivation, tremor or vomiting; wash off and assess after overdose.
  • Keep treated animals away from rabbits, bees, fish and surface water; prevent environmental transfer until dry.
  • Heartworm use prevents susceptible larval stages; it is not adulticide treatment. Assess infection and exposure first.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Fipronil107 mg/ml Praziquantel42.8 mg/ml Moxidectin26.75 mg/ml Pyriproxyfen21.4 mg/ml
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Manufacturer (register)
JSC SPC EKOPROM, Russia
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 650, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 06 May 2027
Veterinary (National Food Agency)
In the register: ინსპექტორ კვადრო C
№ 000151
Verified on: 21 Oct 2026
EU Yes, veterinary
№ 0022-3129
Verified on: 22 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Inspector Quadro C 1 ml, Spot-on

spot-on solution for dogs 4-10 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
7.0/10
Situational / acceptable
vetman assessment

Inspector Quadro C

1 ml, spot-on solution for dogs 4-10 kg
Assessed clinical scopeDog · Labelled canine topical scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention · On the skin
Care settingVeterinary-selected home application to dry intact skin after parasite and heartworm assessment, with diagnosis-specific follow-up
vetman score 7.0/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 000159 · Verified on 21 Oct 2026

Registered exact canine spot-on supported by a public SPC and small exact-product studies. Do not treat every broad combination claim as equally proven; use the exact dog weight band after parasite and heartworm assessment.

Regulatory and scientific credibility7.5/10

Exact strengths have current Georgian registrations and an indefinite Bulgarian authorization with a public product-specific SPC confirming composition, dog-only use and weight bands.

Clinical efficacy7.0/10

An exact-product report found high activity against several natural infestations, but groups were small, control detail limited and an author was affiliated with the producer. The broad label has moderate, not definitive, clinical support.

Safety and tolerability6.5/10

A small exact-product study found no measured abnormalities at up to five times the label dose, but cannot exclude uncommon harms. Licking, overdose, reproduction, age or illness, other antiparasitics, ear integrity and environmental exposure need safeguards.

Clinical practicality7.0/10

A whole weight-banded pipette simplifies routine dosing. Direct-to-skin placement, prevention of licking, keeping dry and separation until dry add practical burden.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with hypersensitivity, infectious disease or debilitation, on wet or damaged skin, or outside the exact labelled species, age and weight band.
  • Do not combine with another antiparasitic unless a veterinarian has checked ingredients, intervals and cumulative toxicity.
  • During pregnancy or lactation and below 1 kg, use only after an individual veterinary benefit-risk assessment.
  • For ear-directed use, confirm tympanic-membrane integrity; with a perforated eardrum the product must not enter the ear canal.
  • Prevent licking and monitor for local irritation, depression, hypersalivation, tremor or vomiting; wash off and assess after overdose.
  • Keep treated animals away from rabbits, bees, fish and surface water; prevent environmental transfer until dry.
  • Heartworm use prevents susceptible larval stages; it is not adulticide treatment. Assess infection and exposure first.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Fipronil107 mg/ml Praziquantel42.8 mg/ml Moxidectin26.75 mg/ml Pyriproxyfen21.4 mg/ml
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Manufacturer (register)
JSC SPC EKOPROM, Russia
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 675, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 06 May 2027
Veterinary (National Food Agency)
In the register: ინსპექტორ კვადრო C
№ 000159
Verified on: 21 Oct 2026
EU Yes, veterinary
№ 0022-3129
Verified on: 22 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Inspector Quadro C 2.5 ml, Spot-on

spot-on solution for dogs 10-25 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
7.0/10
Situational / acceptable
vetman assessment

Inspector Quadro C

2.5 ml, spot-on solution for dogs 10-25 kg
Assessed clinical scopeDog · Labelled canine topical scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention · On the skin
Care settingVeterinary-selected home application to dry intact skin after parasite and heartworm assessment, with diagnosis-specific follow-up
vetman score 7.0/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 000160 · Verified on 21 Oct 2026

Registered exact canine spot-on supported by a public SPC and small exact-product studies. Do not treat every broad combination claim as equally proven; use the exact dog weight band after parasite and heartworm assessment.

Regulatory and scientific credibility7.5/10

Exact strengths have current Georgian registrations and an indefinite Bulgarian authorization with a public product-specific SPC confirming composition, dog-only use and weight bands.

Clinical efficacy7.0/10

An exact-product report found high activity against several natural infestations, but groups were small, control detail limited and an author was affiliated with the producer. The broad label has moderate, not definitive, clinical support.

Safety and tolerability6.5/10

A small exact-product study found no measured abnormalities at up to five times the label dose, but cannot exclude uncommon harms. Licking, overdose, reproduction, age or illness, other antiparasitics, ear integrity and environmental exposure need safeguards.

Clinical practicality7.0/10

A whole weight-banded pipette simplifies routine dosing. Direct-to-skin placement, prevention of licking, keeping dry and separation until dry add practical burden.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with hypersensitivity, infectious disease or debilitation, on wet or damaged skin, or outside the exact labelled species, age and weight band.
  • Do not combine with another antiparasitic unless a veterinarian has checked ingredients, intervals and cumulative toxicity.
  • During pregnancy or lactation and below 1 kg, use only after an individual veterinary benefit-risk assessment.
  • For ear-directed use, confirm tympanic-membrane integrity; with a perforated eardrum the product must not enter the ear canal.
  • Prevent licking and monitor for local irritation, depression, hypersalivation, tremor or vomiting; wash off and assess after overdose.
  • Keep treated animals away from rabbits, bees, fish and surface water; prevent environmental transfer until dry.
  • Heartworm use prevents susceptible larval stages; it is not adulticide treatment. Assess infection and exposure first.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Fipronil107 mg/ml Praziquantel42.8 mg/ml Moxidectin26.75 mg/ml Pyriproxyfen21.4 mg/ml
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Manufacturer (register)
JSC SPC EKOPROM, Russia
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 676, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 06 May 2027
Veterinary (National Food Agency)
In the register: ინსპექტორ კვადრო C
№ 000160
Verified on: 21 Oct 2026
EU Yes, veterinary
№ 0022-3129
Verified on: 22 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Inspector Quadro C 4 ml, Spot-on

spot-on solution for dogs 25-40 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
7.0/10
Situational / acceptable
vetman assessment

Inspector Quadro C

4 ml, spot-on solution for dogs 25-40 kg
Assessed clinical scopeDog · Labelled canine topical scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention · On the skin
Care settingVeterinary-selected home application to dry intact skin after parasite and heartworm assessment, with diagnosis-specific follow-up
vetman score 7.0/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 000158 · Verified on 21 Oct 2026

Registered exact canine spot-on supported by a public SPC and small exact-product studies. Do not treat every broad combination claim as equally proven; use the exact dog weight band after parasite and heartworm assessment.

Regulatory and scientific credibility7.5/10

Exact strengths have current Georgian registrations and an indefinite Bulgarian authorization with a public product-specific SPC confirming composition, dog-only use and weight bands.

Clinical efficacy7.0/10

An exact-product report found high activity against several natural infestations, but groups were small, control detail limited and an author was affiliated with the producer. The broad label has moderate, not definitive, clinical support.

Safety and tolerability6.5/10

A small exact-product study found no measured abnormalities at up to five times the label dose, but cannot exclude uncommon harms. Licking, overdose, reproduction, age or illness, other antiparasitics, ear integrity and environmental exposure need safeguards.

Clinical practicality7.0/10

A whole weight-banded pipette simplifies routine dosing. Direct-to-skin placement, prevention of licking, keeping dry and separation until dry add practical burden.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with hypersensitivity, infectious disease or debilitation, on wet or damaged skin, or outside the exact labelled species, age and weight band.
  • Do not combine with another antiparasitic unless a veterinarian has checked ingredients, intervals and cumulative toxicity.
  • During pregnancy or lactation and below 1 kg, use only after an individual veterinary benefit-risk assessment.
  • For ear-directed use, confirm tympanic-membrane integrity; with a perforated eardrum the product must not enter the ear canal.
  • Prevent licking and monitor for local irritation, depression, hypersalivation, tremor or vomiting; wash off and assess after overdose.
  • Keep treated animals away from rabbits, bees, fish and surface water; prevent environmental transfer until dry.
  • Heartworm use prevents susceptible larval stages; it is not adulticide treatment. Assess infection and exposure first.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Fipronil107 mg/ml Praziquantel42.8 mg/ml Moxidectin26.75 mg/ml Pyriproxyfen21.4 mg/ml
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Manufacturer (register)
JSC SPC EKOPROM, Russia
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 672, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 06 May 2027
Veterinary (National Food Agency)
In the register: ინსპექტორ კვადრო C
№ 000158
Verified on: 21 Oct 2026
EU Yes, veterinary
№ 0022-3129
Verified on: 22 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Inspector Quadro C 6 ml, Spot-on

spot-on solution for dogs 40-60 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
7.0/10
Situational / acceptable
vetman assessment

Inspector Quadro C

6 ml, spot-on solution for dogs 40-60 kg
Assessed clinical scopeDog · Labelled canine topical scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention · On the skin
Care settingVeterinary-selected home application to dry intact skin after parasite and heartworm assessment, with diagnosis-specific follow-up
vetman score 7.0/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 000157 · Verified on 21 Oct 2026

Registered exact canine spot-on supported by a public SPC and small exact-product studies. Do not treat every broad combination claim as equally proven; use the exact dog weight band after parasite and heartworm assessment.

Regulatory and scientific credibility7.5/10

Exact strengths have current Georgian registrations and an indefinite Bulgarian authorization with a public product-specific SPC confirming composition, dog-only use and weight bands.

Clinical efficacy7.0/10

An exact-product report found high activity against several natural infestations, but groups were small, control detail limited and an author was affiliated with the producer. The broad label has moderate, not definitive, clinical support.

Safety and tolerability6.5/10

A small exact-product study found no measured abnormalities at up to five times the label dose, but cannot exclude uncommon harms. Licking, overdose, reproduction, age or illness, other antiparasitics, ear integrity and environmental exposure need safeguards.

Clinical practicality7.0/10

A whole weight-banded pipette simplifies routine dosing. Direct-to-skin placement, prevention of licking, keeping dry and separation until dry add practical burden.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with hypersensitivity, infectious disease or debilitation, on wet or damaged skin, or outside the exact labelled species, age and weight band.
  • Do not combine with another antiparasitic unless a veterinarian has checked ingredients, intervals and cumulative toxicity.
  • During pregnancy or lactation and below 1 kg, use only after an individual veterinary benefit-risk assessment.
  • For ear-directed use, confirm tympanic-membrane integrity; with a perforated eardrum the product must not enter the ear canal.
  • Prevent licking and monitor for local irritation, depression, hypersalivation, tremor or vomiting; wash off and assess after overdose.
  • Keep treated animals away from rabbits, bees, fish and surface water; prevent environmental transfer until dry.
  • Heartworm use prevents susceptible larval stages; it is not adulticide treatment. Assess infection and exposure first.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Fipronil107 mg/ml Praziquantel42.8 mg/ml Moxidectin26.75 mg/ml Pyriproxyfen21.4 mg/ml
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Manufacturer (register)
JSC SPC EKOPROM, Russia
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 674, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 06 May 2027
Veterinary (National Food Agency)
In the register: ინსპექტორ კვადრო C
№ 000157
Verified on: 21 Oct 2026
EU Yes, veterinary
№ 0022-3129
Verified on: 22 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Inspector Quadro K 0.4 ml, Spot-on

spot-on solution for cats 1-4 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Cat
6.0/10
Situational / acceptable
vetman assessment

Inspector Quadro K

0.4 ml, spot-on solution for cats 1-4 kg
Assessed clinical scopeCat · Labelled feline topical scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention · On the skin
Care settingVeterinary-selected home application to dry intact skin after parasite and heartworm assessment, with diagnosis-specific follow-up
vetman score 6.0/10 Situational / acceptable
Evidence confidence: Low Georgia: Yes, veterinary · № 000155 · Verified on 21 Oct 2026

Registered exact feline spot-on with manufacturer instructions and small exact-product studies, but the Bulgarian register links the wrong product SPC. Use only in cats within the exact weight band, with explicit parasite selection and follow-up.

Regulatory and scientific credibility5.5/10

Exact strengths have current Georgian registrations and an indefinite Bulgarian register entry. Confidence is reduced because the Quadro K page links to the Quadro C dog SPC rather than a K-specific feline SPC; the exact K instruction is available from the manufacturer.

Clinical efficacy6.0/10

An exact-product report found high activity against several natural infestations, but groups were small, control detail limited and an author was affiliated with the producer. The broad label has moderate, not definitive, clinical support.

Safety and tolerability6.0/10

A small exact-product study found no measured abnormalities at up to five times the label dose, but cannot exclude uncommon harms. Licking, overdose, reproduction, age or illness, other antiparasitics, ear integrity and environmental exposure need safeguards.

Clinical practicality7.0/10

A whole weight-banded pipette simplifies routine dosing. Direct-to-skin placement, prevention of licking, keeping dry and separation until dry add practical burden.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with hypersensitivity, infectious disease or debilitation, on wet or damaged skin, or outside the exact labelled species, age and weight band.
  • Do not combine with another antiparasitic unless a veterinarian has checked ingredients, intervals and cumulative toxicity.
  • During pregnancy or lactation and below 1 kg, use only after an individual veterinary benefit-risk assessment.
  • For ear-directed use, confirm tympanic-membrane integrity; with a perforated eardrum the product must not enter the ear canal.
  • Prevent licking and monitor for local irritation, depression, hypersalivation, tremor or vomiting; wash off and assess after overdose.
  • Keep treated animals away from rabbits, bees, fish and surface water; prevent environmental transfer until dry.
  • Heartworm use prevents susceptible larval stages; it is not adulticide treatment. Assess infection and exposure first.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Fipronil107 mg/ml Praziquantel42.8 mg/ml Moxidectin10.7 mg/ml Pyriproxyfen21.4 mg/ml
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Manufacturer (register)
JSC SPC EKOPROM, Russia
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 657, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 10 May 2027
Veterinary (National Food Agency)
In the register: ინსპექტორ კვადრო K
№ 000155
Verified on: 21 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Inspector Quadro K 0.8 ml, Spot-on

spot-on solution for cats 4-8 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Cat
6.0/10
Situational / acceptable
vetman assessment

Inspector Quadro K

0.8 ml, spot-on solution for cats 4-8 kg
Assessed clinical scopeCat · Labelled feline topical scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention · On the skin
Care settingVeterinary-selected home application to dry intact skin after parasite and heartworm assessment, with diagnosis-specific follow-up
vetman score 6.0/10 Situational / acceptable
Evidence confidence: Low Georgia: Yes, veterinary · № 000798 · Verified on 21 Oct 2026

Registered exact feline spot-on with manufacturer instructions and small exact-product studies, but the Bulgarian register links the wrong product SPC. Use only in cats within the exact weight band, with explicit parasite selection and follow-up.

Regulatory and scientific credibility5.5/10

Exact strengths have current Georgian registrations and an indefinite Bulgarian register entry. Confidence is reduced because the Quadro K page links to the Quadro C dog SPC rather than a K-specific feline SPC; the exact K instruction is available from the manufacturer.

Clinical efficacy6.0/10

An exact-product report found high activity against several natural infestations, but groups were small, control detail limited and an author was affiliated with the producer. The broad label has moderate, not definitive, clinical support.

Safety and tolerability6.0/10

A small exact-product study found no measured abnormalities at up to five times the label dose, but cannot exclude uncommon harms. Licking, overdose, reproduction, age or illness, other antiparasitics, ear integrity and environmental exposure need safeguards.

Clinical practicality7.0/10

A whole weight-banded pipette simplifies routine dosing. Direct-to-skin placement, prevention of licking, keeping dry and separation until dry add practical burden.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with hypersensitivity, infectious disease or debilitation, on wet or damaged skin, or outside the exact labelled species, age and weight band.
  • Do not combine with another antiparasitic unless a veterinarian has checked ingredients, intervals and cumulative toxicity.
  • During pregnancy or lactation and below 1 kg, use only after an individual veterinary benefit-risk assessment.
  • For ear-directed use, confirm tympanic-membrane integrity; with a perforated eardrum the product must not enter the ear canal.
  • Prevent licking and monitor for local irritation, depression, hypersalivation, tremor or vomiting; wash off and assess after overdose.
  • Keep treated animals away from rabbits, bees, fish and surface water; prevent environmental transfer until dry.
  • Heartworm use prevents susceptible larval stages; it is not adulticide treatment. Assess infection and exposure first.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Fipronil107 mg/ml Praziquantel42.8 mg/ml Moxidectin10.7 mg/ml Pyriproxyfen21.4 mg/ml
Formulation Type
Spot-on
Administration route
On the skin
Manufacturer
Manufacturer (register)
JSC SPF EKOPROM, Russia
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1313, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 11 May 2027
Veterinary (National Food Agency)
In the register: ინსპექტორ კვადრო K
№ 000798
Verified on: 21 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Inspector Quadro Tabs 20/0.6/10 mg, Tablet

tablets for dogs and cats 0.5-2 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog Labelled oral scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention
6.0/10
Situational / acceptable
vetman assessment

Inspector Quadro Tabs

20/0.6/10 mg, tablets for dogs and cats 0.5-2 kg
Assessed clinical scopeDog · Labelled oral scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention · By mouth
Care settingVeterinary-selected oral use after parasite and heartworm assessment, with diagnosis-specific follow-up
vetman score 6.0/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 002597 · Verified on 21 Oct 2026

Registered exact oral product, but broad efficacy rests on limited direct evidence and the public Bulgarian SPC has a route-inconsistent passage. Use for a defined parasite target, exact species and weight band, with monitoring.

Regulatory and scientific credibility6.0/10

Exact strengths have current Georgian registrations and an indefinite Bulgarian authorization with a public SPC. Confidence is reduced because the BFSA Tabs SPC contains a topical pharmacokinetic passage inconsistent with an oral-tablet document.

Clinical efficacy4.5/10

The combination is plausible and has a small exact-product tolerability study, but direct efficacy evidence is sparse. A five-dog cestode report required repeat dosing for full clearance; robust independent trials do not validate every broad claim in both species.

Safety and tolerability6.5/10

A small exact-product study found no measured abnormalities at up to five times the label dose, but cannot exclude uncommon harms. Macrocyclic-lactone susceptibility, age, health, reproduction, interactions and adverse reactions need screening.

Clinical practicality7.5/10

Weight-banded tablets and half-tablet increments simplify routine dosing, but repeated or diagnosis-specific schedules must not be inferred from a one-dose calculator.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with hypersensitivity, renal or hepatic dysfunction, infectious disease or debilitation; do not use below 0.5 kg or below 6 weeks.
  • Do not use during pregnancy or lactation; reproductive safety is not established.
  • Do not combine with other macrocyclic lactones, piperazine compounds or cholinesterase inhibitors without an evidence-based specialist plan.
  • Screen Collies and other ABCB1-susceptible dogs for macrocyclic-lactone risk and monitor neurologic status.
  • Monitor for vomiting, diarrhoea, hypersalivation, appetite change or hypersensitivity; stop and reassess if important signs occur.
  • Heartworm use prevents susceptible larval stages; it is not adulticide treatment. Assess infection and exposure first.
  • Direct efficacy evidence is small and does not validate every broad claim; confirm the parasite and reassess response.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Cat Labelled oral scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention
6.0/10
Situational / acceptable
vetman assessment

Inspector Quadro Tabs

20/0.6/10 mg, tablets for dogs and cats 0.5-2 kg
Assessed clinical scopeCat · Labelled oral scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention · By mouth
Care settingVeterinary-selected oral use after parasite and heartworm assessment, with diagnosis-specific follow-up
vetman score 6.0/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 002597 · Verified on 21 Oct 2026

Registered exact oral product, but broad efficacy rests on limited direct evidence and the public Bulgarian SPC has a route-inconsistent passage. Use for a defined parasite target, exact species and weight band, with monitoring.

Regulatory and scientific credibility6.0/10

Exact strengths have current Georgian registrations and an indefinite Bulgarian authorization with a public SPC. Confidence is reduced because the BFSA Tabs SPC contains a topical pharmacokinetic passage inconsistent with an oral-tablet document.

Clinical efficacy4.5/10

The combination is plausible and has a small exact-product tolerability study, but direct efficacy evidence is sparse. A five-dog cestode report required repeat dosing for full clearance; robust independent trials do not validate every broad claim in both species.

Safety and tolerability6.5/10

A small exact-product study found no measured abnormalities at up to five times the label dose, but cannot exclude uncommon harms. Macrocyclic-lactone susceptibility, age, health, reproduction, interactions and adverse reactions need screening.

Clinical practicality7.5/10

Weight-banded tablets and half-tablet increments simplify routine dosing, but repeated or diagnosis-specific schedules must not be inferred from a one-dose calculator.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with hypersensitivity, renal or hepatic dysfunction, infectious disease or debilitation; do not use below 0.5 kg or below 6 weeks.
  • Do not use during pregnancy or lactation; reproductive safety is not established.
  • Do not combine with other macrocyclic lactones, piperazine compounds or cholinesterase inhibitors without an evidence-based specialist plan.
  • Screen Collies and other ABCB1-susceptible dogs for macrocyclic-lactone risk and monitor neurologic status.
  • Monitor for vomiting, diarrhoea, hypersalivation, appetite change or hypersensitivity; stop and reassess if important signs occur.
  • Heartworm use prevents susceptible larval stages; it is not adulticide treatment. Assess infection and exposure first.
  • Direct efficacy evidence is small and does not validate every broad claim; confirm the parasite and reassess response.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Lufenuron20 mg Moxidectin0.6 mg Praziquantel10 mg
Formulation Type
Tablet
Administration route
By mouth
Manufacturer
Manufacturer (register)
Joint Stock Company NPF Ekoprom, Russia
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 528, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 23 Dec 2026
Veterinary (National Food Agency)
In the register: ინსპექტორ კვადრო ტაბსი
№ 002597
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown

Inspector Quadro Tabs 40/1.2/20 mg, Tablet

tablets for dogs and cats 2-8 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog Labelled oral scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention
6.0/10
Situational / acceptable
vetman assessment

Inspector Quadro Tabs

40/1.2/20 mg, tablets for dogs and cats 2-8 kg
Assessed clinical scopeDog · Labelled oral scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention · By mouth
Care settingVeterinary-selected oral use after parasite and heartworm assessment, with diagnosis-specific follow-up
vetman score 6.0/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 002598 · Verified on 21 Oct 2026

Registered exact oral product, but broad efficacy rests on limited direct evidence and the public Bulgarian SPC has a route-inconsistent passage. Use for a defined parasite target, exact species and weight band, with monitoring.

Regulatory and scientific credibility6.0/10

Exact strengths have current Georgian registrations and an indefinite Bulgarian authorization with a public SPC. Confidence is reduced because the BFSA Tabs SPC contains a topical pharmacokinetic passage inconsistent with an oral-tablet document.

Clinical efficacy4.5/10

The combination is plausible and has a small exact-product tolerability study, but direct efficacy evidence is sparse. A five-dog cestode report required repeat dosing for full clearance; robust independent trials do not validate every broad claim in both species.

Safety and tolerability6.5/10

A small exact-product study found no measured abnormalities at up to five times the label dose, but cannot exclude uncommon harms. Macrocyclic-lactone susceptibility, age, health, reproduction, interactions and adverse reactions need screening.

Clinical practicality7.5/10

Weight-banded tablets and half-tablet increments simplify routine dosing, but repeated or diagnosis-specific schedules must not be inferred from a one-dose calculator.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with hypersensitivity, renal or hepatic dysfunction, infectious disease or debilitation; do not use below 0.5 kg or below 6 weeks.
  • Do not use during pregnancy or lactation; reproductive safety is not established.
  • Do not combine with other macrocyclic lactones, piperazine compounds or cholinesterase inhibitors without an evidence-based specialist plan.
  • Screen Collies and other ABCB1-susceptible dogs for macrocyclic-lactone risk and monitor neurologic status.
  • Monitor for vomiting, diarrhoea, hypersalivation, appetite change or hypersensitivity; stop and reassess if important signs occur.
  • Heartworm use prevents susceptible larval stages; it is not adulticide treatment. Assess infection and exposure first.
  • Direct efficacy evidence is small and does not validate every broad claim; confirm the parasite and reassess response.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Cat Labelled oral scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention
6.0/10
Situational / acceptable
vetman assessment

Inspector Quadro Tabs

40/1.2/20 mg, tablets for dogs and cats 2-8 kg
Assessed clinical scopeCat · Labelled oral scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention · By mouth
Care settingVeterinary-selected oral use after parasite and heartworm assessment, with diagnosis-specific follow-up
vetman score 6.0/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 002598 · Verified on 21 Oct 2026

Registered exact oral product, but broad efficacy rests on limited direct evidence and the public Bulgarian SPC has a route-inconsistent passage. Use for a defined parasite target, exact species and weight band, with monitoring.

Regulatory and scientific credibility6.0/10

Exact strengths have current Georgian registrations and an indefinite Bulgarian authorization with a public SPC. Confidence is reduced because the BFSA Tabs SPC contains a topical pharmacokinetic passage inconsistent with an oral-tablet document.

Clinical efficacy4.5/10

The combination is plausible and has a small exact-product tolerability study, but direct efficacy evidence is sparse. A five-dog cestode report required repeat dosing for full clearance; robust independent trials do not validate every broad claim in both species.

Safety and tolerability6.5/10

A small exact-product study found no measured abnormalities at up to five times the label dose, but cannot exclude uncommon harms. Macrocyclic-lactone susceptibility, age, health, reproduction, interactions and adverse reactions need screening.

Clinical practicality7.5/10

Weight-banded tablets and half-tablet increments simplify routine dosing, but repeated or diagnosis-specific schedules must not be inferred from a one-dose calculator.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with hypersensitivity, renal or hepatic dysfunction, infectious disease or debilitation; do not use below 0.5 kg or below 6 weeks.
  • Do not use during pregnancy or lactation; reproductive safety is not established.
  • Do not combine with other macrocyclic lactones, piperazine compounds or cholinesterase inhibitors without an evidence-based specialist plan.
  • Screen Collies and other ABCB1-susceptible dogs for macrocyclic-lactone risk and monitor neurologic status.
  • Monitor for vomiting, diarrhoea, hypersalivation, appetite change or hypersensitivity; stop and reassess if important signs occur.
  • Heartworm use prevents susceptible larval stages; it is not adulticide treatment. Assess infection and exposure first.
  • Direct efficacy evidence is small and does not validate every broad claim; confirm the parasite and reassess response.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Lufenuron40 mg Moxidectin1.2 mg Praziquantel20 mg
Formulation Type
Tablet
Administration route
By mouth
Manufacturer
Manufacturer (register)
Joint Stock Company NPF Ekoprom, Russia
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 529, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 23 Dec 2026
Veterinary (National Food Agency)
In the register: ინსპექტორ კვადრო ტაბსი
№ 002598
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown

Inspector Quadro Tabs 160/4.8/80 mg, Tablet

tablets for dogs and cats 8-16 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog Labelled oral scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention
6.0/10
Situational / acceptable
vetman assessment

Inspector Quadro Tabs

160/4.8/80 mg, tablets for dogs and cats 8-16 kg
Assessed clinical scopeDog · Labelled oral scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention · By mouth
Care settingVeterinary-selected oral use after parasite and heartworm assessment, with diagnosis-specific follow-up
vetman score 6.0/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 001249 · Verified on 21 Oct 2026

Registered exact oral product, but broad efficacy rests on limited direct evidence and the public Bulgarian SPC has a route-inconsistent passage. Use for a defined parasite target, exact species and weight band, with monitoring.

Regulatory and scientific credibility6.0/10

Exact strengths have current Georgian registrations and an indefinite Bulgarian authorization with a public SPC. Confidence is reduced because the BFSA Tabs SPC contains a topical pharmacokinetic passage inconsistent with an oral-tablet document.

Clinical efficacy4.5/10

The combination is plausible and has a small exact-product tolerability study, but direct efficacy evidence is sparse. A five-dog cestode report required repeat dosing for full clearance; robust independent trials do not validate every broad claim in both species.

Safety and tolerability6.5/10

A small exact-product study found no measured abnormalities at up to five times the label dose, but cannot exclude uncommon harms. Macrocyclic-lactone susceptibility, age, health, reproduction, interactions and adverse reactions need screening.

Clinical practicality7.5/10

Weight-banded tablets and half-tablet increments simplify routine dosing, but repeated or diagnosis-specific schedules must not be inferred from a one-dose calculator.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with hypersensitivity, renal or hepatic dysfunction, infectious disease or debilitation; do not use below 0.5 kg or below 6 weeks.
  • Do not use during pregnancy or lactation; reproductive safety is not established.
  • Do not combine with other macrocyclic lactones, piperazine compounds or cholinesterase inhibitors without an evidence-based specialist plan.
  • Screen Collies and other ABCB1-susceptible dogs for macrocyclic-lactone risk and monitor neurologic status.
  • Monitor for vomiting, diarrhoea, hypersalivation, appetite change or hypersensitivity; stop and reassess if important signs occur.
  • Heartworm use prevents susceptible larval stages; it is not adulticide treatment. Assess infection and exposure first.
  • Direct efficacy evidence is small and does not validate every broad claim; confirm the parasite and reassess response.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Cat Labelled oral scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention
6.0/10
Situational / acceptable
vetman assessment

Inspector Quadro Tabs

160/4.8/80 mg, tablets for dogs and cats 8-16 kg
Assessed clinical scopeCat · Labelled oral scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention · By mouth
Care settingVeterinary-selected oral use after parasite and heartworm assessment, with diagnosis-specific follow-up
vetman score 6.0/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 001249 · Verified on 21 Oct 2026

Registered exact oral product, but broad efficacy rests on limited direct evidence and the public Bulgarian SPC has a route-inconsistent passage. Use for a defined parasite target, exact species and weight band, with monitoring.

Regulatory and scientific credibility6.0/10

Exact strengths have current Georgian registrations and an indefinite Bulgarian authorization with a public SPC. Confidence is reduced because the BFSA Tabs SPC contains a topical pharmacokinetic passage inconsistent with an oral-tablet document.

Clinical efficacy4.5/10

The combination is plausible and has a small exact-product tolerability study, but direct efficacy evidence is sparse. A five-dog cestode report required repeat dosing for full clearance; robust independent trials do not validate every broad claim in both species.

Safety and tolerability6.5/10

A small exact-product study found no measured abnormalities at up to five times the label dose, but cannot exclude uncommon harms. Macrocyclic-lactone susceptibility, age, health, reproduction, interactions and adverse reactions need screening.

Clinical practicality7.5/10

Weight-banded tablets and half-tablet increments simplify routine dosing, but repeated or diagnosis-specific schedules must not be inferred from a one-dose calculator.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with hypersensitivity, renal or hepatic dysfunction, infectious disease or debilitation; do not use below 0.5 kg or below 6 weeks.
  • Do not use during pregnancy or lactation; reproductive safety is not established.
  • Do not combine with other macrocyclic lactones, piperazine compounds or cholinesterase inhibitors without an evidence-based specialist plan.
  • Screen Collies and other ABCB1-susceptible dogs for macrocyclic-lactone risk and monitor neurologic status.
  • Monitor for vomiting, diarrhoea, hypersalivation, appetite change or hypersensitivity; stop and reassess if important signs occur.
  • Heartworm use prevents susceptible larval stages; it is not adulticide treatment. Assess infection and exposure first.
  • Direct efficacy evidence is small and does not validate every broad claim; confirm the parasite and reassess response.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Lufenuron160 mg Moxidectin4.8 mg Praziquantel80 mg
Formulation Type
Tablet
Administration route
By mouth
Manufacturer
Manufacturer (register)
JSC SPC EKOPROM, Russia
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1853, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 04 Sep 2031
Veterinary (National Food Agency)
In the register: ინსპექტორ კვადრო ტაბსი
№ 001249
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown

Inspector Quadro Tabs 320/9.6/160 mg, Tablet

tablets for dogs over 16 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
6.0/10
Situational / acceptable
vetman assessment

Inspector Quadro Tabs

320/9.6/160 mg, tablets for dogs over 16 kg
Assessed clinical scopeDog · Labelled oral scope for the exact weight band: ectoparasites, gastrointestinal nematodes and cestodes, and heartworm-larval prevention · By mouth
Care settingVeterinary-selected oral use after parasite and heartworm assessment, with diagnosis-specific follow-up
vetman score 6.0/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 002596 · Verified on 21 Oct 2026

Registered exact oral product, but broad efficacy rests on limited direct evidence and the public Bulgarian SPC has a route-inconsistent passage. Use for a defined parasite target, exact species and weight band, with monitoring.

Regulatory and scientific credibility6.0/10

Exact strengths have current Georgian registrations and an indefinite Bulgarian authorization with a public SPC. Confidence is reduced because the BFSA Tabs SPC contains a topical pharmacokinetic passage inconsistent with an oral-tablet document.

Clinical efficacy4.5/10

The combination is plausible and has a small exact-product tolerability study, but direct efficacy evidence is sparse. A five-dog cestode report required repeat dosing for full clearance; robust independent trials do not validate every broad claim in both species.

Safety and tolerability6.5/10

A small exact-product study found no measured abnormalities at up to five times the label dose, but cannot exclude uncommon harms. Macrocyclic-lactone susceptibility, age, health, reproduction, interactions and adverse reactions need screening.

Clinical practicality7.5/10

Weight-banded tablets and half-tablet increments simplify routine dosing, but repeated or diagnosis-specific schedules must not be inferred from a one-dose calculator.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with hypersensitivity, renal or hepatic dysfunction, infectious disease or debilitation; do not use below 0.5 kg or below 6 weeks.
  • Do not use during pregnancy or lactation; reproductive safety is not established.
  • Do not combine with other macrocyclic lactones, piperazine compounds or cholinesterase inhibitors without an evidence-based specialist plan.
  • Screen Collies and other ABCB1-susceptible dogs for macrocyclic-lactone risk and monitor neurologic status.
  • Monitor for vomiting, diarrhoea, hypersalivation, appetite change or hypersensitivity; stop and reassess if important signs occur.
  • Heartworm use prevents susceptible larval stages; it is not adulticide treatment. Assess infection and exposure first.
  • Direct efficacy evidence is small and does not validate every broad claim; confirm the parasite and reassess response.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Lufenuron320 mg Moxidectin9.6 mg Praziquantel160 mg
Formulation Type
Tablet
Administration route
By mouth
Manufacturer
Manufacturer (register)
Joint Stock Company NPF Ekoprom, Russia
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 527, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 22 Dec 2026
Veterinary (National Food Agency)
In the register: ინსპექტორ კვადრო ტაბსი
№ 002596
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
6.0/10
Weak evidence support
vetman assessment

OKVET ExpressTabs

150/25/1 mg tablets, N2 for dogs up to 5 kg
Assessed clinical scopeDog · Full labelled canine oral scope in an explicitly printed weight-table cell: treatment and control of susceptible fleas, ticks, lice, mites, gastrointestinal nematodes and cestodes, and prevention of susceptible Dirofilaria larval infection · By mouth
Care settingVeterinary-selected home dosing with parasite and heartworm-risk assessment, exact table-cell selection, administration with or immediately after food and follow-up appropriate to the target parasite
vetman score 6.0/10 Weak evidence support
Evidence confidence: Medium Georgia: Yes, veterinary · № 000608 · Verified on 21 Oct 2026

A locally registered, broad-spectrum dog tablet with exact-product evidence and relatively flexible small-dog dosing. It remains a weak-to-situational choice because evidence is mostly sponsor-linked and safety restrictions are substantial; use only an explicit weight-table cell and diagnose the target parasite.

Regulatory and scientific credibility6.5/10

The exact strengths are actively registered in Georgia, a regulator-hosted Moldovan leaflet independently corroborates identity and use, and multiple exact-product studies are published. However, no EMA/FDA-style public assessment or transparent full dossier was found, and much of the evidence is manufacturer-linked.

Clinical efficacy6.0/10

Exact-product studies report high efficacy against selected naturally or experimentally infested ectoparasites and provide pharmacokinetic support for all three actives. Study groups are generally small, comparator, blinding and sponsor independence are limited, and the very broad label spectrum and every claimed duration are not validated equally well.

Safety and tolerability4.5/10

A 30-dog tolerance study found no important effect at the therapeutic regimen, but five consecutive daily double doses caused salivation, vomiting, incoordination, depression or mydriasis in 30% of dogs. The exact label has extensive age, reproductive, disease, MDR1/macrolactone and drug-combination restrictions; uncommon-event and diverse-patient safety remain incompletely defined.

Clinical practicality7.5/10

Quarter-tablet scoring and explicit small-dog cells make this the most flexible presentation. It must still be given with or just after food and only for printed weight cells; the table contains gaps and alternative-strength overlaps that must not be interpolated.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use below 1.25 kg, under 8 weeks of age, during pregnancy or lactation, or in emaciated, infectious-disease, hyperthermic, hepatic, renal or epileptic patients.
  • Avoid in known MDR1/ABCB1 or macrocyclic-lactone sensitivity unless a specialist has explicitly assessed the individual risk.
  • Do not use within 6 weeks of another macrocyclic lactone and do not combine with cholinesterase inhibitors or piperazine. Review every antiparasitic active ingredient before dosing.
  • Give with a small amount of food or immediately after feeding. If vomiting occurs soon after dosing, do not automatically repeat the dose; assess timing, visible tablet loss and patient risk with a veterinarian.
  • Monitor for anorexia, vomiting, diarrhoea, salivation, ataxia, depression, mydriasis, tremor, excitation, photophobia or convulsions. A repeated double-dose tolerance study produced poisoning signs in 30% of dogs.
  • Use only an explicitly printed weight-table cell. The official table contains gaps and overlapping alternative strengths; do not interpolate a missing band or convert the combination into a continuous mg/kg rule.
  • Heartworm use is prevention against susceptible larval stages, not treatment of adult infection. Assess geographic exposure, test as clinically indicated and follow current canine heartworm guidance.
  • The broad label does not mean every parasite is present or equally supported by evidence. Identify the likely parasite, use appropriate diagnostics and confirm response or clearance where the disease requires it.
  • Most exact-product studies are small and manufacturer-linked. Their positive findings do not replace independent surveillance, transparent regulator assessment or reassessment when expected control fails.
  • Prevent access by cats, children and unintended dogs, record the date and exact strength, and avoid accidental repeat dosing across household parasite-control products.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Spinosad150 mg/tablet Praziquantel25 mg/tablet Moxidectin1 mg/tablet
Formulation Type
Scored tablet
Administration route
By mouth
Manufacturer
AVZ S-P Ltd · Russia
Manufacturer (register)
AVZ S-P Ltd, Russia
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1087, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 20 May 2029
Veterinary (National Food Agency)
In the register: ექსპრესტაბსი®
№ 000608
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
5.9/10
Weak evidence support
vetman assessment

OKVET ExpressTabs

300/50/2 mg tablets, N3 for dogs 5-15 kg
Assessed clinical scopeDog · Full labelled canine oral scope in an explicitly printed weight-table cell: treatment and control of susceptible fleas, ticks, lice, mites, gastrointestinal nematodes and cestodes, and prevention of susceptible Dirofilaria larval infection · By mouth
Care settingVeterinary-selected home dosing with parasite and heartworm-risk assessment, exact table-cell selection, administration with or immediately after food and follow-up appropriate to the target parasite
vetman score 5.9/10 Weak evidence support
Evidence confidence: Medium Georgia: Yes, veterinary · № 000624 · Verified on 21 Oct 2026

A locally registered broad-spectrum option with exact-product studies, but evidence independence and broad-claim coverage are limited. Its discontinuous dosing table and substantial safety restrictions require deliberate veterinary selection rather than a generic monthly all-parasite assumption.

Regulatory and scientific credibility6.5/10

The exact strengths are actively registered in Georgia, a regulator-hosted Moldovan leaflet independently corroborates identity and use, and multiple exact-product studies are published. However, no EMA/FDA-style public assessment or transparent full dossier was found, and much of the evidence is manufacturer-linked.

Clinical efficacy6.0/10

Exact-product studies report high efficacy against selected naturally or experimentally infested ectoparasites and provide pharmacokinetic support for all three actives. Study groups are generally small, comparator, blinding and sponsor independence are limited, and the very broad label spectrum and every claimed duration are not validated equally well.

Safety and tolerability4.5/10

A 30-dog tolerance study found no important effect at the therapeutic regimen, but five consecutive daily double doses caused salivation, vomiting, incoordination, depression or mydriasis in 30% of dogs. The exact label has extensive age, reproductive, disease, MDR1/macrolactone and drug-combination restrictions; uncommon-event and diverse-patient safety remain incompletely defined.

Clinical practicality7.0/10

Quarter-tablet scoring provides useful flexibility across several explicit cells, but the official table is discontinuous and extends this presentation beyond its marketing subtitle. Select the printed cell rather than inferring a continuous mg/kg rule or substituting another strength.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use below 1.25 kg, under 8 weeks of age, during pregnancy or lactation, or in emaciated, infectious-disease, hyperthermic, hepatic, renal or epileptic patients.
  • Avoid in known MDR1/ABCB1 or macrocyclic-lactone sensitivity unless a specialist has explicitly assessed the individual risk.
  • Do not use within 6 weeks of another macrocyclic lactone and do not combine with cholinesterase inhibitors or piperazine. Review every antiparasitic active ingredient before dosing.
  • Give with a small amount of food or immediately after feeding. If vomiting occurs soon after dosing, do not automatically repeat the dose; assess timing, visible tablet loss and patient risk with a veterinarian.
  • Monitor for anorexia, vomiting, diarrhoea, salivation, ataxia, depression, mydriasis, tremor, excitation, photophobia or convulsions. A repeated double-dose tolerance study produced poisoning signs in 30% of dogs.
  • Use only an explicitly printed weight-table cell. The official table contains gaps and overlapping alternative strengths; do not interpolate a missing band or convert the combination into a continuous mg/kg rule.
  • Heartworm use is prevention against susceptible larval stages, not treatment of adult infection. Assess geographic exposure, test as clinically indicated and follow current canine heartworm guidance.
  • The broad label does not mean every parasite is present or equally supported by evidence. Identify the likely parasite, use appropriate diagnostics and confirm response or clearance where the disease requires it.
  • Most exact-product studies are small and manufacturer-linked. Their positive findings do not replace independent surveillance, transparent regulator assessment or reassessment when expected control fails.
  • Prevent access by cats, children and unintended dogs, record the date and exact strength, and avoid accidental repeat dosing across household parasite-control products.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Spinosad300 mg/tablet Praziquantel50 mg/tablet Moxidectin2 mg/tablet
Formulation Type
Scored tablet
Administration route
By mouth
Manufacturer
AVZ S-P Ltd · Russia
Manufacturer (register)
AVZ S-P Ltd, Russia
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1111, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 03 Jun 2029
Veterinary (National Food Agency)
In the register: ექსპრესტაბსი®
№ 000624
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
5.7/10
Weak evidence support
vetman assessment

OKVET ExpressTabs

900/150/6 mg tablets, N2 for dogs 15-60 kg
Assessed clinical scopeDog · Full labelled canine oral scope in an explicitly printed weight-table cell: treatment and control of susceptible fleas, ticks, lice, mites, gastrointestinal nematodes and cestodes, and prevention of susceptible Dirofilaria larval infection · By mouth
Care settingVeterinary-selected home dosing with parasite and heartworm-risk assessment, exact table-cell selection, administration with or immediately after food and follow-up appropriate to the target parasite
vetman score 5.7/10 Weak evidence support
Evidence confidence: Medium Georgia: Yes, veterinary · № 000599 | 000640 · Verified on 21 Oct 2026

A locally registered broad-spectrum option with exact-product studies, but the large-dog presentation has material table gaps and combination requirements, while safety and evidence limitations remain. Use only the explicit cell selected for the dog and do not interpolate missing bands.

Regulatory and scientific credibility6.5/10

The exact strengths are actively registered in Georgia, a regulator-hosted Moldovan leaflet independently corroborates identity and use, and multiple exact-product studies are published. However, no EMA/FDA-style public assessment or transparent full dossier was found, and much of the evidence is manufacturer-linked.

Clinical efficacy6.0/10

Exact-product studies report high efficacy against selected naturally or experimentally infested ectoparasites and provide pharmacokinetic support for all three actives. Study groups are generally small, comparator, blinding and sponsor independence are limited, and the very broad label spectrum and every claimed duration are not validated equally well.

Safety and tolerability4.5/10

A 30-dog tolerance study found no important effect at the therapeutic regimen, but five consecutive daily double doses caused salivation, vomiting, incoordination, depression or mydriasis in 30% of dogs. The exact label has extensive age, reproductive, disease, MDR1/macrolactone and drug-combination restrictions; uncommon-event and diverse-patient safety remain incompletely defined.

Clinical practicality6.0/10

Oral dosing and quarter-tablet scoring are convenient, but the large-dog table has no 21-25 kg cell for this strength and requires another strength there; above 60 kg the label uses combinations not supplied by this single presentation. These gaps materially increase selection and pack-management burden.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use below 1.25 kg, under 8 weeks of age, during pregnancy or lactation, or in emaciated, infectious-disease, hyperthermic, hepatic, renal or epileptic patients.
  • Avoid in known MDR1/ABCB1 or macrocyclic-lactone sensitivity unless a specialist has explicitly assessed the individual risk.
  • Do not use within 6 weeks of another macrocyclic lactone and do not combine with cholinesterase inhibitors or piperazine. Review every antiparasitic active ingredient before dosing.
  • Give with a small amount of food or immediately after feeding. If vomiting occurs soon after dosing, do not automatically repeat the dose; assess timing, visible tablet loss and patient risk with a veterinarian.
  • Monitor for anorexia, vomiting, diarrhoea, salivation, ataxia, depression, mydriasis, tremor, excitation, photophobia or convulsions. A repeated double-dose tolerance study produced poisoning signs in 30% of dogs.
  • Use only an explicitly printed cell. This strength has no 21-25 kg cell; use the labelled alternative strength there. Above 60 kg, follow a veterinarian-selected labelled combination and do not invent a single-strength dose.
  • Heartworm use is prevention against susceptible larval stages, not treatment of adult infection. Assess geographic exposure, test as clinically indicated and follow current canine heartworm guidance.
  • The broad label does not mean every parasite is present or equally supported by evidence. Identify the likely parasite, use appropriate diagnostics and confirm response or clearance where the disease requires it.
  • Most exact-product studies are small and manufacturer-linked. Their positive findings do not replace independent surveillance, transparent regulator assessment or reassessment when expected control fails.
  • Prevent access by cats, children and unintended dogs, record the date and exact strength, and avoid accidental repeat dosing across household parasite-control products.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Spinosad900 mg/tablet Praziquantel150 mg/tablet Moxidectin6 mg/tablet
Formulation Type
Scored tablet
Administration route
By mouth
Manufacturer
AVZ S-P Ltd · Russia
Registration
Georgia Yes, veterinary
In force until 25 Apr 2029
Veterinary (National Food Agency)
In the register: ექსპრესტაბსი®
№ 000599 | 000640
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown

Simparica Trio 3 mg/0.06 mg/12.5 mg, Chewable tablet

sarolaner 3 mg + moxidectin 0.06 mg + pyrantel (as embonate) 12.5 mg, chewable tablet for dogs 1.25-2.5 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
8.2/10
Very good
vetman assessment

Simparica Trio

3 mg/0.06 mg/12.5 mg, sarolaner 3 mg + moxidectin 0.06 mg + pyrantel (as embonate) 12.5 mg, chewable tablet for dogs 1.25-2.5 kg
Assessed clinical scopeDog · Full labelled canine combined-parasite scope when ectoparasite treatment and one or more nematode, heartworm or lungworm indications are concurrently required · By mouth
Care settingMonthly weight-band chewable integrated parasite control after indication, heartworm, age, neurologic and MDR1-risk assessment
vetman score 8.2/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 182-11, 34-11 · Verified on 15 Oct 2026

A highly effective, well-documented integrated monthly option when its combined indication is genuinely present; broader coverage brings more screening and safety obligations than sarolaner alone.

Regulatory and scientific credibility9.0/10

Every exact strength is registered in Georgia and the combination has current central EU/UK and FDA authorisations with detailed public dossiers.

Clinical efficacy9.0/10

Large controlled field and laboratory programmes support fleas, ticks, gastrointestinal nematodes and heartworm prevention, with additional labelled mite and lungworm roles; efficacy depends on matching the combined-indication gate and schedule.

Safety and tolerability6.5/10

The profile is extensively studied but combines isoxazoline neurological risk with macrocyclic-lactone precautions, potential reactions in heavily microfilaraemic dogs and strict dose discipline in MDR1-sensitive breeds.

Clinical practicality8.5/10

One palatable monthly chew integrates several parasite targets, but correct use requires heartworm testing where indicated, exact weight-band selection and confirmation that a combination product is clinically justified.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Isoxazoline-associated tremor, ataxia and seizures can occur, including without prior history; use particular caution in dogs with neurologic disease.
  • In heartworm-endemic settings, test dogs according to the exact label before preventive use; heavily microfilaraemic dogs may develop hypersensitivity-type reactions after treatment.
  • Use only in dogs and only the correct whole-tablet weight band. Strictly observe the dose in MDR1-sensitive breeds and do not split tablets.
  • Use the combination only when ectoparasite treatment and one or more additional labelled nematode, heartworm or lungworm indications are concurrently required.
  • Pregnancy, lactation, breeding and very-young-puppy use require the locally applicable exact-label benefit-risk rules.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Sarolaner3 mg Moxidectin0.06 mg Pyrantel12.5 mg
Formulation Type
Chewable tablet
Administration route
By mouth
Manufacturer
Zoetis · United States
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: სიმპარიკა ტრიო - საღეჭი ტაბლეტები ძაღლებისთვის >1.25-2.5კგ
№ 182-11, 34-11
Verified on: 15 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-521
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Simparica Trio 6 mg/0.12 mg/25 mg, Chewable tablet

sarolaner 6 mg + moxidectin 0.12 mg + pyrantel (as embonate) 25 mg, chewable tablet for dogs 2.5-5 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
8.2/10
Very good
vetman assessment

Simparica Trio

6 mg/0.12 mg/25 mg, sarolaner 6 mg + moxidectin 0.12 mg + pyrantel (as embonate) 25 mg, chewable tablet for dogs 2.5-5 kg
Assessed clinical scopeDog · Full labelled canine combined-parasite scope when ectoparasite treatment and one or more nematode, heartworm or lungworm indications are concurrently required · By mouth
Care settingMonthly weight-band chewable integrated parasite control after indication, heartworm, age, neurologic and MDR1-risk assessment
vetman score 8.2/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 180-11, 404-11 · Verified on 15 Oct 2026

A highly effective, well-documented integrated monthly option when its combined indication is genuinely present; broader coverage brings more screening and safety obligations than sarolaner alone.

Regulatory and scientific credibility9.0/10

Every exact strength is registered in Georgia and the combination has current central EU/UK and FDA authorisations with detailed public dossiers.

Clinical efficacy9.0/10

Large controlled field and laboratory programmes support fleas, ticks, gastrointestinal nematodes and heartworm prevention, with additional labelled mite and lungworm roles; efficacy depends on matching the combined-indication gate and schedule.

Safety and tolerability6.5/10

The profile is extensively studied but combines isoxazoline neurological risk with macrocyclic-lactone precautions, potential reactions in heavily microfilaraemic dogs and strict dose discipline in MDR1-sensitive breeds.

Clinical practicality8.5/10

One palatable monthly chew integrates several parasite targets, but correct use requires heartworm testing where indicated, exact weight-band selection and confirmation that a combination product is clinically justified.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Isoxazoline-associated tremor, ataxia and seizures can occur, including without prior history; use particular caution in dogs with neurologic disease.
  • In heartworm-endemic settings, test dogs according to the exact label before preventive use; heavily microfilaraemic dogs may develop hypersensitivity-type reactions after treatment.
  • Use only in dogs and only the correct whole-tablet weight band. Strictly observe the dose in MDR1-sensitive breeds and do not split tablets.
  • Use the combination only when ectoparasite treatment and one or more additional labelled nematode, heartworm or lungworm indications are concurrently required.
  • Pregnancy, lactation, breeding and very-young-puppy use require the locally applicable exact-label benefit-risk rules.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Sarolaner6 mg Moxidectin0.12 mg Pyrantel25 mg
Formulation Type
Chewable tablet
Administration route
By mouth
Manufacturer
Zoetis · United States
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: სიმპარიკა ტრიო - საღეჭი ტაბლეტები ძაღლებისთვის >2.5-5კგ
№ 180-11, 404-11
Verified on: 15 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-521
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Simparica Trio 12 mg/0.24 mg/50 mg, Chewable tablet

sarolaner 12 mg + moxidectin 0.24 mg + pyrantel (as embonate) 50 mg, chewable tablet for dogs 5-10 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
8.2/10
Very good
vetman assessment

Simparica Trio

12 mg/0.24 mg/50 mg, sarolaner 12 mg + moxidectin 0.24 mg + pyrantel (as embonate) 50 mg, chewable tablet for dogs 5-10 kg
Assessed clinical scopeDog · Full labelled canine combined-parasite scope when ectoparasite treatment and one or more nematode, heartworm or lungworm indications are concurrently required · By mouth
Care settingMonthly weight-band chewable integrated parasite control after indication, heartworm, age, neurologic and MDR1-risk assessment
vetman score 8.2/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 185-11, 406-11 · Verified on 15 Oct 2026

A highly effective, well-documented integrated monthly option when its combined indication is genuinely present; broader coverage brings more screening and safety obligations than sarolaner alone.

Regulatory and scientific credibility9.0/10

Every exact strength is registered in Georgia and the combination has current central EU/UK and FDA authorisations with detailed public dossiers.

Clinical efficacy9.0/10

Large controlled field and laboratory programmes support fleas, ticks, gastrointestinal nematodes and heartworm prevention, with additional labelled mite and lungworm roles; efficacy depends on matching the combined-indication gate and schedule.

Safety and tolerability6.5/10

The profile is extensively studied but combines isoxazoline neurological risk with macrocyclic-lactone precautions, potential reactions in heavily microfilaraemic dogs and strict dose discipline in MDR1-sensitive breeds.

Clinical practicality8.5/10

One palatable monthly chew integrates several parasite targets, but correct use requires heartworm testing where indicated, exact weight-band selection and confirmation that a combination product is clinically justified.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Isoxazoline-associated tremor, ataxia and seizures can occur, including without prior history; use particular caution in dogs with neurologic disease.
  • In heartworm-endemic settings, test dogs according to the exact label before preventive use; heavily microfilaraemic dogs may develop hypersensitivity-type reactions after treatment.
  • Use only in dogs and only the correct whole-tablet weight band. Strictly observe the dose in MDR1-sensitive breeds and do not split tablets.
  • Use the combination only when ectoparasite treatment and one or more additional labelled nematode, heartworm or lungworm indications are concurrently required.
  • Pregnancy, lactation, breeding and very-young-puppy use require the locally applicable exact-label benefit-risk rules.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Sarolaner12 mg Moxidectin0.24 mg Pyrantel50 mg
Formulation Type
Chewable tablet
Administration route
By mouth
Manufacturer
Zoetis · United States
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: სიმპარიკა ტრიო - საღეჭი ტაბლეტები ძაღლებისთვის >5-10კგ
№ 185-11, 406-11
Verified on: 15 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-521
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Simparica Trio 24 mg/0.48 mg/100 mg, Chewable tablet

sarolaner 24 mg + moxidectin 0.48 mg + pyrantel (as embonate) 100 mg, chewable tablet for dogs 10-20 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
8.2/10
Very good
vetman assessment

Simparica Trio

24 mg/0.48 mg/100 mg, sarolaner 24 mg + moxidectin 0.48 mg + pyrantel (as embonate) 100 mg, chewable tablet for dogs 10-20 kg
Assessed clinical scopeDog · Full labelled canine combined-parasite scope when ectoparasite treatment and one or more nematode, heartworm or lungworm indications are concurrently required · By mouth
Care settingMonthly weight-band chewable integrated parasite control after indication, heartworm, age, neurologic and MDR1-risk assessment
vetman score 8.2/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 184-11, 403-11 · Verified on 15 Oct 2026

A highly effective, well-documented integrated monthly option when its combined indication is genuinely present; broader coverage brings more screening and safety obligations than sarolaner alone.

Regulatory and scientific credibility9.0/10

Every exact strength is registered in Georgia and the combination has current central EU/UK and FDA authorisations with detailed public dossiers.

Clinical efficacy9.0/10

Large controlled field and laboratory programmes support fleas, ticks, gastrointestinal nematodes and heartworm prevention, with additional labelled mite and lungworm roles; efficacy depends on matching the combined-indication gate and schedule.

Safety and tolerability6.5/10

The profile is extensively studied but combines isoxazoline neurological risk with macrocyclic-lactone precautions, potential reactions in heavily microfilaraemic dogs and strict dose discipline in MDR1-sensitive breeds.

Clinical practicality8.5/10

One palatable monthly chew integrates several parasite targets, but correct use requires heartworm testing where indicated, exact weight-band selection and confirmation that a combination product is clinically justified.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Isoxazoline-associated tremor, ataxia and seizures can occur, including without prior history; use particular caution in dogs with neurologic disease.
  • In heartworm-endemic settings, test dogs according to the exact label before preventive use; heavily microfilaraemic dogs may develop hypersensitivity-type reactions after treatment.
  • Use only in dogs and only the correct whole-tablet weight band. Strictly observe the dose in MDR1-sensitive breeds and do not split tablets.
  • Use the combination only when ectoparasite treatment and one or more additional labelled nematode, heartworm or lungworm indications are concurrently required.
  • Pregnancy, lactation, breeding and very-young-puppy use require the locally applicable exact-label benefit-risk rules.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Sarolaner24 mg Moxidectin0.48 mg Pyrantel100 mg
Formulation Type
Chewable tablet
Administration route
By mouth
Manufacturer
Zoetis · United States
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: სიმპარიკა ტრიო - საღეჭი ტაბლეტები ძაღლებისთვის >10-20კგ
№ 184-11, 403-11
Verified on: 15 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-521
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Simparica Trio 48 mg/0.96 mg/200 mg, Chewable tablet

sarolaner 48 mg + moxidectin 0.96 mg + pyrantel (as embonate) 200 mg, chewable tablet for dogs 20-40 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
8.2/10
Very good
vetman assessment

Simparica Trio

48 mg/0.96 mg/200 mg, sarolaner 48 mg + moxidectin 0.96 mg + pyrantel (as embonate) 200 mg, chewable tablet for dogs 20-40 kg
Assessed clinical scopeDog · Full labelled canine combined-parasite scope when ectoparasite treatment and one or more nematode, heartworm or lungworm indications are concurrently required · By mouth
Care settingMonthly weight-band chewable integrated parasite control after indication, heartworm, age, neurologic and MDR1-risk assessment
vetman score 8.2/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 179-11, 402-11 · Verified on 15 Oct 2026

A highly effective, well-documented integrated monthly option when its combined indication is genuinely present; broader coverage brings more screening and safety obligations than sarolaner alone.

Regulatory and scientific credibility9.0/10

Every exact strength is registered in Georgia and the combination has current central EU/UK and FDA authorisations with detailed public dossiers.

Clinical efficacy9.0/10

Large controlled field and laboratory programmes support fleas, ticks, gastrointestinal nematodes and heartworm prevention, with additional labelled mite and lungworm roles; efficacy depends on matching the combined-indication gate and schedule.

Safety and tolerability6.5/10

The profile is extensively studied but combines isoxazoline neurological risk with macrocyclic-lactone precautions, potential reactions in heavily microfilaraemic dogs and strict dose discipline in MDR1-sensitive breeds.

Clinical practicality8.5/10

One palatable monthly chew integrates several parasite targets, but correct use requires heartworm testing where indicated, exact weight-band selection and confirmation that a combination product is clinically justified.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Isoxazoline-associated tremor, ataxia and seizures can occur, including without prior history; use particular caution in dogs with neurologic disease.
  • In heartworm-endemic settings, test dogs according to the exact label before preventive use; heavily microfilaraemic dogs may develop hypersensitivity-type reactions after treatment.
  • Use only in dogs and only the correct whole-tablet weight band. Strictly observe the dose in MDR1-sensitive breeds and do not split tablets.
  • Use the combination only when ectoparasite treatment and one or more additional labelled nematode, heartworm or lungworm indications are concurrently required.
  • Pregnancy, lactation, breeding and very-young-puppy use require the locally applicable exact-label benefit-risk rules.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Sarolaner48 mg Moxidectin0.96 mg Pyrantel200 mg
Formulation Type
Chewable tablet
Administration route
By mouth
Manufacturer
Zoetis · United States
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: სიმპარიკა ტრიო - საღეჭი ტაბლეტები ძაღლებისთვის >20-40კგ
№ 179-11, 402-11
Verified on: 15 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-521
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Simparica Trio 72 mg/1.44 mg/300 mg, Chewable tablet

sarolaner 72 mg + moxidectin 1.44 mg + pyrantel (as embonate) 300 mg, chewable tablet for dogs 40-60 kg
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
8.2/10
Very good
vetman assessment

Simparica Trio

72 mg/1.44 mg/300 mg, sarolaner 72 mg + moxidectin 1.44 mg + pyrantel (as embonate) 300 mg, chewable tablet for dogs 40-60 kg
Assessed clinical scopeDog · Full labelled canine combined-parasite scope when ectoparasite treatment and one or more nematode, heartworm or lungworm indications are concurrently required · By mouth
Care settingMonthly weight-band chewable integrated parasite control after indication, heartworm, age, neurologic and MDR1-risk assessment
vetman score 8.2/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 181-11, 33-11 · Verified on 15 Oct 2026

A highly effective, well-documented integrated monthly option when its combined indication is genuinely present; broader coverage brings more screening and safety obligations than sarolaner alone.

Regulatory and scientific credibility9.0/10

Every exact strength is registered in Georgia and the combination has current central EU/UK and FDA authorisations with detailed public dossiers.

Clinical efficacy9.0/10

Large controlled field and laboratory programmes support fleas, ticks, gastrointestinal nematodes and heartworm prevention, with additional labelled mite and lungworm roles; efficacy depends on matching the combined-indication gate and schedule.

Safety and tolerability6.5/10

The profile is extensively studied but combines isoxazoline neurological risk with macrocyclic-lactone precautions, potential reactions in heavily microfilaraemic dogs and strict dose discipline in MDR1-sensitive breeds.

Clinical practicality8.5/10

One palatable monthly chew integrates several parasite targets, but correct use requires heartworm testing where indicated, exact weight-band selection and confirmation that a combination product is clinically justified.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Isoxazoline-associated tremor, ataxia and seizures can occur, including without prior history; use particular caution in dogs with neurologic disease.
  • In heartworm-endemic settings, test dogs according to the exact label before preventive use; heavily microfilaraemic dogs may develop hypersensitivity-type reactions after treatment.
  • Use only in dogs and only the correct whole-tablet weight band. Strictly observe the dose in MDR1-sensitive breeds and do not split tablets.
  • Use the combination only when ectoparasite treatment and one or more additional labelled nematode, heartworm or lungworm indications are concurrently required.
  • Pregnancy, lactation, breeding and very-young-puppy use require the locally applicable exact-label benefit-risk rules.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Sarolaner72 mg Moxidectin1.44 mg Pyrantel300 mg
Formulation Type
Chewable tablet
Administration route
By mouth
Manufacturer
Zoetis · United States
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: სიმპარიკა ტრიო - საღეჭი ტაბლეტები ძაღლებისთვის >40-60კგ
№ 181-11, 33-11
Verified on: 15 Oct 2026
EU Yes, veterinary
Verified on: 15 Oct 2026
UK Yes, veterinary
Verified on: 15 Oct 2026
US Yes, veterinary
№ NADA 141-521
Verified on: 15 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Cat
6.3/10
Situational / acceptable
vetman assessment

Superium Panacea

20/6/0.6/10 mg tablet N1 for cats 0.5-2 kg
Assessed clinical scopeCat · Full labelled feline oral scope: fleas and FAD, listed sarcoptiform and demodectic mites, gastrointestinal nematodes and cestodes, mixed infestations and heartworm-larval prevention · By mouth
Care settingVeterinary-selected home administration after parasite-risk assessment, with diagnostic follow-up when treating established infestation
vetman score 6.3/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 000953 · Verified on 21 Oct 2026

A convenient broad oral option with encouraging exact-product feline data, but not a strongly validated substitute for better-documented parasite-specific choices. Use after confirming the actual parasite spectrum and plan follow-up, especially for cestodes.

Regulatory and scientific credibility6.5/10

The exact feline strengths are currently registered in Georgia and have a valid prescription registration plus a detailed regulator-approved SPC in Moldova. The dossier is much less transparent than an EMA/FDA assessment and the broad label is supported mainly by small regional studies.

Clinical efficacy6.0/10

Small exact-product studies support flea and ear-mite activity and suggest benefit in mixed infestations, while established lufenuron/nitenpyram and moxidectin/praziquantel evidence supports component plausibility. The full mite, nematode, cestode and heartworm-prevention label has not been confirmed by robust controlled trials; one 54-cat report found residual Dipylidium segments requiring separate praziquantel.

Safety and tolerability5.5/10

Small studies report good short-term tolerance, but the approved SPC lists rare tremor, seizures, depression, vomiting and gastrointestinal dysfunction. Robust target-animal safety, reproductive and interaction datasets for the four-drug combination are not publicly available; pregnancy and lactation are restricted.

Clinical practicality7.5/10

A single whole weight-banded tablet can consolidate several parasite targets and is given monthly for continuous flea or heartworm prevention. It must not be split, complete swallowing must be observed, and voluntary tablet acceptance in cats is variable; established infestations may need repeat dosing and laboratory follow-up.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with known hypersensitivity, in emaciated animals or animals with infectious disease, or below 6 weeks of age or 0.5 kg body weight.
  • Do not administer concurrently with another antiparasitic. The regulator-approved feline SPC states that interaction data are unavailable; review all current medicines before use.
  • Rare neurological or gastrointestinal reactions can include tremor, seizures, depression, vomiting and digestive dysfunction. Stop and assess promptly if neurological signs, persistent vomiting or marked depression occurs.
  • Avoid during pregnancy and lactation unless a veterinarian determines that expected benefit outweighs risk; exact-combination reproductive safety is not established.
  • This tablet does not treat adult Dirofilaria and is not protection against ixodid pasture ticks. Test and stage heartworm risk as clinically appropriate and choose separate tick control when exposure exists.
  • Use the exact whole tablet for the current body-weight band; do not divide. Give with food or directly by mouth and observe complete swallowing. Reweigh growing or borderline patients before the next dose.
  • The exact-product feline studies are small and cover only part of the label. Recheck established mixed infection; one 54-cat report found persistent Dipylidium segments in isolated cases and used separate praziquantel.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Lufenuron20 mg/tablet Nitenpyram6 mg/tablet Moxidectin0.6 mg/tablet Praziquantel10 mg/tablet
Formulation Type
Tablet
Administration route
By mouth
Manufacturer (register)
INTER LEK LTD, Ukraine
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1513, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 15 Sep 2030
Veterinary (National Food Agency)
In the register: სუპერიუმ პანაცეა
№ 000953
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
5.6/10
Weak evidence support
vetman assessment

Superium Panacea

20/6/0.6/10 mg tablet N1 for dogs 0.5-2 kg
Assessed clinical scopeDog · Full labelled canine oral scope: fleas and FAD, lice, listed sarcoptiform and demodectic mites, gastrointestinal nematodes and cestodes, mixed infestations and heartworm-larval prevention · By mouth
Care settingVeterinary-selected home administration after parasite-risk assessment, with diagnostic follow-up when treating established infestation
vetman score 5.6/10 Weak evidence support
Evidence confidence: Low Georgia: Yes, veterinary · № 000999 · Verified on 21 Oct 2026

Mechanistically plausible and locally registered, but the exact canine combination has too little independent evidence for its very broad label. Prefer better-documented parasite-specific products when available and use this tablet only with explicit diagnostic and follow-up reasoning.

Regulatory and scientific credibility5.5/10

The exact canine strengths are registered in Georgia and have a current manufacturer instruction, but no EMA/FDA-style public assessment or comparable regulator dossier was found. Exact-product independent evidence for dogs was not identified, so ingredient evidence cannot substitute for the combination dossier.

Clinical efficacy5.0/10

The four ingredients have credible activity against their respective targets, including field evidence for lufenuron plus nitenpyram and separate moxidectin/praziquantel data. However, no robust independent trial of this exact canine four-drug tablet was found, so the unusually broad mite, helminth and heartworm-prevention claims remain incompletely validated.

Safety and tolerability5.0/10

The instruction lists rare neurological and gastrointestinal reactions and restricts use in debilitated, infectious, very young or very small animals and with other antiparasitics. Public target-animal safety and interaction data for the exact four-drug canine combination are sparse, and moxidectin warrants particular caution in ABCB1-sensitive dogs.

Clinical practicality8.0/10

One whole monthly weight-banded tablet can consolidate several parasite targets and avoids topical residue. Five canine weight bands support dose selection, but the tablet must not be split, complete swallowing must be confirmed and treatment schedules differ by parasite, with reassessment or repeat dosing for mites and severe helminth infection.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with known hypersensitivity, in emaciated animals or animals with infectious disease, or below 6 weeks of age or 0.5 kg body weight.
  • Do not administer concurrently with another antiparasitic. The regulator-approved feline SPC states that interaction data are unavailable; review all current medicines before use.
  • Rare neurological or gastrointestinal reactions can include tremor, seizures, depression, vomiting and digestive dysfunction. Stop and assess promptly if neurological signs, persistent vomiting or marked depression occurs.
  • Avoid during pregnancy and lactation unless a veterinarian determines that expected benefit outweighs risk; exact-combination reproductive safety is not established.
  • This tablet does not treat adult Dirofilaria and is not protection against ixodid pasture ticks. Test and stage heartworm risk as clinically appropriate and choose separate tick control when exposure exists.
  • Use the exact whole tablet for the current body-weight band; do not divide. Give with food or directly by mouth and observe complete swallowing. Reweigh growing or borderline patients before the next dose.
  • In Collies and other ABCB1-sensitive dogs, use moxidectin-containing treatment only at the exact labelled dose under veterinary supervision; avoid interacting P-glycoprotein substrates unless the individual risk is resolved.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Lufenuron20 mg/tablet Nitenpyram6 mg/tablet Moxidectin0.6 mg/tablet Praziquantel10 mg/tablet
Formulation Type
Tablet
Administration route
By mouth
Manufacturer (register)
INTER LEK LTD, Ukraine
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1578, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 12 Sep 2030
Veterinary (National Food Agency)
In the register: სუპერიუმ პანაცეა
№ 000999
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Cat
6.3/10
Situational / acceptable
vetman assessment

Superium Panacea

40/12/1.2/20 mg tablet N1 for cats 2-8 kg
Assessed clinical scopeCat · Full labelled feline oral scope: fleas and FAD, listed sarcoptiform and demodectic mites, gastrointestinal nematodes and cestodes, mixed infestations and heartworm-larval prevention · By mouth
Care settingVeterinary-selected home administration after parasite-risk assessment, with diagnostic follow-up when treating established infestation
vetman score 6.3/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 001001 · Verified on 21 Oct 2026

A convenient broad oral option with encouraging exact-product feline data, but not a strongly validated substitute for better-documented parasite-specific choices. Use after confirming the actual parasite spectrum and plan follow-up, especially for cestodes.

Regulatory and scientific credibility6.5/10

The exact feline strengths are currently registered in Georgia and have a valid prescription registration plus a detailed regulator-approved SPC in Moldova. The dossier is much less transparent than an EMA/FDA assessment and the broad label is supported mainly by small regional studies.

Clinical efficacy6.0/10

Small exact-product studies support flea and ear-mite activity and suggest benefit in mixed infestations, while established lufenuron/nitenpyram and moxidectin/praziquantel evidence supports component plausibility. The full mite, nematode, cestode and heartworm-prevention label has not been confirmed by robust controlled trials; one 54-cat report found residual Dipylidium segments requiring separate praziquantel.

Safety and tolerability5.5/10

Small studies report good short-term tolerance, but the approved SPC lists rare tremor, seizures, depression, vomiting and gastrointestinal dysfunction. Robust target-animal safety, reproductive and interaction datasets for the four-drug combination are not publicly available; pregnancy and lactation are restricted.

Clinical practicality7.5/10

A single whole weight-banded tablet can consolidate several parasite targets and is given monthly for continuous flea or heartworm prevention. It must not be split, complete swallowing must be observed, and voluntary tablet acceptance in cats is variable; established infestations may need repeat dosing and laboratory follow-up.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with known hypersensitivity, in emaciated animals or animals with infectious disease, or below 6 weeks of age or 0.5 kg body weight.
  • Do not administer concurrently with another antiparasitic. The regulator-approved feline SPC states that interaction data are unavailable; review all current medicines before use.
  • Rare neurological or gastrointestinal reactions can include tremor, seizures, depression, vomiting and digestive dysfunction. Stop and assess promptly if neurological signs, persistent vomiting or marked depression occurs.
  • Avoid during pregnancy and lactation unless a veterinarian determines that expected benefit outweighs risk; exact-combination reproductive safety is not established.
  • This tablet does not treat adult Dirofilaria and is not protection against ixodid pasture ticks. Test and stage heartworm risk as clinically appropriate and choose separate tick control when exposure exists.
  • Use the exact whole tablet for the current body-weight band; do not divide. Give with food or directly by mouth and observe complete swallowing. Reweigh growing or borderline patients before the next dose.
  • The exact-product feline studies are small and cover only part of the label. Recheck established mixed infection; one 54-cat report found persistent Dipylidium segments in isolated cases and used separate praziquantel.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Lufenuron40 mg/tablet Nitenpyram12 mg/tablet Moxidectin1.2 mg/tablet Praziquantel20 mg/tablet
Formulation Type
Tablet
Administration route
By mouth
Manufacturer (register)
INTER LEK LTD, Ukraine
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1580, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 12 Sep 2030
Veterinary (National Food Agency)
In the register: სუპერიუმ პანაცეა
№ 001001
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
5.6/10
Weak evidence support
vetman assessment

Superium Panacea

40/12/1.2/20 mg tablet N1 for dogs 2-8 kg
Assessed clinical scopeDog · Full labelled canine oral scope: fleas and FAD, lice, listed sarcoptiform and demodectic mites, gastrointestinal nematodes and cestodes, mixed infestations and heartworm-larval prevention · By mouth
Care settingVeterinary-selected home administration after parasite-risk assessment, with diagnostic follow-up when treating established infestation
vetman score 5.6/10 Weak evidence support
Evidence confidence: Low Georgia: Yes, veterinary · № 000946 · Verified on 21 Oct 2026

Mechanistically plausible and locally registered, but the exact canine combination has too little independent evidence for its very broad label. Prefer better-documented parasite-specific products when available and use this tablet only with explicit diagnostic and follow-up reasoning.

Regulatory and scientific credibility5.5/10

The exact canine strengths are registered in Georgia and have a current manufacturer instruction, but no EMA/FDA-style public assessment or comparable regulator dossier was found. Exact-product independent evidence for dogs was not identified, so ingredient evidence cannot substitute for the combination dossier.

Clinical efficacy5.0/10

The four ingredients have credible activity against their respective targets, including field evidence for lufenuron plus nitenpyram and separate moxidectin/praziquantel data. However, no robust independent trial of this exact canine four-drug tablet was found, so the unusually broad mite, helminth and heartworm-prevention claims remain incompletely validated.

Safety and tolerability5.0/10

The instruction lists rare neurological and gastrointestinal reactions and restricts use in debilitated, infectious, very young or very small animals and with other antiparasitics. Public target-animal safety and interaction data for the exact four-drug canine combination are sparse, and moxidectin warrants particular caution in ABCB1-sensitive dogs.

Clinical practicality8.0/10

One whole monthly weight-banded tablet can consolidate several parasite targets and avoids topical residue. Five canine weight bands support dose selection, but the tablet must not be split, complete swallowing must be confirmed and treatment schedules differ by parasite, with reassessment or repeat dosing for mites and severe helminth infection.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with known hypersensitivity, in emaciated animals or animals with infectious disease, or below 6 weeks of age or 0.5 kg body weight.
  • Do not administer concurrently with another antiparasitic. The regulator-approved feline SPC states that interaction data are unavailable; review all current medicines before use.
  • Rare neurological or gastrointestinal reactions can include tremor, seizures, depression, vomiting and digestive dysfunction. Stop and assess promptly if neurological signs, persistent vomiting or marked depression occurs.
  • Avoid during pregnancy and lactation unless a veterinarian determines that expected benefit outweighs risk; exact-combination reproductive safety is not established.
  • This tablet does not treat adult Dirofilaria and is not protection against ixodid pasture ticks. Test and stage heartworm risk as clinically appropriate and choose separate tick control when exposure exists.
  • Use the exact whole tablet for the current body-weight band; do not divide. Give with food or directly by mouth and observe complete swallowing. Reweigh growing or borderline patients before the next dose.
  • In Collies and other ABCB1-sensitive dogs, use moxidectin-containing treatment only at the exact labelled dose under veterinary supervision; avoid interacting P-glycoprotein substrates unless the individual risk is resolved.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Lufenuron40 mg/tablet Nitenpyram12 mg/tablet Moxidectin1.2 mg/tablet Praziquantel20 mg/tablet
Formulation Type
Tablet
Administration route
By mouth
Manufacturer (register)
INTER LEK LTD, Ukraine
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1506, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 12 Sep 2030
Veterinary (National Food Agency)
In the register: სუპერიუმ პანაცეა
№ 000946
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
5.6/10
Weak evidence support
vetman assessment

Superium Panacea

80/24/2.4/40 mg tablet, N1 for dogs 8-16 kg
Assessed clinical scopeDog · Full labelled canine oral scope: fleas and FAD, lice, listed sarcoptiform and demodectic mites, gastrointestinal nematodes and cestodes, mixed infestations and heartworm-larval prevention · By mouth
Care settingVeterinary-selected home administration after parasite-risk assessment, with diagnostic follow-up when treating established infestation
vetman score 5.6/10 Weak evidence support
Evidence confidence: Low Georgia: Yes, veterinary · № 000948 · Verified on 21 Oct 2026

Mechanistically plausible and locally registered, but the exact canine combination has too little independent evidence for its very broad label. Prefer better-documented parasite-specific products when available and use this tablet only with explicit diagnostic and follow-up reasoning.

Regulatory and scientific credibility5.5/10

The exact canine strengths are registered in Georgia and have a current manufacturer instruction, but no EMA/FDA-style public assessment or comparable regulator dossier was found. Exact-product independent evidence for dogs was not identified, so ingredient evidence cannot substitute for the combination dossier.

Clinical efficacy5.0/10

The four ingredients have credible activity against their respective targets, including field evidence for lufenuron plus nitenpyram and separate moxidectin/praziquantel data. However, no robust independent trial of this exact canine four-drug tablet was found, so the unusually broad mite, helminth and heartworm-prevention claims remain incompletely validated.

Safety and tolerability5.0/10

The instruction lists rare neurological and gastrointestinal reactions and restricts use in debilitated, infectious, very young or very small animals and with other antiparasitics. Public target-animal safety and interaction data for the exact four-drug canine combination are sparse, and moxidectin warrants particular caution in ABCB1-sensitive dogs.

Clinical practicality8.0/10

One whole monthly weight-banded tablet can consolidate several parasite targets and avoids topical residue. Five canine weight bands support dose selection, but the tablet must not be split, complete swallowing must be confirmed and treatment schedules differ by parasite, with reassessment or repeat dosing for mites and severe helminth infection.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with known hypersensitivity, in emaciated animals or animals with infectious disease, or below 6 weeks of age or 0.5 kg body weight.
  • Do not administer concurrently with another antiparasitic. The regulator-approved feline SPC states that interaction data are unavailable; review all current medicines before use.
  • Rare neurological or gastrointestinal reactions can include tremor, seizures, depression, vomiting and digestive dysfunction. Stop and assess promptly if neurological signs, persistent vomiting or marked depression occurs.
  • Avoid during pregnancy and lactation unless a veterinarian determines that expected benefit outweighs risk; exact-combination reproductive safety is not established.
  • This tablet does not treat adult Dirofilaria and is not protection against ixodid pasture ticks. Test and stage heartworm risk as clinically appropriate and choose separate tick control when exposure exists.
  • Use the exact whole tablet for the current body-weight band; do not divide. Give with food or directly by mouth and observe complete swallowing. Reweigh growing or borderline patients before the next dose.
  • In Collies and other ABCB1-sensitive dogs, use moxidectin-containing treatment only at the exact labelled dose under veterinary supervision; avoid interacting P-glycoprotein substrates unless the individual risk is resolved.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Lufenuron80 mg/tablet Nitenpyram24 mg/tablet Moxidectin2.4 mg/tablet Praziquantel40 mg/tablet
Formulation Type
Tablet
Administration route
By mouth
Manufacturer
Manufacturer (register)
INTER LEK LTD, Ukraine
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1508, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 15 Sep 2030
Veterinary (National Food Agency)
In the register: სუპერიუმ პანაცეა
№ 000948
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Cat
6.3/10
Situational / acceptable
vetman assessment

Superium Panacea

80/24/2.4/40 mg tablet N1 for cats 8-16 kg
Assessed clinical scopeCat · Full labelled feline oral scope: fleas and FAD, listed sarcoptiform and demodectic mites, gastrointestinal nematodes and cestodes, mixed infestations and heartworm-larval prevention · By mouth
Care settingVeterinary-selected home administration after parasite-risk assessment, with diagnostic follow-up when treating established infestation
vetman score 6.3/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 000948 · Verified on 21 Oct 2026

A convenient broad oral option with encouraging exact-product feline data, but not a strongly validated substitute for better-documented parasite-specific choices. Use after confirming the actual parasite spectrum and plan follow-up, especially for cestodes.

Regulatory and scientific credibility6.5/10

The exact feline strengths are currently registered in Georgia and have a valid prescription registration plus a detailed regulator-approved SPC in Moldova. The dossier is much less transparent than an EMA/FDA assessment and the broad label is supported mainly by small regional studies.

Clinical efficacy6.0/10

Small exact-product studies support flea and ear-mite activity and suggest benefit in mixed infestations, while established lufenuron/nitenpyram and moxidectin/praziquantel evidence supports component plausibility. The full mite, nematode, cestode and heartworm-prevention label has not been confirmed by robust controlled trials; one 54-cat report found residual Dipylidium segments requiring separate praziquantel.

Safety and tolerability5.5/10

Small studies report good short-term tolerance, but the approved SPC lists rare tremor, seizures, depression, vomiting and gastrointestinal dysfunction. Robust target-animal safety, reproductive and interaction datasets for the four-drug combination are not publicly available; pregnancy and lactation are restricted.

Clinical practicality7.5/10

A single whole weight-banded tablet can consolidate several parasite targets and is given monthly for continuous flea or heartworm prevention. It must not be split, complete swallowing must be observed, and voluntary tablet acceptance in cats is variable; established infestations may need repeat dosing and laboratory follow-up.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with known hypersensitivity, in emaciated animals or animals with infectious disease, or below 6 weeks of age or 0.5 kg body weight.
  • Do not administer concurrently with another antiparasitic. The regulator-approved feline SPC states that interaction data are unavailable; review all current medicines before use.
  • Rare neurological or gastrointestinal reactions can include tremor, seizures, depression, vomiting and digestive dysfunction. Stop and assess promptly if neurological signs, persistent vomiting or marked depression occurs.
  • Avoid during pregnancy and lactation unless a veterinarian determines that expected benefit outweighs risk; exact-combination reproductive safety is not established.
  • This tablet does not treat adult Dirofilaria and is not protection against ixodid pasture ticks. Test and stage heartworm risk as clinically appropriate and choose separate tick control when exposure exists.
  • Use the exact whole tablet for the current body-weight band; do not divide. Give with food or directly by mouth and observe complete swallowing. Reweigh growing or borderline patients before the next dose.
  • The exact-product feline studies are small and cover only part of the label. Recheck established mixed infection; one 54-cat report found persistent Dipylidium segments in isolated cases and used separate praziquantel.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Lufenuron80 mg/tablet Nitenpyram24 mg/tablet Moxidectin2.4 mg/tablet Praziquantel40 mg/tablet
Formulation Type
Tablet
Administration route
By mouth
Manufacturer (register)
INTER LEK LTD, Ukraine
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1508, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 15 Sep 2030
Veterinary (National Food Agency)
In the register: სუპერიუმ პანაცეა
№ 000948
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
5.6/10
Weak evidence support
vetman assessment

Superium Panacea

160/48/4.8/80 mg tablet N1 for dogs 16-30 kg
Assessed clinical scopeDog · Full labelled canine oral scope: fleas and FAD, lice, listed sarcoptiform and demodectic mites, gastrointestinal nematodes and cestodes, mixed infestations and heartworm-larval prevention · By mouth
Care settingVeterinary-selected home administration after parasite-risk assessment, with diagnostic follow-up when treating established infestation
vetman score 5.6/10 Weak evidence support
Evidence confidence: Low Georgia: Yes, veterinary · № 001000 · Verified on 21 Oct 2026

Mechanistically plausible and locally registered, but the exact canine combination has too little independent evidence for its very broad label. Prefer better-documented parasite-specific products when available and use this tablet only with explicit diagnostic and follow-up reasoning.

Regulatory and scientific credibility5.5/10

The exact canine strengths are registered in Georgia and have a current manufacturer instruction, but no EMA/FDA-style public assessment or comparable regulator dossier was found. Exact-product independent evidence for dogs was not identified, so ingredient evidence cannot substitute for the combination dossier.

Clinical efficacy5.0/10

The four ingredients have credible activity against their respective targets, including field evidence for lufenuron plus nitenpyram and separate moxidectin/praziquantel data. However, no robust independent trial of this exact canine four-drug tablet was found, so the unusually broad mite, helminth and heartworm-prevention claims remain incompletely validated.

Safety and tolerability5.0/10

The instruction lists rare neurological and gastrointestinal reactions and restricts use in debilitated, infectious, very young or very small animals and with other antiparasitics. Public target-animal safety and interaction data for the exact four-drug canine combination are sparse, and moxidectin warrants particular caution in ABCB1-sensitive dogs.

Clinical practicality8.0/10

One whole monthly weight-banded tablet can consolidate several parasite targets and avoids topical residue. Five canine weight bands support dose selection, but the tablet must not be split, complete swallowing must be confirmed and treatment schedules differ by parasite, with reassessment or repeat dosing for mites and severe helminth infection.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with known hypersensitivity, in emaciated animals or animals with infectious disease, or below 6 weeks of age or 0.5 kg body weight.
  • Do not administer concurrently with another antiparasitic. The regulator-approved feline SPC states that interaction data are unavailable; review all current medicines before use.
  • Rare neurological or gastrointestinal reactions can include tremor, seizures, depression, vomiting and digestive dysfunction. Stop and assess promptly if neurological signs, persistent vomiting or marked depression occurs.
  • Avoid during pregnancy and lactation unless a veterinarian determines that expected benefit outweighs risk; exact-combination reproductive safety is not established.
  • This tablet does not treat adult Dirofilaria and is not protection against ixodid pasture ticks. Test and stage heartworm risk as clinically appropriate and choose separate tick control when exposure exists.
  • Use the exact whole tablet for the current body-weight band; do not divide. Give with food or directly by mouth and observe complete swallowing. Reweigh growing or borderline patients before the next dose.
  • In Collies and other ABCB1-sensitive dogs, use moxidectin-containing treatment only at the exact labelled dose under veterinary supervision; avoid interacting P-glycoprotein substrates unless the individual risk is resolved.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Lufenuron160 mg/tablet Nitenpyram48 mg/tablet Moxidectin4.8 mg/tablet Praziquantel80 mg/tablet
Formulation Type
Tablet
Administration route
By mouth
Manufacturer (register)
INTER LEK LTD, Ukraine
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1579, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 12 Sep 2030
Veterinary (National Food Agency)
In the register: სუპერიუმ პანაცეა
№ 001000
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
5.6/10
Weak evidence support
vetman assessment

Superium Panacea

320/96/9.6/160 mg tablet N1 for dogs 30-60 kg
Assessed clinical scopeDog · Full labelled canine oral scope: fleas and FAD, lice, listed sarcoptiform and demodectic mites, gastrointestinal nematodes and cestodes, mixed infestations and heartworm-larval prevention · By mouth
Care settingVeterinary-selected home administration after parasite-risk assessment, with diagnostic follow-up when treating established infestation
vetman score 5.6/10 Weak evidence support
Evidence confidence: Low Georgia: Yes, veterinary · № 000947 · Verified on 21 Oct 2026

Mechanistically plausible and locally registered, but the exact canine combination has too little independent evidence for its very broad label. Prefer better-documented parasite-specific products when available and use this tablet only with explicit diagnostic and follow-up reasoning.

Regulatory and scientific credibility5.5/10

The exact canine strengths are registered in Georgia and have a current manufacturer instruction, but no EMA/FDA-style public assessment or comparable regulator dossier was found. Exact-product independent evidence for dogs was not identified, so ingredient evidence cannot substitute for the combination dossier.

Clinical efficacy5.0/10

The four ingredients have credible activity against their respective targets, including field evidence for lufenuron plus nitenpyram and separate moxidectin/praziquantel data. However, no robust independent trial of this exact canine four-drug tablet was found, so the unusually broad mite, helminth and heartworm-prevention claims remain incompletely validated.

Safety and tolerability5.0/10

The instruction lists rare neurological and gastrointestinal reactions and restricts use in debilitated, infectious, very young or very small animals and with other antiparasitics. Public target-animal safety and interaction data for the exact four-drug canine combination are sparse, and moxidectin warrants particular caution in ABCB1-sensitive dogs.

Clinical practicality8.0/10

One whole monthly weight-banded tablet can consolidate several parasite targets and avoids topical residue. Five canine weight bands support dose selection, but the tablet must not be split, complete swallowing must be confirmed and treatment schedules differ by parasite, with reassessment or repeat dosing for mites and severe helminth infection.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Do not use with known hypersensitivity, in emaciated animals or animals with infectious disease, or below 6 weeks of age or 0.5 kg body weight.
  • Do not administer concurrently with another antiparasitic. The regulator-approved feline SPC states that interaction data are unavailable; review all current medicines before use.
  • Rare neurological or gastrointestinal reactions can include tremor, seizures, depression, vomiting and digestive dysfunction. Stop and assess promptly if neurological signs, persistent vomiting or marked depression occurs.
  • Avoid during pregnancy and lactation unless a veterinarian determines that expected benefit outweighs risk; exact-combination reproductive safety is not established.
  • This tablet does not treat adult Dirofilaria and is not protection against ixodid pasture ticks. Test and stage heartworm risk as clinically appropriate and choose separate tick control when exposure exists.
  • Use the exact whole tablet for the current body-weight band; do not divide. Give with food or directly by mouth and observe complete swallowing. Reweigh growing or borderline patients before the next dose.
  • In Collies and other ABCB1-sensitive dogs, use moxidectin-containing treatment only at the exact labelled dose under veterinary supervision; avoid interacting P-glycoprotein substrates unless the individual risk is resolved.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Lufenuron320 mg/tablet Nitenpyram96 mg/tablet Moxidectin9.6 mg/tablet Praziquantel160 mg/tablet
Formulation Type
Tablet
Administration route
By mouth
Manufacturer (register)
INTER LEK LTD, Ukraine
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1507, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 12 Sep 2030
Veterinary (National Food Agency)
In the register: სუპერიუმ პანაცეა
№ 000947
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown

All of this shows in vetman as you prescribe

The dose for the patient's weight, registration in Georgia and controlled status, right on the prescription.