Register
Medicines reference
Product

Floximed

Ciprofloxacin · EIPICO

2 forms: eye drops, ointment. In force in Georgia: 2 of 2 (human register).

Forms and doses2 of 2 in force in Georgia

Form Dose Frequency Georgia
3 mg/g (0.3%), Ointment No label dose in the reference yet - Georgia Yes, human
In force until 03 Feb 2027
Human (Ministry of Health, RAMA)
In the register: Floximed 0.3% eye ointment 5 g
№ რ-034300
Verified on: 22 Oct 2026
Details: pack, label wording, sources, registration

Floximed 3 mg/g (0.3%), Ointment

eye ointment 5 g, human medicine
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 Veterinarian-directed ointment treatment of selected superficial susceptible bacterial ocular infection when prolonged surface contact is useful and corneal structural integrity permits safe application
4.8/10
Weak evidence support
vetman assessment

Floximed

3 mg/g (0.3%), eye ointment 5 g, human medicine
Assessed clinical scopeDog · Veterinarian-directed ointment treatment of selected superficial susceptible bacterial ocular infection when prolonged surface contact is useful and corneal structural integrity permits safe application · Into the eye
Care settingVeterinarian-directed clinic/home treatment after complete ocular examination, with early recheck and cytology/culture for deep, melting, recurrent, severe or nonresponsive disease.
vetman score 4.8/10 Weak evidence support
Evidence confidence: Low Georgia: Yes, human · № რ-034300 · Verified on 22 Oct 2026 Off-label use

A potentially useful retained-contact form for selected superficial susceptible infection, but direct veterinary ointment evidence is thin and it should not be used through a dangerously compromised cornea.

Regulatory and scientific credibility4.0/10

Exact strength, form, pack and current Georgian human registration are traceable, but no complete current Floximed regulator label or exact-product veterinary dossier was found; EU/GB/US status remains unknown. Because efficacy evidence is formulation-mismatched, the PLAYBOOK gate caps scientific credibility at 4.0.

Clinical efficacy3.5/10

The active can treat susceptible superficial infection, but ointment comparator evidence is human conjunctivitis-focused and does not establish Floximed canine keratitis outcomes, intensive-ulcer exposure or superiority over solution/other agents.

Safety and tolerability6.0/10

Topical systemic exposure is expected to be low, but exact Floximed excipients and target-animal safety are undocumented; irritation, blur, keratopathy, contamination, hypersensitivity and tube-tip trauma or intraocular ointment entry are clinically important.

Clinical practicality6.5/10

Ointment can prolong surface contact and reduce administration frequency in selected superficial disease, but causes temporary blur, must be applied last and is unsuitable when contact trauma or passage through a compromised cornea is plausible.

Full-course cost-effectiveness-

No verified current Georgian patient-adjusted full-course price is available, so cost is excluded.

Important safety and use flags

  • Human ophthalmic medicine used off-label in dogs and cats. The exact Georgian human registration does not establish veterinary authorisation, animal efficacy or a product-specific animal dose.
  • Do not treat an undifferentiated red or painful eye empirically. Perform complete ocular examination, fluorescein staining and tear-film/ocular-surface assessment; identify trauma, foreign body, dry eye, uveitis, glaucoma, viral, fungal or immune-mediated disease.
  • Obtain cytology and culture/susceptibility for deep, stromal, melting, rapidly progressive, recurrent, previously treated or nonresponsive keratitis, preferably before the first dose when this will not dangerously delay treatment.
  • Ciprofloxacin is strong against many Pseudomonas isolates but does not reliably cover Streptococcus or every ocular isolate. Do not assume class-wide or regional susceptibility; combine, narrow or change treatment from findings and response.
  • No exact Floximed dog/cat regimen is established. Do not transfer the 25–50 mg/kg oral ciprofloxacin dose, a human comparator schedule, another fluoroquinolone schedule or solution frequency to ointment.
  • Apply ointment after all other topical eye medicines and avoid use where tube-tip trauma or passage through a melting, perforated, freshly operated or structurally weak cornea is plausible.
  • Never inject into the eye. Use one container for one patient, preserve tip sterility, close promptly and follow the exact pack discard/storage instruction; these Floximed in-use details were not independently verified.
  • Monitor pain, blepharospasm, discharge, hyperaemia, corneal opacity, staining, crystalline deposit, epitheliopathy, irritation, allergy and vision. Worsening, melting, perforation or vision change needs urgent ophthalmic reassessment.
  • Reassess early and document an objective response. De-escalate, narrow, combine, change or stop according to culture, susceptibility, epithelial healing and diagnosis; do not extend fluoroquinolone exposure solely because redness persists.
  • Exact safety in puppies/kittens, pregnancy, lactation, breeding animals, severe dry eye and prolonged or repeated courses is not established. Low systemic exposure from comparator products is not proof of exact Floximed safety.
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 Veterinarian-directed ointment treatment of selected superficial susceptible bacterial ocular infection when prolonged surface contact is useful and corneal structural integrity permits safe application
4.7/10
Weak evidence support
vetman assessment

Floximed

3 mg/g (0.3%), eye ointment 5 g, human medicine
Assessed clinical scopeCat · Veterinarian-directed ointment treatment of selected superficial susceptible bacterial ocular infection when prolonged surface contact is useful and corneal structural integrity permits safe application · Into the eye
Care settingVeterinarian-directed clinic/home treatment after complete ocular examination, with early recheck and cytology/culture for deep, melting, recurrent, severe or nonresponsive disease.
vetman score 4.7/10 Weak evidence support
Evidence confidence: Low Georgia: Yes, human · № რ-034300 · Verified on 22 Oct 2026 Off-label use

A potentially useful retained-contact form for selected superficial susceptible infection, but direct veterinary ointment evidence is thin and it should not be used through a dangerously compromised cornea.

Regulatory and scientific credibility4.0/10

Exact strength, form, pack and current Georgian human registration are traceable, but no complete current Floximed regulator label or exact-product veterinary dossier was found; EU/GB/US status remains unknown. Because efficacy evidence is formulation-mismatched, the PLAYBOOK gate caps scientific credibility at 4.0.

Clinical efficacy3.0/10

Ciprofloxacin has useful feline isolate activity, but the ointment form lacks direct feline outcome or PK evidence and should not be extrapolated to deep, melting or mixed-pathogen disease from solution susceptibility alone.

Safety and tolerability6.0/10

Topical systemic exposure is expected to be low, but exact Floximed excipients and target-animal safety are undocumented; irritation, blur, keratopathy, contamination, hypersensitivity and tube-tip trauma or intraocular ointment entry are clinically important.

Clinical practicality6.5/10

Ointment can prolong surface contact and reduce administration frequency in selected superficial disease, but causes temporary blur, must be applied last and is unsuitable when contact trauma or passage through a compromised cornea is plausible.

Full-course cost-effectiveness-

No verified current Georgian patient-adjusted full-course price is available, so cost is excluded.

Important safety and use flags

  • Human ophthalmic medicine used off-label in dogs and cats. The exact Georgian human registration does not establish veterinary authorisation, animal efficacy or a product-specific animal dose.
  • Do not treat an undifferentiated red or painful eye empirically. Perform complete ocular examination, fluorescein staining and tear-film/ocular-surface assessment; identify trauma, foreign body, dry eye, uveitis, glaucoma, viral, fungal or immune-mediated disease.
  • Obtain cytology and culture/susceptibility for deep, stromal, melting, rapidly progressive, recurrent, previously treated or nonresponsive keratitis, preferably before the first dose when this will not dangerously delay treatment.
  • Ciprofloxacin is strong against many Pseudomonas isolates but does not reliably cover Streptococcus or every ocular isolate. Do not assume class-wide or regional susceptibility; combine, narrow or change treatment from findings and response.
  • No exact Floximed dog/cat regimen is established. Do not transfer the 25–50 mg/kg oral ciprofloxacin dose, a human comparator schedule, another fluoroquinolone schedule or solution frequency to ointment.
  • Apply ointment after all other topical eye medicines and avoid use where tube-tip trauma or passage through a melting, perforated, freshly operated or structurally weak cornea is plausible.
  • Never inject into the eye. Use one container for one patient, preserve tip sterility, close promptly and follow the exact pack discard/storage instruction; these Floximed in-use details were not independently verified.
  • Monitor pain, blepharospasm, discharge, hyperaemia, corneal opacity, staining, crystalline deposit, epitheliopathy, irritation, allergy and vision. Worsening, melting, perforation or vision change needs urgent ophthalmic reassessment.
  • Reassess early and document an objective response. De-escalate, narrow, combine, change or stop according to culture, susceptibility, epithelial healing and diagnosis; do not extend fluoroquinolone exposure solely because redness persists.
  • Exact safety in puppies/kittens, pregnancy, lactation, breeding animals, severe dry eye and prolonged or repeated courses is not established. Low systemic exposure from comparator products is not proof of exact Floximed safety.
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
Formulation Type
Ointment
Administration route
Into the eye
Manufacturer
EIPICO · Egypt
Registration
Georgia Yes, human
In force until 03 Feb 2027
Human (Ministry of Health, RAMA)
In the register: Floximed 0.3% eye ointment 5 g
№ რ-034300
Verified on: 22 Oct 2026
EU Not confirmed
UK Not confirmed
Verified on: 23 Oct 2026
US Not confirmed
Verified on: 23 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
Information not fully verified No product-specific veterinary dose is established. Do not transfer the oral 25–50 mg/kg ciprofloxacin dose or a human comparator schedule. Select frequency and duration from diagnosis, depth/severity, cytology/culture, susceptibility, response and ophthalmic review.
3 mg/ml (0.3%), Eye drops No label dose in the reference yet - Georgia Yes, human
In force until 09 Feb 2028
Human (Ministry of Health, RAMA)
In the register: Floximed 0.3% eye drops 5 ml
№ რ-037297
Verified on: 22 Oct 2026
Details: pack, label wording, sources, registration

Floximed 3 mg/ml (0.3%), Eye drops

eye drops 5 ml, human medicine
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 Veterinarian-directed topical treatment of a diagnosed susceptible bacterial ocular-surface infection, including selected infected keratitis; culture-led for complicated disease
4.9/10
Weak evidence support
vetman assessment

Floximed

3 mg/ml (0.3%), eye drops 5 ml, human medicine
Assessed clinical scopeDog · Veterinarian-directed topical treatment of a diagnosed susceptible bacterial ocular-surface infection, including selected infected keratitis; culture-led for complicated disease · Into the eye
Care settingVeterinarian-directed clinic/home treatment after complete ocular examination, with early recheck and cytology/culture for deep, melting, recurrent, severe or nonresponsive disease.
vetman score 4.9/10 Weak evidence support
Evidence confidence: Low Georgia: Yes, human · № რ-037297 · Verified on 22 Oct 2026 Off-label use

Useful culture-aware topical fluoroquinolone activity, strongest for susceptible Gram-negative infection, but incomplete exact-product documentation and variable streptococcal/overall coverage prevent routine monotherapy claims.

Regulatory and scientific credibility4.0/10

Exact strength, form, pack and current Georgian human registration are traceable, but no complete current Floximed regulator label or exact-product veterinary dossier was found; EU/GB/US status remains unknown. Because efficacy evidence is formulation-mismatched, the PLAYBOOK gate caps scientific credibility at 4.0.

Clinical efficacy4.0/10

Canine isolate and ocular-PK studies support useful Gram-negative, especially Pseudomonas, activity, but only 69% overall susceptibility in one large cohort, poor Streptococcus coverage, regional variation and absent exact-product outcomes make monotherapy situational.

Safety and tolerability6.5/10

Topical comparator exposure is low and immature-dog ocular study found no articular lesions, but Floximed excipients, sterility/in-use limits and dog/cat safety are incompletely documented; irritation, deposits, keratopathy, contamination and hypersensitivity remain relevant.

Clinical practicality5.5/10

Drops avoid tube contact and allow intensive treatment, but severe keratitis may require dosing every one to few hours, multiple agents, culture and frequent rechecks; no exact Floximed animal schedule or calibrated drop volume is established.

Full-course cost-effectiveness-

No verified current Georgian patient-adjusted full-course price is available, so cost is excluded.

Important safety and use flags

  • Human ophthalmic medicine used off-label in dogs and cats. The exact Georgian human registration does not establish veterinary authorisation, animal efficacy or a product-specific animal dose.
  • Do not treat an undifferentiated red or painful eye empirically. Perform complete ocular examination, fluorescein staining and tear-film/ocular-surface assessment; identify trauma, foreign body, dry eye, uveitis, glaucoma, viral, fungal or immune-mediated disease.
  • Obtain cytology and culture/susceptibility for deep, stromal, melting, rapidly progressive, recurrent, previously treated or nonresponsive keratitis, preferably before the first dose when this will not dangerously delay treatment.
  • Ciprofloxacin is strong against many Pseudomonas isolates but does not reliably cover Streptococcus or every ocular isolate. Do not assume class-wide or regional susceptibility; combine, narrow or change treatment from findings and response.
  • No exact Floximed dog/cat regimen is established. Do not transfer the 25–50 mg/kg oral ciprofloxacin dose, a human comparator schedule, another fluoroquinolone schedule or solution frequency to ointment.
  • Keep topical eye medicines at least five minutes apart; if ointment is also prescribed, use it last. Do not let the dropper tip touch eye, eyelid, hair, fingers or another surface.
  • Never inject into the eye. Use one container for one patient, preserve tip sterility, close promptly and follow the exact pack discard/storage instruction; these Floximed in-use details were not independently verified.
  • Monitor pain, blepharospasm, discharge, hyperaemia, corneal opacity, staining, crystalline deposit, epitheliopathy, irritation, allergy and vision. Worsening, melting, perforation or vision change needs urgent ophthalmic reassessment.
  • Reassess early and document an objective response. De-escalate, narrow, combine, change or stop according to culture, susceptibility, epithelial healing and diagnosis; do not extend fluoroquinolone exposure solely because redness persists.
  • Exact safety in puppies/kittens, pregnancy, lactation, breeding animals, severe dry eye and prolonged or repeated courses is not established. Low systemic exposure from comparator products is not proof of exact Floximed safety.
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 Veterinarian-directed topical treatment of a diagnosed susceptible bacterial ocular-surface infection, including selected infected keratitis; culture-led for complicated disease
4.9/10
Weak evidence support
vetman assessment

Floximed

3 mg/ml (0.3%), eye drops 5 ml, human medicine
Assessed clinical scopeCat · Veterinarian-directed topical treatment of a diagnosed susceptible bacterial ocular-surface infection, including selected infected keratitis; culture-led for complicated disease · Into the eye
Care settingVeterinarian-directed clinic/home treatment after complete ocular examination, with early recheck and cytology/culture for deep, melting, recurrent, severe or nonresponsive disease.
vetman score 4.9/10 Weak evidence support
Evidence confidence: Low Georgia: Yes, human · № რ-037297 · Verified on 22 Oct 2026 Off-label use

Useful culture-aware topical fluoroquinolone activity, strongest for susceptible Gram-negative infection, but incomplete exact-product documentation and variable streptococcal/overall coverage prevent routine monotherapy claims.

Regulatory and scientific credibility4.0/10

Exact strength, form, pack and current Georgian human registration are traceable, but no complete current Floximed regulator label or exact-product veterinary dossier was found; EU/GB/US status remains unknown. Because efficacy evidence is formulation-mismatched, the PLAYBOOK gate caps scientific credibility at 4.0.

Clinical efficacy4.0/10

A feline referral cohort found 94% ciprofloxacin susceptibility and supports it among initial keratitis options, but evidence is retrospective and in-vitro, regional resistance matters and no exact-product feline outcome trial exists.

Safety and tolerability6.5/10

Topical comparator exposure is low and immature-dog ocular study found no articular lesions, but Floximed excipients, sterility/in-use limits and dog/cat safety are incompletely documented; irritation, deposits, keratopathy, contamination and hypersensitivity remain relevant.

Clinical practicality5.5/10

Drops avoid tube contact and allow intensive treatment, but severe keratitis may require dosing every one to few hours, multiple agents, culture and frequent rechecks; no exact Floximed animal schedule or calibrated drop volume is established.

Full-course cost-effectiveness-

No verified current Georgian patient-adjusted full-course price is available, so cost is excluded.

Important safety and use flags

  • Human ophthalmic medicine used off-label in dogs and cats. The exact Georgian human registration does not establish veterinary authorisation, animal efficacy or a product-specific animal dose.
  • Do not treat an undifferentiated red or painful eye empirically. Perform complete ocular examination, fluorescein staining and tear-film/ocular-surface assessment; identify trauma, foreign body, dry eye, uveitis, glaucoma, viral, fungal or immune-mediated disease.
  • Obtain cytology and culture/susceptibility for deep, stromal, melting, rapidly progressive, recurrent, previously treated or nonresponsive keratitis, preferably before the first dose when this will not dangerously delay treatment.
  • Ciprofloxacin is strong against many Pseudomonas isolates but does not reliably cover Streptococcus or every ocular isolate. Do not assume class-wide or regional susceptibility; combine, narrow or change treatment from findings and response.
  • No exact Floximed dog/cat regimen is established. Do not transfer the 25–50 mg/kg oral ciprofloxacin dose, a human comparator schedule, another fluoroquinolone schedule or solution frequency to ointment.
  • Keep topical eye medicines at least five minutes apart; if ointment is also prescribed, use it last. Do not let the dropper tip touch eye, eyelid, hair, fingers or another surface.
  • Never inject into the eye. Use one container for one patient, preserve tip sterility, close promptly and follow the exact pack discard/storage instruction; these Floximed in-use details were not independently verified.
  • Monitor pain, blepharospasm, discharge, hyperaemia, corneal opacity, staining, crystalline deposit, epitheliopathy, irritation, allergy and vision. Worsening, melting, perforation or vision change needs urgent ophthalmic reassessment.
  • Reassess early and document an objective response. De-escalate, narrow, combine, change or stop according to culture, susceptibility, epithelial healing and diagnosis; do not extend fluoroquinolone exposure solely because redness persists.
  • Exact safety in puppies/kittens, pregnancy, lactation, breeding animals, severe dry eye and prolonged or repeated courses is not established. Low systemic exposure from comparator products is not proof of exact Floximed safety.
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
Ciprofloxacin3 mg/ml
Formulation Type
Eye drops
Administration route
Into the eye
Manufacturer
EIPICO · Egypt
Registration
Georgia Yes, human
In force until 09 Feb 2028
Human (Ministry of Health, RAMA)
In the register: Floximed 0.3% eye drops 5 ml
№ რ-037297
Verified on: 22 Oct 2026
EU Not confirmed
UK Not confirmed
Verified on: 23 Oct 2026
US Not confirmed
Verified on: 23 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
Information not fully verified No product-specific veterinary dose is established. Do not transfer the oral 25–50 mg/kg ciprofloxacin dose or a human comparator schedule. Select frequency and duration from diagnosis, depth/severity, cytology/culture, susceptibility, response and ophthalmic review.

Ciprofloxacin: No dose supported by a publicly verifiable source yet

Known Contraindications

  • Critical
    Do not use ciprofloxacin in patients with known hypersensitivity to ciprofloxacin or another fluoroquinolone.
  • Warning
    Both ciprofloxacin and moxifloxacin have been associated with potentially fatal antimicrobial-induced colitis.
    Sources: MSD Vet Manual
  • Warning
    Avoid excessive or prolonged quinolone use in immature animals because cartilage erosion and permanent lameness have occurred in growing dogs and foals.
    Sources: MSD Vet Manual
  • Warning (Cat)
    Not well absorbed in cats
    Sources: MSD Vet Manual

Known Drug Interactions

  • Major warning Ciprofloxacin + Aminophylline
    Serious and fatal reactions have been reported in patients receiving concurrent administration of CIPRO and theophylline. These reactions have included cardiac arrest, seizure, status epilepticus, and respiratory failure. Avoid Use (Plasma Exposure Likely to be Increased and Prolonged)
    Recommendation: Avoid concurrent use when possible. If the combination is unavoidable, monitor serum theophylline and reduce the aminophylline dose as needed. Watch for nausea, vomiting, tremor, excitation, tachycardia, and seizures.
    Sources: FDA
  • Major warning Theophylline + Ciprofloxacin
    Serious and fatal reactions have been reported in patients receiving concurrent administration of CIPRO and theophylline. These reactions have included cardiac arrest, seizure, status epilepticus, and respiratory failure. Avoid Use (Plasma Exposure Likely to be Increased and Prolonged)
    Recommendation: Avoid concurrent use when possible. If the combination is unavoidable, monitor serum theophylline and reduce its dose as needed. Watch for nausea, vomiting, tremor, excitation, tachycardia, and seizures.
    Sources: FDA

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.