Register
Medicines reference
Active substance

Glucose

Carbohydrate infusion solution. Registered in Georgia: 1 veterinary product and 6 human medicines. Forms: emulsion, solution.

Dose and use

Doses

We have no dose with a cited source for this substance yet.

Before use

Safety information

Known Contraindications

  • Critical
    Do not use glucose-containing infusion solutions in animals with hyperglycaemia unless specifically required and closely monitored.
    Sources: VMD SPC · VMD
  • Critical
    Do not use in animals with pre-existing peripheral oedema caused by a reduction in intravascular oncotic pressure.
    Sources: VMD SPC · VMD
  • Warning
    Use with particular caution in diabetes mellitus.
    Sources: VMD SPC · VMD
  • Warning
    Use with particular caution in hypoadrenocorticism (Addison disease).
    Sources: VMD SPC · VMD
  • Warning
    Use with particular caution in anuria. This product contains no electrolytes; monitor electrolyte and phosphate balance.
    Sources: VMD SPC · VMD
Latin name
Glucose
Georgian name
გლუკოზა
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
7 of 7 forms
Human medicines in Georgia
Ardeanutrisol G
Human medicines with this substance in the Georgian register of medicines (Ministry of Health), checked on 18 Oct 2026. They are human medicines, not veterinary products; strengths and forms differ.
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 registration7

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

Glucose Decefrag 10%, Solution

solution for infusion, 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 Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition
6.2/10
Situational / acceptable
vetman assessment

Glucose Decefrag

10%, solution for infusion, human medicine
Assessed clinical scopeDog · Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition · Intravenous
Care settingVeterinary clinic or hospital with immediate point-of-care glucose measurement, central venous access or validated dilution for peripheral use, infusion control and serial glucose, electrolyte, osmolality and fluid-balance monitoring
vetman score 6.2/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, human · № რ-041771 · Verified on 16 Oct 2026 Off-label use

Clinically valuable for measured hypoglycaemia when rapid, titratable glucose is needed, but the exact 10% bag is a hypertonic hospital tool rather than a general-purpose fluid. Use a central line or validate peripheral dilution, monitor glucose and electrolytes closely, treat the cause, and avoid reflex continuation after the endpoint is reached.

Regulatory and scientific credibility5.5/10

The exact 10% human infusion has a sourced current Georgian registration with identifiable manufacturer, strength and IV route, while exhaustive current checks record it as not registered in EU/EEA, GB or US. Veterinary administration is off-label; current foreign class labels and veterinary guidance support dextrose rather than any one of these exact products.

Clinical efficacy7.0/10

IV dextrose is an established, rapidly effective intervention for clinically important hypoglycaemia in dogs and cats and is listed as an essential veterinary medicine. The exact 10% bag can supply a controlled infusion, but routine dog/cat guidance usually targets 1.25–5% after an initial bolus; benefit depends on diagnosing and treating the cause, and comparative exact-product outcome evidence is absent.

Safety and tolerability6.0/10

At 100 mg/ml and about 505 mOsm/L, this is a hypertonic glucose solution. Excess dose or rate can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration, electrolyte shifts and fluid overload; peripheral infusion risks phlebitis and extravasation injury. Rapid glucose-driven insulin release can worsen hypokalaemia or hypophosphataemia and can produce rebound hypoglycaemia in hyperinsulinaemic disease.

Clinical practicality6.5/10

The ready sterile bag permits a controlled central infusion and exact calculation at 0.1 g/ml, but concentrations above 5% are preferably central-line solutions in dogs and cats. Peripheral use generally requires aseptic dilution, compatibility and final-osmolality checks, an infusion pump, frequent bedside glucose measurement and a plan to taper or stop once oral/enteral control or normoglycaemia is sustained.

Full-course cost-effectiveness-

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

Important safety and use flags

  • Do not administer 10% dextrose to a patient with clinically significant hyperglycaemia or known dextrose/excipient hypersensitivity. Confirm a reliable glucose result and the treatment endpoint; neurologic signs alone do not prove hypoglycaemia.
  • Ten-percent dextrose is hypertonic and concentrations above 5% should preferably use a central venous line in dogs and cats. For peripheral delivery, prepare a validated lower final concentration aseptically, use a pump, inspect the catheter frequently and stop immediately for pain, swelling, erythema, phlebitis or extravasation.
  • Do not administer 10% dextrose simultaneously with blood products through the same administration set because pseudoagglutination or haemolysis can occur. Use a separate compatible line and follow the blood component and exact fluid instructions.
  • Measure glucose frequently during initiation and every rate change, then titrate to the lowest concentration and rate that controls clinical signs without marked hyperglycaemia. Excess delivery can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration and potentially fatal neurologic or fluid complications.
  • Monitor potassium, phosphate, sodium, magnesium, osmolality, urine output and total fluid balance. Glucose-stimulated insulin can shift potassium and phosphate intracellularly; after dextrose metabolism the delivered water can contribute to dilutional hyponatraemia and overload, especially with renal, cardiac or pulmonary disease.
  • In insulinoma or another hyperinsulinaemic state, large glucose boluses can provoke further insulin release and rebound hypoglycaemia. Treat symptomatic hypoglycaemia with the lowest effective dose, reassess rapidly, provide definitive disease management and consider alternative support when escalating dextrose fails.
  • Do not use this electrolyte-free 10% solution for volume resuscitation, as a routine maintenance prescription or as complete parenteral nutrition. Correct hypovolaemia with an appropriate crystalloid, supply required electrolytes and nutrition separately, and include dextrose carrier volume in the total daily fluid plan.
  • Before adding a medicine, confirm its prescribed diluent, final concentration, osmolarity, pH, stability and line compatibility from current instructions. Use only a clear intact single-dose container, maintain asepsis, never pool or share remnants and discard unused solution after the allowed handling interval.
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 Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition
6.2/10
Situational / acceptable
vetman assessment

Glucose Decefrag

10%, solution for infusion, human medicine
Assessed clinical scopeCat · Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition · Intravenous
Care settingVeterinary clinic or hospital with immediate point-of-care glucose measurement, central venous access or validated dilution for peripheral use, infusion control and serial glucose, electrolyte, osmolality and fluid-balance monitoring
vetman score 6.2/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, human · № რ-041771 · Verified on 16 Oct 2026 Off-label use

Clinically valuable for measured hypoglycaemia when rapid, titratable glucose is needed, but the exact 10% bag is a hypertonic hospital tool rather than a general-purpose fluid. Use a central line or validate peripheral dilution, monitor glucose and electrolytes closely, treat the cause, and avoid reflex continuation after the endpoint is reached.

Regulatory and scientific credibility5.5/10

The exact 10% human infusion has a sourced current Georgian registration with identifiable manufacturer, strength and IV route, while exhaustive current checks record it as not registered in EU/EEA, GB or US. Veterinary administration is off-label; current foreign class labels and veterinary guidance support dextrose rather than any one of these exact products.

Clinical efficacy7.0/10

IV dextrose is an established, rapidly effective intervention for clinically important hypoglycaemia in dogs and cats and is listed as an essential veterinary medicine. The exact 10% bag can supply a controlled infusion, but routine dog/cat guidance usually targets 1.25–5% after an initial bolus; benefit depends on diagnosing and treating the cause, and comparative exact-product outcome evidence is absent.

Safety and tolerability6.0/10

At 100 mg/ml and about 505 mOsm/L, this is a hypertonic glucose solution. Excess dose or rate can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration, electrolyte shifts and fluid overload; peripheral infusion risks phlebitis and extravasation injury. Rapid glucose-driven insulin release can worsen hypokalaemia or hypophosphataemia and can produce rebound hypoglycaemia in hyperinsulinaemic disease.

Clinical practicality6.5/10

The ready sterile bag permits a controlled central infusion and exact calculation at 0.1 g/ml, but concentrations above 5% are preferably central-line solutions in dogs and cats. Peripheral use generally requires aseptic dilution, compatibility and final-osmolality checks, an infusion pump, frequent bedside glucose measurement and a plan to taper or stop once oral/enteral control or normoglycaemia is sustained.

Full-course cost-effectiveness-

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

Important safety and use flags

  • Do not administer 10% dextrose to a patient with clinically significant hyperglycaemia or known dextrose/excipient hypersensitivity. Confirm a reliable glucose result and the treatment endpoint; neurologic signs alone do not prove hypoglycaemia.
  • Ten-percent dextrose is hypertonic and concentrations above 5% should preferably use a central venous line in dogs and cats. For peripheral delivery, prepare a validated lower final concentration aseptically, use a pump, inspect the catheter frequently and stop immediately for pain, swelling, erythema, phlebitis or extravasation.
  • Do not administer 10% dextrose simultaneously with blood products through the same administration set because pseudoagglutination or haemolysis can occur. Use a separate compatible line and follow the blood component and exact fluid instructions.
  • Measure glucose frequently during initiation and every rate change, then titrate to the lowest concentration and rate that controls clinical signs without marked hyperglycaemia. Excess delivery can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration and potentially fatal neurologic or fluid complications.
  • Monitor potassium, phosphate, sodium, magnesium, osmolality, urine output and total fluid balance. Glucose-stimulated insulin can shift potassium and phosphate intracellularly; after dextrose metabolism the delivered water can contribute to dilutional hyponatraemia and overload, especially with renal, cardiac or pulmonary disease.
  • In insulinoma or another hyperinsulinaemic state, large glucose boluses can provoke further insulin release and rebound hypoglycaemia. Treat symptomatic hypoglycaemia with the lowest effective dose, reassess rapidly, provide definitive disease management and consider alternative support when escalating dextrose fails.
  • Do not use this electrolyte-free 10% solution for volume resuscitation, as a routine maintenance prescription or as complete parenteral nutrition. Correct hypovolaemia with an appropriate crystalloid, supply required electrolytes and nutrition separately, and include dextrose carrier volume in the total daily fluid plan.
  • Before adding a medicine, confirm its prescribed diluent, final concentration, osmolarity, pH, stability and line compatibility from current instructions. Use only a clear intact single-dose container, maintain asepsis, never pool or share remnants and discard unused solution after the allowed handling interval.
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
Glucose100 mg/ml
Formulation Type
Solution
Administration route
Intravenous
Registration
Georgia Yes, human
In force until 06 Aug 2029
Human (Ministry of Health, RAMA)
In the register: გლუკოზა დეცეფრაგი 10%, საინფუზიო ხსნარი
№ რ-041771
Verified on: 16 Oct 2026
EU No
UK No
Verified on: 16 Oct 2026
US No
Verified on: 16 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

Glucose Dentafill Plus 10%, Solution

solution for infusion, 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 Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition
6.2/10
Situational / acceptable
vetman assessment

Glucose Dentafill Plus

10%, solution for infusion, human medicine
Assessed clinical scopeDog · Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition · Intravenous
Care settingVeterinary clinic or hospital with immediate point-of-care glucose measurement, central venous access or validated dilution for peripheral use, infusion control and serial glucose, electrolyte, osmolality and fluid-balance monitoring
vetman score 6.2/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, human · № რ-035628, რ-035629, რ-035630 · Verified on 16 Oct 2026 Off-label use

Clinically valuable for measured hypoglycaemia when rapid, titratable glucose is needed, but the exact 10% bag is a hypertonic hospital tool rather than a general-purpose fluid. Use a central line or validate peripheral dilution, monitor glucose and electrolytes closely, treat the cause, and avoid reflex continuation after the endpoint is reached.

Regulatory and scientific credibility5.5/10

The exact 10% human infusion has a sourced current Georgian registration with identifiable manufacturer, strength and IV route, while exhaustive current checks record it as not registered in EU/EEA, GB or US. Veterinary administration is off-label; current foreign class labels and veterinary guidance support dextrose rather than any one of these exact products.

Clinical efficacy7.0/10

IV dextrose is an established, rapidly effective intervention for clinically important hypoglycaemia in dogs and cats and is listed as an essential veterinary medicine. The exact 10% bag can supply a controlled infusion, but routine dog/cat guidance usually targets 1.25–5% after an initial bolus; benefit depends on diagnosing and treating the cause, and comparative exact-product outcome evidence is absent.

Safety and tolerability6.0/10

At 100 mg/ml and about 505 mOsm/L, this is a hypertonic glucose solution. Excess dose or rate can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration, electrolyte shifts and fluid overload; peripheral infusion risks phlebitis and extravasation injury. Rapid glucose-driven insulin release can worsen hypokalaemia or hypophosphataemia and can produce rebound hypoglycaemia in hyperinsulinaemic disease.

Clinical practicality6.5/10

The ready sterile bag permits a controlled central infusion and exact calculation at 0.1 g/ml, but concentrations above 5% are preferably central-line solutions in dogs and cats. Peripheral use generally requires aseptic dilution, compatibility and final-osmolality checks, an infusion pump, frequent bedside glucose measurement and a plan to taper or stop once oral/enteral control or normoglycaemia is sustained.

Full-course cost-effectiveness-

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

Important safety and use flags

  • Do not administer 10% dextrose to a patient with clinically significant hyperglycaemia or known dextrose/excipient hypersensitivity. Confirm a reliable glucose result and the treatment endpoint; neurologic signs alone do not prove hypoglycaemia.
  • Ten-percent dextrose is hypertonic and concentrations above 5% should preferably use a central venous line in dogs and cats. For peripheral delivery, prepare a validated lower final concentration aseptically, use a pump, inspect the catheter frequently and stop immediately for pain, swelling, erythema, phlebitis or extravasation.
  • Do not administer 10% dextrose simultaneously with blood products through the same administration set because pseudoagglutination or haemolysis can occur. Use a separate compatible line and follow the blood component and exact fluid instructions.
  • Measure glucose frequently during initiation and every rate change, then titrate to the lowest concentration and rate that controls clinical signs without marked hyperglycaemia. Excess delivery can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration and potentially fatal neurologic or fluid complications.
  • Monitor potassium, phosphate, sodium, magnesium, osmolality, urine output and total fluid balance. Glucose-stimulated insulin can shift potassium and phosphate intracellularly; after dextrose metabolism the delivered water can contribute to dilutional hyponatraemia and overload, especially with renal, cardiac or pulmonary disease.
  • In insulinoma or another hyperinsulinaemic state, large glucose boluses can provoke further insulin release and rebound hypoglycaemia. Treat symptomatic hypoglycaemia with the lowest effective dose, reassess rapidly, provide definitive disease management and consider alternative support when escalating dextrose fails.
  • Do not use this electrolyte-free 10% solution for volume resuscitation, as a routine maintenance prescription or as complete parenteral nutrition. Correct hypovolaemia with an appropriate crystalloid, supply required electrolytes and nutrition separately, and include dextrose carrier volume in the total daily fluid plan.
  • Before adding a medicine, confirm its prescribed diluent, final concentration, osmolarity, pH, stability and line compatibility from current instructions. Use only a clear intact single-dose container, maintain asepsis, never pool or share remnants and discard unused solution after the allowed handling interval.
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 Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition
6.2/10
Situational / acceptable
vetman assessment

Glucose Dentafill Plus

10%, solution for infusion, human medicine
Assessed clinical scopeCat · Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition · Intravenous
Care settingVeterinary clinic or hospital with immediate point-of-care glucose measurement, central venous access or validated dilution for peripheral use, infusion control and serial glucose, electrolyte, osmolality and fluid-balance monitoring
vetman score 6.2/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, human · № რ-035628, რ-035629, რ-035630 · Verified on 16 Oct 2026 Off-label use

Clinically valuable for measured hypoglycaemia when rapid, titratable glucose is needed, but the exact 10% bag is a hypertonic hospital tool rather than a general-purpose fluid. Use a central line or validate peripheral dilution, monitor glucose and electrolytes closely, treat the cause, and avoid reflex continuation after the endpoint is reached.

Regulatory and scientific credibility5.5/10

The exact 10% human infusion has a sourced current Georgian registration with identifiable manufacturer, strength and IV route, while exhaustive current checks record it as not registered in EU/EEA, GB or US. Veterinary administration is off-label; current foreign class labels and veterinary guidance support dextrose rather than any one of these exact products.

Clinical efficacy7.0/10

IV dextrose is an established, rapidly effective intervention for clinically important hypoglycaemia in dogs and cats and is listed as an essential veterinary medicine. The exact 10% bag can supply a controlled infusion, but routine dog/cat guidance usually targets 1.25–5% after an initial bolus; benefit depends on diagnosing and treating the cause, and comparative exact-product outcome evidence is absent.

Safety and tolerability6.0/10

At 100 mg/ml and about 505 mOsm/L, this is a hypertonic glucose solution. Excess dose or rate can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration, electrolyte shifts and fluid overload; peripheral infusion risks phlebitis and extravasation injury. Rapid glucose-driven insulin release can worsen hypokalaemia or hypophosphataemia and can produce rebound hypoglycaemia in hyperinsulinaemic disease.

Clinical practicality6.5/10

The ready sterile bag permits a controlled central infusion and exact calculation at 0.1 g/ml, but concentrations above 5% are preferably central-line solutions in dogs and cats. Peripheral use generally requires aseptic dilution, compatibility and final-osmolality checks, an infusion pump, frequent bedside glucose measurement and a plan to taper or stop once oral/enteral control or normoglycaemia is sustained.

Full-course cost-effectiveness-

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

Important safety and use flags

  • Do not administer 10% dextrose to a patient with clinically significant hyperglycaemia or known dextrose/excipient hypersensitivity. Confirm a reliable glucose result and the treatment endpoint; neurologic signs alone do not prove hypoglycaemia.
  • Ten-percent dextrose is hypertonic and concentrations above 5% should preferably use a central venous line in dogs and cats. For peripheral delivery, prepare a validated lower final concentration aseptically, use a pump, inspect the catheter frequently and stop immediately for pain, swelling, erythema, phlebitis or extravasation.
  • Do not administer 10% dextrose simultaneously with blood products through the same administration set because pseudoagglutination or haemolysis can occur. Use a separate compatible line and follow the blood component and exact fluid instructions.
  • Measure glucose frequently during initiation and every rate change, then titrate to the lowest concentration and rate that controls clinical signs without marked hyperglycaemia. Excess delivery can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration and potentially fatal neurologic or fluid complications.
  • Monitor potassium, phosphate, sodium, magnesium, osmolality, urine output and total fluid balance. Glucose-stimulated insulin can shift potassium and phosphate intracellularly; after dextrose metabolism the delivered water can contribute to dilutional hyponatraemia and overload, especially with renal, cardiac or pulmonary disease.
  • In insulinoma or another hyperinsulinaemic state, large glucose boluses can provoke further insulin release and rebound hypoglycaemia. Treat symptomatic hypoglycaemia with the lowest effective dose, reassess rapidly, provide definitive disease management and consider alternative support when escalating dextrose fails.
  • Do not use this electrolyte-free 10% solution for volume resuscitation, as a routine maintenance prescription or as complete parenteral nutrition. Correct hypovolaemia with an appropriate crystalloid, supply required electrolytes and nutrition separately, and include dextrose carrier volume in the total daily fluid plan.
  • Before adding a medicine, confirm its prescribed diluent, final concentration, osmolarity, pH, stability and line compatibility from current instructions. Use only a clear intact single-dose container, maintain asepsis, never pool or share remnants and discard unused solution after the allowed handling interval.
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
Glucose100 mg/ml
Formulation Type
Solution
Administration route
Intravenous
Manufacturer
Dentafill Plus · Uzbekistan
Registration
Georgia Yes, human
In force until 22 Jun 2027
Human (Ministry of Health, RAMA)
In the register: გლუკოზა დენტაფილ პლუსი 10%, საინფუზიო ხსნარი
№ რ-035628, რ-035629, რ-035630
Verified on: 16 Oct 2026
EU No
UK No
Verified on: 16 Oct 2026
US No
Verified on: 16 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

Glucose Pharmatech 10%, Solution

solution for infusion, 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 Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition
6.2/10
Situational / acceptable
vetman assessment

Glucose Pharmatech

10%, solution for infusion, human medicine
Assessed clinical scopeDog · Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition · Intravenous
Care settingVeterinary clinic or hospital with immediate point-of-care glucose measurement, central venous access or validated dilution for peripheral use, infusion control and serial glucose, electrolyte, osmolality and fluid-balance monitoring
vetman score 6.2/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, human · № რ-035638 · Verified on 16 Oct 2026 Off-label use

Clinically valuable for measured hypoglycaemia when rapid, titratable glucose is needed, but the exact 10% bag is a hypertonic hospital tool rather than a general-purpose fluid. Use a central line or validate peripheral dilution, monitor glucose and electrolytes closely, treat the cause, and avoid reflex continuation after the endpoint is reached.

Regulatory and scientific credibility5.5/10

The exact 10% human infusion has a sourced current Georgian registration with identifiable manufacturer, strength and IV route, while exhaustive current checks record it as not registered in EU/EEA, GB or US. Veterinary administration is off-label; current foreign class labels and veterinary guidance support dextrose rather than any one of these exact products.

Clinical efficacy7.0/10

IV dextrose is an established, rapidly effective intervention for clinically important hypoglycaemia in dogs and cats and is listed as an essential veterinary medicine. The exact 10% bag can supply a controlled infusion, but routine dog/cat guidance usually targets 1.25–5% after an initial bolus; benefit depends on diagnosing and treating the cause, and comparative exact-product outcome evidence is absent.

Safety and tolerability6.0/10

At 100 mg/ml and about 505 mOsm/L, this is a hypertonic glucose solution. Excess dose or rate can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration, electrolyte shifts and fluid overload; peripheral infusion risks phlebitis and extravasation injury. Rapid glucose-driven insulin release can worsen hypokalaemia or hypophosphataemia and can produce rebound hypoglycaemia in hyperinsulinaemic disease.

Clinical practicality6.5/10

The ready sterile bag permits a controlled central infusion and exact calculation at 0.1 g/ml, but concentrations above 5% are preferably central-line solutions in dogs and cats. Peripheral use generally requires aseptic dilution, compatibility and final-osmolality checks, an infusion pump, frequent bedside glucose measurement and a plan to taper or stop once oral/enteral control or normoglycaemia is sustained.

Full-course cost-effectiveness-

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

Important safety and use flags

  • Do not administer 10% dextrose to a patient with clinically significant hyperglycaemia or known dextrose/excipient hypersensitivity. Confirm a reliable glucose result and the treatment endpoint; neurologic signs alone do not prove hypoglycaemia.
  • Ten-percent dextrose is hypertonic and concentrations above 5% should preferably use a central venous line in dogs and cats. For peripheral delivery, prepare a validated lower final concentration aseptically, use a pump, inspect the catheter frequently and stop immediately for pain, swelling, erythema, phlebitis or extravasation.
  • Do not administer 10% dextrose simultaneously with blood products through the same administration set because pseudoagglutination or haemolysis can occur. Use a separate compatible line and follow the blood component and exact fluid instructions.
  • Measure glucose frequently during initiation and every rate change, then titrate to the lowest concentration and rate that controls clinical signs without marked hyperglycaemia. Excess delivery can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration and potentially fatal neurologic or fluid complications.
  • Monitor potassium, phosphate, sodium, magnesium, osmolality, urine output and total fluid balance. Glucose-stimulated insulin can shift potassium and phosphate intracellularly; after dextrose metabolism the delivered water can contribute to dilutional hyponatraemia and overload, especially with renal, cardiac or pulmonary disease.
  • In insulinoma or another hyperinsulinaemic state, large glucose boluses can provoke further insulin release and rebound hypoglycaemia. Treat symptomatic hypoglycaemia with the lowest effective dose, reassess rapidly, provide definitive disease management and consider alternative support when escalating dextrose fails.
  • Do not use this electrolyte-free 10% solution for volume resuscitation, as a routine maintenance prescription or as complete parenteral nutrition. Correct hypovolaemia with an appropriate crystalloid, supply required electrolytes and nutrition separately, and include dextrose carrier volume in the total daily fluid plan.
  • Before adding a medicine, confirm its prescribed diluent, final concentration, osmolarity, pH, stability and line compatibility from current instructions. Use only a clear intact single-dose container, maintain asepsis, never pool or share remnants and discard unused solution after the allowed handling interval.
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 Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition
6.2/10
Situational / acceptable
vetman assessment

Glucose Pharmatech

10%, solution for infusion, human medicine
Assessed clinical scopeCat · Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition · Intravenous
Care settingVeterinary clinic or hospital with immediate point-of-care glucose measurement, central venous access or validated dilution for peripheral use, infusion control and serial glucose, electrolyte, osmolality and fluid-balance monitoring
vetman score 6.2/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, human · № რ-035638 · Verified on 16 Oct 2026 Off-label use

Clinically valuable for measured hypoglycaemia when rapid, titratable glucose is needed, but the exact 10% bag is a hypertonic hospital tool rather than a general-purpose fluid. Use a central line or validate peripheral dilution, monitor glucose and electrolytes closely, treat the cause, and avoid reflex continuation after the endpoint is reached.

Regulatory and scientific credibility5.5/10

The exact 10% human infusion has a sourced current Georgian registration with identifiable manufacturer, strength and IV route, while exhaustive current checks record it as not registered in EU/EEA, GB or US. Veterinary administration is off-label; current foreign class labels and veterinary guidance support dextrose rather than any one of these exact products.

Clinical efficacy7.0/10

IV dextrose is an established, rapidly effective intervention for clinically important hypoglycaemia in dogs and cats and is listed as an essential veterinary medicine. The exact 10% bag can supply a controlled infusion, but routine dog/cat guidance usually targets 1.25–5% after an initial bolus; benefit depends on diagnosing and treating the cause, and comparative exact-product outcome evidence is absent.

Safety and tolerability6.0/10

At 100 mg/ml and about 505 mOsm/L, this is a hypertonic glucose solution. Excess dose or rate can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration, electrolyte shifts and fluid overload; peripheral infusion risks phlebitis and extravasation injury. Rapid glucose-driven insulin release can worsen hypokalaemia or hypophosphataemia and can produce rebound hypoglycaemia in hyperinsulinaemic disease.

Clinical practicality6.5/10

The ready sterile bag permits a controlled central infusion and exact calculation at 0.1 g/ml, but concentrations above 5% are preferably central-line solutions in dogs and cats. Peripheral use generally requires aseptic dilution, compatibility and final-osmolality checks, an infusion pump, frequent bedside glucose measurement and a plan to taper or stop once oral/enteral control or normoglycaemia is sustained.

Full-course cost-effectiveness-

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

Important safety and use flags

  • Do not administer 10% dextrose to a patient with clinically significant hyperglycaemia or known dextrose/excipient hypersensitivity. Confirm a reliable glucose result and the treatment endpoint; neurologic signs alone do not prove hypoglycaemia.
  • Ten-percent dextrose is hypertonic and concentrations above 5% should preferably use a central venous line in dogs and cats. For peripheral delivery, prepare a validated lower final concentration aseptically, use a pump, inspect the catheter frequently and stop immediately for pain, swelling, erythema, phlebitis or extravasation.
  • Do not administer 10% dextrose simultaneously with blood products through the same administration set because pseudoagglutination or haemolysis can occur. Use a separate compatible line and follow the blood component and exact fluid instructions.
  • Measure glucose frequently during initiation and every rate change, then titrate to the lowest concentration and rate that controls clinical signs without marked hyperglycaemia. Excess delivery can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration and potentially fatal neurologic or fluid complications.
  • Monitor potassium, phosphate, sodium, magnesium, osmolality, urine output and total fluid balance. Glucose-stimulated insulin can shift potassium and phosphate intracellularly; after dextrose metabolism the delivered water can contribute to dilutional hyponatraemia and overload, especially with renal, cardiac or pulmonary disease.
  • In insulinoma or another hyperinsulinaemic state, large glucose boluses can provoke further insulin release and rebound hypoglycaemia. Treat symptomatic hypoglycaemia with the lowest effective dose, reassess rapidly, provide definitive disease management and consider alternative support when escalating dextrose fails.
  • Do not use this electrolyte-free 10% solution for volume resuscitation, as a routine maintenance prescription or as complete parenteral nutrition. Correct hypovolaemia with an appropriate crystalloid, supply required electrolytes and nutrition separately, and include dextrose carrier volume in the total daily fluid plan.
  • Before adding a medicine, confirm its prescribed diluent, final concentration, osmolarity, pH, stability and line compatibility from current instructions. Use only a clear intact single-dose container, maintain asepsis, never pool or share remnants and discard unused solution after the allowed handling interval.
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
Glucose100 mg/ml
Formulation Type
Solution
Administration route
Intravenous
Manufacturer
Registration
Georgia Yes, human
In force until 22 Jun 2027
Human (Ministry of Health, RAMA)
In the register: გლუკოზა ფარმატექი 10%, საინფუზიო ხსნარი
№ რ-035638
Verified on: 16 Oct 2026
EU No
UK No
Verified on: 16 Oct 2026
US No
Verified on: 16 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

Glucose Reka-Med 10%, Solution

solution for infusion, 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 Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition
6.2/10
Situational / acceptable
vetman assessment

Glucose Reka-Med

10%, solution for infusion, human medicine
Assessed clinical scopeDog · Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition · Intravenous
Care settingVeterinary clinic or hospital with immediate point-of-care glucose measurement, central venous access or validated dilution for peripheral use, infusion control and serial glucose, electrolyte, osmolality and fluid-balance monitoring
vetman score 6.2/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, human · № რ-035421 · Verified on 16 Oct 2026 Off-label use

Clinically valuable for measured hypoglycaemia when rapid, titratable glucose is needed, but the exact 10% bag is a hypertonic hospital tool rather than a general-purpose fluid. Use a central line or validate peripheral dilution, monitor glucose and electrolytes closely, treat the cause, and avoid reflex continuation after the endpoint is reached.

Regulatory and scientific credibility5.5/10

The exact 10% human infusion has a sourced current Georgian registration with identifiable manufacturer, strength and IV route, while exhaustive current checks record it as not registered in EU/EEA, GB or US. Veterinary administration is off-label; current foreign class labels and veterinary guidance support dextrose rather than any one of these exact products.

Clinical efficacy7.0/10

IV dextrose is an established, rapidly effective intervention for clinically important hypoglycaemia in dogs and cats and is listed as an essential veterinary medicine. The exact 10% bag can supply a controlled infusion, but routine dog/cat guidance usually targets 1.25–5% after an initial bolus; benefit depends on diagnosing and treating the cause, and comparative exact-product outcome evidence is absent.

Safety and tolerability6.0/10

At 100 mg/ml and about 505 mOsm/L, this is a hypertonic glucose solution. Excess dose or rate can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration, electrolyte shifts and fluid overload; peripheral infusion risks phlebitis and extravasation injury. Rapid glucose-driven insulin release can worsen hypokalaemia or hypophosphataemia and can produce rebound hypoglycaemia in hyperinsulinaemic disease.

Clinical practicality6.5/10

The ready sterile bag permits a controlled central infusion and exact calculation at 0.1 g/ml, but concentrations above 5% are preferably central-line solutions in dogs and cats. Peripheral use generally requires aseptic dilution, compatibility and final-osmolality checks, an infusion pump, frequent bedside glucose measurement and a plan to taper or stop once oral/enteral control or normoglycaemia is sustained.

Full-course cost-effectiveness-

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

Important safety and use flags

  • Do not administer 10% dextrose to a patient with clinically significant hyperglycaemia or known dextrose/excipient hypersensitivity. Confirm a reliable glucose result and the treatment endpoint; neurologic signs alone do not prove hypoglycaemia.
  • Ten-percent dextrose is hypertonic and concentrations above 5% should preferably use a central venous line in dogs and cats. For peripheral delivery, prepare a validated lower final concentration aseptically, use a pump, inspect the catheter frequently and stop immediately for pain, swelling, erythema, phlebitis or extravasation.
  • Do not administer 10% dextrose simultaneously with blood products through the same administration set because pseudoagglutination or haemolysis can occur. Use a separate compatible line and follow the blood component and exact fluid instructions.
  • Measure glucose frequently during initiation and every rate change, then titrate to the lowest concentration and rate that controls clinical signs without marked hyperglycaemia. Excess delivery can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration and potentially fatal neurologic or fluid complications.
  • Monitor potassium, phosphate, sodium, magnesium, osmolality, urine output and total fluid balance. Glucose-stimulated insulin can shift potassium and phosphate intracellularly; after dextrose metabolism the delivered water can contribute to dilutional hyponatraemia and overload, especially with renal, cardiac or pulmonary disease.
  • In insulinoma or another hyperinsulinaemic state, large glucose boluses can provoke further insulin release and rebound hypoglycaemia. Treat symptomatic hypoglycaemia with the lowest effective dose, reassess rapidly, provide definitive disease management and consider alternative support when escalating dextrose fails.
  • Do not use this electrolyte-free 10% solution for volume resuscitation, as a routine maintenance prescription or as complete parenteral nutrition. Correct hypovolaemia with an appropriate crystalloid, supply required electrolytes and nutrition separately, and include dextrose carrier volume in the total daily fluid plan.
  • Before adding a medicine, confirm its prescribed diluent, final concentration, osmolarity, pH, stability and line compatibility from current instructions. Use only a clear intact single-dose container, maintain asepsis, never pool or share remnants and discard unused solution after the allowed handling interval.
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 Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition
6.2/10
Situational / acceptable
vetman assessment

Glucose Reka-Med

10%, solution for infusion, human medicine
Assessed clinical scopeCat · Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition · Intravenous
Care settingVeterinary clinic or hospital with immediate point-of-care glucose measurement, central venous access or validated dilution for peripheral use, infusion control and serial glucose, electrolyte, osmolality and fluid-balance monitoring
vetman score 6.2/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, human · № რ-035421 · Verified on 16 Oct 2026 Off-label use

Clinically valuable for measured hypoglycaemia when rapid, titratable glucose is needed, but the exact 10% bag is a hypertonic hospital tool rather than a general-purpose fluid. Use a central line or validate peripheral dilution, monitor glucose and electrolytes closely, treat the cause, and avoid reflex continuation after the endpoint is reached.

Regulatory and scientific credibility5.5/10

The exact 10% human infusion has a sourced current Georgian registration with identifiable manufacturer, strength and IV route, while exhaustive current checks record it as not registered in EU/EEA, GB or US. Veterinary administration is off-label; current foreign class labels and veterinary guidance support dextrose rather than any one of these exact products.

Clinical efficacy7.0/10

IV dextrose is an established, rapidly effective intervention for clinically important hypoglycaemia in dogs and cats and is listed as an essential veterinary medicine. The exact 10% bag can supply a controlled infusion, but routine dog/cat guidance usually targets 1.25–5% after an initial bolus; benefit depends on diagnosing and treating the cause, and comparative exact-product outcome evidence is absent.

Safety and tolerability6.0/10

At 100 mg/ml and about 505 mOsm/L, this is a hypertonic glucose solution. Excess dose or rate can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration, electrolyte shifts and fluid overload; peripheral infusion risks phlebitis and extravasation injury. Rapid glucose-driven insulin release can worsen hypokalaemia or hypophosphataemia and can produce rebound hypoglycaemia in hyperinsulinaemic disease.

Clinical practicality6.5/10

The ready sterile bag permits a controlled central infusion and exact calculation at 0.1 g/ml, but concentrations above 5% are preferably central-line solutions in dogs and cats. Peripheral use generally requires aseptic dilution, compatibility and final-osmolality checks, an infusion pump, frequent bedside glucose measurement and a plan to taper or stop once oral/enteral control or normoglycaemia is sustained.

Full-course cost-effectiveness-

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

Important safety and use flags

  • Do not administer 10% dextrose to a patient with clinically significant hyperglycaemia or known dextrose/excipient hypersensitivity. Confirm a reliable glucose result and the treatment endpoint; neurologic signs alone do not prove hypoglycaemia.
  • Ten-percent dextrose is hypertonic and concentrations above 5% should preferably use a central venous line in dogs and cats. For peripheral delivery, prepare a validated lower final concentration aseptically, use a pump, inspect the catheter frequently and stop immediately for pain, swelling, erythema, phlebitis or extravasation.
  • Do not administer 10% dextrose simultaneously with blood products through the same administration set because pseudoagglutination or haemolysis can occur. Use a separate compatible line and follow the blood component and exact fluid instructions.
  • Measure glucose frequently during initiation and every rate change, then titrate to the lowest concentration and rate that controls clinical signs without marked hyperglycaemia. Excess delivery can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration and potentially fatal neurologic or fluid complications.
  • Monitor potassium, phosphate, sodium, magnesium, osmolality, urine output and total fluid balance. Glucose-stimulated insulin can shift potassium and phosphate intracellularly; after dextrose metabolism the delivered water can contribute to dilutional hyponatraemia and overload, especially with renal, cardiac or pulmonary disease.
  • In insulinoma or another hyperinsulinaemic state, large glucose boluses can provoke further insulin release and rebound hypoglycaemia. Treat symptomatic hypoglycaemia with the lowest effective dose, reassess rapidly, provide definitive disease management and consider alternative support when escalating dextrose fails.
  • Do not use this electrolyte-free 10% solution for volume resuscitation, as a routine maintenance prescription or as complete parenteral nutrition. Correct hypovolaemia with an appropriate crystalloid, supply required electrolytes and nutrition separately, and include dextrose carrier volume in the total daily fluid plan.
  • Before adding a medicine, confirm its prescribed diluent, final concentration, osmolarity, pH, stability and line compatibility from current instructions. Use only a clear intact single-dose container, maintain asepsis, never pool or share remnants and discard unused solution after the allowed handling interval.
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
Glucose100 mg/ml
Formulation Type
Solution
Administration route
Intravenous
Manufacturer
Registration
Georgia Yes, human
In force until 01 Jun 2027
Human (Ministry of Health, RAMA)
In the register: გლუკოზა რეკა-მედი 10%, საინფუზიო ხსნარი
№ რ-035421
Verified on: 16 Oct 2026
EU No
UK No
Verified on: 16 Oct 2026
US No
Verified on: 16 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

Neofleks Dextrose 10%, Solution

solution for infusion, 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 Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition
6.2/10
Situational / acceptable
vetman assessment

Neofleks Dextrose

10%, solution for infusion, human medicine
Assessed clinical scopeDog · Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition · Intravenous
Care settingVeterinary clinic or hospital with immediate point-of-care glucose measurement, central venous access or validated dilution for peripheral use, infusion control and serial glucose, electrolyte, osmolality and fluid-balance monitoring
vetman score 6.2/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, human · № რ-039076 · Verified on 16 Oct 2026 Off-label use

Clinically valuable for measured hypoglycaemia when rapid, titratable glucose is needed, but the exact 10% bag is a hypertonic hospital tool rather than a general-purpose fluid. Use a central line or validate peripheral dilution, monitor glucose and electrolytes closely, treat the cause, and avoid reflex continuation after the endpoint is reached.

Regulatory and scientific credibility5.5/10

The exact 10% human infusion has a sourced current Georgian registration with identifiable manufacturer, strength and IV route, while exhaustive current checks record it as not registered in EU/EEA, GB or US. Veterinary administration is off-label; current foreign class labels and veterinary guidance support dextrose rather than any one of these exact products.

Clinical efficacy7.0/10

IV dextrose is an established, rapidly effective intervention for clinically important hypoglycaemia in dogs and cats and is listed as an essential veterinary medicine. The exact 10% bag can supply a controlled infusion, but routine dog/cat guidance usually targets 1.25–5% after an initial bolus; benefit depends on diagnosing and treating the cause, and comparative exact-product outcome evidence is absent.

Safety and tolerability6.0/10

At 100 mg/ml and about 505 mOsm/L, this is a hypertonic glucose solution. Excess dose or rate can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration, electrolyte shifts and fluid overload; peripheral infusion risks phlebitis and extravasation injury. Rapid glucose-driven insulin release can worsen hypokalaemia or hypophosphataemia and can produce rebound hypoglycaemia in hyperinsulinaemic disease.

Clinical practicality6.5/10

The ready sterile bag permits a controlled central infusion and exact calculation at 0.1 g/ml, but concentrations above 5% are preferably central-line solutions in dogs and cats. Peripheral use generally requires aseptic dilution, compatibility and final-osmolality checks, an infusion pump, frequent bedside glucose measurement and a plan to taper or stop once oral/enteral control or normoglycaemia is sustained.

Full-course cost-effectiveness-

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

Important safety and use flags

  • Do not administer 10% dextrose to a patient with clinically significant hyperglycaemia or known dextrose/excipient hypersensitivity. Confirm a reliable glucose result and the treatment endpoint; neurologic signs alone do not prove hypoglycaemia.
  • Ten-percent dextrose is hypertonic and concentrations above 5% should preferably use a central venous line in dogs and cats. For peripheral delivery, prepare a validated lower final concentration aseptically, use a pump, inspect the catheter frequently and stop immediately for pain, swelling, erythema, phlebitis or extravasation.
  • Do not administer 10% dextrose simultaneously with blood products through the same administration set because pseudoagglutination or haemolysis can occur. Use a separate compatible line and follow the blood component and exact fluid instructions.
  • Measure glucose frequently during initiation and every rate change, then titrate to the lowest concentration and rate that controls clinical signs without marked hyperglycaemia. Excess delivery can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration and potentially fatal neurologic or fluid complications.
  • Monitor potassium, phosphate, sodium, magnesium, osmolality, urine output and total fluid balance. Glucose-stimulated insulin can shift potassium and phosphate intracellularly; after dextrose metabolism the delivered water can contribute to dilutional hyponatraemia and overload, especially with renal, cardiac or pulmonary disease.
  • In insulinoma or another hyperinsulinaemic state, large glucose boluses can provoke further insulin release and rebound hypoglycaemia. Treat symptomatic hypoglycaemia with the lowest effective dose, reassess rapidly, provide definitive disease management and consider alternative support when escalating dextrose fails.
  • Do not use this electrolyte-free 10% solution for volume resuscitation, as a routine maintenance prescription or as complete parenteral nutrition. Correct hypovolaemia with an appropriate crystalloid, supply required electrolytes and nutrition separately, and include dextrose carrier volume in the total daily fluid plan.
  • Before adding a medicine, confirm its prescribed diluent, final concentration, osmolarity, pH, stability and line compatibility from current instructions. Use only a clear intact single-dose container, maintain asepsis, never pool or share remnants and discard unused solution after the allowed handling interval.
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 Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition
6.2/10
Situational / acceptable
vetman assessment

Neofleks Dextrose

10%, solution for infusion, human medicine
Assessed clinical scopeCat · Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition · Intravenous
Care settingVeterinary clinic or hospital with immediate point-of-care glucose measurement, central venous access or validated dilution for peripheral use, infusion control and serial glucose, electrolyte, osmolality and fluid-balance monitoring
vetman score 6.2/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, human · № რ-039076 · Verified on 16 Oct 2026 Off-label use

Clinically valuable for measured hypoglycaemia when rapid, titratable glucose is needed, but the exact 10% bag is a hypertonic hospital tool rather than a general-purpose fluid. Use a central line or validate peripheral dilution, monitor glucose and electrolytes closely, treat the cause, and avoid reflex continuation after the endpoint is reached.

Regulatory and scientific credibility5.5/10

The exact 10% human infusion has a sourced current Georgian registration with identifiable manufacturer, strength and IV route, while exhaustive current checks record it as not registered in EU/EEA, GB or US. Veterinary administration is off-label; current foreign class labels and veterinary guidance support dextrose rather than any one of these exact products.

Clinical efficacy7.0/10

IV dextrose is an established, rapidly effective intervention for clinically important hypoglycaemia in dogs and cats and is listed as an essential veterinary medicine. The exact 10% bag can supply a controlled infusion, but routine dog/cat guidance usually targets 1.25–5% after an initial bolus; benefit depends on diagnosing and treating the cause, and comparative exact-product outcome evidence is absent.

Safety and tolerability6.0/10

At 100 mg/ml and about 505 mOsm/L, this is a hypertonic glucose solution. Excess dose or rate can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration, electrolyte shifts and fluid overload; peripheral infusion risks phlebitis and extravasation injury. Rapid glucose-driven insulin release can worsen hypokalaemia or hypophosphataemia and can produce rebound hypoglycaemia in hyperinsulinaemic disease.

Clinical practicality6.5/10

The ready sterile bag permits a controlled central infusion and exact calculation at 0.1 g/ml, but concentrations above 5% are preferably central-line solutions in dogs and cats. Peripheral use generally requires aseptic dilution, compatibility and final-osmolality checks, an infusion pump, frequent bedside glucose measurement and a plan to taper or stop once oral/enteral control or normoglycaemia is sustained.

Full-course cost-effectiveness-

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

Important safety and use flags

  • Do not administer 10% dextrose to a patient with clinically significant hyperglycaemia or known dextrose/excipient hypersensitivity. Confirm a reliable glucose result and the treatment endpoint; neurologic signs alone do not prove hypoglycaemia.
  • Ten-percent dextrose is hypertonic and concentrations above 5% should preferably use a central venous line in dogs and cats. For peripheral delivery, prepare a validated lower final concentration aseptically, use a pump, inspect the catheter frequently and stop immediately for pain, swelling, erythema, phlebitis or extravasation.
  • Do not administer 10% dextrose simultaneously with blood products through the same administration set because pseudoagglutination or haemolysis can occur. Use a separate compatible line and follow the blood component and exact fluid instructions.
  • Measure glucose frequently during initiation and every rate change, then titrate to the lowest concentration and rate that controls clinical signs without marked hyperglycaemia. Excess delivery can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration and potentially fatal neurologic or fluid complications.
  • Monitor potassium, phosphate, sodium, magnesium, osmolality, urine output and total fluid balance. Glucose-stimulated insulin can shift potassium and phosphate intracellularly; after dextrose metabolism the delivered water can contribute to dilutional hyponatraemia and overload, especially with renal, cardiac or pulmonary disease.
  • In insulinoma or another hyperinsulinaemic state, large glucose boluses can provoke further insulin release and rebound hypoglycaemia. Treat symptomatic hypoglycaemia with the lowest effective dose, reassess rapidly, provide definitive disease management and consider alternative support when escalating dextrose fails.
  • Do not use this electrolyte-free 10% solution for volume resuscitation, as a routine maintenance prescription or as complete parenteral nutrition. Correct hypovolaemia with an appropriate crystalloid, supply required electrolytes and nutrition separately, and include dextrose carrier volume in the total daily fluid plan.
  • Before adding a medicine, confirm its prescribed diluent, final concentration, osmolarity, pH, stability and line compatibility from current instructions. Use only a clear intact single-dose container, maintain asepsis, never pool or share remnants and discard unused solution after the allowed handling interval.
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
Glucose100 mg/ml
Formulation Type
Solution
Administration route
Intravenous
Manufacturer
Turktipsan · Türkiye
Registration
Georgia Yes, human
In force until 14 Sep 2028
Human (Ministry of Health, RAMA)
In the register: ნეოფლექსი დექსტროზა 10%, საინფუზიო ხსნარი
№ რ-039076
Verified on: 16 Oct 2026
EU No
UK No
Verified on: 16 Oct 2026
US No
Verified on: 16 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

Polifleks Dextrose 10%, Solution

solution for infusion, 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 Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition
6.2/10
Situational / acceptable
vetman assessment

Polifleks Dextrose

10%, solution for infusion, human medicine
Assessed clinical scopeDog · Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition · Intravenous
Care settingVeterinary clinic or hospital with immediate point-of-care glucose measurement, central venous access or validated dilution for peripheral use, infusion control and serial glucose, electrolyte, osmolality and fluid-balance monitoring
vetman score 6.2/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, human · № რ-046076 · Verified on 16 Oct 2026 Off-label use

Clinically valuable for measured hypoglycaemia when rapid, titratable glucose is needed, but the exact 10% bag is a hypertonic hospital tool rather than a general-purpose fluid. Use a central line or validate peripheral dilution, monitor glucose and electrolytes closely, treat the cause, and avoid reflex continuation after the endpoint is reached.

Regulatory and scientific credibility5.5/10

The exact 10% human infusion has a sourced current Georgian registration with identifiable manufacturer, strength and IV route, while exhaustive current checks record it as not registered in EU/EEA, GB or US. Veterinary administration is off-label; current foreign class labels and veterinary guidance support dextrose rather than any one of these exact products.

Clinical efficacy7.0/10

IV dextrose is an established, rapidly effective intervention for clinically important hypoglycaemia in dogs and cats and is listed as an essential veterinary medicine. The exact 10% bag can supply a controlled infusion, but routine dog/cat guidance usually targets 1.25–5% after an initial bolus; benefit depends on diagnosing and treating the cause, and comparative exact-product outcome evidence is absent.

Safety and tolerability6.0/10

At 100 mg/ml and about 505 mOsm/L, this is a hypertonic glucose solution. Excess dose or rate can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration, electrolyte shifts and fluid overload; peripheral infusion risks phlebitis and extravasation injury. Rapid glucose-driven insulin release can worsen hypokalaemia or hypophosphataemia and can produce rebound hypoglycaemia in hyperinsulinaemic disease.

Clinical practicality6.5/10

The ready sterile bag permits a controlled central infusion and exact calculation at 0.1 g/ml, but concentrations above 5% are preferably central-line solutions in dogs and cats. Peripheral use generally requires aseptic dilution, compatibility and final-osmolality checks, an infusion pump, frequent bedside glucose measurement and a plan to taper or stop once oral/enteral control or normoglycaemia is sustained.

Full-course cost-effectiveness-

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

Important safety and use flags

  • Do not administer 10% dextrose to a patient with clinically significant hyperglycaemia or known dextrose/excipient hypersensitivity. Confirm a reliable glucose result and the treatment endpoint; neurologic signs alone do not prove hypoglycaemia.
  • Ten-percent dextrose is hypertonic and concentrations above 5% should preferably use a central venous line in dogs and cats. For peripheral delivery, prepare a validated lower final concentration aseptically, use a pump, inspect the catheter frequently and stop immediately for pain, swelling, erythema, phlebitis or extravasation.
  • Do not administer 10% dextrose simultaneously with blood products through the same administration set because pseudoagglutination or haemolysis can occur. Use a separate compatible line and follow the blood component and exact fluid instructions.
  • Measure glucose frequently during initiation and every rate change, then titrate to the lowest concentration and rate that controls clinical signs without marked hyperglycaemia. Excess delivery can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration and potentially fatal neurologic or fluid complications.
  • Monitor potassium, phosphate, sodium, magnesium, osmolality, urine output and total fluid balance. Glucose-stimulated insulin can shift potassium and phosphate intracellularly; after dextrose metabolism the delivered water can contribute to dilutional hyponatraemia and overload, especially with renal, cardiac or pulmonary disease.
  • In insulinoma or another hyperinsulinaemic state, large glucose boluses can provoke further insulin release and rebound hypoglycaemia. Treat symptomatic hypoglycaemia with the lowest effective dose, reassess rapidly, provide definitive disease management and consider alternative support when escalating dextrose fails.
  • Do not use this electrolyte-free 10% solution for volume resuscitation, as a routine maintenance prescription or as complete parenteral nutrition. Correct hypovolaemia with an appropriate crystalloid, supply required electrolytes and nutrition separately, and include dextrose carrier volume in the total daily fluid plan.
  • Before adding a medicine, confirm its prescribed diluent, final concentration, osmolarity, pH, stability and line compatibility from current instructions. Use only a clear intact single-dose container, maintain asepsis, never pool or share remnants and discard unused solution after the allowed handling interval.
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 Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition
6.2/10
Situational / acceptable
vetman assessment

Polifleks Dextrose

10%, solution for infusion, human medicine
Assessed clinical scopeCat · Controlled IV 10% dextrose for documented symptomatic or persistent hypoglycaemia, central-line glucose support, or dilution as a compatible drug/energy carrier; not volume resuscitation, routine maintenance fluid or complete parenteral nutrition · Intravenous
Care settingVeterinary clinic or hospital with immediate point-of-care glucose measurement, central venous access or validated dilution for peripheral use, infusion control and serial glucose, electrolyte, osmolality and fluid-balance monitoring
vetman score 6.2/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, human · № რ-046076 · Verified on 16 Oct 2026 Off-label use

Clinically valuable for measured hypoglycaemia when rapid, titratable glucose is needed, but the exact 10% bag is a hypertonic hospital tool rather than a general-purpose fluid. Use a central line or validate peripheral dilution, monitor glucose and electrolytes closely, treat the cause, and avoid reflex continuation after the endpoint is reached.

Regulatory and scientific credibility5.5/10

The exact 10% human infusion has a sourced current Georgian registration with identifiable manufacturer, strength and IV route, while exhaustive current checks record it as not registered in EU/EEA, GB or US. Veterinary administration is off-label; current foreign class labels and veterinary guidance support dextrose rather than any one of these exact products.

Clinical efficacy7.0/10

IV dextrose is an established, rapidly effective intervention for clinically important hypoglycaemia in dogs and cats and is listed as an essential veterinary medicine. The exact 10% bag can supply a controlled infusion, but routine dog/cat guidance usually targets 1.25–5% after an initial bolus; benefit depends on diagnosing and treating the cause, and comparative exact-product outcome evidence is absent.

Safety and tolerability6.0/10

At 100 mg/ml and about 505 mOsm/L, this is a hypertonic glucose solution. Excess dose or rate can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration, electrolyte shifts and fluid overload; peripheral infusion risks phlebitis and extravasation injury. Rapid glucose-driven insulin release can worsen hypokalaemia or hypophosphataemia and can produce rebound hypoglycaemia in hyperinsulinaemic disease.

Clinical practicality6.5/10

The ready sterile bag permits a controlled central infusion and exact calculation at 0.1 g/ml, but concentrations above 5% are preferably central-line solutions in dogs and cats. Peripheral use generally requires aseptic dilution, compatibility and final-osmolality checks, an infusion pump, frequent bedside glucose measurement and a plan to taper or stop once oral/enteral control or normoglycaemia is sustained.

Full-course cost-effectiveness-

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

Important safety and use flags

  • Do not administer 10% dextrose to a patient with clinically significant hyperglycaemia or known dextrose/excipient hypersensitivity. Confirm a reliable glucose result and the treatment endpoint; neurologic signs alone do not prove hypoglycaemia.
  • Ten-percent dextrose is hypertonic and concentrations above 5% should preferably use a central venous line in dogs and cats. For peripheral delivery, prepare a validated lower final concentration aseptically, use a pump, inspect the catheter frequently and stop immediately for pain, swelling, erythema, phlebitis or extravasation.
  • Do not administer 10% dextrose simultaneously with blood products through the same administration set because pseudoagglutination or haemolysis can occur. Use a separate compatible line and follow the blood component and exact fluid instructions.
  • Measure glucose frequently during initiation and every rate change, then titrate to the lowest concentration and rate that controls clinical signs without marked hyperglycaemia. Excess delivery can cause hyperglycaemia, hyperosmolality, osmotic diuresis, dehydration and potentially fatal neurologic or fluid complications.
  • Monitor potassium, phosphate, sodium, magnesium, osmolality, urine output and total fluid balance. Glucose-stimulated insulin can shift potassium and phosphate intracellularly; after dextrose metabolism the delivered water can contribute to dilutional hyponatraemia and overload, especially with renal, cardiac or pulmonary disease.
  • In insulinoma or another hyperinsulinaemic state, large glucose boluses can provoke further insulin release and rebound hypoglycaemia. Treat symptomatic hypoglycaemia with the lowest effective dose, reassess rapidly, provide definitive disease management and consider alternative support when escalating dextrose fails.
  • Do not use this electrolyte-free 10% solution for volume resuscitation, as a routine maintenance prescription or as complete parenteral nutrition. Correct hypovolaemia with an appropriate crystalloid, supply required electrolytes and nutrition separately, and include dextrose carrier volume in the total daily fluid plan.
  • Before adding a medicine, confirm its prescribed diluent, final concentration, osmolarity, pH, stability and line compatibility from current instructions. Use only a clear intact single-dose container, maintain asepsis, never pool or share remnants and discard unused solution after the allowed handling interval.
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
Glucose100 mg/ml
Formulation Type
Solution
Administration route
Intravenous
Manufacturer
Polifarma Ilac · Türkiye
Registration
Georgia Yes, human
In force until 03 Aug 2031
Human (Ministry of Health, RAMA)
In the register: პოლიფლექსი დექსტროზა 10%, საინფუზიო ხსნარი
№ რ-046076
Verified on: 16 Oct 2026
EU No
UK No
Verified on: 16 Oct 2026
US No
Verified on: 16 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.
Dog Full dog label: parenteral supportive therapy with glucose, sorbitol and vitamins A, D3, B1, nicotinamide and C at a fixed 10-15 ml per animal
4.9/10
Weak evidence support
vetman assessment

VITATOX

50 ml emulsion for injection for dogs and cats
Assessed clinical scopeDog · Full dog label: parenteral supportive therapy with glucose, sorbitol and vitamins A, D3, B1, nicotinamide and C at a fixed 10-15 ml per animal · SC,IM,IV,IP
Care settingClinic supportive care, given slowly IV or by another labelled route, alongside diagnosis and specific treatment
vetman score 4.9/10 Weak evidence support
Evidence confidence: Low Georgia: Yes, veterinary · № 61-11 · Verified on 22 Oct 2026

A weak option: an authorised but old-style sugar and vitamin emulsion with little evidence of benefit and a fixed dose that ignores body size. Give targeted fluids, dextrose or a specific vitamin only when a need is shown.

Regulatory and scientific credibility5.5/10

The dog and cat product holds an Italian national authorisation listed in the EU database (UPD 600000097476), a real regulator record, but it is an older authorisation with no published efficacy data; Georgia lists it as 61-11 with no validity date.

Clinical efficacy3.5/10

Glucose gives short-lived energy and vitamins help only a true deficiency; no controlled study shows clinical benefit for the labelled supportive uses, and current fluid guidelines use measured fluids and dextrose instead.

Safety and tolerability5.5/10

The dose is fixed at 10-15 ml regardless of size, giving 20,000-30,000 IU of vitamin D3 and 500-750 mg of glucose per dose; the label excludes hyperglycaemia and the first third of pregnancy and warns of vitamin excess.

Clinical practicality5.5/10

Slow IV injection in clinic is straightforward, but the emulsion must not be mixed with other drugs and an opened vial lasts 28 days.

Full-course cost-effectiveness-

No verified current Georgian price or patient-adjusted course cost was found; foreign prices were not substituted.

Important safety and use flags

  • Do not use with hyperglycaemia, including diabetes, or hypersensitivity to an ingredient; avoid in the first third of pregnancy because vitamin A can be teratogenic.
  • Each dose contains 20,000-30,000 IU of vitamin D3; do not repeat routinely, and check calcium if doses are repeated.
  • Inject IV slowly; do not mix with other medicines because compatibility has not been studied.
  • The dose is per animal, not per kg; use the lower 10 ml dose for small dogs.
  • Use within 28 days of opening; protect from light and heat.
Assessment sources
Assessed: 23 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Cat Full cat label: parenteral supportive therapy with glucose, sorbitol and vitamins A, D3, B1, nicotinamide and C at a fixed 10-15 ml per animal
4.6/10
Weak evidence support
vetman assessment

VITATOX

50 ml emulsion for injection for dogs and cats
Assessed clinical scopeCat · Full cat label: parenteral supportive therapy with glucose, sorbitol and vitamins A, D3, B1, nicotinamide and C at a fixed 10-15 ml per animal · SC,IM,IV,IP
Care settingClinic supportive care, given slowly IV or by another labelled route, alongside diagnosis and specific treatment
vetman score 4.6/10 Weak evidence support
Evidence confidence: Low Georgia: Yes, veterinary · № 61-11 · Verified on 22 Oct 2026

A weak option for cats: an old-style sugar and vitamin emulsion with little evidence of benefit and a dog-sized fixed dose that delivers a high vitamin D load to a small cat. Use measured fluids, dextrose or a specific vitamin when a need is shown.

Regulatory and scientific credibility5.5/10

The dog and cat product holds an Italian national authorisation listed in the EU database (UPD 600000097476), a real regulator record, but it is an older authorisation with no published efficacy data; Georgia lists it as 61-11 with no validity date.

Clinical efficacy3.5/10

Glucose gives short-lived energy and vitamins help only a true deficiency; no controlled study shows clinical benefit for the labelled supportive uses, and current fluid guidelines use measured fluids and dextrose instead.

Safety and tolerability4.5/10

The same fixed 10-15 ml dose as for dogs gives a 3-4 kg cat roughly 5,000-10,000 IU/kg of vitamin D3 and a large glucose load in one injection; the label excludes hyperglycaemia and the first third of pregnancy and warns of vitamin excess.

Clinical practicality5.0/10

10-15 ml is a large single volume for a cat by any route, the IV injection must be slow, and the emulsion must not be mixed with other drugs.

Full-course cost-effectiveness-

No verified current Georgian price or patient-adjusted course cost was found; foreign prices were not substituted.

Important safety and use flags

  • Do not use with hyperglycaemia, including diabetes, or hypersensitivity to an ingredient; avoid in the first third of pregnancy because vitamin A can be teratogenic.
  • Each dose contains 20,000-30,000 IU of vitamin D3, a high load for a cat; use the lower 10 ml dose, do not repeat routinely, and check calcium if repeated.
  • Check blood glucose in sick or stressed cats before giving 500-750 mg of glucose plus sorbitol.
  • Inject IV slowly; do not mix with other medicines because compatibility has not been studied.
  • Use within 28 days of opening; protect from light and heat.
Assessment sources
Assessed: 23 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
Glucose50 mg/ml Sorbitol50 mg/ml Nicotinamide1.2 mg/ml Ascorbic Acid8 mg/ml Thiamine0.36 mg/ml Cholecalciferol2000 IU/ml Vitamin A400 IU/ml
Formulation Type
Emulsion
Administration route
Subcutaneous, Intramuscular, Intravenous, IP
Manufacturer
Fatro S.p.A. · Italy
Manufacturer (register)
Fatro S.P.A., Italy
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1334, 19 Oct 2026.
Registration
Georgia Yes, veterinary
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.