Veterinary drug · Drug monograph
Glipizide: veterinary dose and monograph
Glipizide is a veterinary drug. Oral sulfonylurea hypoglycaemic used in CATS with type-2-like (non-insulin-dependent) diabetes mellitus as an alternative to insulin in selected, otherwise-stable patients. Indications include feline non-insulin-dependent (type-2-like) diabetes mellitus — stable, well-selected cats; owner-declined-insulin cases where oral therapy is attempted (with informed limitations). This monograph lists 1 reference dose for cats, each with route, frequency and source.
At a glance
- Drug class
- Veterinary drug
- Also known as
- Glucotrol, Glynase (glipizide), Glytop
- Species with doses
- Cats
- Routes
- PO
- Last reviewed
- 1 October 2026
Indications
- Feline non-insulin-dependent (type-2-like) diabetes mellitus — stable, well-selected cats
- Owner-declined-insulin cases where oral therapy is attempted (with informed limitations)
Glipizide dose by species
Doses are per administration unless stated. mg/kg doses scale with body weight; per-animal, per-quarter and infusion-rate doses are shown as the reference writes them.
Cats
| Indication | Dose | Route | Frequency | Duration |
|---|---|---|---|---|
| Type-2 diabetes mellitus (non-ketotic, well cat) | 2.5–5 mg/cat | PO | q12h with a meal | — |
- Type-2 diabetes mellitus (non-ketotic, well cat): Papich 5e: 2.5–7.5 mg per cat q12h PO — usually 2.5 mg initially, then 5 mg q12h. Plumb’s p.574: 2.5 mg twice daily with food, check glucose every 3–4 h for the first 12–18 h, increase to 5 mg twice daily after 2 weeks if still hyperglycaemic (Herrtage 2009); maximum 7.5 mg twice daily (Feldman 2005). Switch to insulin if ketotic, ill, or glucose >270 mg/dL after 1–2 months. Fewer than half of cats respond.
Contraindications
Diabetic ketoacidosis or any unstable/ill diabetic (use insulin). Insulin-dependent diabetes / non-functional β-cells. Significant hepatic or renal impairment. Pregnancy. Sulfonamide hypersensitivity. Known hypersensitivity. Not for dogs.
Species-specific warnings
Cats: Only for non-ketotic, stable type-2-like diabetics; if the cat is unwell, ketotic or losing weight, switch to insulin. Stop if hepatotoxicity develops.
Adverse effects
- Hypoglycaemia
- Vomiting/anorexia (give with food)
- Hepatotoxicity (raised liver enzymes, icterus) — may necessitate stopping
- Does not halt ongoing β-cell loss; many cats ultimately need insulin
Drug interactions
- Other hypoglycaemics / insulin: additive hypoglycaemia
- Beta-blockers: mask hypoglycaemia signs and may impair recovery
- Corticosteroids / progestins: antagonise glucose control (raise glucose)
- Hepatically metabolised — CYP interactions can alter levels
Pregnancy and lactation
Avoid in pregnancy (use insulin if a diabetic queen requires glycaemic control).
Monitoring
- Blood glucose / fructosamine and clinical signs (PU/PD, weight, appetite)
- Hypoglycaemia signs (warn owner)
- Liver enzymes (hepatotoxicity)
- Reassess need to switch to insulin if control is inadequate
Toxicity and overdose
The main acute risk is HYPOGLYCAEMIA (weakness, ataxia, seizures, coma) — including from accidental overdose or a cat that eats poorly after dosing. Chronic concern is hepatotoxicity. Overdose of sulfonylureas can cause prolonged, recurrent hypoglycaemia.
Management: Treat hypoglycaemia: oral glucose/Karo syrup if conscious, IV dextrose bolus then a dextrose CRI for sustained/severe cases (sulfonylurea hypoglycaemia can be prolonged and recurrent — monitor for hours). Octreotide can blunt refractory sulfonylurea-induced insulin release. Supportive care; monitor glucose closely and check liver values.
Clinical pearls
- An oral option ONLY for stable feline type-2-like diabetes with residual β-cell function — insulin remains more effective and is required for sick/ketotic cats
- Always give with food and counsel owners on hypoglycaemia (and to skip a dose if the cat isn't eating)
- Watch liver enzymes — hepatotoxicity is a recognised reason to discontinue
- Octreotide is a useful adjunct for refractory sulfonylurea overdose hypoglycaemia
- Not for dogs (canine diabetes is insulin-dependent)
Mechanism of action
A sulfonylurea that binds the SUR1 subunit of ATP-sensitive potassium channels on pancreatic β-cells, closing them; the resulting depolarisation opens voltage-gated calcium channels and triggers insulin secretion. It therefore augments endogenous insulin release and requires functioning β-cells — it cannot work in true insulin-deficient diabetes. Extra-pancreatic effects on insulin sensitivity are minor.
Formulations and products
- 2.5 mg tablet
- 5 mg tablet
- Glynase — 5 mg tablet, Tablet (human-label)
- Glytop — 2.5 / 5 mg tablet, Tablet (human-label)
Storage
Tablets: 15–30 °C, dry, protect from light/moisture.
Before you use this dose
Reference doses for veterinary professionals. Confirm the dose against the product label, the patient’s condition, current guidance and local regulations before use; the attending veterinarian remains responsible for every clinical decision.
Frequently asked questions
What is the dose of Glipizide for cats?
Reference doses for Glipizide in cats: 2.5–5 mg/cat PO q12h with a meal (Type-2 diabetes mellitus (non-ketotic, well cat)). Confirm against the label and the patient before use.
When should Glipizide not be used?
Diabetic ketoacidosis or any unstable/ill diabetic (use insulin). Insulin-dependent diabetes / non-functional β-cells. Significant hepatic or renal impairment. Pregnancy. Sulfonamide hypersensitivity. Known hypersensitivity. Not for dogs.
What are the side effects of Glipizide in animals?
Hypoglycaemia; Vomiting/anorexia (give with food); Hepatotoxicity (raised liver enzymes, icterus) — may necessitate stopping; Does not halt ongoing β-cell loss; many cats ultimately need insulin.
Sources
- Plumb's Veterinary Drug Handbook
- Merck Veterinary Manual, 11th edition
- Papich, Papich Handbook of Veterinary Drugs, 5th edition
Last reviewed · VetMasterJi