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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

Glipizide doses for cats
IndicationDoseRouteFrequencyDuration
Type-2 diabetes mellitus (non-ketotic, well cat)2.5–5 mg/catPOq12h 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