VetMasterJi

Cardiovascular · Drug monograph

Telmisartan: veterinary dose and monograph

Telmisartan is a veterinary cardiovascular drug. Angiotensin II receptor blocker (ARB) — selectively blocks the AT1 receptor (the pathological receptor for angiotensin II). Indications include feline CKD-associated proteinuria (PRIMARY indication); feline systemic hypertension (alternative to amlodipine); canine proteinuric kidney disease (extra-label). This monograph lists 4 reference doses for dogs and cats, each with route, frequency and source.

At a glance

Drug class
Cardiovascular
Also known as
Semintra, Micardis
Species with doses
Dogs and Cats
General dose range
1–3 mg/kg PO q24h — check the species tables for the indication
Routes
PO
Last reviewed
1 October 2026

Indications

  • Feline CKD-associated proteinuria (PRIMARY indication)
  • Feline systemic hypertension (alternative to amlodipine)
  • Canine proteinuric kidney disease (extra-label)
  • Canine MMVD / DCM (alternative to ACE-I in ACE-intolerant patients)
  • Canine hypertension

Telmisartan 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.

Dogs

Telmisartan doses for dogs
IndicationDoseRouteFrequencyDuration
Proteinuria / hypertension (extra-label)1–3 mg/kgPOq24h (may increase to q12h)—
  • Proteinuria / hypertension (extra-label): Papich 5e: 1 mg/kg PO once daily as a starting dose; increase to 3 mg/kg once daily and then twice daily if needed. Monitor creatinine, potassium and blood pressure.

Cats

Telmisartan doses for cats
IndicationDoseRouteFrequencyDuration
CKD proteinuria (Semintra)1 mg/kgPOq24h—
Systemic hypertension — first 14 days1.5 mg/kgPOq12h14 days
Systemic hypertension — maintenance1–2 mg/kgPOq24h—
  • CKD proteinuria (Semintra): Label dose (Semintra, oral solution): 1 mg/kg PO once daily for proteinuria in feline CKD. Give directly or with a small amount of food.
  • Systemic hypertension — first 14 days: Papich 5e: 1.5 mg/kg PO q12h for the first 14 days, then 2 mg/kg PO q24h. Monitor blood pressure.
  • Systemic hypertension — maintenance: Papich 5e: 2 mg/kg PO q24h after the 14-day induction (0.2 mL/kg of the 10 mg/mL solution). Adjust in 0.5 mg/kg steps by blood pressure; hypotensive cats usually go down to 1 mg/kg.

Contraindications

Severe hepatic impairment (telmisartan metabolised by liver). Pregnancy / breeding (fetal renal failure). Hypotension, dehydration, hypovolaemia. Hyperkalaemia. Concurrent ACE-I (excessive RAAS blockade — additive hyperkalaemia / hypotension). Concurrent K-sparing diuretic (hyperkalaemia).

Species-specific warnings

Cats: First-line for CKD proteinuria and hypertension per IRIS 2024 guidelines. Semintra is highly palatable; preferred over ACE-I in most cases. NEVER combine with enalapril.

Dogs: Extra-label use for proteinuric CKD and ACE-intolerant MMVD. 0.5–1 mg/kg PO q24h. Same pregnancy contraindication as ACE-I.

Adverse effects

  • Hypotension (mild)
  • GI upset (vomiting, anorexia) — uncommon
  • Hyperkalaemia (mild — monitor if combined with spironolactone)
  • Mild azotaemia (much less than ACE-I)
  • Rare hepatic enzyme elevation
  • Dizziness / sedation (very uncommon)

Drug interactions

  • ACE inhibitors (enalapril, benazepril): additive RAAS blockade — hyperkalaemia / hypotension risk. AVOID combination unless under specialist supervision.
  • K-sparing diuretics (spironolactone): additive hyperkalaemia
  • K supplements / KCl salt substitutes: hyperkalaemia
  • NSAIDs: blunt antihypertensive effect; additive nephrotoxicity in dehydration
  • Diuretics (furosemide): synergistic antihypertensive effect — caution for first-dose hypotension
  • Lithium: reduced clearance (rarely relevant in vet practice)

Pregnancy and lactation

CONTRAINDICATED in pregnancy — fetal renal failure, oligohydramnios, pulmonary hypoplasia, skull deformities (similar to ACE-I). FDA Category D (1st tri) / X (2nd–3rd tri). NEVER initiate in pregnant animals; discontinue if pregnancy diagnosed.

Monitoring

  • Blood pressure at baseline, 1 week after starting, then every 3 months
  • Renal function (BUN, creatinine, urinalysis with UPC ratio) baseline, 1 week, then every 3 months
  • Electrolytes (K+, Na+) on same schedule
  • Hepatic enzymes if used >6 months
  • Pregnancy status documented before every prescription in intact females
  • Proteinuria response — UPC at 4–6 weeks; target <0.5

Toxicity and overdose

Wide therapeutic margin. Overdose: hypotension, dizziness, mild azotaemia. Hyperkalaemia rare in vet patients. No teratogenicity reported at therapeutic doses in adult animals (but contraindicated in pregnancy).

Management: Supportive — IV fluids for hypotension, electrolyte correction for K abnormality. No specific antidote. Most overdoses resolve within 24–48 h. Vasopressor (norepinephrine) for refractory hypotension.

Clinical pearls

  • Cats with CKD-associated proteinuria (IRIS stage 2–4 with UPC >0.4): Semintra 1 mg/kg PO q24h — first-line per IRIS 2024 guidelines
  • Cats with systemic hypertension: 1.5–3 mg/kg PO q24h — comparable to amlodipine for BP control with proteinuria reduction
  • Cats palatability is excellent — many cats voluntarily accept Semintra liquid
  • Renoprotective effect independent of BP — reduces glomerular hyperfiltration
  • No dose reduction needed in CKD (biliary excretion) — advantage over ACE-I
  • NEVER combine with ACE-I (enalapril) routinely — hyperkalaemia / hypotension risk; specialist-only combo for refractory cases
  • Pregnancy contraindicated — fetal renal failure same as ACE-I
  • Replaces benazepril / enalapril in many feline CKD practices due to better tolerability
  • Cats often need higher doses for BP than for proteinuria (1.5–3 vs 1 mg/kg)

Mechanism of action

Angiotensin II type 1 receptor (AT1) blocker. Selectively binds AT1 — blocks vasoconstriction, aldosterone secretion, sympathetic activation, and pathological cardiac/renal remodelling driven by angiotensin II. Leaves AT2 receptor unopposed (potentially beneficial — AT2 may promote tissue repair). Hepatically metabolised; biliary excretion (no dose reduction needed in CKD — major advantage in renal patients).

Formulations and products

  • Semintra 4 mg/mL oral solution (cats)
  • Semintra 10 mg/mL oral solution (cats, higher concentration)
  • Micardis 20 / 40 / 80 mg human tablet
  • Semintra 4 mg/mL (Boehringer Ingelheim) — 4 mg/mL, Oral solution (cats)
  • Semintra 10 mg/mL (Boehringer Ingelheim) — 10 mg/mL, Oral solution (cats, higher conc.)
  • Micardis — 20 / 40 / 80 mg, Tablet (human-label)

Storage

Semintra oral solution: 15–25 °C, do not refrigerate, discard 6 months after opening. Tablets: 15–30 °C, dry, protected from light.

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 Telmisartan for dogs?

Reference doses for Telmisartan in dogs: 1–3 mg/kg PO q24h (may increase to q12h) (Proteinuria / hypertension (extra-label)). Confirm against the label and the patient before use.

What is the dose of Telmisartan for cats?

Reference doses for Telmisartan in cats: 1 mg/kg PO q24h (CKD proteinuria (Semintra)); 1.5 mg/kg PO q12h for 14 days (Systemic hypertension — first 14 days); 1–2 mg/kg PO q24h (Systemic hypertension — maintenance). Confirm against the label and the patient before use.

When should Telmisartan not be used?

Severe hepatic impairment (telmisartan metabolised by liver). Pregnancy / breeding (fetal renal failure). Hypotension, dehydration, hypovolaemia. Hyperkalaemia. Concurrent ACE-I (excessive RAAS blockade — additive hyperkalaemia / hypotension). Concurrent K-sparing diuretic (hyperkalaemia).

What are the side effects of Telmisartan in animals?

Hypotension (mild); GI upset (vomiting, anorexia) — uncommon; Hyperkalaemia (mild — monitor if combined with spironolactone); Mild azotaemia (much less than ACE-I); Rare hepatic enzyme elevation; Dizziness / sedation (very uncommon).

Sources

  • Plumb's Veterinary Drug Handbook
  • IRIS CKD Guidelines 2024; ACVIM 2018 systemic hypertension consensus
  • Papich, Papich Handbook of Veterinary Drugs, 5th edition

Last reviewed · VetMasterJi