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
| Indication | Dose | Route | Frequency | Duration |
|---|---|---|---|---|
| Proteinuria / hypertension (extra-label) | 1–3 mg/kg | PO | q24h (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
| Indication | Dose | Route | Frequency | Duration |
|---|---|---|---|---|
| CKD proteinuria (Semintra) | 1 mg/kg | PO | q24h | — |
| Systemic hypertension — first 14 days | 1.5 mg/kg | PO | q12h | 14 days |
| Systemic hypertension — maintenance | 1–2 mg/kg | PO | q24h | — |
- 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