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Telmisartan + Amlodipine

Antihypertensive fixed-dose combination (ARB + DHP calcium channel blocker) · Antihypertensive

Also known as Telma AM, Telmikind AM, Telsartan AM, Amtel

START
Telmisartan 40 / amlodipine 5 mg PO once daily
TYPICAL MAX
Telmisartan 80 mg + amlodipine 10 mg once daily
STOP IF
Pregnancy, angioedema, severe hyperkalaemia, or symptomatic hypotension
WATCH
K, creatinine, BP, peripheral oedema; baseline + after dose changes
CDSCO approvedSchedule HATC C09DB04
Dose laddermg/d
40low telm/d80max telm
Renal dose adjustmenteGFR mL/min/1.73m²
FULLStandard dosing30CAUTIONCaution; monitor K/creatinine closely90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
1hONSET6hPEAK1.7d1dDURATION
ONSET
1h · absorption
PEAK
6h · combined
1.7d · amlod t½
DURATION
1d · once-daily
EXCRETION
Telmisartan biliary; amlodipine hepatic / renal metabolites
route + CYP
INTERACTIONS
12 major
incl. contraindicated
PREGNANCY
Contraindicated (ARB component).
FDA category + note
Top interactionssee all 12
  • AliskirenContraindicatedTextbookG&G 14e · p603
  • Sacubitril ValsartanContraindicatedTextbookG&G 14e · p602
  • Aliskiren In DiabetesContraindicatedDatabaseKimi deep-research + Cla
  • Angiotensin Converting Enzyme InhibitorsSevereTextbookHarrison 22e · p2396

Mechanism

Telmisartan blocks AT1 angiotensin II receptors (reducing vasoconstriction and aldosterone); amlodipine blocks L-type calcium channels in vascular smooth muscle (peripheral arteriolar vasodilation) — complementary BP-lowering mechanisms with strong evidence base.

Indications

Hypertension (when both components appropriate)

Dosing

Adult
Telmisartan 40 mg / amlodipine 5 mg PO once daily; titrate to 80/5, 40/10, or 80/10 PO once daily.
Pediatric
Not established for combination.
Renal adjustment
No specific adjustment (telmisartan biliary; amlodipine hepatic).
Hepatic adjustment
Severe hepatic impairment: avoid.
Geriatric
Start low (e.g., 40/2.5 or 40/5); monitor BP.
Max dose
Telmisartan 80 mg + amlodipine 10 mg once daily

Pharmacokinetics

Onset
BP effect within hours
Peak effect
Telmisartan Tmax ~0.5–1 h; amlodipine ~6–12 h
Duration
~24 h (once-daily)
Half-life
Telmisartan ~24 h; amlodipine ~30–50 h
Bioavailability
Telmisartan ~50%; amlodipine ~64%
Protein binding
Telmisartan >99%; amlodipine ~93%
Metabolism
Telmisartan glucuronidation; amlodipine CYP3A4
Excretion
Telmisartan biliary/faecal; amlodipine hepatic metabolites + renal

Contraindications

  • Pregnancy (RAAS-blocker fetotoxicity 2nd–3rd trimester)
  • Bilateral renal artery stenosis
  • Concomitant aliskiren in diabetes
  • Significant aortic stenosis
  • Severe hepatic impairment
  • Cardiogenic shock
  • Hypersensitivity

Side effects

Common
Peripheral oedema (amlodipine)DizzinessHeadacheFlushingHyperkalaemiaFatigue
Serious
  • Severe hypotension (volume-depleted)
  • Hyperkalaemia
  • Angioedema (rare with ARB)
  • Acute kidney injury (volume depletion / RAS)
  • Severe peripheral oedema

Pregnancy & lactation

Pregnancy

Contraindicated (ARB component).

Lactation

Limited combination data; alternatives preferred.

Drug interactions

Aliskiren
Contraindicated
Textbook

Increased risk of hypotension, hyperkalemia, and renal impairment.

Avoid concomitant use.

Source: G&G 14e · p603

Sacubitril Valsartan
Contraindicated
Textbook

Potentially excessive hypotension, increased risk of adverse effects.

Do not use in conjunction with other ARBs.

Source: G&G 14e · p602

Aliskiren In Diabetes
Contraindicated
Database

Dual RAAS blockade

Avoid combination

Source: Kimi deep-research + Cla

Angiotensin Converting Enzyme Inhibitors
Severe
Textbook

Greater incidence of acute kidney injury (AKI) and adverse cardiac events.

The combination of these two classes should be avoided.

Source: Harrison 22e · p2396

Benazepril
Severe
Textbook

Increased worsening of renal function, hypotension, syncope, and hyperkalemia without increased efficacy.

Not recommended for the treatment of hypertension. Previous studies indicate more harm than benefit.

Source: G&G 14e

Captopril
Severe
Textbook

Increased worsening of renal function, hypotension, syncope, and hyperkalemia without increased efficacy.

Not recommended for the treatment of hypertension. Previous studies indicate more harm than benefit.

Source: G&G 14e

Enalapril
Severe
Textbook

Increased worsening of renal function, hypotension, syncope, and hyperkalemia without increased efficacy.

Not recommended for the treatment of hypertension. Previous studies indicate more harm than benefit.

Source: G&G 14e

Enalaprilat
Severe
Textbook

Increased worsening of renal function, hypotension, syncope, and hyperkalemia without increased efficacy.

Not recommended for the treatment of hypertension. Previous studies indicate more harm than benefit.

Source: G&G 14e

Fosinopril
Severe
Textbook

Increased worsening of renal function, hypotension, syncope, and hyperkalemia without increased efficacy.

Not recommended for the treatment of hypertension. Previous studies indicate more harm than benefit.

Source: G&G 14e

Imidapril
Severe
Textbook

Greater incidence of acute kidney injury (AKI) and adverse cardiac events.

The combination of these two classes should be avoided.

Source: Harrison 22e · p2396

Lisinopril
Severe
Textbook

Increased worsening of renal function, hypotension, syncope, and hyperkalemia without increased efficacy.

Not recommended for the treatment of hypertension. Previous studies indicate more harm than benefit.

Source: G&G 14e

Moexipril
Severe
Textbook

Increased worsening of renal function, hypotension, syncope, and hyperkalemia without increased efficacy.

Not recommended for the treatment of hypertension. Previous studies indicate more harm than benefit.

Source: G&G 14e

Related guidelines

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