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Telmisartan + Chlorthalidone

Antihypertensive fixed-dose combination (ARB + thiazide-like diuretic) · Antihypertensive

Also known as Telmikind-CH, Tazloc-CT, Telsartan-CH, Arbitel-CH, Telma-CH, Cortel-LN

START
Telmisartan 40 mg / chlorthalidone 12.5 mg PO once daily
TYPICAL MAX
Telmisartan 80 mg / chlorthalidone 25 mg once daily
STOP IF
Pregnancy, severe electrolyte disturbance, or AKI
WATCH
K, Na, creatinine/eGFR, urate, BP at baseline and after changes
CDSCO approvedSchedule HATC C09DA07
Dose laddermg/d
40low/day80max telm
Renal dose adjustmenteGFR mL/min/1.73m²
FULLUsual combination dosing30REDUCEReduced thiazide efficacy — prefer l…90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
1hONSET2hPEAK1.7d1dDURATION
ONSET
1h · absorption
PEAK
2h · combined peak
1.7d · chlorthalidone t½
DURATION
1d · once-daily
EXCRETION
Telmisartan biliary; chlorthalidone renal
route + CYP
INTERACTIONS
12 major
incl. contraindicated
PREGNANCY
Contraindicated.
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 angiotensin II type-1 (AT1) receptors, reducing vasoconstriction and aldosterone; chlorthalidone inhibits Na/Cl reabsorption in the distal tubule, producing mild diuresis — complementary BP lowering with synergistic efficacy.

Indications

Hypertension when telmisartan + chlorthalidone components are appropriate

Dosing

Adult
Telmisartan 40 mg/chlorthalidone 12.5 mg PO once daily; titrate to telmisartan 80 mg/chlorthalidone 12.5 or 25 mg once daily.
Pediatric
Not established for combination.
Renal adjustment
Reduced efficacy of thiazide at CrCl <30; use loop diuretic in advanced CKD.
Hepatic adjustment
Severe hepatic impairment: avoid (telmisartan).
Geriatric
Start low; volume/electrolyte monitoring.
Max dose
Telmisartan 80 mg + chlorthalidone 25 mg once daily

Pharmacokinetics

Onset
BP effect within hours; full effect 2–4 weeks
Peak effect
Telmisartan Tmax 0.5–1 h; chlorthalidone ~2 h
Duration
~24 h (once-daily)
Half-life
Telmisartan ~24 h; chlorthalidone ~40–60 h
Bioavailability
Telmisartan ~50%; chlorthalidone ~64%
Protein binding
Telmisartan >99%; chlorthalidone ~75%
Metabolism
Telmisartan hepatic glucuronidation; chlorthalidone minimal
Excretion
Telmisartan biliary/faecal; chlorthalidone renal

Contraindications

  • Pregnancy (RAAS-blocker fetotoxicity)
  • Bilateral renal artery stenosis
  • Anuria
  • Concomitant aliskiren in diabetes
  • Sulfonamide hypersensitivity (thiazide)
  • Severe hepatic impairment

Side effects

Common
DizzinessHyperuricaemiaHypokalaemiaHyperglycaemiaHeadacheFatigue
Serious
  • Hyperkalaemia (with K-sparing/RAAS combination) or hypokalaemia (thiazide)
  • Acute kidney injury (volume depletion)
  • Severe electrolyte/acid-base disturbance
  • Angioedema (rare with ARB)

Pregnancy & lactation

Pregnancy

Contraindicated.

Lactation

Avoid; thiazide may reduce milk supply.

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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