Telmisartan (telmisartan)

Advertisement

Last reviewed · Source: First Databank (FDB) drug data

Overview

Telmisartan is a nonpeptide, benzimidazole-derivative angiotensin II type 1 (AT1) receptor antagonist (also referred to as an angiotensin II receptor blocker (ARB)).

Telmisartan is a nonpeptide, angiotensin II receptor (AT1) antagonist. Telmisartan blocks the vasoconstriction and aldosterone-secreting effects of angiotensin II by blocking the binding of angiotensin II to the AT1 receptor in many tissues. Angiotensin II is the primary pressor agent from the renin-angiotensin system that causes vasoconstriction, stimulation of the synthesis and release of aldosterone, cardiac stimulation, and renal reabsorption of sodium.

Telmisartan does not inhibit the degradation of bradykinin like angiotensin converting enzyme (ACE) inhibitors.

Following oral administration, peak plasma concentrations of telmisartan occur after 0.5-1 hour. Administration of telmisartan with food slightly reduces the bioavailability of the drug. At 40 mg and 160 mg doses, the bioavailability of telmisartan is 42% and 58%, respectively.

Telmisartan has an accumulation index of 1.5-2.0 with repeated once daily dosing. Antihypertensive effects of telmisartan are evident within 2 weeks of initiation, with maximum blood pressure lowering observed after 4 weeks. Telmisartan is highly bound to plasma proteins (>99.5%), principally albumin and alpha1-acid glycoprotein.

Telmisartan is excreted mainly (>97%) as unchanged drug in feces via biliary elimination; only small amounts (less than 1% of an administered dose) are excreted in urine. The drug undergoes conjugation with glucuronic acid, forming pharmacologically inactive metabolites. Telmisartan is not metabolized by the cytochrome P-450 (CYP) microsomal enzyme system.

In addition, in vitro studies indicate that telmisartan does not appear to have an inhibitory effect on CYP isoenzymes except for CYP2C19. The elimination half-life of telmisartan is approximately 24 hours.

USES: This medication is used to treat high blood pressure. Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. Telmisartan belongs to a class of drugs known as angiotensin receptor blockers (ARBs).

It works by relaxing blood vessels so blood can flow more easily.

Generic name: telmisartan
Pronunciation: (tel-mi-SAR-tan)

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

Today’s intelligence on Telmisartan

Intelligence content is not available yet.

Indications

The following indications are listed for Telmisartan:

  • Hypertension
  • Myocardial Infarction Prevention
  • Prevention Of Cerebrovascular Accident

Also known as: Acute Mi Prophylaxis, Acute Myocardial Infarction Prophylaxis, Ami Prophylaxis, Cardiac Infarct Prophylaxis, Cardiac Infarction Prophylaxis, Cva Prophylaxis, Elevated Blood Pressure, Essential Hypertension, Hyperpiesia, Hyperpiesis, Hypertensive Disorder, Mi Prophylaxis, Myocardial Infarct Prophylaxis, Myocardial Infarction Prophylaxis, Stroke Prophylaxis, Systemic Arterial Hypertension.

Dosing

No dosing information is available for this tab.

Drug interactions

Telmisartan is not metabolized by cytochrome P-450 (CYP) isoenzymes and has no effect on CYP isoenzymes except for some inhibition of CYP2C19 in vitro.

Contraindications

*Known hypersensitivity (e.g., anaphylaxis or angioedema) to telmisartan or any ingredient in the formulation.

*Concomitant use of telmisartan and aliskiren in patients with diabetes mellitus.

Adverse reactions

Adverse effects occurring in >=1% of patients receiving telmisartan in clinical trials include back pain, sinusitis, diarrhea, intermittent claudication, and skin ulcer.

Precautions

No enhanced messaging available.

ICD codes

No ICD codes are available for this drug.

Formulary status

Search health-plan coverage for this drug by ZIP code.

Enter a ZIP code to view available health plans.

Last reviewed · Source: First Databank (FDB) drug data