Telmisartan
| Clinical data | |
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| Pronunciation | /tɛlmɪˈsɑːrtən/ |
| Trade names | Micardis, others |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a601249 |
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| Routes of administration | By mouth |
| Drug class | Angiotensin II receptor antagonist |
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| Pharmacokinetic data | |
| Bioavailability | 42–100% |
| Protein binding | >99.5% |
| Metabolism | Minimal liver (glucuronidation) |
| Elimination half-life | 24 hours |
| Excretion | Feces 97% |
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| ECHA InfoCard | 100.149.347 |
| Chemical and physical data | |
| Formula | C33H30N4O2 |
| Molar mass | 514.629 g·mol−1 |
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Telmisartan, sold under the brand name Micardis among others, is a medication used to treat high blood pressure and heart failure. It is a reasonable initial treatment for high blood pressure. It is taken by mouth.
Common side effects include upper respiratory tract infections, diarrhea, and back pain. Serious side effects may include kidney problems, low blood pressure, and angioedema. Use in pregnancy may harm the baby and use when breastfeeding is not recommended. It is an angiotensin II receptor blocker and works by blocking the effects of angiotensin II.
Telmisartan was patented in 1991 and came into medical use in 1999. It is available as a generic medication. In 2022, it was the 228th most commonly prescribed medication in the United States, with more than 1 million prescriptions. It is available in combination with hydrochlorothiazide as telmisartan/hydrochlorothiazide; with cilnidipine as telmisartan/cilnidipine; and with amlodipine as telmisartan/amlodipine.