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Telmisartan

Telmisartan tablets, USP are an angiotensin II receptor blocker (ARB) indicated for: Treatment of hypertension, to lower blood pressure. Lowering bloo.

Checked against the official label · Updated

MEDICAMENTO SUJEITO A RECEITA MÉDICA Oral Alertas de segurança registados

How to use Telmisartan

O que diz a bula oficial. Se um médico receitou, siga a receita. Se a bula da sua caixa for diferente, vale a da sua caixa.

Advertência grave: FETAL TOXICITY When pregnancy is detected, discontinue telmisartan as soon as possible [see Warnings and Precautions (5.1) and Use in Specific Populations (8.1) ]. Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus [see Warnings and Precautions (5.1) and Use in Specific Populations (8.1) ] WARNING: FETAL TOXICITY See full prescribing information for complete boxed warning. …
Para quem é

Telmisartan tablets, USP are an angiotensin II receptor blocker (ARB) indicated for: Treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) Cardiovascular (CV) risk reduction in patients unable to take ACE inhibitors ( 1.2 ) 1.1 Hypertension Telmisartan tablets, USP are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. …

Como tomar e com que frequência
  • May be administered with or without food When used for cardiovascular risk reduction, monitoring of blood pressure is recommended, and if appropriate, adjustment of medications that lower blood pressure may be necessary Indication Starting Dose Dose Range Hypertension 40 mg once daily 40 to 80 mg once daily Cardiovascular Risk Reduction 80 mg once daily 80 mg once daily Hypertension Dosage must be individualized
  • The usual starting dose of telmisartan tablets is 40 mg once a day
  • Blood pressure response is dose-related over the range of 20 to 80 mg [see Clinical Studies ]
  • Most of the antihypertensive effect is apparent within 2 weeks and maximal reduction is generally attained after 4 weeks
  • No initial dosage adjustment is necessary for elderly patients or patients with renal impairment, including those on hemodialysis
  • Patients on dialysis may develop orthostatic hypotension; their blood pressure should be closely monitored
  • Telmisartan tablets may be administered with other antihypertensive agents
  • Telmisartan tablets may be administered with or without food
  • Cardiovascular Risk Reduction The recommended dose of telmisartan tablets is 80 mg once a day and can be administered with or without food
  • It is not known whether doses lower than 80 mg of telmisartan are effective in reducing the risk of cardiovascular morbidity and mortality. …
Strengths it comes in

80 mg, white to off-white, uncoated oval shaped tablets, biconvex with beveled edges, plain on one side and debossed “038” on other side. Tablets: 80mg ( 3 )

Children
  • Safety and effectiveness
  • In pediatric patients have not been established [see Clinical Pharmacology ]
  • Neonates with a history of in utero exposure to telmisartan If oliguria or hypotension occurs, support blood pressure and renal perfusion
  • Exchange transfusions or dialysis may be required as a means of reversing hypotension and/or substituting for disordered renal function
Older adults

Of the total number of patients receiving telmisartan in hypertension clinical studies, 551 (19%) were 65 to 74 years of age and 130 (4%) were 75 years or older. No overall differences in effectiveness and safety were observed in these patients compared to younger patients and other reported clinical experience has not identified differences in responses between the elderly and younger patients, but greater sensitivity of some older individuals c …

While you are taking it
  • Advise the patient to read the FDA-approved patient labeling (Patient Information) Pregnancy Advise female patients of childbearing age about the consequences of exposure to telmisartan during pregnancy
  • Discuss treatment options with women planning to become pregnant
  • Tell patients to report pregnancies to their physicians as soon as possible [see Warnings and Precautions and Use in Specific Populations ]
  • Lactation Advise nursing women not to breastfeed during treatment with telmisartan [see Use in Specific Populations ] . …
Talk to a doctor first if
  • Telmisartan is contraindicated in patients with known hypersensitivity (e.g., anaphylaxis or angioedema) to telmisartan or any other component of this product [see Adverse Reactions ]
  • Do not co-administer aliskiren with telmisartan in patients with diabetes. [see Drug interactions ]
  • Known hypersensitivity (e.g., anaphylaxis or angioedema) to telmisartan or any other component of this product Do not co-administer aliskiren with telmisartan in patients with diabetes
Medicines it may not mix with

Aliskiren: Do not co-administer aliskiren with telmisartan in patients with diabetes. Avoid use of aliskiren with telmisartan in patients with renal impairment (GFR

Warnings

Avoid fetal or neonatal exposure ( 5.1 ) Hypotension: Correct any volume or salt depletion before initiating therapy. Observe for signs and symptoms of hypotension ( 5.2 ) Monitor carefully in patients with impaired hepatic ( 5.4 ) or renal function ( 5.5 ) Avoid concomitant use of an ACE inhibitor and angiotensin receptor blocker ( 5.6) 5.1 Fetal Toxicity Use of drugs that act on the renin-angiotensin system during the second and third trimesters of pregnancy reduces fetal renal function and increases fetal and neonatal morbidity and death. Resulting oligohydramnios can be associated with fetal lung hypoplasia and skeletal deformations. …

Possíveis efeitos colaterais

The following adverse reaction is described elsewhere in labeling: Renal dysfunction upon use with ramipril [see Warnings and Precautions (5.6) ] Hypertension: The most common adverse events (≥1%) reported in hypertension trials are back pain, sinusitis, and diarrhea ( 6.1 ) Cardiovascular risk reduction: The serious adverse events (≥1%) reported in cardiovascular risk reduction trials were intermittent claudication and skin ulcer ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Ascend Laboratories, LLC at 1-877-272-7901 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. …

Pregnancy and breastfeeding

8.1 Pregnancy Risk Summary Telmisartan can cause fetal harm when administered to a pregnant woman. Use of drugs that act on the renin-angiotensin system during the second and third trimesters of pregnancy reduces fetal renal function and increases fetal and neonatal morbidity and death (see Clinical Considerations ). …

If you take too much

Limited data are available with regard to overdosage in humans. The most likely manifestation of overdosage with telmisartan tablets would be hypotension, dizziness and tachycardia; bradycardia could occur from parasympathetic (vagal) stimulation. If symptomatic hypotension should occur, supportive treatment should be instituted. Telmisartan is not removed by hemodialysis.

Se esquecer uma dose

Tome assim que lembrar, a menos que esteja quase na hora da próxima dose. Nesse caso, pule a dose esquecida. Nunca tome duas doses de uma vez para compensar. Confira a bula, pois alguns medicamentos são diferentes.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2026-06-05.

Marcas pelo mundo

Products with Telmisartan as the active ingredient. Names differ between countries.

Registered products

United States (FDA)

TelmisartanTELMISARTAN 20 mg/1 · Tablet · Jubilant Cadista Pharmacuticals Inc.
NDC 59746-439Label
Telmisartan And HydrochlorothiazideTELMISARTAN 40 mg/1, HYDROCHLOROTHIAZIDE 12.5 mg/1 · Tablet · Lifestar Pharma LLC
NDC 70756-315Label
TelmisartanTELMISARTAN 80 mg/1 · Tablet · Solco Healthcare US, LLC
NDC 43547-285Label
TelmisartanTELMISARTAN 20 mg/1 · Tablet · Lifestar Pharma LLC
NDC 70756-312Label
TelmisartanTELMISARTAN 40 mg/1 · Tablet · Bryant Ranch Prepack
NDC 63629-5682Label

Nigeria (NAFDAC)

NAFDACTelmisartan 40 Tablet A4-100144NAFDACTelmisartan 80 Tablet A4-100145NAFDACTelmisartan Tablet 80 mg B4-9069NAFDACTelmisartan 40 mg Tablets C4-1226NAFDACTelmisartan 80 mg Tablets A4-100064NAFDACTelmisartan 80 mg Tablets C4-1227NAFDACTelmisartan 40 mg Tablets A4-100791NAFDACTelmisartan Tablets 40 mg A4-101286NAFDACTelmisartan 80 mg Tablets_ A4-100920NAFDACTelmisartan + Hydrochlorothiazide 80/12.5 mg Tablet A4-100646NAFDACTelmisartan + Hydrochlorothiazide 40/12.5 mg Tablets A4-100647NAFDACTelmisartan & Hydrochlorothiazide Tablets USP 80 + 12.5 mg A4-100610

Other countries: check your pack's registration number and we point you to your regulator.

Safety alerts and recalls

Telmisartan and Amlodipine, Tablets, USP, 40mg/5 mg, 30-count Bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA, Made in India, NDC 0378-1075-U.S. FDA Class III
1 Oct 2026 · Viatris, Inc. · OngoingSuperpotent Drug: potential for the Telmisartan content in these lots to exceed specifications
Telmisartan Tablets, USP 40mg, Rx Only, 30 Tablets per bottle, Manufactured by: Micro Labs Limited Goa-403 722, INDIA, Manufactured for: Micro Labs USA Inc., Somerset, NJ 08873, NDU.S. FDA Class II
9 Feb 2024 · Micro Labs Limited · TerminatedFailed Stability Specifications: Out of specification for blend uniformity.
Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg, 30 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Plot no 2, Phase-2, Pharma Zone, SEZ Pithampur, DU.S. FDA Class II
29 Jun 2022 · Glenmark Pharmaceuticals Inc., USA · TerminatedDefective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .
Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/12.5 mg, 30 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Plot no 2, Phase-2, Pharma Zone, SEZ Pithampur,U.S. FDA Class II
29 Jun 2022 · Glenmark Pharmaceuticals Inc., USA · TerminatedDefective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .

A recall usually affects certain batches only. Compare the lot number on your pack.

Check your pack of Telmisartan

Type the registration number on the pack, or scan it with your camera.

Ou tire fotos da caixa
Restam 3 verificações grátis hoje Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

Questions about Telmisartan

What is Telmisartan used for?

Telmisartan tablets, USP are an angiotensin II receptor blocker (ARB) indicated for: Treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) Cardiovascular (CV) risk reduction in patients unable to take ACE inhibitors ( 1.2 ) 1.1 Hypertension Telmisartan tablets, USP are indicated fo (From the official U.S. FDA label.)

How do I take Telmisartan?

Follow your prescription or the leaflet in your pack. The official label says: May be administered with or without food ( 2.1 ) When used for cardiovascular risk reduction, monitoring of blood pressure is recommended, and if appropriate, adjustment of medications that lower blood pressure may be necessary ( 2.2 ) Indication Starting Dose Dose Range Hypertension ( 2.1 ) 40 mg once daily 40 to 80 mg once daily Cardiovascular Risk Reduction ( 2.2 ) 80 mg onc…

Do I need a prescription for Telmisartan?

Usually yes. Telmisartan is a prescription medicine in most countries. Rules differ by country.

What brands contain Telmisartan?

Telmisartan is sold under names such as Twynsta, Semintra, Micardis, Widaplik, Micardis-hct. Brand names differ between countries.

What are the side effects of Telmisartan?

The official label lists: The following adverse reaction is described elsewhere in labeling: Renal dysfunction upon use with ramipril [see Warnings and Precautions (5.6) ] Hypertension: The most common adverse events (≥1%) reported in hypertension trials are back pain, sinusitis, and diarrhea ( 6.1 ) Cardiovascular risk reduction: The serious adverse events (≥1%) reported in cardiovascular risk reductio… Tell your doctor about any side effect that bothers you or does not go away.

Can children take Telmisartan?

Safety and effectiveness in pediatric patients have not been established [see Clinical Pharmacology (12.3) ]. Neonates with a history of in utero exposure to telmisartan If oliguria or hypotension occurs, support blood pressure and renal perfusion. Exchange transfusions or dialysis may be required as a means of reversing hypotension and/or substituting for disordered renal func… Always use the dose for the child's age or weight on the pack or prescription.

Can I take Telmisartan when pregnant or breastfeeding?

8.1 Pregnancy Risk Summary Telmisartan can cause fetal harm when administered to a pregnant woman. Use of drugs that act on the renin-angiotensin system during the second and third trimesters of pregnancy reduces fetal renal function and increases fetal and neonatal morbidity and death (see Clinical Considerations ). … Ask your doctor or midwife first.

What medicines interact with Telmisartan?

Aliskiren: Do not co-administer aliskiren with telmisartan in patients with diabetes. Avoid use of aliskiren with telmisartan in patients with renal impairment (GFR Use the free interaction checker before combining medicines.

What happens if I take too much Telmisartan?

Limited data are available with regard to overdosage in humans. The most likely manifestation of overdosage with telmisartan tablets would be hypotension, dizziness and tachycardia; bradycardia could occur from parasympathetic (vagal) stimulation. If symptomatic hypotension should occur, supportive… Get medical help right away.

How can I check that my Telmisartan is genuine?

Scan the registration number on your pack with PillVera (NAFDAC number in Nigeria, NDC in the United States, DIN in Canada), check the expiry date and buy only from licensed pharmacies.

Sources

This page shows what official sources say, in plain words. It is not medical advice: your prescription and your doctor or pharmacist come first. Brand names, strengths and rules differ between countries.