eprosartan
Brand names: Teveten
Eprosartan (Teveten) is a medicine that lowers high blood pressure. It can be used alone or with other blood pressure medicines.
What it does
Eprosartan is used to treat high blood pressure (hypertension).
Common side effects
Viral infection, Injury, Fatigue
Key warnings
If you become pregnant, stop taking eprosartan right away.
How It Works
Eprosartan belongs to a class of drugs called angiotensin II receptor blockers (ARBs). It works by blocking a substance in your body that tightens blood vessels. This helps blood vessels relax, which lowers blood pressure.
How to Take It
The usual starting dose is 600 mg once a day. Your doctor may adjust your dose between 400 mg and 800 mg per day. You can take eprosartan once or twice a day, with or without food. It may take 2 to 3 weeks to see the full effect on your blood pressure.
Pregnancy & Breastfeeding
Eprosartan can harm your unborn baby, even causing death. Stop taking this medicine as soon as you know you are pregnant. It is not known if eprosartan passes into breast milk, so talk to your doctor about the best way to feed your baby if you are taking this medicine.
Missed Dose
If you miss a dose, take it as soon as you remember. If it is close to your next dose, skip the missed dose and continue with your regular schedule.
Storage
Store eprosartan tablets at room temperature (68° to 77°F) in a tightly closed, light-resistant container.
Serious Warnings
If you become pregnant, stop taking eprosartan right away. This medicine can cause serious harm or death to your unborn baby.
Known Drug Interactions
Drug Interactions Dual Blockade of the Renin-Angiotensin System (RAS) Dual blockade of the RAS with angiotensin receptor blockers, ACE inhibitors, or aliskiren is associated with increased risks of hypotension, hyperkalemia, and changes in renal function (including acute renal failure) compared to monotherapy. Do not co-administer aliskiren with eprosartan in patients with diabetes. Avoid use of aliskiren with eprosartan in patients with renal impairment (GFR < 60 mL/min).
Mechanism: Both drugs work on the same system to lower blood pressure, which can cause blood pressure to drop too low or harm the kidneys.
What to do: Do not use these drugs together if you have diabetes, and avoid this combination if you have kidney problems.
or 800 mg q.d.) doses have been safely used concomitantly with a thiazide diuretic (hydrochlorothiazide).
Mechanism: These two drugs work together to lower blood pressure and have been shown to be safe when used at the same time.
What to do: No special changes are usually needed, but you should still follow your doctor's instructions for blood pressure monitoring.
Concomitant administration of eprosartan and warfarin had no effect on steady-state prothrombin time ratios (INR) in healthy volunteers. Eprosartan has been shown to have no effect on the pharmacokinetics of digoxin and the pharmacodynamics of warfarin and glyburide.
Mechanism: Eprosartan does not change how warfarin works or how it affects your blood's ability to clot.
What to do: You can typically take these medications together without needing to adjust your warfarin dose.
have been safely used concomitantly with sustained-release calcium channel blockers (sustained-release nifedipine) with no clinically significant adverse interactions.
Mechanism: These two blood pressure medicines do not have a negative effect on each other when taken together.
What to do: You can safely take these medications together as prescribed by your doctor.
Eprosartan is not metabolized by the cytochrome P450 system; eprosartan steady-state concentrations were not affected by concomitant administration of ketoconazole or fluconazole, potent inhibitors of CYP3A and 2C9, respectively. Because eprosartan is not metabolized by the cytochrome P450 system, inhibitors of CYP450 enzyme would not be expected to affect its metabolism, and ketoconazole and fluconazole, potent inhibitors of CYP3A and 2C9, respectively, have been shown to have no effect on eprosartan pharmacokinetics.
Mechanism: Ketoconazole blocks certain liver proteins, but eprosartan is not processed by those proteins, so its levels do not change.
What to do: No special precautions are needed when taking these two drugs together.
Common Questions
Can I take eprosartan with other medications?
What should I do if I feel dizzy after taking eprosartan?
Can I drink alcohol while taking eprosartan?
Does eprosartan have any effect on my kidneys?
Can eprosartan cause allergic reactions?
How long do I need to take eprosartan?
Can I stop taking eprosartan if my blood pressure is under control?
Are there any foods I should avoid while taking eprosartan?
Will eprosartan cure my high blood pressure?
What if I have diabetes?
What are the common side effects of eprosartan?
Does eprosartan interact with other medications?
What drug class is eprosartan?
Is eprosartan safe during pregnancy?
Related Medications in Angiotensin II Receptor Blocker (ARB)
Other drugs grouped near eprosartan — same-class peers and common alternatives.
acebutolol
Sectral
Acebutolol is a medicine that helps lower blood pressure and control irregular heartbeats.
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aliskiren
Tekturna
Tekturna is a medicine used to treat high blood pressure.
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amiloride
Midamor
Amiloride is a water pill that helps your body hold onto potassium.
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amlodipine
Norvasc
Amlodipine (Norvasc) is a drug that lowers blood pressure and treats chest pain.
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amlodipine/benazepril
Lotrel
Lotrel is a combination medicine that contains amlodipine and benazepril.
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Medication Guides
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What the FDA Data Shows for eprosartan
The FDA label for eprosartan (sold under brand names such as Teveten) classifies it as a prescription-only medication in the Angiotensin II Receptor Blocker (ARB) class. Eprosartan is used to treat high blood pressure (hypertension). Official labeling lists 11 commonly reported side effects, including Viral infection, Injury, Fatigue.
Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. Voluntary reports accumulate over the lifetime of a drug and reflect wide-ranging clinical use. The database also lists 9 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated major severity. Acquisition-cost data is surveyed weekly by CMS and updated as manufacturers report changes.
Report counts do not establish causation — a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice — always consult a licensed healthcare provider before starting, stopping, or changing any medication.
Data Sources
Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS).
FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.
Last updated: December 5, 2014
Read our methodology — how this data is sourced, computed, and verified.
All federal data sources used on this page
- FDA Orange Book — approved drug products with therapeutic equivalence. accessdata.fda.gov/cder/ob
- FDA DailyMed — NIH-hosted drug labeling for FDA-approved meds. dailymed.nlm.nih.gov
- FDA Adverse Event Reporting System (FAERS) — post-marketing safety surveillance. fda.gov/drugs/faers
- NLM RxNorm — standardized clinical drug nomenclature. nlm.nih.gov/research/umls/rxnorm
- CMS Medicare Part B Drug Average Sales Price Files — federal drug pricing data. cms.gov/medicare/part-b-drugs/asp
- FDA Drug Shortages Database — current and resolved drug shortage tracking. accessdata.fda.gov/drugshortages