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Angiotensin 2 Receptor Blocker · Brand: Avapro

Irbesartan Side Effects: Common, Serious & FDA Warnings

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Quick answer

Based on 48,000+ FDA adverse event reports, the most-reported irbesartan reactions include fatigue, nausea, and diarrhoea. FDA reports 1 active Class II recall of irbesartan, primarily for failed dissolution specifications. The FDA-approved label carries a boxed warning.

For information only. MedivaScan summarizes public FDA data and is not medical advice. Consult a healthcare professional before changing any medication. If you experience a serious reaction, contact your doctor or call 911.

Common Side Effects of Irbesartan

The most-reported reactions in the FDA Adverse Event Reporting System (FAERS) for irbesartan. Percentages reflect the share of reports mentioning each reaction; a single report may include multiple reactions. Reports indicate co-occurrence, not causation.

ReactionReports% of total
Fatigue2,7735.7%
Nausea2,7825.7%
Diarrhoea2,4865.1%
Dizziness2,3224.8%
Dyspnoea2,2304.6%
Acute Kidney Injury2,1664.5%
Headache2,1304.4%
Asthenia1,8853.9%
Malaise1,7903.7%
Blood Pressure Increased1,7083.5%
Source: FDA FAERS·Updated ·n=48,661+·verify on FDA →·Methodology

Serious Outcomes and FDA Warnings

FAERS reports flagged with a serious outcome (death, hospitalization, life-threatening, disability, or congenital anomaly), plus reactions surfaced in the FDA-approved label's Warnings section. Reports indicate co-occurrence, not causation.

Outcome flagReports% of total
Serious reports (any flag)
Hospitalization

From the FDA-approved label, Section 5.1: Fetal Toxicity

Irbesartan tablets 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. Resulting oligohydramnios can be associated with fetal lung hypoplasia and skeletal deformations. Potential neonatal adverse effects include skull hypoplasia, anuria, hypotension, renal failure, and death. When pregnancy is detected, discontinue irbesartan tablets as soon as possible [see Use in Specific Populations (8.1) ].
Source: DailyMed (irbesartan label)·Updated

Irbesartan Recalls

FDA enforcement actions matched to irbesartan via openFDA's structured generic_name field and the NDC bridge. Ongoing recalls are listed below (verify on FDA →); closed recalls are grouped in the disclosure that follows.

DateReasonClassQuantityStatus
2025-02-19Out of Specification for Dissolution
AvKARE
Class II341 cartonsOngoing
Source: FDA Drug Enforcement Reports·Updated ·Refreshes every 6 hours·verify on FDA →
Show 6 closed recalls (2019 to 2022)

Includes resolved and terminated recalls matched to irbesartan. Most recent first.

DateReasonClassQuantityStatus
2022-08-03Failed dissolution specifications.
Jubilant Cadista Pharmaceuticals, Inc.
Class II9,600 bottlesTerminated
2022-08-03Failed Dissolution Specifications
Jubilant Cadista Pharmaceuticals, Inc.
Class II28,560 bottlesTerminated
2021-11-10CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Lupin Pharmaceuticals Inc.
Class II51,144 bottlesTerminated
2021-11-10CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Lupin Pharmaceuticals Inc.
Class II119,544 bottlesTerminated
2021-11-10CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Lupin Pharmaceuticals Inc.
Class II134,016 bottlesTerminated
2019-02-06CGMP Deviations: FDA lab confirmed presence an impurity, N-nitrosodimethylamine (NDEA) contained in the API used to manufacture the product above the interim acceptable daily intake level of 0.083 parts per million.
Prinston Pharmaceutical Inc
Class II19800 bottlesResolved

Irbesartan Shortages

FDA-listed shortages of irbesartan products. Strength and dosage-form level detail.

No active or recent shortages of irbesartan are listed. We refresh this view daily.
Source: FDA Drug Shortages·Updated

Is Irbesartan Safe?

Irbesartan is FDA-approved. The label's Warnings and Precautions section covers fetal toxicity (Section 5.1), hypotension in volume or salt-depleted (Section 5.2), impaired renal function (Section 5.3).

As with any prescription, the assessment of safety is individual; consult a clinician about your own risk profile.

Source: DailyMed (irbesartan label)·Updated

FDA-Approved Indications

Irbesartan is FDA-approved for use in the condition categories below. The FDA-approved label’s Indications and Usage section is shown verbatim.

Irbesartan tablets 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 ) Treatment of diabetic nephropathy in hypertensive patients with type 2 diabetes, an elevated serum creatinine, and proteinuria. ( 1.2 ) 1.1 Hypertension Irbesartan tablets are indicated for the treatment of hypertension, to lower blood pressure.
Show full Indications and UsageSee less
Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular (CV) events, primarily strokes and myocardial infarction. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including this drug. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than 1 drug to achieve blood pressure goals. For specific advice on goals and management, see published guidelines, such as those of the National High Blood Pressure Education Program’s Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC). Numerous antihypertensive drugs, from a variety of pharmacologic classes and with different mechanisms of action, have been shown in randomized controlled trials to reduce cardiovascular morbidity and mortality, and it can be concluded that it is blood pressure reduction, and not some other pharmacologic property of the drugs, that is largely responsible for those benefits. The largest and most consistent cardiovascular outcome benefit has been a reduction in the risk of stroke, but reductions in myocardial infarction and cardiovascular mortality also have been seen regularly. Elevated systolic or diastolic pressure causes increased cardiovascular risk, and the absolute risk increase per mmHg is greater at higher blood pressures, so that even modest reductions of severe hypertension can provide substantial benefit. Relative risk reduction from blood pressure reduction is similar across populations with varying absolute risk, so the absolute benefit is greater in patients who are at higher risk independent of their hypertension (for example, patients with diabetes or hyperlipidemia), and such patients would be expected to benefit from more aggressive treatment to a lower blood pressure goal. Some antihypertensive drugs have smaller blood pressure effects (as monotherapy) in black patients, and many antihypertensive drugs have additional approved indications and effects (e.g., on angina, heart failure, or diabetic kidney disease). These considerations may guide selection of therapy. Irbesartan tablets may be used alone or in combination with other antihypertensive agents. 1.2 Nephropathy in Type 2 Diabetic Patients Irbesartan tablets are indicated for the treatment of diabetic nephropathy in patients with type 2 diabetes and hypertension, an elevated serum creatinine, and proteinuria (>300 mg/day). In this population, irbesartan tablets reduce the rate of progression of nephropathy as measured by the occurrence of doubling of serum creatinine or end-stage renal disease (need for dialysis or renal transplantation) [see Clinical Studies (14.2) ].
Source: DailyMed (irbesartan label)·Updated ·Section 1 (Indications and Usage)

Frequently Asked Questions

What are the most-reported side effects of irbesartan?
Fatigue, nausea, and diarrhoea are among the most-reported reactions in FDA FAERS data for irbesartan. The full ranking, with reaction counts and the share of total reports, is in the Common Side Effects table above. Reports indicate co-occurrence, not causation; consult a clinician about your specific case.
Is irbesartan the same as Avapro?
Irbesartan is the generic name; Avapro is a brand name for the same active ingredient. The active ingredient is identical; formulation and inactive ingredients may vary by manufacturer.
Has irbesartan been recalled?
Yes. Irbesartan has active and closed recalls on record in the FDA enforcement database. Reasons are dominated by CGMP deviations and failed dissolution specifications. See the recalls table on this page for current counts, firm names, dates, and lot quantities.
What are irbesartan's current ongoing recalls about?
Active irbesartan recalls are listed in the recalls table above with their class, reason, firm, and affected lots. The dominant reason across these recalls is failed dissolution specifications. For lot numbers, distribution patterns, and the FDA enforcement record for any individual recall, follow the verify-on-FDA link from each row.
What do FDA recall classes mean?
Class I means a reasonable probability of serious adverse health consequences or death. Class II means temporary or medically reversible adverse health consequences with remote probability of serious harm. Class III means use of the product is unlikely to cause adverse health consequences. The class assignment is the FDA's, not the manufacturer's.
Does irbesartan have an FDA boxed warning?
Yes. The FDA-approved label for irbesartan carries a boxed warning. Boxed warnings are the FDA's strongest cautions. See the "FDA Boxed Warning" section above for the verbatim warning text.

Data Sources & Methodology

How each section of this page is sourced, and how often the data is refreshed.

SourceEndpointRefresh
FAERS reactionsopenFDA /drug/event.json count API. Aggregated per drug per reaction term; we do not store individual reports.Daily
RecallsopenFDA /drug/enforcement.json. Drugs matched via three confidence-tracked strategies: structured generic name (HIGH), NDC code bridge (MEDIUM), text token parse (LOW). Only HIGH and MEDIUM matches surface here.6 hours
ShortagesFDA Drug Shortages list.Daily
Boxed warnings & label sectionsopenFDA /drug/label.json. Labels are stable; monthly cadence is sufficient.Monthly
Condition categoriesSynonym-mapped from drug_labels.indications. Methodology at /methodology/.Per-drug

What we do not do. We do not invent, paraphrase, or extrapolate drug claims. Every figure on this page comes from a query against an openFDA endpoint. If the data is unavailable, the section gracefully omits rather than filling the space with editorial guesswork.