Irbesartan Side Effects: Common, Serious & FDA Warnings
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.
WARNING: FETAL TOXICITY When pregnancy is detected, discontinue irbesartan tablets 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. When pregnancy is detected, discontinue irbesartan tablets as soon as possible. ( 5.1 , 8.1 ) Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus. ( 5.1 , 8.1 )
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.
| Reaction | Reports | % of total |
|---|---|---|
| Fatigue | 2,773 | 5.7% |
| Nausea | 2,782 | 5.7% |
| Diarrhoea | 2,486 | 5.1% |
| Dizziness | 2,322 | 4.8% |
| Dyspnoea | 2,230 | 4.6% |
| Acute Kidney Injury | 2,166 | 4.5% |
| Headache | 2,130 | 4.4% |
| Asthenia | 1,885 | 3.9% |
| Malaise | 1,790 | 3.7% |
| Blood Pressure Increased | 1,708 | 3.5% |
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 flag | Reports | % 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) ].
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.
| Date | Reason | Class | Quantity | Status |
|---|---|---|---|---|
| 2025-02-19 | Out of Specification for Dissolution AvKARE | Class II | 341 cartons | Ongoing |
Show 6 closed recalls (2019 to 2022)
Includes resolved and terminated recalls matched to irbesartan. Most recent first.
| Date | Reason | Class | Quantity | Status |
|---|---|---|---|---|
| 2022-08-03 | Failed dissolution specifications. Jubilant Cadista Pharmaceuticals, Inc. | Class II | 9,600 bottles | Terminated |
| 2022-08-03 | Failed Dissolution Specifications Jubilant Cadista Pharmaceuticals, Inc. | Class II | 28,560 bottles | Terminated |
| 2021-11-10 | CGMP Deviations: impurity N-nitrosoirbesartan detected in API Lupin Pharmaceuticals Inc. | Class II | 51,144 bottles | Terminated |
| 2021-11-10 | CGMP Deviations: impurity N-nitrosoirbesartan detected in API Lupin Pharmaceuticals Inc. | Class II | 119,544 bottles | Terminated |
| 2021-11-10 | CGMP Deviations: impurity N-nitrosoirbesartan detected in API Lupin Pharmaceuticals Inc. | Class II | 134,016 bottles | Terminated |
| 2019-02-06 | CGMP 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 II | 19800 bottles | Resolved |
Irbesartan Shortages
FDA-listed shortages of irbesartan products. Strength and dosage-form level detail.
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.
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 Usage
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) ].
Frequently Asked Questions
What are the most-reported side effects of irbesartan?
Is irbesartan the same as Avapro?
Has irbesartan been recalled?
What are irbesartan's current ongoing recalls about?
What do FDA recall classes mean?
Does irbesartan have an FDA boxed warning?
Data Sources & Methodology
How each section of this page is sourced, and how often the data is refreshed.
| Source | Endpoint | Refresh |
|---|---|---|
| FAERS reactions | openFDA /drug/event.json count API. Aggregated per drug per reaction term; we do not store individual reports. | Daily |
| Recalls | openFDA /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 |
| Shortages | FDA Drug Shortages list. | Daily |
| Boxed warnings & label sections | openFDA /drug/label.json. Labels are stable; monthly cadence is sufficient. | Monthly |
| Condition categories | Synonym-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.