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Enalapril Maleate side effects: what 24,644 FDA adverse event reports show

Enalapril Maleate · Enalapril Maleate · 1,201 reaction terms · 103,728 drug–reaction co-reports · data 2026-09-14
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Drug class

Angiotensin-converting enzyme inhibitor

FDA label, Indications wording

Brand names

Enalapril Maleate

openFDA label

Who reports

24,644 reports · 81% serious · 2,774 with death outcome · 52% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Enalapril maleate oral solution is an angiotensin-converting enzyme inhibitor indicated for: treatment of hypertension in adults and children older than one month, 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 symptomatic heart failure.

FDA label, Indications and Usage

What it is

Enalapril maleate (enalapril maleate) oral solution is the maleate salt of enalapril, the ethyl ester prodrug of a long-acting angiotensin-converting enzyme inhibitor, enalaprilat. Enalapril m.

FDA label, Description section

Boxed warning

FETAL TOXICITY When pregnancy is detected, discontinue enalapril maleate as soon as possible [see Warnings and Precautions (5.1) ]. Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus [see Warnings and Precautions (5.1) ].

FDA label
How to read this page. FAERS is a spontaneous-reporting system: counts are not incidence rates and a signal is not proof of causation. Each reaction below is run through an automated screen — is the term in the FDA label (known), in the indications (the disease being treated), an administrative/coding term, or none of these (unlabeled)? That screen is mechanical text matching, not a causality assessment. The 30 hand-written Bradford Hill assessments are on the causality assessment page. Not medical advice.

Causality screen of the 40 strongest signals

Labeled — boxed warning 1Labeled adverse reaction 1Labeled (related wording) 4Likely indication confounding 8Lab value / disease marker 2Not in label — unassessed 24
What the badges mean

Strongest disproportionality signals

Flagged terms (PRR ≥ 2, χ² ≥ 4, n ≥ 10), ranked by PRR; infinite PRRs (no comparator reports) excluded. The EBGM column is a second, shrinkage-based estimate (MGPS) with its 5th percentile EB05 and the BCPNN IC025; a pair flagged by PRR alone is marked PRR-only and should be read as fragile. The strata column recomputes the PRR on serious reports only (and, for the 300 most-reported drugs, adjusted for age band), and flags pairs whose reports are unusually skewed by sex or come mostly from consumers. Each row also shows the PRR against the other drugs of the same FDA class, which removes most confounding by the condition being treated, and a calibrated p-value: on validation, known non-causes average an ROR of about 2, so significance is judged against that empirical null (✓ = p < 0.05 after calibration). 1,161 further terms are in the interactive explorer. Reaction links open the term's cross-drug page.

Show:
ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Mitral valve calcification2534.3
23.0–51.1ROR 34.3 · calibrated p 2e-4 ✓
32.2 EB05 23.0 · IC025 +3.7
3/3 methods agree
Not in label — unassessedserious n=25no trial data cached
Clear cell renal cell carcinoma2430.9
20.5–46.4ROR 30.9 · calibrated p 4e-4 ✓
29.2 EB05 20.6 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=24 · ♀ 0% (drug 52%) · 100% clinicianno trial data cached
Anoxic encephalopathy2229.7
19.4–45.4ROR 29.7 · calibrated p 5e-4 ✓
28.1 EB05 19.6 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=22no trial data cached
Cardioactive drug level increased4227.8
20.4–37.7ROR 27.8 · calibrated p 5e-4 ✓
26.6 EB05 20.5 · IC025 +3.9
3/3 methods agree
Lab value / disease markerserious n=42no trial data cached
Dyspnoea paroxysmal nocturnal2327.4
18.1–41.4ROR 27.4 · calibrated p 7e-4 ✓
26.0 EB05 18.2 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=23no trial data cached
Acute prerenal failure3627.0
19.3–37.6ROR 27.0 · calibrated p 6e-4 ✓
25.8 EB05 19.5 · IC025 +3.7
3/3 methods agree
Not in label — unassessedserious n=36 · 100% clinicianno trial data cached
Angioneurotic oedema7423.9
19.0–30.1ROR 24.0 · calibrated p 1e-3 ✓
23.2 EB05 19.1 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious n=72 · 90% clinicianno trial data cached
Dilatation atrial3122.9
16.0–32.7ROR 23.0 · calibrated p 0.001 ✓
22.1 EB05 16.3 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=30no trial data cached
Therapeutic agent toxicity8521.9
17.7–27.2ROR 22.0 · calibrated p 0.001 ✓
21.3 EB05 17.8 · IC025 +3.9
3/3 methods agree
Not in label — unassessedserious n=84no trial data cached
Sick sinus syndrome2921.7
15.0–31.4ROR 21.7 · calibrated p 0.002 ✓
20.9 EB05 15.2 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=29no trial data cached
Dilatation ventricular4518.4
13.7–24.7ROR 18.4 · calibrated p 0.004 ✓
17.9 EB05 13.8 · IC025 +3.4
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=45 · 100% clinicianno trial data cached
Left atrial dilatation2617.6
11.9–25.9ROR 17.6 · calibrated p 0.005 ✓
16.9 EB05 12.0 · IC025 +3.1
3/3 methods agree
Not in label — unassessedserious n=26no trial data cached
Loss of employment5816.5
12.7–21.4ROR 16.5 · calibrated p 0.005 ✓
16.1 EB05 12.8 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=58 · ♀ 100% (drug 52%)no trial data cached
Ventricular hypertrophy4816.4
12.3–21.8ROR 16.5 · calibrated p 0.006 ✓
16.0 EB05 12.5 · IC025 +3.3
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=46 · 100% clinicianno trial data cached
Left ventricular hypertrophy8116.4
13.1–20.4ROR 16.4 · calibrated p 0.005 ✓
16.0 EB05 13.3 · IC025 +3.5
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=80no trial data cached
Renal artery stenosis2415.0
10.0–22.4ROR 15.0 · calibrated p 0.009 ✓
14.3 EB05 9.8 · IC025 +2.8
3/3 methods agree
Labeled adverse reaction
exact term
serious n=24no trial data cached
Nodal rhythm2514.7
9.9–21.9ROR 14.7 · calibrated p 0.010 ✓
14.1 EB05 9.7 · IC025 +2.8
3/3 methods agree
Not in label — unassessedserious n=24no trial data cached
Aortic valve incompetence7114.4
11.4–18.2ROR 14.4 · calibrated p 0.009 ✓
14.0 EB05 11.4 · IC025 +3.3
3/3 methods agree
Not in label — unassessedserious n=72no trial data cached
Pulmonary valve incompetence2313.9
9.2–21.0ROR 13.9 · calibrated p 0.013 ✓
13.1 EB05 8.8 · IC025 +2.7
3/3 methods agree
Not in label — unassessedserious n=23no trial data cached
Nephrogenic systemic fibrosis4913.8
10.4–18.3ROR 13.9 · calibrated p 0.011 ✓
13.4 EB05 10.4 · IC025 +3.1
3/3 methods agree
Not in label — unassessedserious n=48no trial data cached
Lacunar infarction3813.7
10.0–18.9ROR 13.7 · calibrated p 0.012 ✓
13.2 EB05 9.9 · IC025 +3.0
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=38no trial data cached
Bundle branch block left6713.5
10.6–17.2ROR 13.6 · calibrated p 0.012 ✓
13.2 EB05 10.7 · IC025 +3.2
3/3 methods agree
Not in label — unassessedserious n=67no trial data cached
Intermittent claudication2513.5
9.1–20.1ROR 13.5 · calibrated p 0.014 ✓
12.8 EB05 8.8 · IC025 +2.8
3/3 methods agree
Not in label — unassessedserious n=23no trial data cached
Hyperkalaemia (high potassium)54613.5
12.4–14.7ROR 13.8 · calibrated p 0.010 ✓
13.3 EB05 12.4 · IC025 +3.6
3/3 methods agree
Labeled — boxed warning
exact term
serious PRR 9.6 · 94% clinicianno trial data cached
Carotid artery stenosis5413.3
10.2–17.4ROR 13.3 · calibrated p 0.013 ✓
12.9 EB05 10.1 · IC025 +3.1
3/3 methods agree
Not in label — unassessedserious n=54no trial data cached
Rhonchi2113.1
8.5–20.1ROR 13.1 · calibrated p 0.016 ✓
12.2 EB05 7.9 · IC025 +2.6
3/3 methods agree
Not in label — unassessedserious n=21no trial data cached
Diabetic nephropathy3312.9
9.1–18.1ROR 12.9 · calibrated p 0.016 ✓
12.3 EB05 8.9 · IC025 +2.9
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=33no trial data cached
Tricuspid valve incompetence11412.4
10.3–15.0ROR 12.5 · calibrated p 0.015 ✓
12.2 EB05 10.4 · IC025 +3.2
3/3 methods agree
Not in label — unassessedserious PRR 8.8no trial data cached
Essential hypertension3712.3
8.9–17.0ROR 12.3 · calibrated p 0.018 ✓
11.8 EB05 8.7 · IC025 +2.9
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=30no trial data cached
Mitral valve incompetence15912.1
10.4–14.2ROR 12.2 · calibrated p 0.016 ✓
11.9 EB05 10.4 · IC025 +3.3
3/3 methods agree
Not in label — unassessedserious PRR 8.6no trial data cached
Diabetic neuropathy6811.8
9.3–14.9ROR 11.8 · calibrated p 0.019 ✓
11.4 EB05 9.2 · IC025 +3.0
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=68no trial data cached
Blood urea increased22411.5
10.0–13.1ROR 11.6 · calibrated p 0.020 ✓
11.3 EB05 10.1 · IC025 +3.2
3/3 methods agree
Lab value / disease markerserious PRR 8.5no trial data cached
Atrioventricular block first degree5811.5
8.8–14.8ROR 11.5 · calibrated p 0.022 ✓
11.0 EB05 8.7 · IC025 +2.9
3/3 methods agree
Not in label — unassessedserious n=57 · 100% clinicianno trial data cached
Hypertensive heart disease2511.4
7.7–17.0ROR 11.4 · calibrated p 0.025 ✓
10.6 EB05 7.2 · IC025 +2.6
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious n=24no trial data cached
Colonic polyp2211.3
7.4–17.2ROR 11.3 · calibrated p 0.027 ✓
10.3 EB05 6.8 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious n=21no trial data cached
Skin induration2711.3
7.7–16.5ROR 11.3 · calibrated p 0.026 ✓
10.4 EB05 7.3 · IC025 +2.6
3/3 methods agree
Not in label — unassessedserious n=26no trial data cached

Trial evidence (ClinicalTrials.gov)

Trial cross-check not yet run for this drug (ClinicalTrials.gov pull covers the 800 most-reported drugs first).

Most frequently reported reactions

By raw co-report count, regardless of disproportionality. Common terms here are often the illness itself or generic outcomes.

ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Nausea1,3811.5
1.4–1.6ROR 1.5 · calibrated p 0.654
1.5 EB05 1.4 · IC025 +0.5Labeled — boxed warning
exact term
serious PRR 1.6no trial data cached
Dyspnoea (shortness of breath)1,2891.9
1.8–2.0ROR 2.0 · calibrated p 0.940
1.9 EB05 1.9 · IC025 +0.9Not in label — unassessedserious PRR 1.7no trial data cached
Diarrhoea (diarrhea)1,2741.7
1.6–1.8ROR 1.7 · calibrated p 0.784
1.7 EB05 1.6 · IC025 +0.7Not in label — unassessedserious PRR 1.7no trial data cached
Fatigue (tiredness)1,1381.2
1.2–1.3ROR 1.3 · calibrated p 0.480
1.2 EB05 1.2 · IC025 +0.2Labeled adverse reaction
exact term
serious PRR 1.2no trial data cached
Dizziness1,1041.9
1.8–2.0ROR 1.9 · calibrated p 0.905
1.9 EB05 1.8 · IC025 +0.8Labeled adverse reaction
exact term
serious PRR 1.9no trial data cached
Drug ineffective (drug did not work)1,0070.7
0.6–0.7ROR 0.6 · calibrated p 0.100
0.7 EB05 0.6 · IC025 -0.7
PRR-only: not supported by EBGM or IC
Reporting / coding artifactserious PRR 0.8no trial data cached
Pain9511.3
1.2–1.4ROR 1.3 · calibrated p 0.527
1.3 EB05 1.2 · IC025 +0.3Labeled — boxed warning
exact term
serious PRR 1.3no trial data cached
Vomiting9301.7
1.6–1.8ROR 1.7 · calibrated p 0.779
1.7 EB05 1.6 · IC025 +0.6Labeled — boxed warning
exact term
serious PRR 1.6no trial data cached
Asthenia (weakness)8972.0
1.9–2.2ROR 2.1 · calibrated p 0.982
2.0 EB05 1.9 · IC025 +0.9Labeled adverse reaction
exact term
serious PRR 1.8no trial data cached
Hypertension (high blood pressure)8903.6
3.4–3.8ROR 3.7 · calibrated p 0.443
3.6 EB05 3.4 · IC025 +1.7
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious PRR 3.0no trial data cached
Headache8761.2
1.1–1.3ROR 1.2 · calibrated p 0.439
1.2 EB05 1.1 · IC025 +0.1Not in label — unassessedserious PRR 1.3no trial data cached
Drug interaction8444.5
4.3–4.9ROR 4.7 · calibrated p 0.274
4.5 EB05 4.3 · IC025 +2.1
3/3 methods agree
Reporting / coding artifactserious PRR 3.5no trial data cached
Fall8232.1
2.0–2.3ROR 2.1 · calibrated p 0.978
2.1 EB05 2.0 · IC025 +1.0Not in label — unassessedserious PRR 1.7no trial data cached
Hypotension (low blood pressure)7903.4
3.1–3.6ROR 3.4 · calibrated p 0.499
3.3 EB05 3.2 · IC025 +1.6
3/3 methods agree
Labeled — boxed warning
exact term
serious PRR 2.7no trial data cached
Myocardial infarction (heart attack)7763.8
3.5–4.0ROR 3.9 · calibrated p 0.406
3.7 EB05 3.5 · IC025 +1.8
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious PRR 2.7no trial data cached

Unlabeled candidate signals

These flagged terms were not found in the FDA label text and do not match an artifact pattern. They are the pairs that would merit a structured assessment (temporality, dose-response, biological plausibility, consistency across databases, trial or cohort evidence). The screen has not done that; string-matching misses label wording, and a strong PRR can still be stimulated reporting, co-medication, or the disease itself.

Want to assess one of these properly? The runbook describes the Bradford Hill / trial-evidence workflow used on the assessment page, and handoff_top1000_signals.csv lists the strongest unassessed pairs across all drugs.

Common questions

What are the most reported side effects of Enalapril Maleate?

In FDA FAERS, the most frequently co-reported reaction terms for Enalapril Maleate are nausea, dyspnoea, diarrhoea, fatigue, dizziness, pain. These are report counts, not rates: FAERS has no denominator, reporting is voluntary and uneven, and a term can be reported because of the illness being treated rather than the drug.

Does Enalapril Maleate have an FDA boxed warning?

Yes. The current FDA label carries a boxed warning: FETAL TOXICITY When pregnancy is detected, discontinue enalapril maleate as soon as possible [see Warnings and Precautions (5.1) ]. Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus [see Warnings and Precautions (5.1) ].

Do FAERS signals prove that Enalapril Maleate causes these side effects?

No. A disproportionality signal (PRR, ROR) means a reaction is reported more often with this drug than with others in the database. That can reflect a real effect, but also the disease being treated, stimulated reporting after news or litigation, co-medications, or how reports are coded. Causality needs temporality, dose-response, biological plausibility, consistency across data sources and, ideally, trial or cohort evidence. This page screens each term against the FDA label and ClinicalTrials.gov results; it does not establish causation.

Sources & methods

Page generated 2026-10-14. Label and PubChem text are retrieved automatically and may lag the current label; always check the current prescribing information. OpenPV is a beta research tool of the Open Source Medicine Foundation.