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Enalapril side effects: what 55,275 FDA adverse event reports show

Enalapril · Enalapril Maleate · 1,197 reaction terms · 205,656 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

55,275 reports · 84% serious · 5,996 with death outcome · 50% 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 (related wording) 6Likely indication confounding 10Lab value / disease marker 2Not in label — unassessed 21
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). 1,157 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
Clear cell renal cell carcinoma5432.4
24.5–42.8ROR 32.4 · calibrated p 2e-4 ✓
29.6 EB05 23.6 · IC025 +4.1
3/3 methods agree
Not in label — unassessedserious n=54 · ♀ 0% (drug 50%)NCT01035255: 1/4,229 (0.0%) on Enalapril (serious AE)
Loss of employment11314.6
12.1–17.6ROR 14.6 · calibrated p 0.008 ✓
14.0 EB05 11.9 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=113 · ♀ 100% (drug 50%)not reported in cached trials
Cardioactive drug level increased4814.2
10.6–18.9ROR 14.2 · calibrated p 0.010 ✓
13.5 EB05 10.5 · IC025 +3.1
3/3 methods agree
Lab value / disease markerserious n=48 · 100% clinicianNCT00853658: 1/2,348 (0.0%) on Enalapril (serious AE)
Atrioventricular block complete20912.2
10.7–14.0ROR 12.3 · calibrated p 0.016 ✓
11.8 EB05 10.5 · IC025 +3.3
3/3 methods agree
Not in label — unassessedserious n=209NCT01035255: 10/4,229 (0.2%) on Enalapril (serious AE)
Hyperkalaemia (high potassium)1,08612.2
11.4–12.9ROR 12.4 · calibrated p 0.015 ✓
11.8 EB05 11.2 · IC025 +3.5
3/3 methods agree
Labeled — boxed warning
exact term
serious PRR 8.2 · 94% clinicianNCT01035255: 42/4,229 (1.0%) on Enalapril (serious AE)
Vascular stent thrombosis6011.5
8.9–14.9ROR 11.5 · calibrated p 0.022 ✓
10.9 EB05 8.7 · IC025 +2.9
3/3 methods agree
Not in label — unassessedserious n=60 · ♀ 0% (drug 50%) · 100% clinicianNCT00853658: 2/2,345 (0.1%) on Enalapril (serious AE)
Angioneurotic oedema7310.5
8.3–13.3ROR 10.5 · calibrated p 0.029 ✓
10.0 EB05 8.1 · IC025 +2.9
3/3 methods agree
Not in label — unassessedserious n=71 · 100% cliniciannot reported in cached trials
Nephrogenic anaemia12210.1
8.5–12.1ROR 10.2 · calibrated p 0.032 ✓
9.7 EB05 8.3 · IC025 +3.0
3/3 methods agree
Not in label — unassessedserious n=122NCT01035255: 1/4,203 (0.0%) on Enalapril (serious AE)
Therapeutic agent toxicity8810.1
8.2–12.5ROR 10.1 · calibrated p 0.033 ✓
9.7 EB05 8.0 · IC025 +2.9
3/3 methods agree
Not in label — unassessedserious n=87not reported in cached trials
Gingival hypertrophy379.6
6.9–13.2ROR 9.6 · calibrated p 0.043 ✓
8.8 EB05 6.5 · IC025 +2.5
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
♀ 0% (drug 50%) · 100% cliniciannot reported in cached trials
Left ventricular hypertrophy1009.0
7.4–11.0ROR 9.1 · calibrated p 0.047 ✓
8.6 EB05 7.3 · IC025 +2.8
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=99not reported in cached trials
Bradyarrhythmia389.0
6.5–12.4ROR 9.0 · calibrated p 0.052
8.2 EB05 6.2 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious n=38 · ♀ 0% (drug 50%) · 100% clinicianNCT01035255: 4/4,229 (0.1%) on Enalapril (serious AE)
Venous occlusion428.9
6.5–12.1ROR 8.9 · calibrated p 0.053
8.2 EB05 6.2 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious n=42 · 100% consumernot reported in cached trials
Orthopnoea728.7
6.9–11.0ROR 8.7 · calibrated p 0.053
8.3 EB05 6.7 · IC025 +2.6
3/3 methods agree
Not in label — unassessedserious n=71NCT01035255: 3/4,229 (0.1%) on Enalapril (serious AE)
Hypertensive heart disease418.4
6.2–11.5ROR 8.4 · calibrated p 0.062
7.8 EB05 5.9 · IC025 +2.4
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious n=40 · ♀ 100% (drug 50%) · 100% clinicianNCT01035255: 2/4,229 (0.0%) on Enalapril (serious AE)
Lymphoproliferative disorder618.0
6.2–10.3ROR 8.0 · calibrated p 0.070
7.5 EB05 6.0 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious n=61 · ♀ 0% (drug 50%)not reported in cached trials
Hypertensive crisis2207.6
6.7–8.7ROR 7.6 · calibrated p 0.078
7.4 EB05 6.6 · IC025 +2.7
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious PRR 5.1NCT01035255: 2/4,229 (0.0%) on Enalapril (serious AE)
Bundle branch block left837.5
6.0–9.3ROR 7.5 · calibrated p 0.084
7.1 EB05 5.9 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious n=83NCT01035255: 3/4,229 (0.1%) on Enalapril (serious AE)
Hyperparathyroidism secondary497.5
5.6–9.9ROR 7.5 · calibrated p 0.088
6.9 EB05 5.4 · IC025 +2.3
3/3 methods agree
Not in label — unassessedserious n=49not reported in cached trials
Dilatation ventricular417.4
5.5–10.1ROR 7.4 · calibrated p 0.090
6.8 EB05 5.2 · IC025 +2.2
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=41 · ♀ 0% (drug 50%) · 100% clinicianNCT01035255: 1/4,203 (0.0%) on Enalapril (serious AE)
Hypovolaemic shock907.3
5.9–9.0ROR 7.3 · calibrated p 0.091
7.0 EB05 5.8 · IC025 +2.4
3/3 methods agree
Not in label — unassessedserious n=90 · 100% clinicianNCT01035255: 2/4,229 (0.0%) on Enalapril (serious AE)
Inappropriate antidiuretic hormone secretion1897.2
6.2–8.3ROR 7.2 · calibrated p 0.093
6.9 EB05 6.1 · IC025 +2.6
3/3 methods agree
Not in label — unassessedserious PRR 4.9 · 92% cliniciannot reported in cached trials
Ventricular hypertrophy477.2
5.4–9.5ROR 7.2 · calibrated p 0.099
6.6 EB05 5.2 · IC025 +2.2
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=46 · 100% cliniciannot reported in cached trials
Pancreatitis necrotising427.1
5.3–9.7ROR 7.1 · calibrated p 0.101
6.6 EB05 5.0 · IC025 +2.2
3/3 methods agree
Not in label — unassessedserious n=42 · ♀ 0% (drug 50%) · 100% clinicianNCT00853658: 1/2,345 (0.0%) on Enalapril (serious AE)
Diabetic retinopathy627.0
5.5–9.0ROR 7.0 · calibrated p 0.102
6.6 EB05 5.3 · IC025 +2.3
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=62NCT01035255: 1/4,229 (0.0%) on Enalapril (serious AE)
Blood urea increased3026.9
6.2–7.7ROR 6.9 · calibrated p 0.102
6.7 EB05 6.1 · IC025 +2.6
3/3 methods agree
Lab value / disease markerserious PRR 5.0 · 91% cliniciannot reported in cached trials
Rebound acid hypersecretion556.9
5.3–9.0ROR 6.9 · calibrated p 0.108
6.5 EB05 5.1 · IC025 +2.2
3/3 methods agree
Not in label — unassessedserious n=55not reported in cached trials
Cardiomegaly2186.8
5.9–7.7ROR 6.8 · calibrated p 0.109
6.6 EB05 5.9 · IC025 +2.5
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious PRR 4.6NCT01035255: 5/4,229 (0.1%) on Enalapril (serious AE)
Angina unstable1136.6
5.5–8.0ROR 6.6 · calibrated p 0.117
6.4 EB05 5.4 · IC025 +2.4
3/3 methods agree
Not in label — unassessedserious n=111NCT01035255: 51/4,229 (1.2%) on Enalapril (serious AE)
Diabetic nephropathy386.6
4.8–9.1ROR 6.6 · calibrated p 0.125
6.1 EB05 4.6 · IC025 +2.1
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=37NCT01035255: 2/4,229 (0.0%) on Enalapril (serious AE)
Aortic valve incompetence736.6
5.2–8.3ROR 6.6 · calibrated p 0.121
6.3 EB05 5.1 · IC025 +2.3
3/3 methods agree
Not in label — unassessedserious n=74NCT01035255: 4/4,229 (0.1%) on Enalapril (serious AE)
Left ventricular failure576.4
4.9–8.3ROR 6.4 · calibrated p 0.131
6.0 EB05 4.8 · IC025 +2.2
3/3 methods agree
Likely indication confounding
term in indications
serious n=57 · 100% clinicianNCT01035255: 5/4,229 (0.1%) on Enalapril (serious AE)
Hypovolaemia966.3
5.2–7.7ROR 6.3 · calibrated p 0.134
6.1 EB05 5.1 · IC025 +2.3
3/3 methods agree
Not in label — unassessedserious n=95NCT01035255: 2/4,229 (0.0%) on Enalapril (serious AE)
Haemorrhagic anaemia736.3
5.0–7.9ROR 6.3 · calibrated p 0.137
6.0 EB05 4.9 · IC025 +2.2
3/3 methods agree
Not in label — unassessedserious n=73NCT01035255: 3/4,229 (0.1%) on Enalapril (serious AE)

Trial evidence (ClinicalTrials.gov)

✓ Trial adverse-event data found on ClinicalTrials.gov

Largest completed trials with posted results that list Enalapril as a study intervention. The right-hand column of the signal table shows whether each FAERS term was also recorded in these trials, with a real denominator (27 of 40 signal terms matched).

Caveats: trial populations, doses and follow-up differ from the reporting population; AE terms are sponsor-coded and matched here by wording; absence from a trial list means the term was not reported above the sponsor's frequency threshold, not that it cannot occur.

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
Diarrhoea (diarrhea)2,8751.7
1.6–1.8ROR 1.7 · calibrated p 0.792
1.7 EB05 1.6 · IC025 +0.7Not in label — unassessedserious PRR 1.7NCT01035255: 15/4,229 (0.4%) on Enalapril (serious AE)
Dyspnoea (shortness of breath)2,7021.8
1.8–1.9ROR 1.9 · calibrated p 0.864
1.8 EB05 1.8 · IC025 +0.8Not in label — unassessedserious PRR 1.6NCT01035255: 57/4,229 (1.3%) on Enalapril (serious AE)
Nausea2,6161.3
1.2–1.3ROR 1.3 · calibrated p 0.489
1.3 EB05 1.2 · IC025 +0.3Labeled — boxed warning
exact term
serious PRR 1.3NCT01035255: 6/4,229 (0.1%) on Enalapril (serious AE)
Drug ineffective (drug did not work)2,5970.7
0.7–0.8ROR 0.7 · calibrated p 0.148
0.7 EB05 0.7 · IC025 -0.5
PRR-only: not supported by EBGM or IC
Reporting / coding artifactserious PRR 1.0not reported in cached trials
Fatigue (tiredness)2,4231.2
1.1–1.2ROR 1.2 · calibrated p 0.435
1.2 EB05 1.1 · IC025 +0.2Labeled adverse reaction
exact term
serious PRR 1.2NCT01035255: 10/4,229 (0.2%) on Enalapril (serious AE)
Drug interaction2,3785.8
5.5–6.0ROR 6.0 · calibrated p 0.152
5.7 EB05 5.5 · IC025 +2.4
3/3 methods agree
Reporting / coding artifactserious PRR 4.3not reported in cached trials
Dizziness2,2611.7
1.7–1.8ROR 1.8 · calibrated p 0.804
1.7 EB05 1.7 · IC025 +0.7Labeled adverse reaction
exact term
serious PRR 1.7NCT01035255: 5/4,229 (0.1%) on Enalapril (serious AE)
Acute kidney injury (sudden kidney damage)2,0835.2
5.0–5.5ROR 5.4 · calibrated p 0.194
5.2 EB05 5.0 · IC025 +2.3
3/3 methods agree
Labeled — boxed warning
synonym match
serious PRR 3.6 · 91% clinicianNCT00853658: 38/2,345 (1.6%) on Enalapril (serious AE)
Vomiting2,0131.6
1.6–1.7ROR 1.7 · calibrated p 0.741
1.6 EB05 1.6 · IC025 +0.6Labeled — boxed warning
exact term
serious PRR 1.5NCT01035255: 14/4,229 (0.3%) on Enalapril (serious AE)
Headache1,8571.1
1.1–1.2ROR 1.1 · calibrated p 0.393
1.1 EB05 1.1 · IC025 +0.1Not in label — unassessedserious PRR 1.2NCT01035255: 3/4,203 (0.1%) on Enalapril (serious AE)
Pain1,8381.1
1.1–1.2ROR 1.1 · calibrated p 0.398
1.1 EB05 1.1 · IC025 +0.1Labeled — boxed warning
exact term
serious PRR 1.0NCT01035255: 23/4,229 (0.5%) on Enalapril (serious AE)
Asthenia (weakness)1,7821.8
1.7–1.9ROR 1.8 · calibrated p 0.846
1.8 EB05 1.7 · IC025 +0.8Labeled adverse reaction
exact term
serious PRR 1.5NCT01035255: 9/4,229 (0.2%) on Enalapril (serious AE)
Off label use (used outside approved label)1,7760.8
0.7–0.8ROR 0.8 · calibrated p 0.166
0.8 EB05 0.7 · IC025 -0.4
PRR-only: not supported by EBGM or IC
Reporting / coding artifactserious PRR 0.8not reported in cached trials
Hypotension (low blood pressure)1,7313.3
3.1–3.5ROR 3.4 · calibrated p 0.517
3.3 EB05 3.1 · IC025 +1.6
3/3 methods agree
Labeled — boxed warning
exact term
serious PRR 2.5NCT01035255: 68/4,229 (1.6%) on Enalapril (serious AE)
Hypertension (high blood pressure)1,7223.1
3.0–3.2ROR 3.2 · calibrated p 0.575
3.1 EB05 3.0 · IC025 +1.5
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious PRR 2.5NCT01035255: 1/4,229 (0.0%) on Enalapril (serious AE)

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?

In FDA FAERS, the most frequently co-reported reaction terms for Enalapril are diarrhoea, dyspnoea, nausea, fatigue, dizziness, acute kidney injury. 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 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 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.