Enalapril side effects: what 55,275 FDA adverse event reports show
Drug class
Angiotensin-converting enzyme inhibitor
Brand names
Enalapril Maleate
Who reports
55,275 reports · 84% serious · 5,996 with death outcome · 50% female
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.
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.
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) ].
Causality screen of the 40 strongest signals
What the badges mean
- Labeled — boxed warning The term (or its clinical synonym) appears in the FDA boxed warning: causality is regulator-recognised and considered serious.
- Labeled (related wording) The label describes this effect under different wording (e.g. 'neutropenia' for 'neutrophil count decreased'). Treated as known.
- Likely indication confounding The term appears in the label's indications: reports probably describe the disease being treated (or its progression), not a drug effect. Classic confounding by indication.
- Lab value / disease marker A laboratory result, investigation or disease-activity marker (antibody positive, CRP abnormal, swollen joint count) not described in the label. These usually mirror the monitored disease or testing protocol rather than a drug effect; not screened further.
- Not in label — unassessed Not found in the label text, not an artifact pattern. This is a genuine candidate for a formal causality assessment (Bradford Hill / WHO-UMC); it has NOT had one here.
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.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Clear cell renal cell carcinoma | 54 | 32.4 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 — unassessed | serious n=54 · ♀ 0% (drug 50%) | NCT01035255: 1/4,229 (0.0%) on Enalapril (serious AE) |
| Loss of employment | 113 | 14.6 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 — unassessed | serious n=113 · ♀ 100% (drug 50%) | not reported in cached trials |
| Cardioactive drug level increased | 48 | 14.2 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 marker | serious n=48 · 100% clinician | NCT00853658: 1/2,348 (0.0%) on Enalapril (serious AE) |
| Atrioventricular block complete | 209 | 12.2 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 — unassessed | serious n=209 | NCT01035255: 10/4,229 (0.2%) on Enalapril (serious AE) |
| Hyperkalaemia (high potassium) | 1,086 | 12.2 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% clinician | NCT01035255: 42/4,229 (1.0%) on Enalapril (serious AE) |
| Concomitant disease progression | 61 | 12.1 9.3–15.6ROR 12.1 · calibrated p 0.018 ✓ | 11.5 EB05 9.2 · IC025 +3.0 3/3 methods agree | Labeled (related wording) related wording | serious n=61 · 100% clinician | not reported in cached trials |
| Vascular stent thrombosis | 60 | 11.5 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 — unassessed | serious n=60 · ♀ 0% (drug 50%) · 100% clinician | NCT00853658: 2/2,345 (0.1%) on Enalapril (serious AE) |
| Angioneurotic oedema | 73 | 10.5 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 — unassessed | serious n=71 · 100% clinician | not reported in cached trials |
| Nephrogenic anaemia | 122 | 10.1 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 — unassessed | serious n=122 | NCT01035255: 1/4,203 (0.0%) on Enalapril (serious AE) |
| Therapeutic agent toxicity | 88 | 10.1 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 — unassessed | serious n=87 | not reported in cached trials |
| Gingival hypertrophy | 37 | 9.6 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% clinician | not reported in cached trials |
| Cardiac failure chronic | 103 | 9.4 7.7–11.4ROR 9.4 · calibrated p 0.042 ✓ | 9.0 EB05 7.6 · IC025 +2.8 3/3 methods agree | Labeled (related wording) related wording | serious n=103 · ♀ 27% (drug 50%) · 100% clinician | NCT01035255: 649/4,229 (15.3%) on Enalapril (serious AE) |
| Left ventricular hypertrophy | 100 | 9.0 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=99 | not reported in cached trials |
| Tongue oedema | 89 | 9.0 7.3–11.1ROR 9.0 · calibrated p 0.048 ✓ | 8.6 EB05 7.1 · IC025 +2.7 3/3 methods agree | Labeled (related wording) related wording | serious n=89 · 100% clinician | NCT00853658: 1/2,347 (0.0%) on Enalapril (serious AE) |
| Bradyarrhythmia | 38 | 9.0 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 — unassessed | serious n=38 · ♀ 0% (drug 50%) · 100% clinician | NCT01035255: 4/4,229 (0.1%) on Enalapril (serious AE) |
| Venous occlusion | 42 | 8.9 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 — unassessed | serious n=42 · 100% consumer | not reported in cached trials |
| Orthopnoea | 72 | 8.7 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 — unassessed | serious n=71 | NCT01035255: 3/4,229 (0.1%) on Enalapril (serious AE) |
| Hypertensive heart disease | 41 | 8.4 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% clinician | NCT01035255: 2/4,229 (0.0%) on Enalapril (serious AE) |
| Renal failure acute | 925 | 8.3 7.8–8.9ROR 8.4 · calibrated p 0.057 | 8.1 EB05 7.7 · IC025 +2.9 3/3 methods agree | Labeled (related wording) related wording | serious PRR 5.6 · 91% clinician | NCT01035255: 1/4,203 (0.0%) on Enalapril (serious AE) |
| Lymphoproliferative disorder | 61 | 8.0 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 — unassessed | serious n=61 · ♀ 0% (drug 50%) | not reported in cached trials |
| Hypertensive crisis | 220 | 7.6 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 5.1 | NCT01035255: 2/4,229 (0.0%) on Enalapril (serious AE) |
| Bundle branch block left | 83 | 7.5 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 — unassessed | serious n=83 | NCT01035255: 3/4,229 (0.1%) on Enalapril (serious AE) |
| Hyperparathyroidism secondary | 49 | 7.5 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 — unassessed | serious n=49 | not reported in cached trials |
| Dilatation ventricular | 41 | 7.4 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% clinician | NCT01035255: 1/4,203 (0.0%) on Enalapril (serious AE) |
| Hypovolaemic shock | 90 | 7.3 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 — unassessed | serious n=90 · 100% clinician | NCT01035255: 2/4,229 (0.0%) on Enalapril (serious AE) |
| Inappropriate antidiuretic hormone secretion | 189 | 7.2 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 — unassessed | serious PRR 4.9 · 92% clinician | not reported in cached trials |
| Ventricular hypertrophy | 47 | 7.2 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% clinician | not reported in cached trials |
| Pancreatitis necrotising | 42 | 7.1 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 — unassessed | serious n=42 · ♀ 0% (drug 50%) · 100% clinician | NCT00853658: 1/2,345 (0.0%) on Enalapril (serious AE) |
| Diabetic retinopathy | 62 | 7.0 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=62 | NCT01035255: 1/4,229 (0.0%) on Enalapril (serious AE) |
| Ischaemic cardiomyopathy | 56 | 7.0 5.3–9.1ROR 7.0 · calibrated p 0.105 | 6.5 EB05 5.2 · IC025 +2.3 3/3 methods agree | Labeled (related wording) related wording | serious n=56 · ♀ 0% (drug 50%) · 100% clinician | NCT01035255: 14/4,229 (0.3%) on Enalapril (serious AE) |
| Blood urea increased | 302 | 6.9 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 marker | serious PRR 5.0 · 91% clinician | not reported in cached trials |
| Rebound acid hypersecretion | 55 | 6.9 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 — unassessed | serious n=55 | not reported in cached trials |
| Cardiomegaly | 218 | 6.8 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 4.6 | NCT01035255: 5/4,229 (0.1%) on Enalapril (serious AE) |
| Angina unstable | 113 | 6.6 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 — unassessed | serious n=111 | NCT01035255: 51/4,229 (1.2%) on Enalapril (serious AE) |
| Diabetic nephropathy | 38 | 6.6 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=37 | NCT01035255: 2/4,229 (0.0%) on Enalapril (serious AE) |
| Aortic valve incompetence | 73 | 6.6 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 — unassessed | serious n=74 | NCT01035255: 4/4,229 (0.1%) on Enalapril (serious AE) |
| Left ventricular failure | 57 | 6.4 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% clinician | NCT01035255: 5/4,229 (0.1%) on Enalapril (serious AE) |
| Cardiac failure acute | 110 | 6.4 5.3–7.7ROR 6.4 · calibrated p 0.131 | 6.1 EB05 5.2 · IC025 +2.3 3/3 methods agree | Labeled (related wording) related wording | serious n=110 · 100% clinician | NCT01035255: 649/4,229 (15.3%) on Enalapril (serious AE) |
| Hypovolaemia | 96 | 6.3 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 — unassessed | serious n=95 | NCT01035255: 2/4,229 (0.0%) on Enalapril (serious AE) |
| Haemorrhagic anaemia | 73 | 6.3 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 — unassessed | serious n=73 | NCT01035255: 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).
- NCT01035255 — This Study Will Evaluate the Efficacy and Safety of LCZ696 Compared to Enalapril on Morbidity and Mortality of (N=8442, PHASE3; 1208 AE terms posted; arms: LCZ696; Enalapril)
- NCT00853658 — Efficacy and Safety of Aliskiren and Aliskiren/Enalapril Combination on Morbidity-mortality in Patients With C (N=7064, PHASE3; 1382 AE terms posted; arms: Combination of Aliskiren and Enalapril; Aliskiren; Enalapril)
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.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Diarrhoea (diarrhea) | 2,875 | 1.7 1.6–1.8ROR 1.7 · calibrated p 0.792 | 1.7 EB05 1.6 · IC025 +0.7 | Not in label — unassessed | serious PRR 1.7 | NCT01035255: 15/4,229 (0.4%) on Enalapril (serious AE) |
| Dyspnoea (shortness of breath) | 2,702 | 1.8 1.8–1.9ROR 1.9 · calibrated p 0.864 | 1.8 EB05 1.8 · IC025 +0.8 | Not in label — unassessed | serious PRR 1.6 | NCT01035255: 57/4,229 (1.3%) on Enalapril (serious AE) |
| Nausea | 2,616 | 1.3 1.2–1.3ROR 1.3 · calibrated p 0.489 | 1.3 EB05 1.2 · IC025 +0.3 | Labeled — boxed warning exact term | serious PRR 1.3 | NCT01035255: 6/4,229 (0.1%) on Enalapril (serious AE) |
| Drug ineffective (drug did not work) | 2,597 | 0.7 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 artifact | serious PRR 1.0 | not reported in cached trials |
| Fatigue (tiredness) | 2,423 | 1.2 1.1–1.2ROR 1.2 · calibrated p 0.435 | 1.2 EB05 1.1 · IC025 +0.2 | Labeled adverse reaction exact term | serious PRR 1.2 | NCT01035255: 10/4,229 (0.2%) on Enalapril (serious AE) |
| Drug interaction | 2,378 | 5.8 5.5–6.0ROR 6.0 · calibrated p 0.152 | 5.7 EB05 5.5 · IC025 +2.4 3/3 methods agree | Reporting / coding artifact | serious PRR 4.3 | not reported in cached trials |
| Dizziness | 2,261 | 1.7 1.7–1.8ROR 1.8 · calibrated p 0.804 | 1.7 EB05 1.7 · IC025 +0.7 | Labeled adverse reaction exact term | serious PRR 1.7 | NCT01035255: 5/4,229 (0.1%) on Enalapril (serious AE) |
| Acute kidney injury (sudden kidney damage) | 2,083 | 5.2 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% clinician | NCT00853658: 38/2,345 (1.6%) on Enalapril (serious AE) |
| Vomiting | 2,013 | 1.6 1.6–1.7ROR 1.7 · calibrated p 0.741 | 1.6 EB05 1.6 · IC025 +0.6 | Labeled — boxed warning exact term | serious PRR 1.5 | NCT01035255: 14/4,229 (0.3%) on Enalapril (serious AE) |
| Headache | 1,857 | 1.1 1.1–1.2ROR 1.1 · calibrated p 0.393 | 1.1 EB05 1.1 · IC025 +0.1 | Not in label — unassessed | serious PRR 1.2 | NCT01035255: 3/4,203 (0.1%) on Enalapril (serious AE) |
| Pain | 1,838 | 1.1 1.1–1.2ROR 1.1 · calibrated p 0.398 | 1.1 EB05 1.1 · IC025 +0.1 | Labeled — boxed warning exact term | serious PRR 1.0 | NCT01035255: 23/4,229 (0.5%) on Enalapril (serious AE) |
| Asthenia (weakness) | 1,782 | 1.8 1.7–1.9ROR 1.8 · calibrated p 0.846 | 1.8 EB05 1.7 · IC025 +0.8 | Labeled adverse reaction exact term | serious PRR 1.5 | NCT01035255: 9/4,229 (0.2%) on Enalapril (serious AE) |
| Off label use (used outside approved label) | 1,776 | 0.8 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 artifact | serious PRR 0.8 | not reported in cached trials |
| Hypotension (low blood pressure) | 1,731 | 3.3 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 2.5 | NCT01035255: 68/4,229 (1.6%) on Enalapril (serious AE) |
| Hypertension (high blood pressure) | 1,722 | 3.1 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 2.5 | NCT01035255: 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.
- Clear cell renal cell carcinoma — n=54, PRR 32.4 (also seen in trial arm)
- Loss of employment — n=113, PRR 14.6
- Atrioventricular block complete — n=209, PRR 12.2 (also seen in trial arm)
- Vascular stent thrombosis — n=60, PRR 11.5 (also seen in trial arm)
- Angioneurotic oedema — n=73, PRR 10.5
- Nephrogenic anaemia — n=122, PRR 10.1 (also seen in trial arm)
- Therapeutic agent toxicity — n=88, PRR 10.1
- Bradyarrhythmia — n=38, PRR 9.0 (also seen in trial arm)
- Venous occlusion — n=42, PRR 8.9
- Orthopnoea — n=72, PRR 8.7 (also seen in trial arm)
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
- FDA label via openFDA (set ID e81a8aca-0e7c-4a02-b596-09e4ac22c70e, effective 20190329; matched on
openfda.generic_name.exact:"ENALAPRIL") - Bayesian shrinkage measures computed offline over all 1,317,300 cached pairs: BCPNN information component (IC, with Norén closed-form IC025) and MGPS empirical-Bayes geometric mean (EBGM, EB05) with a two-component gamma prior fitted by maximum marginal likelihood (α₁=0.57, β₁=0.02, α₂=1.42, β₂=0.70, w=0.17); unstratified
- FAERS pair statistics from the OpenPV build of 2026-09-14 (openFDA
count=aggregation, fieldpatient.drug.openfda.generic_name.exact, 1,197 reaction terms, min 3 co-reports); PRR/ROR with 95% CI, chi-square with Yates correction - Serious-only and stratified counts (serious:1, patient.patientsex, primarysource.qualification) from openFDA count queries; serious-only PRR uses the drug serious report total and the term global serious total (N_serious=11,882,979); strata shown only when n ≥ 20
- Seriousness and sex counts from openFDA
count=serious,patient.patientsex,seriousnessdeath - ClinicalTrials.gov API v2 (query
ENALAPRIL, results-bearing studies sorted by enrollment)
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.