Nifedipine side effects: what 41,044 FDA adverse event reports show
Drug class
Dihydropyridine Calcium Channel Blocker
Who reports
41,044 reports · 80% serious · 4,780 with death outcome · 56% female
Used for
I. Vasospastic Angina Nifedipine extended-release tablets are indicated for the management of vasospastic angina confirmed by any of the following criteria: 1) classical pattern of angina at rest accompanied by ST segment elevation, 2) angina or coronary artery spasm provoked by ergonovine, or 3) angiographically demonstrated coronary artery spasm.
What it is
DESCRIPTION Nifedipine is a drug belonging to a class of pharmacological agents known as the calcium channel blockers. Nifedipine is 3,5-pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(.
Boxed warning
None in the current label
Causality screen of the 40 strongest signals
What the badges mean
- Labeled adverse reaction The exact term appears in the label's warnings or adverse-reactions sections: a known, expected effect. The FAERS signal confirms the label rather than discovering anything.
- 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.
- 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). 1,159 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 |
|---|---|---|---|---|---|---|
| Neovascularisation | 64 | 149.0 112.3–197.8ROR 149.2 · calibrated p 9e-9 ✓ | 108.1 EB05 87.6 · IC025 +5.5 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=64 · ♀ 100% (drug 56%) · 100% clinician | not reported in cached trials |
| Dysplastic naevus | 34 | 46.8 32.8–66.6ROR 46.8 · calibrated p 4e-5 ✓ | 41.5 EB05 31.0 · IC025 +4.2 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=34 · ♀ 0% (drug 56%) · 100% clinician | not reported in cached trials |
| Photodermatosis | 39 | 44.9 32.3–62.5ROR 45.0 · calibrated p 4e-5 ✓ | 40.1 EB05 30.6 · IC025 +4.2 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=38 · ♀ 0% (drug 56%) · 100% clinician | not reported in cached trials |
| Chronic kidney disease-mineral and bone disorder | 86 | 38.8 31.1–48.3ROR 38.8 · calibrated p 7e-5 ✓ | 35.5 EB05 29.6 · IC025 +4.5 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=78 | not reported in cached trials |
| Nephrogenic anaemia | 305 | 31.1 27.7–35.0ROR 31.3 · calibrated p 2e-4 ✓ | 29.1 EB05 26.5 · IC025 +4.6 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: PRR 77.5 (52.3–114.8) | Not in label — unassessed | serious n=280 | not reported in cached trials |
| Hyperparathyroidism secondary | 155 | 29.1 24.7–34.2ROR 29.2 · calibrated p 3e-4 ✓ | 27.3 EB05 23.9 · IC025 +4.4 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: PRR 88.6 (49.2–159.4) | Not in label — unassessed | serious n=144 | not reported in cached trials |
| Wrist deformity | 37 | 28.3 20.3–39.5ROR 28.3 · calibrated p 5e-4 ✓ | 26.3 EB05 20.0 · IC025 +3.8 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=38 · ♀ 100% (drug 56%) · 100% clinician | not reported in cached trials |
| Hellp syndrome | 36 | 27.6 19.7–38.6ROR 27.6 · calibrated p 6e-4 ✓ | 25.7 EB05 19.4 · IC025 +3.7 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=33 · ♀ 100% (drug 56%) · 100% clinician | not reported in cached trials |
| Gingival hypertrophy | 81 | 25.4 20.3–31.8ROR 25.5 · calibrated p 7e-4 ✓ | 24.0 EB05 19.9 · IC025 +4.0 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: PRR 37.0 (21.4–64.2) | Likely indication confounding shares a disease stem with the indications wording | serious n=70 · ♀ 24% (drug 56%) · 100% clinician | not reported in cached trials |
| Blood pressure systolic abnormal | 129 | 24.4 20.4–29.1ROR 24.4 · calibrated p 8e-4 ✓ | 23.1 EB05 19.9 · IC025 +4.1 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: PRR 98.3 (50.0–193.2) | Likely indication confounding term in indications | serious n=128 · ♀ 100% (drug 56%) | not reported in cached trials |
| Low birth weight baby | 410 | 24.3 22.0–26.8ROR 24.5 · calibrated p 8e-4 ✓ | 23.0 EB05 21.2 · IC025 +4.3 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious PRR 19.2 · 93% clinician | not reported in cached trials |
| Pre-eclampsia | 232 | 23.0 20.1–26.2ROR 23.1 · calibrated p 0.001 ✓ | 21.9 EB05 19.6 · IC025 +4.2 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=209 · ♀ 100% (drug 56%) · 90% clinician | not reported in cached trials |
| Brash syndrome | 63 | 21.7 16.9–28.0ROR 21.8 · calibrated p 0.002 ✓ | 20.6 EB05 16.7 · IC025 +3.7 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=63 · 100% clinician | not reported in cached trials |
| Polydactyly | 53 | 21.5 16.3–28.3ROR 21.5 · calibrated p 0.002 ✓ | 20.4 EB05 16.2 · IC025 +3.7 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=53 · ♀ 0% (drug 56%) | not reported in cached trials |
| Blood pressure diastolic abnormal | 114 | 20.7 17.2–25.0ROR 20.8 · calibrated p 0.002 ✓ | 19.8 EB05 16.9 · IC025 +3.9 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Likely indication confounding term in indications | serious n=114 · ♀ 100% (drug 56%) · 94% clinician | not reported in cached trials |
| Bradycardia foetal | 36 | 20.5 14.7–28.7ROR 20.5 · calibrated p 0.002 ✓ | 19.5 EB05 14.6 · IC025 +3.4 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=36 · 100% clinician | not reported in cached trials |
| Premature delivery | 700 | 20.4 18.9–22.0ROR 20.7 · calibrated p 0.002 ✓ | 19.5 EB05 18.4 · IC025 +4.1 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: PRR 1,600.4 (514.9–4,973.8) | Not in label — unassessed | serious PRR 15.2 · ♀ 100% (drug 56%) · 91% clinician | not reported in cached trials |
| Hypertensive emergency | 48 | 19.1 14.3–25.5ROR 19.1 · calibrated p 0.003 ✓ | 18.2 EB05 14.3 · IC025 +3.5 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Likely indication confounding shares a disease stem with the indications wording | serious n=43 · 100% clinician | not reported in cached trials |
| Renal artery stenosis | 53 | 17.7 13.5–23.3ROR 17.8 · calibrated p 0.004 ✓ | 17.0 EB05 13.4 · IC025 +3.4 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=45 | not reported in cached trials |
| Joint contracture | 40 | 17.3 12.6–23.7ROR 17.3 · calibrated p 0.005 ✓ | 16.5 EB05 12.5 · IC025 +3.3 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=29 | not reported in cached trials |
| Solar lentigo | 35 | 16.9 12.1–23.7ROR 16.9 · calibrated p 0.005 ✓ | 16.1 EB05 12.0 · IC025 +3.2 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: PRR 18.5 (9.8–34.9) | Not in label — unassessed | serious n=34 · ♀ 0% (drug 56%) · 100% clinician | not reported in cached trials |
| End stage renal disease | 646 | 16.2 15.0–17.5ROR 16.4 · calibrated p 0.005 ✓ | 15.7 EB05 14.7 · IC025 +3.8 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: PRR 67.1 (52.1–86.5) | Not in label — unassessed | serious PRR 11.9 | not reported in cached trials |
| Premature baby | 1,033 | 15.8 14.9–16.8ROR 16.1 · calibrated p 0.005 ✓ | 15.3 EB05 14.5 · IC025 +3.8 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: PRR 244.3 (169.0–353.3) | Not in label — unassessed | serious PRR 12.2 | not reported in cached trials |
| Foetal growth restriction | 198 | 15.1 13.1–17.4ROR 15.2 · calibrated p 0.007 ✓ | 14.6 EB05 13.0 · IC025 +3.6 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=194 · 91% clinician | not reported in cached trials |
| Blood pressure inadequately controlled | 194 | 14.7 12.8–17.0ROR 14.8 · calibrated p 0.008 ✓ | 14.3 EB05 12.6 · IC025 +3.6 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: PRR 63.4 (40.4–99.4) | Likely indication confounding shares a disease stem with the indications wording | serious n=108 | not reported in cached trials |
| Rebound acid hypersecretion | 91 | 13.6 11.1–16.8ROR 13.7 · calibrated p 0.011 ✓ | 13.2 EB05 11.0 · IC025 +3.3 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=80 | not reported in cached trials |
| Aplastic anaemia | 150 | 13.1 11.2–15.4ROR 13.2 · calibrated p 0.012 ✓ | 12.7 EB05 11.1 · IC025 +3.4 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=147 · 92% clinician | NCT01788358: 1/508 (0.2%) on Nifedipine (serious AE) |
| Apgar score low | 36 | 12.8 9.2–17.8ROR 12.8 · calibrated p 0.016 ✓ | 12.1 EB05 8.9 · IC025 +2.9 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=35 · 100% clinician | not reported in cached trials |
| Rectal prolapse | 33 | 12.5 8.9–17.7ROR 12.5 · calibrated p 0.017 ✓ | 11.8 EB05 8.5 · IC025 +2.8 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=33 · ♀ 100% (drug 56%) · 100% clinician | not reported in cached trials |
| Scleroderma | 98 | 12.3 10.1–15.1ROR 12.3 · calibrated p 0.016 ✓ | 11.9 EB05 10.0 · IC025 +3.2 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=86 · ♀ 82% (drug 56%) | not reported in cached trials |
| Bezoar | 37 | 12.3 8.9–17.0ROR 12.3 · calibrated p 0.018 ✓ | 11.6 EB05 8.6 · IC025 +2.8 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Labeled adverse reaction exact term | serious n=37 · ♀ 0% (drug 56%) · 100% clinician | not reported in cached trials |
| Kidney transplant rejection | 128 | 12.2 10.2–14.5ROR 12.2 · calibrated p 0.017 ✓ | 11.8 EB05 10.1 · IC025 +3.2 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=112 · ♀ 30% (drug 56%) | not reported in cached trials |
| Nephrogenic systemic fibrosis | 79 | 11.8 9.5–14.8ROR 11.8 · calibrated p 0.019 ✓ | 11.4 EB05 9.3 · IC025 +3.1 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: PRR 60.2 (30.2–120.0) | Not in label — unassessed | serious n=42 | not reported in cached trials |
| Premature separation of placenta | 37 | 10.9 7.9–15.1ROR 10.9 · calibrated p 0.027 ✓ | 10.2 EB05 7.5 · IC025 +2.7 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=33 · ♀ 100% (drug 56%) · 100% clinician | not reported in cached trials |
| Premature labour | 130 | 10.4 8.7–12.4ROR 10.4 · calibrated p 0.029 ✓ | 10.0 EB05 8.6 · IC025 +3.0 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=109 · ♀ 100% (drug 56%) · 92% clinician | not reported in cached trials |
| Oligohydramnios | 76 | 10.3 8.2–13.0ROR 10.4 · calibrated p 0.030 ✓ | 9.9 EB05 8.1 · IC025 +2.9 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=71 · ♀ 100% (drug 56%) · 100% clinician | not reported in cached trials |
| Complications of transplanted kidney | 48 | 9.8 7.4–13.1ROR 9.8 · calibrated p 0.038 ✓ | 9.2 EB05 7.1 · IC025 +2.7 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: PRR 29.9 (15.5–57.6) | Not in label — unassessed | serious n=43 · ♀ 0% (drug 56%) | not reported in cached trials |
| Patent ductus arteriosus | 84 | 9.6 7.7–11.9ROR 9.6 · calibrated p 0.039 ✓ | 9.2 EB05 7.6 · IC025 +2.8 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=70 · 100% clinician | not reported in cached trials |
| Intra-uterine death | 33 | 9.2 6.5–13.0ROR 9.2 · calibrated p 0.048 ✓ | 8.4 EB05 6.1 · IC025 +2.4 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=31 · ♀ 100% (drug 56%) | not reported in cached trials |
| Neonatal respiratory distress syndrome | 71 | 9.1 7.2–11.5ROR 9.1 · calibrated p 0.047 ✓ | 8.6 EB05 7.0 · IC025 +2.7 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: only this drug | Not in label — unassessed | serious n=67 · 100% clinician | not reported in cached trials |
Trial evidence (ClinicalTrials.gov)
✓ Trial adverse-event data found on ClinicalTrials.gov
Largest completed trials with posted results that list Nifedipine 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 (1 of 40 signal terms matched).
- NCT01167153 — Effectiveness of Valsartan/Amlodipine (EXforge®) and Nifedipine treAtment coMparison in Treating Chinese Hyper (N=564, PHASE4; 3 AE terms posted; arms: Valsartan/Amlodipine; Nifedipine)
- NCT01788358 — Open-Label Long-Term Safety and Efficacy Study of Fixed Dose Combination of Nifedipine Gastrointestinal Therap (N=508, PHASE3; 22 AE terms posted; arms: Nifedipine GITS/Candesartan Cilexetil FD)
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 |
|---|---|---|---|---|---|---|
| Drug ineffective (drug did not work) | 2,597 | 0.9 0.8–0.9ROR 0.9 · calibrated p 0.227 | 0.9 EB05 0.9 · IC025 -0.2 PRR-only: not supported by EBGM or IC vs other Dihydropyridine Calcium Channel Blockers: PRR 35.8 (32.5–39.3) | Reporting / coding artifact | serious PRR 1.3 | not reported in cached trials |
| Dyspnoea (shortness of breath) | 2,484 | 2.0 1.9–2.0ROR 2.0 · calibrated p 0.956 | 2.0 EB05 1.9 · IC025 +0.9 vs other Dihydropyridine Calcium Channel Blockers: PRR 17.0 (15.8–18.3) | Labeled adverse reaction exact term | serious PRR 1.7 | not reported in cached trials |
| Fatigue (tiredness) | 2,386 | 1.4 1.3–1.4ROR 1.4 · calibrated p 0.571 | 1.4 EB05 1.3 · IC025 +0.4 vs other Dihydropyridine Calcium Channel Blockers: PRR 14.8 (13.8–15.8) | Labeled adverse reaction exact term | serious PRR 1.3 | NCT01788358: 18/508 (3.5%) on Nifedipine |
| Diarrhoea (diarrhea) | 2,355 | 1.6 1.6–1.7ROR 1.7 · calibrated p 0.752 | 1.6 EB05 1.6 · IC025 +0.6 vs other Dihydropyridine Calcium Channel Blockers: PRR 18.2 (16.9–19.6) | Labeled adverse reaction exact term | serious PRR 1.5 | not reported in cached trials |
| Nausea | 2,297 | 1.3 1.3–1.4ROR 1.3 · calibrated p 0.520 | 1.3 EB05 1.3 · IC025 +0.3 vs other Dihydropyridine Calcium Channel Blockers: PRR 17.8 (16.5–19.2) | Labeled adverse reaction exact term | serious PRR 1.3 | not reported in cached trials |
| Off label use (used outside approved label) | 2,126 | 1.1 1.1–1.1ROR 1.1 · calibrated p 0.372 | 1.1 EB05 1.1 · IC025 +0.1 vs other Dihydropyridine Calcium Channel Blockers: PRR 21.0 (19.3–22.9) | Reporting / coding artifact | serious PRR 1.3 | not reported in cached trials |
| Headache | 2,074 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.645 | 1.5 EB05 1.4 · IC025 +0.5 vs other Dihydropyridine Calcium Channel Blockers: PRR 16.1 (14.9–17.4) | Labeled adverse reaction exact term | serious PRR 1.5 | NCT01167153: 20/282 (7.1%) on Nifedipine |
| Dizziness | 1,822 | 1.6 1.6–1.7ROR 1.7 · calibrated p 0.747 | 1.6 EB05 1.6 · IC025 +0.6 vs other Dihydropyridine Calcium Channel Blockers: PRR 12.5 (11.6–13.5) | Labeled adverse reaction exact term | serious PRR 1.5 | NCT01788358: 47/508 (9.3%) on Nifedipine |
| Hypertension (high blood pressure) | 1,812 | 3.8 3.7–4.0ROR 4.0 · calibrated p 0.385 | 3.8 EB05 3.7 · IC025 +1.9 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: PRR 45.0 (39.7–51.1) | Likely indication confounding term in indications; also in warnings | serious PRR 3.1 | not reported in cached trials |
| Pain | 1,730 | 1.3 1.2–1.3ROR 1.3 · calibrated p 0.486 | 1.3 EB05 1.2 · IC025 +0.3 vs other Dihydropyridine Calcium Channel Blockers: PRR 13.9 (12.8–15.1) | Likely indication confounding term in indications; also in warnings | serious PRR 1.1 | NCT01788358: 1/508 (0.2%) on Nifedipine (serious AE) |
| Death | 1,552 | 0.8 0.8–0.8ROR 0.8 · calibrated p 0.183 | 0.8 EB05 0.8 · IC025 -0.4 PRR-only: not supported by EBGM or IC vs other Dihydropyridine Calcium Channel Blockers: PRR 65.3 (55.6–76.7) | Outcome field, not a reaction | serious PRR 0.6 | not reported in cached trials |
| Asthenia (weakness) | 1,525 | 1.8 1.7–1.9ROR 1.8 · calibrated p 0.855 | 1.8 EB05 1.7 · IC025 +0.8 vs other Dihydropyridine Calcium Channel Blockers: PRR 29.1 (25.9–32.6) | Labeled adverse reaction exact term | serious PRR 1.5 | not reported in cached trials |
| Pneumonia (lung infection) | 1,524 | 2.1 2.0–2.2ROR 2.2 · calibrated p 0.977 | 2.1 EB05 2.0 · IC025 +1.0 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: PRR 38.7 (34.0–44.0) | Labeled (related wording) related wording | serious PRR 1.6 | not reported in cached trials |
| Acute kidney injury (sudden kidney damage) | 1,490 | 4.4 4.2–4.6ROR 4.5 · calibrated p 0.294 | 4.4 EB05 4.2 · IC025 +2.0 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: PRR 39.3 (34.5–44.8) | Not in label — unassessed | serious PRR 3.4 | not reported in cached trials |
| Hypotension (low blood pressure) | 1,465 | 3.3 3.1–3.5ROR 3.4 · calibrated p 0.521 | 3.3 EB05 3.1 · IC025 +1.6 3/3 methods agree vs other Dihydropyridine Calcium Channel Blockers: PRR 32.7 (29.0–37.0) | Likely indication confounding term in indications; also in warnings | serious PRR 2.7 | not reported in cached trials |
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.
- Neovascularisation — n=64, PRR 149.0
- Dysplastic naevus — n=34, PRR 46.8
- Photodermatosis — n=39, PRR 44.9
- Chronic kidney disease-mineral and bone disorder — n=86, PRR 38.8
- Nephrogenic anaemia — n=305, PRR 31.1
- Hyperparathyroidism secondary — n=155, PRR 29.1
- Wrist deformity — n=37, PRR 28.3
- Hellp syndrome — n=36, PRR 27.6
- Low birth weight baby — n=410, PRR 24.3
- Pre-eclampsia — n=232, PRR 23.0
✓ A hand-written Bradford Hill causality assessment exists for this drug: Nifedipine (dihydropyridine CCBs) ↔ Peripheral oedema.
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 Nifedipine?
In FDA FAERS, the most frequently co-reported reaction terms for Nifedipine are dyspnoea, fatigue, diarrhoea, nausea, headache, dizziness. 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 Nifedipine have an FDA boxed warning?
No. The FDA label retrieved for Nifedipine has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Nifedipine 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 09a04e5f-d3b0-4ee3-b12d-f74203262179, effective 20190606; matched on
openfda.generic_name.exact:"NIFEDIPINE") - 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, 1,199 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
NIFEDIPINE, 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.