Diltiazem side effects: what 34,205 FDA adverse event reports show
Drug class
Not stated in label
Label matched
Diltiazem Hydrochloride (Diltiazem Hydrochloride)
Who reports
34,205 reports · 74% serious · 5,131 with death outcome · 64% female
Used for
Diltiazem hydrochloride extended-release capsules are indicated for the treatment of hypertension. Diltiazem hydrochloride may be used alone or in combination with other antihypertensive medications, such as diuretics. Diltiazem hydrochloride extended-release capsules are indicated for the management of chronic stable angina.
What it is
DESCRIPTION Diltiazem hydrochloride, USP is a calcium ion influx inhibitor (slow channel blocker or calcium antagonist).
Boxed warning
None in the current label
Causality screen of the 40 strongest signals
What the badges mean
- Reporting / coding artifact An administrative, monitoring or exposure term (product issue, off-label use, 'test normal', overdose...). Not a biological reaction; a high PRR here reflects how reports are coded.
- 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). 1,187 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 |
|---|---|---|---|---|---|---|
| Heart sounds | 49 | 626.2 419.8–934.2ROR 627.1 · calibrated p 5e-14 ✓ | 274.2 EB05 215.6 · IC025 +5.8 3/3 methods agree | Not in label — unassessed | serious n=49 · ♀ 100% (drug 64%) | no trial arm names this drug |
| Spirometry abnormal | 161 | 230.8 192.5–276.7ROR 231.9 · calibrated p 1e-10 ✓ | 163.8 EB05 143.6 · IC025 +6.5 3/3 methods agree | Lab value / disease marker | serious n=161 · ♀ 0% (drug 64%) | no trial arm names this drug |
| Mite allergy | 160 | 204.5 171.0–244.6ROR 205.4 · calibrated p 4e-10 ✓ | 150.1 EB05 131.6 · IC025 +6.4 3/3 methods agree | Not in label — unassessed | serious n=160 · ♀ 0% (drug 64%) | no trial arm names this drug |
| Pulmonary vasculitis | 115 | 169.7 138.0–208.7ROR 170.3 · calibrated p 2e-9 ✓ | 129.7 EB05 111.0 · IC025 +6.1 3/3 methods agree | Not in label — unassessed | serious n=115 · ♀ 0% (drug 64%) | no trial arm names this drug |
| Anti-cyclic citrullinated peptide antibody | 136 | 156.2 129.4–188.6ROR 156.8 · calibrated p 4e-9 ✓ | 122.1 EB05 105.8 · IC025 +6.1 3/3 methods agree | Lab value / disease marker | serious n=136 · ♀ 100% (drug 64%) · 100% clinician | no trial arm names this drug |
| Mycotic allergy | 162 | 145.2 122.4–172.4ROR 145.9 · calibrated p 7e-9 ✓ | 115.6 EB05 101.4 · IC025 +6.2 3/3 methods agree | Not in label — unassessed | serious n=162 · ♀ 0% (drug 64%) | no trial arm names this drug |
| Prolonged expiration | 50 | 142.3 104.6–193.7ROR 142.5 · calibrated p 1e-8 ✓ | 110.5 EB05 87.1 · IC025 +5.3 3/3 methods agree | Not in label — unassessed | serious n=50 · ♀ 100% (drug 64%) | no trial arm names this drug |
| Total lung capacity abnormal | 70 | 137.4 106.0–178.1ROR 137.7 · calibrated p 2e-8 ✓ | 108.8 EB05 89.0 · IC025 +5.6 3/3 methods agree | Not in label — unassessed | serious n=70 · ♀ 0% (drug 64%) | no trial arm names this drug |
| Lupus vulgaris | 207 | 128.4 110.6–149.2ROR 129.2 · calibrated p 2e-8 ✓ | 105.0 EB05 93.5 · IC025 +6.2 3/3 methods agree | Not in label — unassessed | serious n=207 · ♀ 100% (drug 64%) · 100% clinician | no trial arm names this drug |
| Sedation complication | 433 | 127.8 115.3–141.7ROR 129.4 · calibrated p 2e-8 ✓ | 105.1 EB05 97.0 · IC025 +6.4 3/3 methods agree | Reporting / coding artifact | serious n=432 · ♀ 100% (drug 64%) | no trial arm names this drug |
| Amaurosis fugax | 185 | 127.6 108.9–149.5ROR 128.3 · calibrated p 2e-8 ✓ | 104.3 EB05 92.3 · IC025 +6.1 3/3 methods agree | Not in label — unassessed | serious n=185 · 91% clinician | no trial arm names this drug |
| Capillaritis | 46 | 126.2 91.8–173.3ROR 126.3 · calibrated p 4e-8 ✓ | 100.2 EB05 78.2 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious n=46 · ♀ 0% (drug 64%) | no trial arm names this drug |
| Dust allergy | 162 | 123.2 104.0–145.8ROR 123.8 · calibrated p 3e-8 ✓ | 101.2 EB05 88.8 · IC025 +6.0 3/3 methods agree | Not in label — unassessed | serious n=162 · ♀ 0% (drug 64%) | no trial arm names this drug |
| Gastrointestinal procedural complication | 35 | 93.0 65.2–132.8ROR 93.1 · calibrated p 4e-7 ✓ | 77.4 EB05 58.2 · IC025 +4.7 3/3 methods agree | Reporting / coding artifact | serious n=35 · ♀ 100% (drug 64%) · 100% clinician | no trial arm names this drug |
| Creatinine renal clearance decreased | 462 | 78.9 71.7–86.9ROR 80.0 · calibrated p 6e-7 ✓ | 69.7 EB05 64.5 · IC025 +5.9 3/3 methods agree | Lab value / disease marker | serious n=461 · ♀ 100% (drug 64%) | no trial arm names this drug |
| Conjunctivitis allergic | 166 | 78.0 66.4–91.7ROR 78.4 · calibrated p 8e-7 ✓ | 68.6 EB05 60.3 · IC025 +5.6 3/3 methods agree | Not in label — unassessed | serious n=166 · ♀ 0% (drug 64%) | no trial arm names this drug |
| Deep vein thrombosis postoperative | 218 | 76.2 66.2–87.7ROR 76.7 · calibrated p 9e-7 ✓ | 67.4 EB05 60.2 · IC025 +5.7 3/3 methods agree | Not in label — unassessed | serious n=218 · ♀ 100% (drug 64%) · 100% clinician | no trial arm names this drug |
| Adjustment disorder with depressed mood | 211 | 71.2 61.8–82.1ROR 71.7 · calibrated p 1e-6 ✓ | 63.4 EB05 56.6 · IC025 +5.6 3/3 methods agree | Not in label — unassessed | serious n=211 · ♀ 100% (drug 64%) · 95% clinician | no trial arm names this drug |
| Dislocation of vertebra | 229 | 69.9 61.0–80.2ROR 70.4 · calibrated p 2e-6 ✓ | 62.4 EB05 55.9 · IC025 +5.6 3/3 methods agree | Not in label — unassessed | serious n=229 · ♀ 100% (drug 64%) · 93% clinician | no trial arm names this drug |
| Retinitis | 171 | 69.5 59.4–81.4ROR 69.9 · calibrated p 2e-6 ✓ | 62.0 EB05 54.6 · IC025 +5.5 3/3 methods agree | Not in label — unassessed | serious n=171 · ♀ 100% (drug 64%) · 100% clinician | no trial arm names this drug |
| Antineutrophil cytoplasmic antibody positive | 73 | 67.9 53.3–86.4ROR 68.0 · calibrated p 2e-6 ✓ | 60.2 EB05 49.5 · IC025 +5.1 3/3 methods agree | Lab value / disease marker | serious n=73 · ♀ 0% (drug 64%) | no trial arm names this drug |
| Systemic lupus erythematosus rash | 78 | 65.6 52.0–82.9ROR 65.8 · calibrated p 3e-6 ✓ | 58.4 EB05 48.3 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious n=78 · ♀ 100% (drug 64%) · 100% clinician | no trial arm names this drug |
| Seronegative arthritis | 103 | 61.6 50.3–75.4ROR 61.7 · calibrated p 4e-6 ✓ | 55.4 EB05 47.0 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious n=103 · ♀ 100% (drug 64%) · 100% clinician | no trial arm names this drug |
| Multiple drug therapy | 63 | 60.4 46.7–78.3ROR 60.6 · calibrated p 6e-6 ✓ | 54.2 EB05 43.8 · IC025 +4.9 3/3 methods agree | Reporting / coding artifact | serious n=63 · ♀ 100% (drug 64%) · 100% clinician | no trial arm names this drug |
| X-ray abnormal | 152 | 56.7 48.0–66.9ROR 57.0 · calibrated p 7e-6 ✓ | 51.6 EB05 45.1 · IC025 +5.2 3/3 methods agree | Lab value / disease marker | serious n=152 · ♀ 100% (drug 64%) · 92% clinician | no trial arm names this drug |
| Bunion operation | 43 | 50.5 37.0–69.0ROR 50.6 · calibrated p 2e-5 ✓ | 45.8 EB05 35.4 · IC025 +4.4 3/3 methods agree | Reporting / coding artifact | serious n=43 · ♀ 100% (drug 64%) · 100% clinician | no trial arm names this drug |
| Neuritis | 117 | 50.1 41.5–60.5ROR 50.3 · calibrated p 2e-5 ✓ | 46.0 EB05 39.4 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | serious n=117 · ♀ 0% (drug 64%) | no trial arm names this drug |
| Alveolar osteitis | 32 | 49.4 34.5–70.8ROR 49.5 · calibrated p 3e-5 ✓ | 44.6 EB05 33.1 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious n=32 · ♀ 100% (drug 64%) | no trial arm names this drug |
| Creatinine renal clearance increased | 55 | 48.1 36.5–63.3ROR 48.2 · calibrated p 2e-5 ✓ | 44.0 EB05 35.0 · IC025 +4.6 3/3 methods agree | Lab value / disease marker | serious n=54 · ♀ 100% (drug 64%) · 100% clinician | no trial arm names this drug |
| Porphyria acute | 100 | 47.6 38.8–58.3ROR 47.7 · calibrated p 2e-5 ✓ | 43.8 EB05 37.1 · IC025 +4.9 3/3 methods agree | Not in label — unassessed | serious n=100 · ♀ 100% (drug 64%) · 100% clinician | no trial arm names this drug |
| Urinary tract discomfort | 31 | 44.8 31.1–64.5ROR 44.8 · calibrated p 5e-5 ✓ | 40.8 EB05 30.1 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=31 · ♀ 100% (drug 64%) · 100% clinician | no trial arm names this drug |
| Body tinea | 36 | 41.5 29.6–58.2ROR 41.5 · calibrated p 7e-5 ✓ | 38.2 EB05 28.8 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=35 · ♀ 100% (drug 64%) · 100% clinician | no trial arm names this drug |
| Normochromic normocytic anaemia | 173 | 37.2 32.0–43.4ROR 37.4 · calibrated p 8e-5 ✓ | 35.0 EB05 30.8 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=173 · ♀ 0% (drug 64%) | no trial arm names this drug |
| Rheumatic fever | 246 | 36.3 32.0–41.3ROR 36.6 · calibrated p 9e-5 ✓ | 34.2 EB05 30.8 · IC025 +4.8 3/3 methods agree | Not in label — unassessed | serious n=246 · ♀ 100% (drug 64%) · 94% clinician | no trial arm names this drug |
| Eosinophilic granulomatosis with polyangiitis | 112 | 35.8 29.6–43.3ROR 35.9 · calibrated p 1e-4 ✓ | 33.6 EB05 28.7 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious n=112 · ♀ 0% (drug 64%) | no trial arm names this drug |
| Swollen joint count increased | 173 | 35.8 30.7–41.7ROR 35.9 · calibrated p 1e-4 ✓ | 33.7 EB05 29.7 · IC025 +4.7 3/3 methods agree | Lab value / disease marker | serious n=173 · ♀ 100% (drug 64%) · 100% clinician | no trial arm names this drug |
| Duodenal ulcer perforation | 404 | 35.5 32.1–39.2ROR 35.9 · calibrated p 1e-4 ✓ | 33.5 EB05 30.8 · IC025 +4.8 3/3 methods agree | Not in label — unassessed | serious PRR 26.2 · ♀ 100% (drug 64%) · 96% clinician | no trial arm names this drug |
| Muscle injury | 442 | 34.7 31.5–38.1ROR 35.1 · calibrated p 1e-4 ✓ | 32.8 EB05 30.3 · IC025 +4.8 3/3 methods agree | Not in label — unassessed | serious PRR 27.8 · ♀ 100% (drug 64%) · 97% clinician | no trial arm names this drug |
| Bone erosion | 190 | 34.5 29.8–39.9ROR 34.7 · calibrated p 1e-4 ✓ | 32.6 EB05 28.9 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=190 · ♀ 100% (drug 64%) · 91% clinician | no trial arm names this drug |
| Facet joint syndrome | 166 | 33.8 29.0–39.6ROR 34.0 · calibrated p 1e-4 ✓ | 32.0 EB05 28.1 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious n=166 · ♀ 100% (drug 64%) | no trial arm names this drug |
Trial evidence (ClinicalTrials.gov)
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 |
|---|---|---|---|---|---|---|
| Dyspnoea (shortness of breath) | 3,310 | 3.6 3.5–3.7ROR 3.9 · calibrated p 0.405 | 3.6 EB05 3.5 · IC025 +1.8 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 3.3 | no trial arm names this drug |
| Fatigue (tiredness) | 2,733 | 2.1 2.1–2.2ROR 2.2 · calibrated p 0.928 | 2.1 EB05 2.1 · IC025 +1.0 3/3 methods agree | Labeled (related wording) related wording | serious PRR 2.4 | no trial arm names this drug |
| Nausea | 2,455 | 1.9 1.8–2.0ROR 2.0 · calibrated p 0.927 | 1.9 EB05 1.8 · IC025 +0.9 | Labeled adverse reaction exact term | serious PRR 2.2 | no trial arm names this drug |
| Pain | 2,422 | 2.4 2.3–2.5ROR 2.5 · calibrated p 0.808 | 2.4 EB05 2.3 · IC025 +1.2 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.7 | no trial arm names this drug |
| Dizziness | 2,173 | 2.7 2.6–2.8ROR 2.8 · calibrated p 0.702 | 2.7 EB05 2.6 · IC025 +1.3 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.9 | no trial arm names this drug |
| Diarrhoea (diarrhea) | 2,113 | 2.0 1.9–2.1ROR 2.1 · calibrated p 0.983 | 2.0 EB05 1.9 · IC025 +0.9 | Labeled adverse reaction exact term | serious PRR 2.1 | no trial arm names this drug |
| Drug ineffective (drug did not work) | 2,066 | 1.0 0.9–1.0ROR 1.0 · calibrated p 0.277 | 1.0 EB05 0.9 · IC025 -0.1 PRR-only: not supported by EBGM or IC | Reporting / coding artifact | serious PRR 1.3 | no trial arm names this drug |
| Headache | 2,024 | 2.0 1.9–2.1ROR 2.0 · calibrated p 0.963 | 2.0 EB05 1.9 · IC025 +0.9 | Labeled adverse reaction exact term | serious PRR 2.4 | no trial arm names this drug |
| Fall | 1,984 | 3.7 3.5–3.8ROR 3.8 · calibrated p 0.413 | 3.6 EB05 3.5 · IC025 +1.8 3/3 methods agree | Not in label — unassessed | serious PRR 3.2 | no trial arm names this drug |
| Atrial fibrillation | 1,783 | 11.3 10.8–11.9ROR 11.9 · calibrated p 0.017 ✓ | 11.1 EB05 10.7 · IC025 +3.4 3/3 methods agree | Labeled (related wording) related wording | serious PRR 8.7 | no trial arm names this drug |
| Asthenia (weakness) | 1,745 | 2.8 2.7–3.0ROR 2.9 · calibrated p 0.647 | 2.8 EB05 2.7 · IC025 +1.4 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.7 | no trial arm names this drug |
| Pneumonia (lung infection) | 1,639 | 3.1 3.0–3.3ROR 3.2 · calibrated p 0.563 | 3.1 EB05 3.0 · IC025 +1.5 3/3 methods agree | Labeled (related wording) related wording | serious PRR 2.5 | no trial arm names this drug |
| Arthralgia (joint pain) | 1,618 | 2.4 2.3–2.5ROR 2.5 · calibrated p 0.833 | 2.4 EB05 2.3 · IC025 +1.2 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.8 | no trial arm names this drug |
| Hypotension (low blood pressure) | 1,513 | 4.6 4.4–4.9ROR 4.8 · calibrated p 0.257 | 4.6 EB05 4.4 · IC025 +2.1 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 4.0 | no trial arm names this drug |
| Pain in extremity | 1,492 | 3.1 2.9–3.3ROR 3.2 · calibrated p 0.569 | 3.1 EB05 3.0 · IC025 +1.5 3/3 methods agree | Not in label — unassessed | serious PRR 3.6 | no trial arm names this drug |
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.
- Heart sounds — n=49, PRR 626.2
- Mite allergy — n=160, PRR 204.5
- Pulmonary vasculitis — n=115, PRR 169.7
- Mycotic allergy — n=162, PRR 145.2
- Prolonged expiration — n=50, PRR 142.3
- Total lung capacity abnormal — n=70, PRR 137.4
- Lupus vulgaris — n=207, PRR 128.4
- Amaurosis fugax — n=185, PRR 127.6
- Capillaritis — n=46, PRR 126.2
- Dust allergy — n=162, PRR 123.2
✓ A hand-written Bradford Hill causality assessment exists for this drug: Diltiazem (non-dihydropyridine CCBs) ↔ Bradycardia / AV block.
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 Diltiazem?
In FDA FAERS, the most frequently co-reported reaction terms for Diltiazem are dyspnoea, fatigue, nausea, pain, dizziness, diarrhoea. 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 Diltiazem have an FDA boxed warning?
No. The FDA label retrieved for Diltiazem has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Diltiazem 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 04a85be5-f746-418e-8e37-292703f16934, effective 20260429; matched on
openfda.generic_name.exact:"DILTIAZEM HYDROCHLORIDE") - 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, 1,227 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
DILTIAZEM, 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.