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Diltiazem side effects: what 34,205 FDA adverse event reports show

Diltiazem Hydrochloride · 1,227 reaction terms · 218,577 drug–reaction co-reports · data 2026-09-14
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Drug class

Not stated in label

Label matched

Diltiazem Hydrochloride (Diltiazem Hydrochloride)

closest FDA label found for this product string; brand list suppressed because the label is a related product, not an exact match

Who reports

34,205 reports · 74% serious · 5,131 with death outcome · 64% female

openFDA FAERS counts, all years, deduplication not applied

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.

FDA label, Indications and Usage

What it is

DESCRIPTION Diltiazem hydrochloride, USP is a calcium ion influx inhibitor (slow channel blocker or calcium antagonist).

FDA label, Description section

Boxed warning

None in the current 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

Reporting / coding artifact 4Lab value / disease marker 7Not in label — unassessed 29
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). 1,187 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
Heart sounds49626.2
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 — unassessedserious n=49 · ♀ 100% (drug 64%)no trial arm names this drug
Spirometry abnormal161230.8
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 markerserious n=161 · ♀ 0% (drug 64%)no trial arm names this drug
Mite allergy160204.5
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 — unassessedserious n=160 · ♀ 0% (drug 64%)no trial arm names this drug
Pulmonary vasculitis115169.7
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 — unassessedserious n=115 · ♀ 0% (drug 64%)no trial arm names this drug
Anti-cyclic citrullinated peptide antibody136156.2
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 markerserious n=136 · ♀ 100% (drug 64%) · 100% clinicianno trial arm names this drug
Mycotic allergy162145.2
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 — unassessedserious n=162 · ♀ 0% (drug 64%)no trial arm names this drug
Prolonged expiration50142.3
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 — unassessedserious n=50 · ♀ 100% (drug 64%)no trial arm names this drug
Total lung capacity abnormal70137.4
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 — unassessedserious n=70 · ♀ 0% (drug 64%)no trial arm names this drug
Lupus vulgaris207128.4
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 — unassessedserious n=207 · ♀ 100% (drug 64%) · 100% clinicianno trial arm names this drug
Sedation complication433127.8
115.3–141.7ROR 129.4 · calibrated p 2e-8 ✓
105.1 EB05 97.0 · IC025 +6.4
3/3 methods agree
Reporting / coding artifactserious n=432 · ♀ 100% (drug 64%)no trial arm names this drug
Amaurosis fugax185127.6
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 — unassessedserious n=185 · 91% clinicianno trial arm names this drug
Capillaritis46126.2
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 — unassessedserious n=46 · ♀ 0% (drug 64%)no trial arm names this drug
Dust allergy162123.2
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 — unassessedserious n=162 · ♀ 0% (drug 64%)no trial arm names this drug
Gastrointestinal procedural complication3593.0
65.2–132.8ROR 93.1 · calibrated p 4e-7 ✓
77.4 EB05 58.2 · IC025 +4.7
3/3 methods agree
Reporting / coding artifactserious n=35 · ♀ 100% (drug 64%) · 100% clinicianno trial arm names this drug
Creatinine renal clearance decreased46278.9
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 markerserious n=461 · ♀ 100% (drug 64%)no trial arm names this drug
Conjunctivitis allergic16678.0
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 — unassessedserious n=166 · ♀ 0% (drug 64%)no trial arm names this drug
Deep vein thrombosis postoperative21876.2
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 — unassessedserious n=218 · ♀ 100% (drug 64%) · 100% clinicianno trial arm names this drug
Adjustment disorder with depressed mood21171.2
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 — unassessedserious n=211 · ♀ 100% (drug 64%) · 95% clinicianno trial arm names this drug
Dislocation of vertebra22969.9
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 — unassessedserious n=229 · ♀ 100% (drug 64%) · 93% clinicianno trial arm names this drug
Retinitis17169.5
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 — unassessedserious n=171 · ♀ 100% (drug 64%) · 100% clinicianno trial arm names this drug
Antineutrophil cytoplasmic antibody positive7367.9
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 markerserious n=73 · ♀ 0% (drug 64%)no trial arm names this drug
Systemic lupus erythematosus rash7865.6
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 — unassessedserious n=78 · ♀ 100% (drug 64%) · 100% clinicianno trial arm names this drug
Seronegative arthritis10361.6
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 — unassessedserious n=103 · ♀ 100% (drug 64%) · 100% clinicianno trial arm names this drug
Multiple drug therapy6360.4
46.7–78.3ROR 60.6 · calibrated p 6e-6 ✓
54.2 EB05 43.8 · IC025 +4.9
3/3 methods agree
Reporting / coding artifactserious n=63 · ♀ 100% (drug 64%) · 100% clinicianno trial arm names this drug
X-ray abnormal15256.7
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 markerserious n=152 · ♀ 100% (drug 64%) · 92% clinicianno trial arm names this drug
Bunion operation4350.5
37.0–69.0ROR 50.6 · calibrated p 2e-5 ✓
45.8 EB05 35.4 · IC025 +4.4
3/3 methods agree
Reporting / coding artifactserious n=43 · ♀ 100% (drug 64%) · 100% clinicianno trial arm names this drug
Neuritis11750.1
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 — unassessedserious n=117 · ♀ 0% (drug 64%)no trial arm names this drug
Alveolar osteitis3249.4
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 — unassessedserious n=32 · ♀ 100% (drug 64%)no trial arm names this drug
Creatinine renal clearance increased5548.1
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 markerserious n=54 · ♀ 100% (drug 64%) · 100% clinicianno trial arm names this drug
Porphyria acute10047.6
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 — unassessedserious n=100 · ♀ 100% (drug 64%) · 100% clinicianno trial arm names this drug
Urinary tract discomfort3144.8
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 — unassessedserious n=31 · ♀ 100% (drug 64%) · 100% clinicianno trial arm names this drug
Body tinea3641.5
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 — unassessedserious n=35 · ♀ 100% (drug 64%) · 100% clinicianno trial arm names this drug
Normochromic normocytic anaemia17337.2
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 — unassessedserious n=173 · ♀ 0% (drug 64%)no trial arm names this drug
Rheumatic fever24636.3
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 — unassessedserious n=246 · ♀ 100% (drug 64%) · 94% clinicianno trial arm names this drug
Eosinophilic granulomatosis with polyangiitis11235.8
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 — unassessedserious n=112 · ♀ 0% (drug 64%)no trial arm names this drug
Swollen joint count increased17335.8
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 markerserious n=173 · ♀ 100% (drug 64%) · 100% clinicianno trial arm names this drug
Duodenal ulcer perforation40435.5
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 — unassessedserious PRR 26.2 · ♀ 100% (drug 64%) · 96% clinicianno trial arm names this drug
Muscle injury44234.7
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 — unassessedserious PRR 27.8 · ♀ 100% (drug 64%) · 97% clinicianno trial arm names this drug
Bone erosion19034.5
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 — unassessedserious n=190 · ♀ 100% (drug 64%) · 91% clinicianno trial arm names this drug
Facet joint syndrome16633.8
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 — unassessedserious n=166 · ♀ 100% (drug 64%)no trial arm names this drug

Trial evidence (ClinicalTrials.gov)

ClinicalTrials.gov returned results-bearing trials mentioning Diltiazem only as a background or rescue medication (NCT00000620, NCT00911508); no trial listing it as the tested intervention was cached, so no trial cross-check is shown.

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
Dyspnoea (shortness of breath)3,3103.6
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 3.3no trial arm names this drug
Nausea2,4551.9
1.8–2.0ROR 2.0 · calibrated p 0.927
1.9 EB05 1.8 · IC025 +0.9Labeled adverse reaction
exact term
serious PRR 2.2no trial arm names this drug
Pain2,4222.4
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 2.7no trial arm names this drug
Dizziness2,1732.7
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 2.9no trial arm names this drug
Diarrhoea (diarrhea)2,1132.0
1.9–2.1ROR 2.1 · calibrated p 0.983
2.0 EB05 1.9 · IC025 +0.9Labeled adverse reaction
exact term
serious PRR 2.1no trial arm names this drug
Drug ineffective (drug did not work)2,0661.0
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 artifactserious PRR 1.3no trial arm names this drug
Headache2,0242.0
1.9–2.1ROR 2.0 · calibrated p 0.963
2.0 EB05 1.9 · IC025 +0.9Labeled adverse reaction
exact term
serious PRR 2.4no trial arm names this drug
Fall1,9843.7
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 — unassessedserious PRR 3.2no trial arm names this drug
Asthenia (weakness)1,7452.8
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 2.7no trial arm names this drug
Arthralgia (joint pain)1,6182.4
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 2.8no trial arm names this drug
Hypotension (low blood pressure)1,5134.6
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 4.0no trial arm names this drug
Pain in extremity1,4923.1
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 — unassessedserious PRR 3.6no 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.

✓ 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

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.