Ranitidine Hydrochloride side effects: what 54,034 FDA adverse event reports show
Drug class
Not stated in label
Who reports
54,034 reports · 95% serious · 4,399 with death outcome · 51% female
Used for
Ranitidine Tablets are indicated in: Short- term treatment of active duodenal ulcer. Most patients heal within 4 weeks. Studies available to date have not assessed the safety of Ranitidine in uncomplicated duodenal ulcer for periods of more than 8 weeks. Maintenance therapy for duodenal ulcer patients at reduced dosage after healing of acute ulcers.
What it is
DESCRIPTION Ranitidine Tablets USP are available for oral administration containing 150 mg or 300 mg of ranitidine. The active ingredient in Ranitidine Tablets USP, 150 mg and 300 mg is Ranitidine hydrochloride (HCl), USP, a histamine H 2 -receptor antagonist.
Boxed warning
None in the current label
Causality screen of the 40 strongest signals
What the badges mean
- 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.
- 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.
- 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). 1,088 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 |
|---|---|---|---|---|---|---|
| Computerised tomogram thorax | 26 | 292.1 175.3–486.7ROR 292.2 · calibrated p 2e-10 ✓ | 148.1 EB05 106.2 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=26 · ♀ 100% (drug 51%) · 100% clinician | not reported in cached trials |
| Junctional ectopic tachycardia | 20 | 206.5 119.8–355.7ROR 206.5 · calibrated p 4e-9 ✓ | 119.3 EB05 81.6 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious n=20 · ♀ 100% (drug 51%) | not reported in cached trials |
| Synovial fluid analysis | 25 | 156.5 98.3–249.3ROR 156.6 · calibrated p 2e-8 ✓ | 102.8 EB05 73.2 · IC025 +4.5 3/3 methods agree | Reporting / coding artifact | serious n=25 · ♀ 100% (drug 51%) · 100% clinician | not reported in cached trials |
| Haemorrhage foetal | 15 | 146.9 81.0–266.5ROR 146.9 · calibrated p 7e-8 ✓ | 94.0 EB05 60.5 · IC025 +3.7 3/3 methods agree | Not in label — unassessed | serious n=15 | not reported in cached trials |
| Hepatic enzyme | 37 | 139.9 96.0–203.9ROR 140.0 · calibrated p 2e-8 ✓ | 97.6 EB05 74.0 · IC025 +4.9 3/3 methods agree | Not in label — unassessed | serious n=37 · ♀ 100% (drug 51%) · 100% clinician | not reported in cached trials |
| Hypocholesterolaemia | 75 | 125.1 96.4–162.3ROR 125.3 · calibrated p 3e-8 ✓ | 92.3 EB05 76.1 · IC025 +5.5 3/3 methods agree | Not in label — unassessed | serious n=75 · ♀ 100% (drug 51%) · 100% clinician | not reported in cached trials |
| Nasal cavity cancer | 170 | 87.6 74.2–103.5ROR 87.9 · calibrated p 3e-7 ✓ | 70.9 EB05 62.4 · IC025 +5.6 3/3 methods agree | Not in label — unassessed | serious n=170 · ♀ 30% (drug 51%) · 100% consumer | not reported in cached trials |
| Foramen magnum stenosis | 13 | 63.7 35.4–114.5ROR 63.7 · calibrated p 1e-5 ✓ | 50.9 EB05 31.6 · IC025 +3.3 3/3 methods agree | Not in label — unassessed | serious n=13 | not reported in cached trials |
| Bladder cancer stage i, with cancer in situ | 30 | 61.6 41.9–90.6ROR 61.6 · calibrated p 7e-6 ✓ | 51.5 EB05 37.8 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious n=30 · ♀ 0% (drug 51%) | not reported in cached trials |
| Temperature regulation disorder | 297 | 61.0 54.0–68.9ROR 61.3 · calibrated p 4e-6 ✓ | 52.6 EB05 47.7 · IC025 +5.4 3/3 methods agree | Not in label — unassessed | serious n=297 · ♀ 100% (drug 51%) | not reported in cached trials |
| Neoplasm of appendix | 15 | 61.0 35.3–105.1ROR 61.0 · calibrated p 2e-5 ✓ | 49.6 EB05 31.9 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | serious n=14 | not reported in cached trials |
| Osteoporosis postmenopausal | 19 | 60.5 37.3–98.1ROR 60.5 · calibrated p 1e-5 ✓ | 49.9 EB05 33.8 · IC025 +3.7 3/3 methods agree | Not in label — unassessed | serious n=19 | not reported in cached trials |
| Foetal anaemia | 15 | 49.8 29.1–85.3ROR 49.8 · calibrated p 5e-5 ✓ | 42.0 EB05 27.0 · IC025 +3.3 3/3 methods agree | Not in label — unassessed | serious n=15 | not reported in cached trials |
| Small intestine carcinoma | 254 | 49.3 43.2–56.1ROR 49.5 · calibrated p 2e-5 ✓ | 43.6 EB05 39.3 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious n=254 · 100% consumer | not reported in cached trials |
| Sinobronchitis | 17 | 49.2 29.7–81.5ROR 49.2 · calibrated p 4e-5 ✓ | 41.8 EB05 27.6 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=17 | not reported in cached trials |
| Colorectal cancer | 5,102 | 45.7 44.5–47.0ROR 50.4 · calibrated p 1e-5 ✓ | 40.9 EB05 40.0 · IC025 +5.3 3/3 methods agree | Not in label — unassessed | serious PRR 24.7 · 99% consumer | not reported in cached trials |
| Airway remodelling | 13 | 45.1 25.4–80.2ROR 45.2 · calibrated p 9e-5 ✓ | 38.4 EB05 23.9 · IC025 +3.1 3/3 methods agree | Not in label — unassessed | serious n=13 | not reported in cached trials |
| Renal cancer | 4,846 | 43.3 42.1–44.5ROR 47.5 · calibrated p 2e-5 ✓ | 39.0 EB05 38.1 · IC025 +5.2 3/3 methods agree | Not in label — unassessed | serious PRR 23.8 · 98% consumer | not reported in cached trials |
| Oesophageal carcinoma | 2,998 | 43.0 41.4–44.6ROR 45.5 · calibrated p 2e-5 ✓ | 38.7 EB05 37.6 · IC025 +5.2 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious PRR 23.4 · ♀ 27% (drug 51%) · 98% consumer | not reported in cached trials |
| Hepatic cancer | 2,343 | 41.4 39.7–43.2ROR 43.2 · calibrated p 3e-5 ✓ | 37.4 EB05 36.2 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious PRR 22.7 · 97% consumer | not reported in cached trials |
| Gallbladder cancer | 136 | 39.4 33.0–46.9ROR 39.5 · calibrated p 6e-5 ✓ | 35.6 EB05 30.9 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=136 · 100% consumer | not reported in cached trials |
| Gastric cancer | 2,321 | 38.6 37.0–40.3ROR 40.3 · calibrated p 5e-5 ✓ | 35.1 EB05 34.0 · IC025 +5.1 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious PRR 21.2 · 98% consumer | NCT00401752: 2/107 (1.9%) on Ranitidine Hydrochloride (serious AE) |
| Gastrointestinal carcinoma | 810 | 37.5 34.9–40.3ROR 38.1 · calibrated p 7e-5 ✓ | 34.2 EB05 32.3 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | serious PRR 20.7 · 98% consumer | not reported in cached trials |
| Prostate cancer | 7,126 | 37.3 36.4–38.1ROR 42.8 · calibrated p 3e-5 ✓ | 34.0 EB05 33.4 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | serious PRR 20.6 · ♀ 1% (drug 51%) · 98% consumer | not reported in cached trials |
| Bladder cancer | 5,173 | 36.8 35.9–37.9ROR 40.6 · calibrated p 5e-5 ✓ | 33.7 EB05 32.9 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | serious PRR 20.4 · ♀ 26% (drug 51%) · 97% consumer | not reported in cached trials |
| Breast cancer | 7,734 | 34.7 34.0–35.5ROR 40.4 · calibrated p 5e-5 ✓ | 31.9 EB05 31.3 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | serious PRR 19.4 · ♀ 98% (drug 51%) · 99% consumer | not reported in cached trials |
| Facet joint syndrome | 258 | 34.5 30.4–39.2ROR 34.7 · calibrated p 1e-4 ✓ | 31.7 EB05 28.6 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=258 · ♀ 100% (drug 51%) · 93% clinician | not reported in cached trials |
| Appendix cancer | 76 | 34.1 27.0–43.1ROR 34.2 · calibrated p 2e-4 ✓ | 31.2 EB05 25.7 · IC025 +4.3 3/3 methods agree | Not in label — unassessed | serious n=76 · 100% consumer | not reported in cached trials |
| Paranasal sinus inflammation | 17 | 33.0 20.1–54.1ROR 33.0 · calibrated p 4e-4 ✓ | 29.5 EB05 19.5 · IC025 +3.2 3/3 methods agree | Not in label — unassessed | serious n=17 | not reported in cached trials |
| Carbuncle | 22 | 32.7 21.2–50.5ROR 32.7 · calibrated p 3e-4 ✓ | 29.5 EB05 20.5 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=22 · ♀ 100% (drug 51%) | not reported in cached trials |
| Throat cancer | 329 | 32.5 29.0–36.3ROR 32.7 · calibrated p 2e-4 ✓ | 30.0 EB05 27.4 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=329 · 100% consumer | not reported in cached trials |
| Pancreatic carcinoma | 2,244 | 32.4 31.1–33.8ROR 33.8 · calibrated p 1e-4 ✓ | 30.0 EB05 28.9 · IC025 +4.8 3/3 methods agree | Not in label — unassessed | serious PRR 18.1 · 98% consumer | not reported in cached trials |
| Splenic neoplasm malignancy unspecified | 10 | 31.6 16.6–60.2ROR 31.6 · calibrated p 7e-4 ✓ | 27.7 EB05 15.9 · IC025 +2.6 3/3 methods agree | Not in label — unassessed | serious n=10 | not reported in cached trials |
| Overlap syndrome | 50 | 30.3 22.7–40.4ROR 30.3 · calibrated p 3e-4 ✓ | 27.9 EB05 22.0 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious n=50 · ♀ 100% (drug 51%) · 100% clinician | not reported in cached trials |
| Peripheral venous disease | 282 | 29.4 26.1–33.2ROR 29.6 · calibrated p 3e-4 ✓ | 27.4 EB05 24.8 · IC025 +4.5 3/3 methods agree | Not in label — unassessed | serious n=282 · ♀ 100% (drug 51%) · 96% clinician | not reported in cached trials |
| Oesophageal polyp | 13 | 28.4 16.2–49.8ROR 28.4 · calibrated p 9e-4 ✓ | 25.5 EB05 15.8 · IC025 +2.8 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=13 | not reported in cached trials |
| Urethral cancer | 14 | 26.5 15.4–45.5ROR 26.5 · calibrated p 0.001 ✓ | 24.0 EB05 15.1 · IC025 +2.9 3/3 methods agree | Not in label — unassessed | serious n=14 | not reported in cached trials |
| Renal cancer stage i | 169 | 26.3 22.5–30.8ROR 26.4 · calibrated p 5e-4 ✓ | 24.6 EB05 21.7 · IC025 +4.3 3/3 methods agree | Not in label — unassessed | serious n=169 | not reported in cached trials |
| Breast cancer stage iii | 403 | 25.9 23.4–28.6ROR 26.1 · calibrated p 6e-4 ✓ | 24.3 EB05 22.4 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious n=403 · ♀ 100% (drug 51%) · 97% clinician | not reported in cached trials |
| Schizoaffective disorder | 112 | 25.8 21.3–31.2ROR 25.9 · calibrated p 6e-4 ✓ | 24.1 EB05 20.6 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=112 · ♀ 100% (drug 51%) | 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 Ranitidine Hydrochloride 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).
- NCT00401752 — Efficacy and Safety Study of Esomeprazole 20mg qd vs Ranitidine 150mg Bid in Patients With an NSAID-induced Ga (N=397, PHASE3; 12 AE terms posted; arms: Esomeprazole; Ranitidine)
- NCT00838526 — Rabeprazole Extended-Release 50 mg vs. Ranitidine 150 mg for Maintenance of Healed Erosive Gastroesophageal Re (N=240, PHASE3; 19 AE terms posted; arms: RAN 150mg BID; RAB ER 50mg QD)
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 |
|---|---|---|---|---|---|---|
| Breast cancer | 7,734 | 34.7 34.0–35.5ROR 40.4 · calibrated p 5e-5 ✓ | 31.9 EB05 31.3 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | serious PRR 19.4 · ♀ 98% (drug 51%) · 99% consumer | not reported in cached trials |
| Prostate cancer | 7,126 | 37.3 36.4–38.1ROR 42.8 · calibrated p 3e-5 ✓ | 34.0 EB05 33.4 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | serious PRR 20.6 · ♀ 1% (drug 51%) · 98% consumer | not reported in cached trials |
| Bladder cancer | 5,173 | 36.8 35.9–37.9ROR 40.6 · calibrated p 5e-5 ✓ | 33.7 EB05 32.9 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | serious PRR 20.4 · ♀ 26% (drug 51%) · 97% consumer | not reported in cached trials |
| Colorectal cancer | 5,102 | 45.7 44.5–47.0ROR 50.4 · calibrated p 1e-5 ✓ | 40.9 EB05 40.0 · IC025 +5.3 3/3 methods agree | Not in label — unassessed | serious PRR 24.7 · 99% consumer | not reported in cached trials |
| Renal cancer | 4,846 | 43.3 42.1–44.5ROR 47.5 · calibrated p 2e-5 ✓ | 39.0 EB05 38.1 · IC025 +5.2 3/3 methods agree | Not in label — unassessed | serious PRR 23.8 · 98% consumer | not reported in cached trials |
| Oesophageal carcinoma | 2,998 | 43.0 41.4–44.6ROR 45.5 · calibrated p 2e-5 ✓ | 38.7 EB05 37.6 · IC025 +5.2 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious PRR 23.4 · ♀ 27% (drug 51%) · 98% consumer | not reported in cached trials |
| Neoplasm malignant | 2,749 | 16.6 16.0–17.3ROR 17.5 · calibrated p 0.004 ✓ | 16.0 EB05 15.5 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious PRR 9.9 · 97% consumer | not reported in cached trials |
| Hepatic cancer | 2,343 | 41.4 39.7–43.2ROR 43.2 · calibrated p 3e-5 ✓ | 37.4 EB05 36.2 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious PRR 22.7 · 97% consumer | not reported in cached trials |
| Gastric cancer | 2,321 | 38.6 37.0–40.3ROR 40.3 · calibrated p 5e-5 ✓ | 35.1 EB05 34.0 · IC025 +5.1 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious PRR 21.2 · 98% consumer | NCT00401752: 2/107 (1.9%) on Ranitidine Hydrochloride (serious AE) |
| Pancreatic carcinoma | 2,244 | 32.4 31.1–33.8ROR 33.8 · calibrated p 1e-4 ✓ | 30.0 EB05 28.9 · IC025 +4.8 3/3 methods agree | Not in label — unassessed | serious PRR 18.1 · 98% consumer | not reported in cached trials |
| Lung neoplasm malignant | 1,963 | 19.3 18.5–20.2ROR 20.0 · calibrated p 0.002 ✓ | 18.4 EB05 17.8 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious PRR 11.2 · 98% consumer | not reported in cached trials |
| Injury | 1,780 | 10.0 9.6–10.5ROR 10.3 · calibrated p 0.029 ✓ | 9.8 EB05 9.4 · IC025 +3.2 3/3 methods agree | Not in label — unassessed | serious PRR 6.5 | not reported in cached trials |
| Pain | 1,541 | 1.0 0.9–1.0ROR 1.0 · calibrated p 0.288 | 1.0 EB05 0.9 · IC025 -0.1 PRR-only: not supported by EBGM or IC | Likely indication confounding term in indications; also in warnings | serious PRR 0.9 · ♀ 90% (drug 51%) | NCT00401752: 2/110 (1.8%) on Ranitidine Hydrochloride |
| Off label use (used outside approved label) | 1,444 | 0.6 0.6–0.7ROR 0.6 · calibrated p 0.100 | 0.6 EB05 0.6 · IC025 -0.7 PRR-only: not supported by EBGM or IC | Reporting / coding artifact | serious PRR 0.6 · ♀ 89% (drug 51%) | not reported in cached trials |
| Drug ineffective (drug did not work) | 1,254 | 0.4 0.3–0.4ROR 0.4 · calibrated p 0.014 ✓ | 0.4 EB05 0.4 · IC025 -1.5 PRR-only: not supported by EBGM or IC | Reporting / coding artifact | serious PRR 0.5 · ♀ 83% (drug 51%) | 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.
- Computerised tomogram thorax — n=26, PRR 292.1
- Junctional ectopic tachycardia — n=20, PRR 206.5
- Hepatic enzyme — n=37, PRR 139.9
- Hypocholesterolaemia — n=75, PRR 125.1
- Nasal cavity cancer — n=170, PRR 87.6
- Bladder cancer stage i, with cancer in situ — n=30, PRR 61.6
- Temperature regulation disorder — n=297, PRR 61.0
- Small intestine carcinoma — n=254, PRR 49.3
- Colorectal cancer — n=5,102, PRR 45.7
- Renal cancer — n=4,846, PRR 43.3
✓ A hand-written Bradford Hill causality assessment exists for this drug: Ranitidine (Zantac) ↔ Cancer (breast, prostate, bladder, colorectal, renal).
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 Ranitidine Hydrochloride?
In FDA FAERS, the most frequently co-reported reaction terms for Ranitidine Hydrochloride are breast cancer, prostate cancer, bladder cancer, colorectal cancer, renal cancer, oesophageal carcinoma. 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 Ranitidine Hydrochloride have an FDA boxed warning?
No. The FDA label retrieved for Ranitidine Hydrochloride has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Ranitidine Hydrochloride 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 0fba6615-37c2-4ba6-b6e5-09599369a5bc, effective 20251205; matched on
openfda.generic_name.exact:"RANITIDINE") - 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, 1,128 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
RANITIDINE, 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.