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Rabeprazole side effects: what 22,026 FDA adverse event reports show

Rabeprazole · Rabeprazole Sodium · 1,210 reaction terms · 113,792 drug–reaction co-reports · data 2026-09-14
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Drug class

Not stated in label

Brand names

Rabeprazole Sodium

openFDA label

Who reports

22,026 reports · 92% serious · 2,526 with death outcome · 58% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Rabeprazole sodium delayed-release tablets are a proton pump inhibitor (PPI) indicated in adults for: Healing of Erosive or Ulcerative Gastroesophageal Reflux Disease (GERD). ( 1.1 ) Maintenance of Healing of Erosive or Ulcerative GERD. ( 1.2 ) Treatment of Symptomatic GERD. ( 1.3 ) Healing of Duodenal Ulcers. ( 1.4 ) Helicobacter pylori Eradication to Reduce Risk of Duodenal Ulcer Recurrence.

FDA label, Indications and Usage

What it is

The active ingredient in rabeprazole sodium delayed-release tablets is rabeprazole sodium, USP which is a proton pump inhibitor. It is a substituted benzimidazole known chemically as 2-[[[4-(3-­methoxypropoxy)-3-methyl-2-pyridinyl]-methyl]sulfinyl]-1 H –benzimidazole sodium salt.

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

Labeled adverse reaction 1Labeled (related wording) 5Likely indication confounding 1Reporting / coding artifact 2Lab value / disease marker 7Not in label — unassessed 24
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). 1,170 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
Sputum culture231,541.4
793.3–2,995.1ROR 1,543.0 · calibrated p 2e-16 ✓
392.6 EB05 275.5 · IC025 +4.7
3/3 methods agree
Lab value / disease markerserious n=23not reported in cached trials
Eosinophilic bronchitis83665.6
502.6–881.5ROR 668.1 · calibrated p 8e-15 ✓
357.6 EB05 297.6 · IC025 +6.5
3/3 methods agree
Not in label — unassessedserious n=83 · ♀ 100% (drug 58%)not reported in cached trials
Cestode infection18324.8
190.1–555.0ROR 325.0 · calibrated p 9e-11 ✓
192.5 EB05 128.8 · IC025 +4.2
3/3 methods agree
Not in label — unassessedserious n=18not reported in cached trials
Gait spastic86314.0
246.0–400.7ROR 315.2 · calibrated p 1e-11 ✓
223.8 EB05 186.9 · IC025 +6.3
3/3 methods agree
Not in label — unassessedserious n=86 · ♀ 0% (drug 58%)not reported in cached trials
Vital capacity decreased90237.9
188.8–299.7ROR 238.8 · calibrated p 1e-10 ✓
182.6 EB05 153.1 · IC025 +6.2
3/3 methods agree
Not in label — unassessedserious n=90 · ♀ 100% (drug 58%)not reported in cached trials
Needle fatigue86220.5
174.4–278.7ROR 221.3 · calibrated p 3e-10 ✓
171.9 EB05 143.5 · IC025 +6.1
3/3 methods agree
Not in label — unassessedserious n=86 · ♀ 0% (drug 58%)not reported in cached trials
Reversible airways obstruction96218.6
175.1–272.9ROR 219.6 · calibrated p 3e-10 ✓
171.5 EB05 144.6 · IC025 +6.2
3/3 methods agree
Not in label — unassessedserious n=96 · ♀ 100% (drug 58%)not reported in cached trials
Parathyroid gland enlargement23179.8
115.1–280.9ROR 180.0 · calibrated p 5e-9 ✓
134.4 EB05 94.4 · IC025 +4.5
3/3 methods agree
Not in label — unassessedserious n=23 · ♀ 0% (drug 58%) · 100% cliniciannot reported in cached trials
Cerebral hypoperfusion67162.9
125.7–211.0ROR 163.4 · calibrated p 4e-9 ✓
133.7 EB05 108.9 · IC025 +5.7
3/3 methods agree
Not in label — unassessedserious n=67 · ♀ 0% (drug 58%)not reported in cached trials
Sputum culture positive94122.5
98.8–151.8ROR 123.0 · calibrated p 3e-8 ✓
106.2 EB05 89.3 · IC025 +5.8
3/3 methods agree
Lab value / disease markerserious n=93 · ♀ 100% (drug 58%)not reported in cached trials
Binocular eye movement disorder28105.5
71.4–155.9ROR 105.6 · calibrated p 2e-7 ✓
89.3 EB05 64.9 · IC025 +4.5
3/3 methods agree
Not in label — unassessedserious n=28 · ♀ 0% (drug 58%)not reported in cached trials
Relapsing-remitting multiple sclerosis86105.3
84.3–131.6ROR 105.7 · calibrated p 1e-7 ✓
92.9 EB05 77.6 · IC025 +5.6
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=86 · ♀ 0% (drug 58%)not reported in cached trials
Muscle tone disorder2892.8
63.0–136.8ROR 92.9 · calibrated p 5e-7 ✓
80.1 EB05 58.2 · IC025 +4.5
3/3 methods agree
Not in label — unassessedserious n=28not reported in cached trials
Bronchial secretion retention10989.8
73.8–109.2ROR 90.2 · calibrated p 3e-7 ✓
80.9 EB05 68.9 · IC025 +5.6
3/3 methods agree
Not in label — unassessedserious n=109 · ♀ 100% (drug 58%)not reported in cached trials
Cerebellar stroke2979.8
54.6–116.6ROR 79.9 · calibrated p 1e-6 ✓
70.3 EB05 51.4 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=29 · ♀ 0% (drug 58%)not reported in cached trials
Blood folate decreased4461.5
45.4–83.4ROR 61.6 · calibrated p 6e-6 ✓
56.5 EB05 43.8 · IC025 +4.6
3/3 methods agree
Lab value / disease markerserious n=44 · ♀ 100% (drug 58%) · 91% cliniciannot reported in cached trials
Sputum purulent3451.5
36.4–72.6ROR 51.5 · calibrated p 2e-5 ✓
47.6 EB05 35.6 · IC025 +4.3
3/3 methods agree
Not in label — unassessedserious n=34 · ♀ 100% (drug 58%) · 100% cliniciannot reported in cached trials
Lung diffusion test decreased2050.6
32.3–79.3ROR 50.6 · calibrated p 3e-5 ✓
46.1 EB05 31.5 · IC025 +3.7
3/3 methods agree
Not in label — unassessedserious n=20not reported in cached trials
Blood pressure systolic abnormal12550.3
42.0–60.2ROR 50.6 · calibrated p 1e-5 ✓
47.4 EB05 40.9 · IC025 +5.0
3/3 methods agree
Lab value / disease markerserious n=124not reported in cached trials
Monoparesis8647.2
38.0–58.5ROR 47.3 · calibrated p 2e-5 ✓
44.5 EB05 37.2 · IC025 +4.8
3/3 methods agree
Not in label — unassessedserious n=86 · ♀ 0% (drug 58%)not reported in cached trials
Hypertonic bladder13346.1
38.7–54.8ROR 46.4 · calibrated p 2e-5 ✓
43.7 EB05 37.8 · IC025 +5.0
3/3 methods agree
Not in label — unassessedserious n=133 · ♀ 31% (drug 58%)not reported in cached trials
Lichen sclerosus3044.5
30.8–64.1ROR 44.5 · calibrated p 5e-5 ✓
41.5 EB05 30.4 · IC025 +4.1
3/3 methods agree
Not in label — unassessedserious n=30 · ♀ 100% (drug 58%) · 100% cliniciannot reported in cached trials
Bronchopulmonary aspergillosis allergic3436.6
26.0–51.6ROR 36.7 · calibrated p 1e-4 ✓
34.7 EB05 25.9 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious n=34 · ♀ 32% (drug 58%)not reported in cached trials
Blood pressure diastolic abnormal9436.1
29.4–44.3ROR 36.3 · calibrated p 1e-4 ✓
34.6 EB05 29.1 · IC025 +4.5
3/3 methods agree
Lab value / disease markerserious n=94not reported in cached trials
Pneumothorax spontaneous2231.8
20.8–48.6ROR 31.8 · calibrated p 3e-4 ✓
30.0 EB05 20.9 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=22 · 100% cliniciannot reported in cached trials
Tonsillar disorder3429.5
21.0–41.5ROR 29.5 · calibrated p 4e-4 ✓
28.2 EB05 21.1 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious n=34 · ♀ 100% (drug 58%) · 100% cliniciannot reported in cached trials
Hypoparathyroidism2329.5
19.5–44.6ROR 29.5 · calibrated p 5e-4 ✓
28.0 EB05 19.7 · IC025 +3.5
3/3 methods agree
Labeled adverse reaction
exact term
serious n=23 · 100% cliniciannot reported in cached trials
Obstructive airways disorder30326.5
23.7–29.7ROR 26.9 · calibrated p 5e-4 ✓
25.8 EB05 23.5 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious PRR 16.8 · ♀ 84% (drug 58%)not reported in cached trials
Loss of employment7524.0
19.1–30.2ROR 24.1 · calibrated p 9e-4 ✓
23.3 EB05 19.2 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious n=75 · ♀ 100% (drug 58%)not reported in cached trials
Eosinophil count increased19623.0
20.0–26.5ROR 23.2 · calibrated p 0.001 ✓
22.4 EB05 19.9 · IC025 +4.2
3/3 methods agree
Lab value / disease markerserious PRR 16.8 · ♀ 95% (drug 58%)not reported in cached trials
Dyschromatopsia1922.7
14.4–35.8ROR 22.8 · calibrated p 0.002 ✓
21.8 EB05 14.6 · IC025 +3.1
3/3 methods agree
Not in label — unassessedserious n=19not reported in cached trials
Pulmonary function test abnormal3421.2
15.1–29.7ROR 21.2 · calibrated p 0.002 ✓
20.5 EB05 15.3 · IC025 +3.4
3/3 methods agree
Reporting / coding artifactserious n=34not reported in cached trials
Product ineffective for unapproved use3020.9
14.5–29.9ROR 20.9 · calibrated p 0.002 ✓
20.2 EB05 14.8 · IC025 +3.3
3/3 methods agree
Reporting / coding artifactserious n=30 · ♀ 100% (drug 58%)not reported in cached trials
Lymphadenitis5020.1
15.2–26.6ROR 20.1 · calibrated p 0.002 ✓
19.5 EB05 15.4 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=49 · ♀ 0% (drug 58%)not reported in cached trials
Blood pressure diastolic decreased15219.9
17.0–23.4ROR 20.0 · calibrated p 0.002 ✓
19.5 EB05 17.0 · IC025 +3.9
3/3 methods agree
Lab value / disease markerserious PRR 13.0not reported in cached trials

Trial evidence (ClinicalTrials.gov)

✓ Trial adverse-event data found on ClinicalTrials.gov

Largest completed trials with posted results that list Rabeprazole 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 (0 of 40 signal terms matched).

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.

ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Drug ineffective (drug did not work)1,9261.4
1.3–1.5ROR 1.4 · calibrated p 0.596
1.4 EB05 1.3 · IC025 +0.4Reporting / coding artifactserious PRR 2.2 · ♀ 80% (drug 58%)not reported in cached trials
Off label use (used outside approved label)1,8672.0
2.0–2.1ROR 2.1 · calibrated p 0.978
2.0 EB05 2.0 · IC025 +1.0Reporting / coding artifactserious PRR 2.3not reported in cached trials
Nausea1,5831.9
1.8–2.0ROR 2.0 · calibrated p 0.934
1.9 EB05 1.8 · IC025 +0.9Labeled adverse reaction
exact term
serious PRR 2.2not reported in cached trials
Diarrhoea (diarrhea)1,3682.0
1.9–2.1ROR 2.1 · calibrated p 0.995
2.0 EB05 1.9 · IC025 +0.9Labeled adverse reaction
exact term
serious PRR 2.1not reported in cached trials
Headache1,3572.1
2.0–2.2ROR 2.1 · calibrated p 0.984
2.1 EB05 2.0 · IC025 +1.0Labeled adverse reaction
exact term
serious PRR 2.5 · ♀ 78% (drug 58%)NCT00658632: 1/676 (0.1%) on Rabeprazole (serious AE)
Pain1,3392.1
2.0–2.2ROR 2.1 · calibrated p 0.980
2.1 EB05 2.0 · IC025 +1.0Labeled adverse reaction
exact term
serious PRR 2.0NCT00464308: 1/459 (0.2%) on Rabeprazole (serious AE)
Dyspnoea (shortness of breath)1,3232.2
2.1–2.3ROR 2.3 · calibrated p 0.899
2.2 EB05 2.1 · IC025 +1.1
3/3 methods agree
Not in label — unassessedserious PRR 1.9not reported in cached trials
Arthralgia (joint pain)1,3053.0
2.8–3.2ROR 3.1 · calibrated p 0.586
3.0 EB05 2.9 · IC025 +1.5
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 3.3not reported in cached trials
Fatigue (tiredness)1,2411.5
1.4–1.6ROR 1.6 · calibrated p 0.676
1.5 EB05 1.5 · IC025 +0.5Not in label — unassessedserious PRR 1.7not reported in cached trials
Malaise (feeling unwell)1,1932.6
2.4–2.7ROR 2.7 · calibrated p 0.741
2.6 EB05 2.5 · IC025 +1.3
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 2.6not reported in cached trials
Pneumonia (lung infection)1,1433.4
3.2–3.6ROR 3.5 · calibrated p 0.484
3.4 EB05 3.2 · IC025 +1.7
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 2.2NCT00658632: 1/676 (0.1%) on Rabeprazole (serious AE)
Fall9732.8
2.6–3.0ROR 2.9 · calibrated p 0.669
2.8 EB05 2.6 · IC025 +1.4
3/3 methods agree
Not in label — unassessedserious PRR 2.1not reported in cached trials
Cough9623.3
3.1–3.5ROR 3.4 · calibrated p 0.514
3.3 EB05 3.1 · IC025 +1.6
3/3 methods agree
Not in label — unassessedserious PRR 3.5not reported in cached trials
Dizziness9151.8
1.6–1.9ROR 1.8 · calibrated p 0.820
1.7 EB05 1.7 · IC025 +0.7Labeled adverse reaction
exact term
serious PRR 1.8not 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.

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 Rabeprazole?

In FDA FAERS, the most frequently co-reported reaction terms for Rabeprazole are nausea, diarrhoea, headache, pain, dyspnoea, arthralgia. 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 Rabeprazole have an FDA boxed warning?

No. The FDA label retrieved for Rabeprazole has no boxed warning; see the label's Warnings and Precautions for the recognised risks.

Do FAERS signals prove that Rabeprazole 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.