Loperamide Hydrochloride side effects: what 44,397 FDA adverse event reports show
Drug class
Not stated in label
Label matched
Loperamide Hydrochloride (Loperamide Hydrochloride)
Who reports
44,397 reports · 62% serious · 3,872 with death outcome · 62% female
Used for
Loperamide hydrochloride capsules are indicated for the control and symptomatic relief of acute nonspecific diarrhea in patients 2 years of age and older and of chronic diarrhea in adults associated with inflammatory bowel disease. Loperamide hydrochloride capsules are also indicated for reducing the volume of discharge from ileostomies.
What it is
DESCRIPTION Loperamide hydrochloride, 4-(p-chlorophenyl)-4-hydroxy-N, N-dimethyl-α,α-diphenyl-piperidinebutyramide monohydrochloride, is a synthetic antidiarrheal for oral use. Loperamide hydrochloride is available in 2 mg capsules.
Boxed warning
TORSADES DE POINTES AND SUDDEN DEATH Cases of Torsades de Pointes, cardiac arrest, and death have been reported with the use of a higher than recommended dosage of loperamide hydrochloride capsules (see WARNINGS and OVERDOSAGE ). Loperamide hydrochloride capsules are contraindicated in pediatric patients less than 2 years of age (see CONTRAINDICATIONS ).
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). 1,159 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 |
|---|---|---|---|---|---|---|
| Total lung capacity increased | 119 | 366.1 287.9–465.4ROR 367.0 · calibrated p 3e-12 ✓ | 198.7 EB05 170.5 · IC025 +6.5 3/3 methods agree | Not in label — unassessed | serious n=119 · ♀ 100% (drug 62%) · 100% clinician | not reported in cached trials |
| Blood mercury abnormal | 41 | 340.1 227.3–508.7ROR 340.4 · calibrated p 2e-11 ✓ | 180.3 EB05 138.6 · IC025 +5.4 3/3 methods agree | Lab value / disease marker | serious n=41 · ♀ 0% (drug 62%) | not reported in cached trials |
| Vaginal flatulence | 111 | 269.9 213.7–341.0ROR 270.6 · calibrated p 4e-11 ✓ | 166.2 EB05 141.9 · IC025 +6.3 3/3 methods agree | Not in label — unassessed | serious n=110 · ♀ 100% (drug 62%) | not reported in cached trials |
| Asthma-chronic obstructive pulmonary disease overlap syndrome | 100 | 112.2 90.2–139.6ROR 112.5 · calibrated p 6e-8 ✓ | 89.1 EB05 75.4 · IC025 +5.6 3/3 methods agree | Not in label — unassessed | serious n=100 · ♀ 100% (drug 62%) · 100% clinician | not reported in cached trials |
| Presbyacusis | 56 | 103.6 77.6–138.4ROR 103.8 · calibrated p 2e-7 ✓ | 82.6 EB05 66.0 · IC025 +5.2 3/3 methods agree | Not in label — unassessed | serious n=56 · ♀ 100% (drug 62%) | not reported in cached trials |
| Gastrointestinal procedural complication | 36 | 74.3 52.3–105.6ROR 74.4 · calibrated p 2e-6 ✓ | 62.2 EB05 46.9 · IC025 +4.5 3/3 methods agree | Reporting / coding artifact | serious n=36 · ♀ 100% (drug 62%) · 100% clinician | not reported in cached trials |
| Gastrointestinal stoma output increased | 45 | 50.7 37.3–69.0ROR 50.8 · calibrated p 2e-5 ✓ | 45.0 EB05 35.0 · IC025 +4.4 3/3 methods agree | Lab value / disease marker | serious n=45 | not reported in cached trials |
| Female genital tract fistula | 128 | 37.8 31.6–45.3ROR 38.0 · calibrated p 8e-5 ✓ | 34.9 EB05 30.1 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=127 · ♀ 100% (drug 62%) | not reported in cached trials |
| Product blister packaging issue | 74 | 36.5 28.8–46.3ROR 36.6 · calibrated p 1e-4 ✓ | 33.7 EB05 27.7 · IC025 +4.4 3/3 methods agree | Reporting / coding artifact | 100% consumer | not reported in cached trials |
| Pleural thickening | 44 | 32.5 23.9–44.1ROR 32.5 · calibrated p 2e-4 ✓ | 30.1 EB05 23.3 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious n=44 · ♀ 100% (drug 62%) · 100% clinician | not reported in cached trials |
| Product package associated injury | 138 | 31.3 26.3–37.1ROR 31.4 · calibrated p 2e-4 ✓ | 29.3 EB05 25.4 · IC025 +4.5 3/3 methods agree | Reporting / coding artifact | 100% consumer | not reported in cached trials |
| Pleural fibrosis | 63 | 30.7 23.8–39.6ROR 30.7 · calibrated p 3e-4 ✓ | 28.6 EB05 23.2 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=63 · ♀ 100% (drug 62%) | not reported in cached trials |
| Blood magnesium increased | 51 | 28.2 21.2–37.4ROR 28.2 · calibrated p 5e-4 ✓ | 26.4 EB05 20.8 · IC025 +3.9 3/3 methods agree | Lab value / disease marker | serious n=50 · ♀ 100% (drug 62%) | not reported in cached trials |
| Product packaging difficult to open | 134 | 27.0 22.7–32.1ROR 27.1 · calibrated p 5e-4 ✓ | 25.5 EB05 22.1 · IC025 +4.3 3/3 methods agree | Reporting / coding artifact | 100% consumer | not reported in cached trials |
| Anticholinergic syndrome | 81 | 25.2 20.2–31.5ROR 25.3 · calibrated p 7e-4 ✓ | 23.9 EB05 19.8 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious n=81 · 100% clinician | not reported in cached trials |
| Jaundice cholestatic | 178 | 24.9 21.4–29.0ROR 25.0 · calibrated p 7e-4 ✓ | 23.7 EB05 20.9 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious n=178 · ♀ 100% (drug 62%) · 100% clinician | not reported in cached trials |
| Hypomania | 182 | 24.4 21.1–28.4ROR 24.5 · calibrated p 8e-4 ✓ | 23.2 EB05 20.5 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious n=182 · ♀ 100% (drug 62%) · 100% clinician | not reported in cached trials |
| Bronchial wall thickening | 35 | 23.9 17.0–33.5ROR 23.9 · calibrated p 0.001 ✓ | 22.5 EB05 16.9 · IC025 +3.6 3/3 methods agree | Not in label — unassessed | serious n=35 · ♀ 100% (drug 62%) | not reported in cached trials |
| Bacterial disease carrier | 35 | 23.8 16.9–33.4ROR 23.8 · calibrated p 0.001 ✓ | 22.4 EB05 16.8 · IC025 +3.6 3/3 methods agree | Reporting / coding artifact | serious n=35 · ♀ 100% (drug 62%) | not reported in cached trials |
| Proctitis | 133 | 23.4 19.7–27.9ROR 23.5 · calibrated p 1e-3 ✓ | 22.3 EB05 19.3 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=131 · ♀ 100% (drug 62%) | not reported in cached trials |
| Chronic sinusitis | 170 | 22.4 19.2–26.1ROR 22.5 · calibrated p 0.001 ✓ | 21.4 EB05 18.8 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=168 · ♀ 100% (drug 62%) | not reported in cached trials |
| Radiculopathy | 116 | 21.7 18.0–26.1ROR 21.7 · calibrated p 0.001 ✓ | 20.7 EB05 17.7 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious n=116 · ♀ 100% (drug 62%) | not reported in cached trials |
| Gastrointestinal stoma complication | 59 | 18.5 14.3–24.0ROR 18.5 · calibrated p 0.003 ✓ | 17.7 EB05 14.2 · IC025 +3.5 3/3 methods agree | Reporting / coding artifact | serious n=58 | not reported in cached trials |
| Pouchitis | 32 | 18.1 12.8–25.8ROR 18.2 · calibrated p 0.004 ✓ | 17.3 EB05 12.7 · IC025 +3.2 3/3 methods agree | Not in label — unassessed | serious n=32 · 100% clinician | not reported in cached trials |
| Product difficult to swallow | 38 | 18.0 13.1–25.0ROR 18.1 · calibrated p 0.004 ✓ | 17.2 EB05 13.0 · IC025 +3.3 3/3 methods agree | Reporting / coding artifact | ♀ 100% (drug 62%) · 100% consumer | not reported in cached trials |
| Product packaging issue | 330 | 17.4 15.6–19.4ROR 17.5 · calibrated p 0.004 ✓ | 16.8 EB05 15.3 · IC025 +3.9 3/3 methods agree | Reporting / coding artifact | 100% consumer | not reported in cached trials |
| Stoma complication | 35 | 16.7 11.9–23.4ROR 16.7 · calibrated p 0.006 ✓ | 16.0 EB05 11.9 · IC025 +3.2 3/3 methods agree | Reporting / coding artifact | serious n=34 | not reported in cached trials |
| Bronchial secretion retention | 39 | 15.0 10.9–20.6ROR 15.0 · calibrated p 0.008 ✓ | 14.3 EB05 10.8 · IC025 +3.1 3/3 methods agree | Not in label — unassessed | serious n=39 · ♀ 100% (drug 62%) | not reported in cached trials |
| Vascular device infection | 136 | 14.6 12.3–17.3ROR 14.7 · calibrated p 0.008 ✓ | 14.2 EB05 12.2 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=136 | not reported in cached trials |
| Rhinitis allergic | 130 | 14.2 11.9–16.9ROR 14.2 · calibrated p 0.009 ✓ | 13.7 EB05 11.8 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | serious n=124 · ♀ 100% (drug 62%) | not reported in cached trials |
| Low density lipoprotein decreased | 41 | 14.0 10.3–19.1ROR 14.0 · calibrated p 0.011 ✓ | 13.4 EB05 10.1 · IC025 +3.0 3/3 methods agree | Lab value / disease marker | serious n=41 · ♀ 0% (drug 62%) | not reported in cached trials |
| Tumour pain | 38 | 13.9 10.1–19.2ROR 13.9 · calibrated p 0.011 ✓ | 13.3 EB05 9.9 · IC025 +3.0 3/3 methods agree | Not in label — unassessed | serious n=36 · 100% clinician | not reported in cached trials |
| Incorrect product administration duration | 578 | 13.8 12.7–15.0ROR 14.0 · calibrated p 0.009 ✓ | 13.4 EB05 12.5 · IC025 +3.6 3/3 methods agree | Reporting / coding artifact | 100% consumer | not reported in cached trials |
| Infrequent bowel movements | 71 | 13.8 10.9–17.5ROR 13.8 · calibrated p 0.011 ✓ | 13.3 EB05 10.8 · IC025 +3.2 3/3 methods agree | Not in label — unassessed | 100% consumer | not reported in cached trials |
| Macular degeneration | 315 | 12.8 11.4–14.3ROR 12.9 · calibrated p 0.013 ✓ | 12.4 EB05 11.3 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | serious PRR 12.6 · ♀ 100% (drug 62%) | not reported in cached trials |
| Therapeutic reaction time decreased | 74 | 12.1 9.6–15.3ROR 12.2 · calibrated p 0.017 ✓ | 11.7 EB05 9.5 · IC025 +3.1 3/3 methods agree | Lab value / disease marker | serious n=71 | not reported in cached trials |
| Blood pressure diastolic abnormal | 64 | 12.0 9.4–15.4ROR 12.0 · calibrated p 0.018 ✓ | 11.5 EB05 9.2 · IC025 +3.0 3/3 methods agree | Lab value / disease marker | serious n=64 · 100% clinician | not reported in cached trials |
| Colitis microscopic | 113 | 11.6 9.6–14.0ROR 11.6 · calibrated p 0.020 ✓ | 11.2 EB05 9.6 · IC025 +3.1 3/3 methods agree | Not in label — unassessed | serious n=112 · ♀ 83% (drug 62%) | not reported in cached trials |
| Blood pressure systolic abnormal | 57 | 11.0 8.5–14.3ROR 11.0 · calibrated p 0.025 ✓ | 10.5 EB05 8.3 · IC025 +2.9 3/3 methods agree | Lab value / disease marker | serious n=57 · 100% clinician | not reported in cached trials |
| Osteosclerosis | 36 | 11.0 7.9–15.3ROR 11.0 · calibrated p 0.027 ✓ | 10.3 EB05 7.5 · IC025 +2.7 3/3 methods agree | Not in label — unassessed | serious n=36 · ♀ 100% (drug 62%) | 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 Loperamide 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).
- NCT02400476 — An Open-Label Study to Characterize the Incidence and Severity of Diarrhea in Patients With Early-Stage HER2+ (N=563, PHASE2; 91 AE terms posted; arms: Loperamide; Budesonide and Loperamide; Colestipol and Loperamide; Colestipol With Loperamide as Needed)
- NCT02008565 — Controlling Anal Incontinence by Performing Anal Exercises With Biofeedback or Loperamide (CAPABLe) (N=300, PHASE3; 36 AE terms posted; arms: Loperamide - Exercise Plus Biofeedback; Placebo - Exercise Plus Biofeedback; Loperamide - Education Only; Placebo - Education Only)
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 |
|---|---|---|---|---|---|---|
| Diarrhoea (diarrhea) | 8,858 | 6.6 6.5–6.7ROR 8.0 · calibrated p 0.067 | 6.5 EB05 6.4 · IC025 +2.7 3/3 methods agree | Labeled — boxed warning exact term | serious PRR 7.0 | NCT02400476: 2/137 (1.5%) on Loperamide (serious AE) |
| Nausea | 4,290 | 2.6 2.5–2.6ROR 2.7 · calibrated p 0.716 | 2.6 EB05 2.5 · IC025 +1.3 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 3.4 | NCT02400476: 1/137 (0.7%) on Loperamide (serious AE) |
| Drug ineffective (drug did not work) | 4,064 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.644 | 1.5 EB05 1.4 · IC025 +0.5 | Reporting / coding artifact | serious PRR 1.3 · 73% consumer | not reported in cached trials |
| Fatigue (tiredness) | 3,881 | 2.4 2.3–2.4ROR 2.5 · calibrated p 0.816 | 2.4 EB05 2.3 · IC025 +1.2 3/3 methods agree | Labeled (related wording) related wording | serious PRR 2.9 | NCT02400476: 41/104 (39.4%) on Loperamide |
| Off label use (used outside approved label) | 3,215 | 1.8 1.7–1.8ROR 1.8 · calibrated p 0.835 | 1.7 EB05 1.7 · IC025 +0.7 | Reporting / coding artifact | serious PRR 2.0 | not reported in cached trials |
| Vomiting | 2,778 | 2.8 2.7–2.9ROR 2.9 · calibrated p 0.651 | 2.8 EB05 2.7 · IC025 +1.4 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 3.2 | NCT02400476: 25/104 (24.0%) on Loperamide |
| Constipation | 2,475 | 5.4 5.2–5.7ROR 5.7 · calibrated p 0.170 | 5.4 EB05 5.2 · IC025 +2.4 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 4.8 | NCT02400476: 39/104 (37.5%) on Loperamide |
| Weight decreased (weight loss) | 2,092 | 3.6 3.4–3.7ROR 3.7 · calibrated p 0.442 | 3.5 EB05 3.4 · IC025 +1.7 3/3 methods agree | Not in label — unassessed | serious PRR 4.1 | NCT02400476: 4/104 (3.8%) on Loperamide |
| Headache | 2,025 | 1.5 1.5–1.6ROR 1.6 · calibrated p 0.676 | 1.5 EB05 1.5 · IC025 +0.5 | Labeled adverse reaction exact term | serious PRR 2.0 | NCT02400476: 24/104 (23.1%) on Loperamide |
| Dyspnoea (shortness of breath) | 1,986 | 1.7 1.6–1.7ROR 1.7 · calibrated p 0.763 | 1.7 EB05 1.6 · IC025 +0.7 | Not in label — unassessed | serious PRR 1.8 | NCT02400476: 4/104 (3.8%) on Loperamide |
| Asthenia (weakness) | 1,836 | 2.3 2.2–2.4ROR 2.4 · calibrated p 0.872 | 2.3 EB05 2.2 · IC025 +1.1 3/3 methods agree | Not in label — unassessed | serious PRR 2.5 | NCT02400476: 4/104 (3.8%) on Loperamide |
| Abdominal pain | 1,827 | 3.7 3.6–3.9ROR 3.8 · calibrated p 0.408 | 3.7 EB05 3.6 · IC025 +1.8 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 3.9 | NCT02400476: 1/136 (0.7%) on Loperamide (serious AE) |
| Decreased appetite (loss of appetite) | 1,814 | 3.7 3.6–3.9ROR 3.8 · calibrated p 0.410 | 3.7 EB05 3.6 · IC025 +1.8 3/3 methods agree | Not in label — unassessed | serious PRR 4.0 | NCT02400476: 1/137 (0.7%) on Loperamide (serious AE) |
| Dizziness | 1,713 | 1.6 1.6–1.7ROR 1.7 · calibrated p 0.738 | 1.6 EB05 1.6 · IC025 +0.6 | Labeled adverse reaction exact term | serious PRR 1.9 | NCT02400476: 20/104 (19.2%) on Loperamide |
| Pain | 1,659 | 1.3 1.2–1.3ROR 1.3 · calibrated p 0.497 | 1.3 EB05 1.2 · IC025 +0.3 | Labeled adverse reaction exact term | serious PRR 1.5 | NCT02400476: 1/136 (0.7%) on Loperamide (serious AE) |
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.
- Total lung capacity increased — n=119, PRR 366.1
- Vaginal flatulence — n=111, PRR 269.9
- Asthma-chronic obstructive pulmonary disease overlap syndrome — n=100, PRR 112.2
- Presbyacusis — n=56, PRR 103.6
- Female genital tract fistula — n=128, PRR 37.8
- Pleural thickening — n=44, PRR 32.5
- Pleural fibrosis — n=63, PRR 30.7
- Anticholinergic syndrome — n=81, PRR 25.2
- Jaundice cholestatic — n=178, PRR 24.9
- Hypomania — n=182, PRR 24.4
✓ A hand-written Bradford Hill causality assessment exists for this drug: Loperamide ↔ QT prolongation.
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 Loperamide?
In FDA FAERS, the most frequently co-reported reaction terms for Loperamide are diarrhoea, nausea, fatigue, vomiting, constipation, weight decreased. 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 Loperamide have an FDA boxed warning?
Yes. The current FDA label carries a boxed warning: TORSADES DE POINTES AND SUDDEN DEATH Cases of Torsades de Pointes, cardiac arrest, and death have been reported with the use of a higher than recommended dosage of loperamide hydrochloride capsules (see WARNINGS and OVERDOSAGE ). Loperamide hydrochloride capsules are contraindicated in pediatric patients less than 2 years of age (see CONTRAINDICATIONS ).
Do FAERS signals prove that Loperamide 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 03c907d5-87f8-47a6-9544-5a24f5272739, effective 20260105; matched on
openfda.generic_name.exact:"LOPERAMIDE 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, 1,199 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
LOPERAMIDE, 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.