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Loperamide Hydrochloride side effects: what 44,397 FDA adverse event reports show

Loperamide Hydrochloride · 1,199 reaction terms · 195,463 drug–reaction co-reports · data 2026-09-14
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Drug class

Not stated in label

Label matched

Loperamide Hydrochloride (Loperamide 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

44,397 reports · 62% serious · 3,872 with death outcome · 62% female

openFDA FAERS counts, all years, deduplication not applied

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.

FDA label, Indications and Usage

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.

FDA label, Description section

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 ).

FDA 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 10Lab value / disease marker 7Not in label — unassessed 23
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). 1,159 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
Total lung capacity increased119366.1
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 — unassessedserious n=119 · ♀ 100% (drug 62%) · 100% cliniciannot reported in cached trials
Blood mercury abnormal41340.1
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 markerserious n=41 · ♀ 0% (drug 62%)not reported in cached trials
Vaginal flatulence111269.9
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 — unassessedserious n=110 · ♀ 100% (drug 62%)not reported in cached trials
Asthma-chronic obstructive pulmonary disease overlap syndrome100112.2
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 — unassessedserious n=100 · ♀ 100% (drug 62%) · 100% cliniciannot reported in cached trials
Presbyacusis56103.6
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 — unassessedserious n=56 · ♀ 100% (drug 62%)not reported in cached trials
Gastrointestinal procedural complication3674.3
52.3–105.6ROR 74.4 · calibrated p 2e-6 ✓
62.2 EB05 46.9 · IC025 +4.5
3/3 methods agree
Reporting / coding artifactserious n=36 · ♀ 100% (drug 62%) · 100% cliniciannot reported in cached trials
Gastrointestinal stoma output increased4550.7
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 markerserious n=45not reported in cached trials
Female genital tract fistula12837.8
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 — unassessedserious n=127 · ♀ 100% (drug 62%)not reported in cached trials
Product blister packaging issue7436.5
28.8–46.3ROR 36.6 · calibrated p 1e-4 ✓
33.7 EB05 27.7 · IC025 +4.4
3/3 methods agree
Reporting / coding artifact100% consumernot reported in cached trials
Pleural thickening4432.5
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 — unassessedserious n=44 · ♀ 100% (drug 62%) · 100% cliniciannot reported in cached trials
Product package associated injury13831.3
26.3–37.1ROR 31.4 · calibrated p 2e-4 ✓
29.3 EB05 25.4 · IC025 +4.5
3/3 methods agree
Reporting / coding artifact100% consumernot reported in cached trials
Pleural fibrosis6330.7
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 — unassessedserious n=63 · ♀ 100% (drug 62%)not reported in cached trials
Blood magnesium increased5128.2
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 markerserious n=50 · ♀ 100% (drug 62%)not reported in cached trials
Product packaging difficult to open13427.0
22.7–32.1ROR 27.1 · calibrated p 5e-4 ✓
25.5 EB05 22.1 · IC025 +4.3
3/3 methods agree
Reporting / coding artifact100% consumernot reported in cached trials
Anticholinergic syndrome8125.2
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 — unassessedserious n=81 · 100% cliniciannot reported in cached trials
Jaundice cholestatic17824.9
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 — unassessedserious n=178 · ♀ 100% (drug 62%) · 100% cliniciannot reported in cached trials
Hypomania18224.4
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 — unassessedserious n=182 · ♀ 100% (drug 62%) · 100% cliniciannot reported in cached trials
Bronchial wall thickening3523.9
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 — unassessedserious n=35 · ♀ 100% (drug 62%)not reported in cached trials
Bacterial disease carrier3523.8
16.9–33.4ROR 23.8 · calibrated p 0.001 ✓
22.4 EB05 16.8 · IC025 +3.6
3/3 methods agree
Reporting / coding artifactserious n=35 · ♀ 100% (drug 62%)not reported in cached trials
Proctitis13323.4
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 — unassessedserious n=131 · ♀ 100% (drug 62%)not reported in cached trials
Chronic sinusitis17022.4
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 — unassessedserious n=168 · ♀ 100% (drug 62%)not reported in cached trials
Radiculopathy11621.7
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 — unassessedserious n=116 · ♀ 100% (drug 62%)not reported in cached trials
Gastrointestinal stoma complication5918.5
14.3–24.0ROR 18.5 · calibrated p 0.003 ✓
17.7 EB05 14.2 · IC025 +3.5
3/3 methods agree
Reporting / coding artifactserious n=58not reported in cached trials
Pouchitis3218.1
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 — unassessedserious n=32 · 100% cliniciannot reported in cached trials
Product difficult to swallow3818.0
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% consumernot reported in cached trials
Product packaging issue33017.4
15.6–19.4ROR 17.5 · calibrated p 0.004 ✓
16.8 EB05 15.3 · IC025 +3.9
3/3 methods agree
Reporting / coding artifact100% consumernot reported in cached trials
Stoma complication3516.7
11.9–23.4ROR 16.7 · calibrated p 0.006 ✓
16.0 EB05 11.9 · IC025 +3.2
3/3 methods agree
Reporting / coding artifactserious n=34not reported in cached trials
Bronchial secretion retention3915.0
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 — unassessedserious n=39 · ♀ 100% (drug 62%)not reported in cached trials
Vascular device infection13614.6
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 — unassessedserious n=136not reported in cached trials
Rhinitis allergic13014.2
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 — unassessedserious n=124 · ♀ 100% (drug 62%)not reported in cached trials
Low density lipoprotein decreased4114.0
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 markerserious n=41 · ♀ 0% (drug 62%)not reported in cached trials
Tumour pain3813.9
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 — unassessedserious n=36 · 100% cliniciannot reported in cached trials
Incorrect product administration duration57813.8
12.7–15.0ROR 14.0 · calibrated p 0.009 ✓
13.4 EB05 12.5 · IC025 +3.6
3/3 methods agree
Reporting / coding artifact100% consumernot reported in cached trials
Infrequent bowel movements7113.8
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 — unassessed100% consumernot reported in cached trials
Macular degeneration31512.8
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 — unassessedserious PRR 12.6 · ♀ 100% (drug 62%)not reported in cached trials
Therapeutic reaction time decreased7412.1
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 markerserious n=71not reported in cached trials
Blood pressure diastolic abnormal6412.0
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 markerserious n=64 · 100% cliniciannot reported in cached trials
Colitis microscopic11311.6
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 — unassessedserious n=112 · ♀ 83% (drug 62%)not reported in cached trials
Blood pressure systolic abnormal5711.0
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 markerserious n=57 · 100% cliniciannot reported in cached trials
Osteosclerosis3611.0
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 — unassessedserious 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).

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
Diarrhoea (diarrhea)8,8586.6
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 7.0NCT02400476: 2/137 (1.5%) on Loperamide (serious AE)
Nausea4,2902.6
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 3.4NCT02400476: 1/137 (0.7%) on Loperamide (serious AE)
Drug ineffective (drug did not work)4,0641.5
1.4–1.5ROR 1.5 · calibrated p 0.644
1.5 EB05 1.4 · IC025 +0.5Reporting / coding artifactserious PRR 1.3 · 73% consumernot reported in cached trials
Off label use (used outside approved label)3,2151.8
1.7–1.8ROR 1.8 · calibrated p 0.835
1.7 EB05 1.7 · IC025 +0.7Reporting / coding artifactserious PRR 2.0not reported in cached trials
Vomiting2,7782.8
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 3.2NCT02400476: 25/104 (24.0%) on Loperamide
Constipation2,4755.4
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 4.8NCT02400476: 39/104 (37.5%) on Loperamide
Weight decreased (weight loss)2,0923.6
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 — unassessedserious PRR 4.1NCT02400476: 4/104 (3.8%) on Loperamide
Headache2,0251.5
1.5–1.6ROR 1.6 · calibrated p 0.676
1.5 EB05 1.5 · IC025 +0.5Labeled adverse reaction
exact term
serious PRR 2.0NCT02400476: 24/104 (23.1%) on Loperamide
Dyspnoea (shortness of breath)1,9861.7
1.6–1.7ROR 1.7 · calibrated p 0.763
1.7 EB05 1.6 · IC025 +0.7Not in label — unassessedserious PRR 1.8NCT02400476: 4/104 (3.8%) on Loperamide
Asthenia (weakness)1,8362.3
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 — unassessedserious PRR 2.5NCT02400476: 4/104 (3.8%) on Loperamide
Abdominal pain1,8273.7
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 3.9NCT02400476: 1/136 (0.7%) on Loperamide (serious AE)
Decreased appetite (loss of appetite)1,8143.7
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 — unassessedserious PRR 4.0NCT02400476: 1/137 (0.7%) on Loperamide (serious AE)
Dizziness1,7131.6
1.6–1.7ROR 1.7 · calibrated p 0.738
1.6 EB05 1.6 · IC025 +0.6Labeled adverse reaction
exact term
serious PRR 1.9NCT02400476: 20/104 (19.2%) on Loperamide
Pain1,6591.3
1.2–1.3ROR 1.3 · calibrated p 0.497
1.3 EB05 1.2 · IC025 +0.3Labeled adverse reaction
exact term
serious PRR 1.5NCT02400476: 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.

✓ 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

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.