Docusate Sodium side effects: what 57,370 FDA adverse event reports show
Drug class
Not stated in label
Label matched
Docusate Sodium (Stool Softener Laxative)
Who reports
57,370 reports · 74% serious · 7,474 with death outcome · 59% female
Used for
relieves occasional constipation (irregularity) generally produces bowel movement in 12 to 72 hours
Boxed warning
None in the current label
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.
- No label text to screen No validated FDA label was retrievable for this product, so the screen could not run. Disproportionality only.
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). 1,151 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 |
|---|---|---|---|---|---|---|
| Antacid therapy | 47 | 234.7 162.5–338.9ROR 234.9 · calibrated p 3e-10 ✓ | 134.7 EB05 105.4 · IC025 +5.4 3/3 methods agree | Reporting / coding artifact | serious n=47 · ♀ 0% (drug 59%) · 100% clinician | no trial arm names this drug |
| Sleep disorder therapy | 68 | 210.8 156.3–284.3ROR 211.0 · calibrated p 6e-10 ✓ | 128.5 EB05 104.9 · IC025 +5.7 3/3 methods agree | Reporting / coding artifact | serious n=68 · ♀ 0% (drug 59%) · 100% clinician | no trial arm names this drug |
| Appendicolith | 100 | 130.7 104.0–164.3ROR 131.0 · calibrated p 2e-8 ✓ | 94.5 EB05 79.9 · IC025 +5.7 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=100 · ♀ 0% (drug 59%) · 100% clinician | no trial arm names this drug |
| Analgesic therapy | 71 | 110.0 84.4–143.5ROR 110.2 · calibrated p 9e-8 ✓ | 82.7 EB05 67.7 · IC025 +5.3 3/3 methods agree | Reporting / coding artifact | serious n=71 · ♀ 0% (drug 59%) · 100% clinician | no trial arm names this drug |
| Drug therapy | 71 | 104.2 80.0–135.7ROR 104.3 · calibrated p 1e-7 ✓ | 79.3 EB05 65.0 · IC025 +5.3 3/3 methods agree | Reporting / coding artifact | serious n=70 · ♀ 0% (drug 59%) · 100% clinician | no trial arm names this drug |
| Pulmonary malformation | 65 | 82.0 62.6–107.3ROR 82.1 · calibrated p 7e-7 ✓ | 65.7 EB05 53.4 · IC025 +5.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=65 · ♀ 100% (drug 59%) · 100% clinician | no trial arm names this drug |
| Anticoagulant therapy | 50 | 80.3 59.1–109.0ROR 80.3 · calibrated p 1e-6 ✓ | 64.3 EB05 50.6 · IC025 +4.9 3/3 methods agree | Reporting / coding artifact | serious n=50 · ♀ 0% (drug 59%) · 100% clinician | no trial arm names this drug |
| Chronic kidney disease-mineral and bone disorder | 84 | 30.9 24.7–38.6ROR 30.9 · calibrated p 3e-4 ✓ | 28.4 EB05 23.6 · IC025 +4.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=84 | no trial arm names this drug |
| Sinusitis fungal | 55 | 27.4 20.8–36.0ROR 27.4 · calibrated p 5e-4 ✓ | 25.3 EB05 20.2 · IC025 +3.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=55 · ♀ 100% (drug 59%) · 100% clinician | no trial arm names this drug |
| Hyperparathyroidism secondary | 162 | 24.9 21.3–29.2ROR 25.0 · calibrated p 7e-4 ✓ | 23.3 EB05 20.5 · IC025 +4.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=162 | no trial arm names this drug |
| Nephrogenic anaemia | 283 | 23.5 20.8–26.5ROR 23.6 · calibrated p 9e-4 ✓ | 22.1 EB05 20.0 · IC025 +4.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=283 | no trial arm names this drug |
| Hyperphosphataemia | 116 | 21.1 17.5–25.4ROR 21.1 · calibrated p 0.002 ✓ | 19.9 EB05 17.1 · IC025 +3.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=116 · ♀ 0% (drug 59%) · 100% clinician | no trial arm names this drug |
| Blood phosphorus increased | 113 | 15.8 13.1–19.0ROR 15.8 · calibrated p 0.006 ✓ | 15.1 EB05 12.9 · IC025 +3.5 3/3 methods agree | Lab value / disease marker | serious n=106 · ♀ 27% (drug 59%) · 100% clinician | no trial arm names this drug |
| Female genital tract fistula | 60 | 13.2 10.2–17.0ROR 13.2 · calibrated p 0.013 ✓ | 12.5 EB05 10.0 · IC025 +3.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=60 · ♀ 100% (drug 59%) · 100% clinician | no trial arm names this drug |
| Failure to thrive | 172 | 12.4 10.7–14.5ROR 12.5 · calibrated p 0.015 ✓ | 12.0 EB05 10.5 · IC025 +3.3 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=171 | no trial arm names this drug |
| Osteosclerosis | 51 | 12.2 9.2–16.1ROR 12.2 · calibrated p 0.018 ✓ | 11.5 EB05 9.0 · IC025 +3.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=51 · 100% consumer | no trial arm names this drug |
| Diastolic dysfunction | 100 | 12.1 9.9–14.8ROR 12.2 · calibrated p 0.017 ✓ | 11.6 EB05 9.8 · IC025 +3.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=99 · ♀ 100% (drug 59%) | no trial arm names this drug |
| Total lung capacity decreased | 50 | 11.7 8.9–15.6ROR 11.8 · calibrated p 0.020 ✓ | 11.1 EB05 8.6 · IC025 +2.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=49 · ♀ 0% (drug 59%) · 100% clinician | no trial arm names this drug |
| Sputum increased | 65 | 11.6 9.0–14.8ROR 11.6 · calibrated p 0.021 ✓ | 11.0 EB05 8.8 · IC025 +3.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=62 · ♀ 100% (drug 59%) · 100% clinician | no trial arm names this drug |
| Chronic sinusitis | 114 | 11.4 9.5–13.8ROR 11.5 · calibrated p 0.021 ✓ | 11.0 EB05 9.3 · IC025 +3.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=111 · ♀ 100% (drug 59%) | no trial arm names this drug |
| Iron deficiency | 133 | 11.2 9.5–13.3ROR 11.3 · calibrated p 0.022 ✓ | 10.8 EB05 9.3 · IC025 +3.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=127 | no trial arm names this drug |
| Respiratory symptom | 83 | 11.1 8.9–13.8ROR 11.1 · calibrated p 0.024 ✓ | 10.6 EB05 8.8 · IC025 +3.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=82 · 100% clinician | no trial arm names this drug |
| Rebound acid hypersecretion | 87 | 10.6 8.6–13.2ROR 10.7 · calibrated p 0.027 ✓ | 10.2 EB05 8.4 · IC025 +2.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=87 | no trial arm names this drug |
| Atelectasis | 275 | 10.6 9.4–12.0ROR 10.7 · calibrated p 0.026 ✓ | 10.3 EB05 9.3 · IC025 +3.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 9.5 · serious PRR 8.2 | no trial arm names this drug |
| Metabolic encephalopathy | 83 | 10.4 8.3–12.9ROR 10.4 · calibrated p 0.030 ✓ | 9.9 EB05 8.2 · IC025 +2.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=83 · 100% clinician | no trial arm names this drug |
| Aortic stenosis | 96 | 10.3 8.4–12.6ROR 10.3 · calibrated p 0.030 ✓ | 9.9 EB05 8.3 · IC025 +2.9 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=96 | no trial arm names this drug |
| Kyphosis | 48 | 10.1 7.6–13.5ROR 10.1 · calibrated p 0.034 ✓ | 9.5 EB05 7.3 · IC025 +2.7 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=47 · ♀ 100% (drug 59%) · 100% consumer | no trial arm names this drug |
| Pleuritic pain | 74 | 10.0 7.9–12.6ROR 10.0 · calibrated p 0.034 ✓ | 9.5 EB05 7.7 · IC025 +2.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=73 · 100% clinician | no trial arm names this drug |
| End stage renal disease | 486 | 9.9 9.0–10.8ROR 10.0 · calibrated p 0.033 ✓ | 9.6 EB05 8.9 · IC025 +3.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious PRR 7.5 | no trial arm names this drug |
| Blood pressure diastolic abnormal | 67 | 9.8 7.7–12.4ROR 9.8 · calibrated p 0.038 ✓ | 9.2 EB05 7.4 · IC025 +2.8 3/3 methods agree | Lab value / disease marker | serious n=66 · ♀ 100% (drug 59%) · 100% clinician | no trial arm names this drug |
| Tricuspid valve incompetence | 202 | 9.6 8.3–11.0ROR 9.6 · calibrated p 0.038 ✓ | 9.2 EB05 8.2 · IC025 +3.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious PRR 7.3 | no trial arm names this drug |
| Atrial tachycardia | 53 | 9.4 7.2–12.3ROR 9.4 · calibrated p 0.043 ✓ | 8.8 EB05 6.9 · IC025 +2.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=53 · ♀ 100% (drug 59%) · 100% clinician | no trial arm names this drug |
| Essential hypertension | 64 | 9.2 7.2–11.8ROR 9.2 · calibrated p 0.045 ✓ | 8.7 EB05 7.0 · IC025 +2.7 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=60 | no trial arm names this drug |
| Haemorrhagic anaemia | 110 | 9.2 7.6–11.1ROR 9.2 · calibrated p 0.044 ✓ | 8.8 EB05 7.5 · IC025 +2.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=110 | no trial arm names this drug |
| Neurogenic bladder | 51 | 9.0 6.8–11.9ROR 9.0 · calibrated p 0.050 | 8.4 EB05 6.6 · IC025 +2.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=48 · ♀ 0% (drug 59%) · 100% clinician | no trial arm names this drug |
| Sedation complication | 59 | 8.8 6.8–11.4ROR 8.8 · calibrated p 0.053 | 8.3 EB05 6.6 · IC025 +2.6 3/3 methods agree | Reporting / coding artifact | serious n=58 · ♀ 100% (drug 59%) · 100% clinician | no trial arm names this drug |
| Activated partial thromboplastin time prolonged | 119 | 8.7 7.3–10.5ROR 8.8 · calibrated p 0.052 | 8.4 EB05 7.2 · IC025 +2.7 3/3 methods agree | Lab value / disease marker | serious n=115 · ♀ 0% (drug 59%) · 100% clinician | no trial arm names this drug |
| Bone lesion | 84 | 8.7 7.0–10.8ROR 8.7 · calibrated p 0.054 | 8.3 EB05 6.8 · IC025 +2.7 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=78 | no trial arm names this drug |
| Aortic arteriosclerosis | 60 | 8.7 6.7–11.2ROR 8.7 · calibrated p 0.055 | 8.1 EB05 6.5 · IC025 +2.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious n=60 · 100% consumer | no trial arm names this drug |
| Hypophosphataemia | 170 | 8.6 7.4–10.0ROR 8.7 · calibrated p 0.053 | 8.3 EB05 7.3 · IC025 +2.8 3/3 methods agree | No label text to screen label has no adverse-reaction text | serious PRR 6.9 · ♀ 33% (drug 59%) · 100% clinician | no trial arm names this drug |
Clinical concept groups
MedDRA splits one clinical problem across several terms (e.g. "neutropenia", "neutrophil count decreased", "agranulocytosis"), which dilutes term-level signals. These rows count reports with any term in a concept group (an exact union, not a sum), compared with all other drugs. Groups are hand-built and listed in the methods.
| Concept | Reports | PRR 95% CI | Reading |
|---|---|---|---|
| Hyponatraemia | 768 | 3.53.3–3.8 | signal |
| Anaemia | 2,595 | 3.23.1–3.3 | signal |
| Venous thromboembolism | 1,841 | 3.13.0–3.3 | signal |
| Gi bleeding | 1,474 | 3.02.8–3.1 | signal |
| Fall / fracture | 3,026 | 2.92.8–3.0 | signal |
| Serious infection | 6,007 | 2.92.8–2.9 | signal |
| Kidney injury | 3,328 | 2.72.6–2.8 | signal |
| Heart failure | 1,220 | 2.52.4–2.6 | signal |
| Neutropenia / agranulocytosis | 1,631 | 2.42.3–2.5 | signal |
| Thrombocytopenia | 1,449 | 2.42.3–2.5 | signal |
| Arrhythmia / qt | 1,272 | 2.42.3–2.5 | signal |
| Depression | 1,445 | 1.91.8–2.0 | raised |
| Pancreatitis | 394 | 1.81.6–2.0 | raised |
| Opportunistic infection | 647 | 1.71.6–1.9 | raised |
| Hyperglycaemia / diabetes | 1,620 | 1.71.6–1.8 | raised |
| Hypoglycaemia | 439 | 1.71.5–1.8 | raised |
Trial evidence (ClinicalTrials.gov)
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 |
|---|---|---|---|---|---|---|
| Fatigue (tiredness) | 4,814 | 2.3 2.2–2.3ROR 2.4 · calibrated p 0.862 | 2.3 EB05 2.2 · IC025 +1.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.0 · serious PRR 2.3 | no trial arm names this drug |
| Nausea | 4,604 | 2.1 2.1–2.2ROR 2.2 · calibrated p 0.933 | 2.1 EB05 2.1 · IC025 +1.0 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.0 · serious PRR 2.4 | no trial arm names this drug |
| Dyspnoea (shortness of breath) | 3,592 | 2.3 2.3–2.4ROR 2.4 · calibrated p 0.849 | 2.3 EB05 2.3 · IC025 +1.2 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.1 · serious PRR 2.2 | no trial arm names this drug |
| Diarrhoea (diarrhea) | 3,551 | 2.0 2.0–2.1ROR 2.1 · calibrated p 0.992 | 2.0 EB05 2.0 · IC025 +1.0 | No label text to screen label has no adverse-reaction text | age-adj. PRR 1.7 · serious PRR 1.9 | no trial arm names this drug |
| Constipation | 3,516 | 6.0 5.8–6.2ROR 6.3 · calibrated p 0.129 | 5.9 EB05 5.8 · IC025 +2.5 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 5.1 · serious PRR 5.8 | no trial arm names this drug |
| Pain | 3,206 | 1.9 1.8–2.0ROR 2.0 · calibrated p 0.923 | 1.9 EB05 1.8 · IC025 +0.9 | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.2 · serious PRR 1.9 | no trial arm names this drug |
| Death | 3,153 | 1.3 1.3–1.4ROR 1.4 · calibrated p 0.547 | 1.3 EB05 1.3 · IC025 +0.4 | Outcome field, not a reaction | age-adj. PRR 1.3 · serious PRR 1.0 | no trial arm names this drug |
| Vomiting | 2,921 | 2.3 2.2–2.4ROR 2.4 · calibrated p 0.878 | 2.3 EB05 2.2 · IC025 +1.1 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.2 · serious PRR 2.2 | no trial arm names this drug |
| Asthenia (weakness) | 2,859 | 2.8 2.7–2.9ROR 2.9 · calibrated p 0.665 | 2.8 EB05 2.7 · IC025 +1.4 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.3 · serious PRR 2.6 | no trial arm names this drug |
| Fall | 2,835 | 3.1 3.0–3.2ROR 3.2 · calibrated p 0.552 | 3.1 EB05 3.0 · IC025 +1.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.4 · serious PRR 2.6 | no trial arm names this drug |
| Pneumonia (lung infection) | 2,718 | 3.1 3.0–3.2ROR 3.2 · calibrated p 0.567 | 3.1 EB05 3.0 · IC025 +1.6 3/3 methods agree | No label text to screen label has no adverse-reaction text | age-adj. PRR 2.6 · serious PRR 2.5 | no trial arm names this drug |
| Headache | 2,553 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.651 | 1.5 EB05 1.4 · IC025 +0.5 | No label text to screen label has no adverse-reaction text | age-adj. PRR 1.4 · serious PRR 1.7 | no trial arm names this drug |
| Off label use (used outside approved label) | 2,511 | 1.1 1.0–1.1ROR 1.1 · calibrated p 0.346 | 1.1 EB05 1.0 · IC025 +0.0 | Reporting / coding artifact | age-adj. PRR 1.0 · serious PRR 1.1 | no trial arm names this drug |
| Drug ineffective (drug did not work) | 2,385 | 0.7 0.6–0.7ROR 0.6 · calibrated p 0.105 | 0.7 EB05 0.6 · IC025 -0.7 PRR-only: not supported by EBGM or IC | Reporting / coding artifact | age-adj. PRR 0.8 · serious PRR 0.8 | no trial arm names this drug |
| Dizziness | 2,385 | 1.8 1.7–1.8ROR 1.8 · calibrated p 0.822 | 1.8 EB05 1.7 · IC025 +0.7 | No label text to screen label has no adverse-reaction text | age-adj. PRR 1.6 · serious PRR 1.8 | no trial arm names this drug |
Unlabeled candidate signals
Every screened signal with n ≥ 20 was either labeled, an indication term, or an artifact pattern — no unlabeled candidate stood out in the top signals.
✓ A hand-written Bradford Hill causality assessment exists for this drug: Methotrexate Sodium ↔ Rheumatoid Arthritis.
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 Docusate?
In FDA FAERS, the most frequently co-reported reaction terms for Docusate are fatigue, nausea, dyspnoea, diarrhoea, constipation, pain. 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 Docusate have an FDA boxed warning?
No. The FDA label retrieved for Docusate has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Docusate 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 098d2377-0019-45fe-b995-700b1b1241c4, effective 20260805; matched on
openfda.generic_name.exact:"DOCUSATE SODIUM") - 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, 1,191 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
DOCUSATE, 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.