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Docusate Sodium side effects: what 57,370 FDA adverse event reports show

Docusate Sodium · 1,191 reaction terms · 273,320 drug–reaction co-reports · data 2026-09-14
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Drug class

Not stated in label

Label matched

Docusate Sodium (Stool Softener Laxative)

closest FDA label found for this product string; brand list suppressed because the label is a related product, not an exact match

Who reports

57,370 reports · 74% serious · 7,474 with death outcome · 59% female

openFDA FAERS counts, all years, deduplication not applied

Used for

relieves occasional constipation (irregularity) generally produces bowel movement in 12 to 72 hours

FDA label, Indications and Usage

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

Reporting / coding artifact 6Lab value / disease marker 3No label text to screen 31
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). 1,151 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
Antacid therapy47234.7
162.5–338.9ROR 234.9 · calibrated p 3e-10 ✓
134.7 EB05 105.4 · IC025 +5.4
3/3 methods agree
Reporting / coding artifactserious n=47 · ♀ 0% (drug 59%) · 100% clinicianno trial arm names this drug
Sleep disorder therapy68210.8
156.3–284.3ROR 211.0 · calibrated p 6e-10 ✓
128.5 EB05 104.9 · IC025 +5.7
3/3 methods agree
Reporting / coding artifactserious n=68 · ♀ 0% (drug 59%) · 100% clinicianno trial arm names this drug
Appendicolith100130.7
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% clinicianno trial arm names this drug
Analgesic therapy71110.0
84.4–143.5ROR 110.2 · calibrated p 9e-8 ✓
82.7 EB05 67.7 · IC025 +5.3
3/3 methods agree
Reporting / coding artifactserious n=71 · ♀ 0% (drug 59%) · 100% clinicianno trial arm names this drug
Drug therapy71104.2
80.0–135.7ROR 104.3 · calibrated p 1e-7 ✓
79.3 EB05 65.0 · IC025 +5.3
3/3 methods agree
Reporting / coding artifactserious n=70 · ♀ 0% (drug 59%) · 100% clinicianno trial arm names this drug
Pulmonary malformation6582.0
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% clinicianno trial arm names this drug
Anticoagulant therapy5080.3
59.1–109.0ROR 80.3 · calibrated p 1e-6 ✓
64.3 EB05 50.6 · IC025 +4.9
3/3 methods agree
Reporting / coding artifactserious n=50 · ♀ 0% (drug 59%) · 100% clinicianno trial arm names this drug
Chronic kidney disease-mineral and bone disorder8430.9
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=84no trial arm names this drug
Sinusitis fungal5527.4
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% clinicianno trial arm names this drug
Hyperparathyroidism secondary16224.9
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=162no trial arm names this drug
Nephrogenic anaemia28323.5
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=283no trial arm names this drug
Hyperphosphataemia11621.1
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% clinicianno trial arm names this drug
Blood phosphorus increased11315.8
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 markerserious n=106 · ♀ 27% (drug 59%) · 100% clinicianno trial arm names this drug
Female genital tract fistula6013.2
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% clinicianno trial arm names this drug
Failure to thrive17212.4
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=171no trial arm names this drug
Osteosclerosis5112.2
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% consumerno trial arm names this drug
Diastolic dysfunction10012.1
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 decreased5011.7
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% clinicianno trial arm names this drug
Sputum increased6511.6
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% clinicianno trial arm names this drug
Chronic sinusitis11411.4
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 deficiency13311.2
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=127no trial arm names this drug
Respiratory symptom8311.1
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% clinicianno trial arm names this drug
Rebound acid hypersecretion8710.6
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=87no trial arm names this drug
Atelectasis27510.6
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 8.2no trial arm names this drug
Metabolic encephalopathy8310.4
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% clinicianno trial arm names this drug
Aortic stenosis9610.3
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=96no trial arm names this drug
Kyphosis4810.1
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% consumerno trial arm names this drug
Pleuritic pain7410.0
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% clinicianno trial arm names this drug
End stage renal disease4869.9
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 7.5no trial arm names this drug
Blood pressure diastolic abnormal679.8
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 markerserious n=66 · ♀ 100% (drug 59%) · 100% clinicianno trial arm names this drug
Tricuspid valve incompetence2029.6
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 7.3no trial arm names this drug
Atrial tachycardia539.4
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% clinicianno trial arm names this drug
Essential hypertension649.2
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=60no trial arm names this drug
Haemorrhagic anaemia1109.2
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=110no trial arm names this drug
Neurogenic bladder519.0
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% clinicianno trial arm names this drug
Sedation complication598.8
6.8–11.4ROR 8.8 · calibrated p 0.053
8.3 EB05 6.6 · IC025 +2.6
3/3 methods agree
Reporting / coding artifactserious n=58 · ♀ 100% (drug 59%) · 100% clinicianno trial arm names this drug
Activated partial thromboplastin time prolonged1198.7
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 markerserious n=115 · ♀ 0% (drug 59%) · 100% clinicianno trial arm names this drug
Bone lesion848.7
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=78no trial arm names this drug
Aortic arteriosclerosis608.7
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% consumerno trial arm names this drug
Hypophosphataemia1708.6
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% clinicianno 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.

ConceptReportsPRR 95% CIReading
Hyponatraemia7683.53.3–3.8signal
Anaemia2,5953.23.1–3.3signal
Venous thromboembolism1,8413.13.0–3.3signal
Gi bleeding1,4743.02.8–3.1signal
Fall / fracture3,0262.92.8–3.0signal
Serious infection6,0072.92.8–2.9signal
Kidney injury3,3282.72.6–2.8signal
Heart failure1,2202.52.4–2.6signal
Neutropenia / agranulocytosis1,6312.42.3–2.5signal
Thrombocytopenia1,4492.42.3–2.5signal
Arrhythmia / qt1,2722.42.3–2.5signal
Depression1,4451.91.8–2.0raised
Pancreatitis3941.81.6–2.0raised
Opportunistic infection6471.71.6–1.9raised
Hyperglycaemia / diabetes1,6201.71.6–1.8raised
Hypoglycaemia4391.71.5–1.8raised

Trial evidence (ClinicalTrials.gov)

ClinicalTrials.gov returned results-bearing trials mentioning Docusate only as a background or rescue medication (NCT00001337); no trial listing it as the tested intervention was cached, so no trial cross-check is shown.

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
Fatigue (tiredness)4,8142.3
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 2.3no trial arm names this drug
Nausea4,6042.1
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 2.4no trial arm names this drug
Dyspnoea (shortness of breath)3,5922.3
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 2.2no trial arm names this drug
Diarrhoea (diarrhea)3,5512.0
2.0–2.1ROR 2.1 · calibrated p 0.992
2.0 EB05 2.0 · IC025 +1.0No label text to screen
label has no adverse-reaction text
age-adj. PRR 1.7 · serious PRR 1.9no trial arm names this drug
Constipation3,5166.0
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 5.8no trial arm names this drug
Pain3,2061.9
1.8–2.0ROR 2.0 · calibrated p 0.923
1.9 EB05 1.8 · IC025 +0.9No label text to screen
label has no adverse-reaction text
age-adj. PRR 2.2 · serious PRR 1.9no trial arm names this drug
Death3,1531.3
1.3–1.4ROR 1.4 · calibrated p 0.547
1.3 EB05 1.3 · IC025 +0.4Outcome field, not a reactionage-adj. PRR 1.3 · serious PRR 1.0no trial arm names this drug
Vomiting2,9212.3
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 2.2no trial arm names this drug
Asthenia (weakness)2,8592.8
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 2.6no trial arm names this drug
Fall2,8353.1
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 2.6no trial arm names this drug
Pneumonia (lung infection)2,7183.1
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 2.5no trial arm names this drug
Headache2,5531.5
1.4–1.5ROR 1.5 · calibrated p 0.651
1.5 EB05 1.4 · IC025 +0.5No label text to screen
label has no adverse-reaction text
age-adj. PRR 1.4 · serious PRR 1.7no trial arm names this drug
Off label use (used outside approved label)2,5111.1
1.0–1.1ROR 1.1 · calibrated p 0.346
1.1 EB05 1.0 · IC025 +0.0Reporting / coding artifactage-adj. PRR 1.0 · serious PRR 1.1no trial arm names this drug
Drug ineffective (drug did not work)2,3850.7
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 artifactage-adj. PRR 0.8 · serious PRR 0.8no trial arm names this drug
Dizziness2,3851.8
1.7–1.8ROR 1.8 · calibrated p 0.822
1.8 EB05 1.7 · IC025 +0.7No label text to screen
label has no adverse-reaction text
age-adj. PRR 1.6 · serious PRR 1.8no 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

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.