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Warfarin Sodium side effects: what 46,105 FDA adverse event reports show

Warfarin Sodium · Warfarin Sodium · 1,251 reaction terms · 178,963 drug–reaction co-reports · data 2026-09-14
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Drug class

Not stated in label

Brand names

Warfarin Sodium

openFDA label

Who reports

46,105 reports · 79% serious · 5,435 with death outcome · 48% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Warfarin sodium tablets are indicated for: Prophylaxis and treatment of venous thrombosis and its extension, pulmonary embolism (PE). Prophylaxis and treatment of thromboembolic complications associated with atrial fibrillation (AF) and/or cardiac valve replacement.

FDA label, Indications and Usage

What it is

Crystalline warfarin sodium is an anticoagulant that acts by inhibiting vitamin K-dependent coagulation factors.

FDA label, Description section

Boxed warning

BLEEDING RISK Warfarin sodium can cause major or fatal bleeding [see Warnings and Precautions (5.1) ] . Perform regular monitoring of INR in all treated patients [see Dosage and Administration (2.1) ] . Drugs, dietary changes, and other factors affect INR levels achieved with warfarin sodium therapy [see Drug Interactions (7) ] .

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

Labeled — boxed warning 2Labeled adverse reaction 1Labeled (related wording) 1Reporting / coding artifact 6Lab value / disease marker 13Not in label — unassessed 17
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). 1,211 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
Appendicolith128232.0
187.5–287.2ROR 232.7 · calibrated p 2e-10 ✓
149.8 EB05 129.2 · IC025 +6.3
3/3 methods agree
Not in label — unassessedserious n=128 · ♀ 13% (drug 48%) · 100% clinicianno trial arm names this drug
Antacid therapy38210.0
142.9–308.8ROR 210.2 · calibrated p 1e-9 ✓
133.8 EB05 101.8 · IC025 +5.1
3/3 methods agree
Reporting / coding artifactserious n=38 · 100% clinicianno trial arm names this drug
Sleep disorder therapy39120.4
84.6–171.5ROR 120.5 · calibrated p 7e-8 ✓
91.0 EB05 69.5 · IC025 +4.9
3/3 methods agree
Reporting / coding artifactserious n=39 · ♀ 0% (drug 48%) · 100% clinicianno trial arm names this drug
Anticoagulation drug level above therapeutic322120.0
106.2–135.7ROR 120.9 · calibrated p 3e-8 ✓
94.4 EB05 86.0 · IC025 +6.2
3/3 methods agree
Lab value / disease markerserious n=205 · 94% clinicianno trial arm names this drug
International normalised ratio abnormal683111.4
102.5–121.1ROR 113.1 · calibrated p 5e-8 ✓
89.2 EB05 83.7 · IC025 +6.3
3/3 methods agree
Lab value / disease markerserious n=480no trial arm names this drug
International normalised ratio decreased767105.1
97.2–113.7ROR 106.9 · calibrated p 7e-8 ✓
85.1 EB05 80.2 · IC025 +6.2
3/3 methods agree
Lab value / disease markerserious n=585no trial arm names this drug
International normalised ratio increased5,08897.7
94.9–100.5ROR 109.6 · calibrated p 6e-8 ✓
80.3 EB05 78.5 · IC025 +6.3
3/3 methods agree
Labeled — boxed warning
synonym match
serious PRR 59.5no trial arm names this drug
Analgesic therapy5394.9
70.6–127.6ROR 95.0 · calibrated p 3e-7 ✓
76.4 EB05 60.6 · IC025 +5.1
3/3 methods agree
Reporting / coding artifactserious n=53 · 100% clinicianno trial arm names this drug
International normalised ratio fluctuation35191.5
81.6–102.6ROR 92.2 · calibrated p 2e-7 ✓
75.8 EB05 69.4 · IC025 +5.9
3/3 methods agree
Lab value / disease markerserious n=177no trial arm names this drug
Steroid dependence13888.1
73.5–105.8ROR 88.4 · calibrated p 3e-7 ✓
73.1 EB05 63.4 · IC025 +5.6
3/3 methods agree
Not in label — unassessedserious n=138 · ♀ 22% (drug 48%) · 92% clinicianno trial arm names this drug
Drug therapy5084.2
62.2–113.8ROR 84.2 · calibrated p 7e-7 ✓
69.2 EB05 54.5 · IC025 +4.9
3/3 methods agree
Reporting / coding artifactserious n=50 · 100% clinicianno trial arm names this drug
Anticoagulant therapy3769.9
49.4–98.8ROR 70.0 · calibrated p 3e-6 ✓
58.8 EB05 44.6 · IC025 +4.5
3/3 methods agree
Reporting / coding artifactserious n=37 · 100% clinicianno trial arm names this drug
Catarrh11768.8
56.7–83.6ROR 69.0 · calibrated p 2e-6 ✓
59.2 EB05 50.8 · IC025 +5.3
3/3 methods agree
Not in label — unassessedserious n=117 · ♀ 26% (drug 48%) · 93% clinicianno trial arm names this drug
Anticoagulation drug level below therapeutic10168.4
55.5–84.3ROR 68.6 · calibrated p 2e-6 ✓
58.8 EB05 49.8 · IC025 +5.2
3/3 methods agree
Lab value / disease markerserious n=65no trial arm names this drug
Calciphylaxis22463.4
55.1–72.9ROR 63.7 · calibrated p 3e-6 ✓
55.4 EB05 49.6 · IC025 +5.4
3/3 methods agree
Labeled — boxed warning
exact term
serious n=224 · ♀ 72% (drug 48%) · 100% clinicianno trial arm names this drug
Central nervous system haemorrhage5763.2
47.9–83.3ROR 63.2 · calibrated p 4e-6 ✓
54.5 EB05 43.6 · IC025 +4.8
3/3 methods agree
Labeled adverse reaction
exact term
serious n=57 · 100% clinicianno trial arm names this drug
Prothrombin time abnormal7252.8
41.3–67.3ROR 52.8 · calibrated p 1e-5 ✓
46.8 EB05 38.4 · IC025 +4.8
3/3 methods agree
Lab value / disease markerserious n=42no trial arm names this drug
Blue toe syndrome3139.3
27.2–56.8ROR 39.3 · calibrated p 1e-4 ✓
35.5 EB05 26.2 · IC025 +3.9
3/3 methods agree
Not in label — unassessed♀ 0% (drug 48%)no trial arm names this drug
Cardiospasm4438.9
28.6–52.9ROR 38.9 · calibrated p 9e-5 ✓
35.3 EB05 27.4 · IC025 +4.2
3/3 methods agree
Not in label — unassessedserious n=44 · ♀ 100% (drug 48%)no trial arm names this drug
Prothrombin time prolonged42634.4
31.2–38.0ROR 34.7 · calibrated p 1e-4 ✓
32.0 EB05 29.5 · IC025 +4.8
3/3 methods agree
Lab value / disease markerserious n=382no trial arm names this drug
Immunisation3033.7
23.3–48.9ROR 33.8 · calibrated p 2e-4 ✓
30.9 EB05 22.7 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious n=30 · ♀ 100% (drug 48%)no trial arm names this drug
Burns second degree12033.4
27.8–40.2ROR 33.5 · calibrated p 2e-4 ✓
31.0 EB05 26.7 · IC025 +4.5
3/3 methods agree
Not in label — unassessedserious n=120 · 92% clinicianno trial arm names this drug
Coagulation time prolonged10031.1
25.4–38.1ROR 31.2 · calibrated p 2e-4 ✓
29.0 EB05 24.5 · IC025 +4.3
3/3 methods agree
Lab value / disease markerserious n=94 · 100% clinicianno trial arm names this drug
Palmoplantar keratoderma4530.3
22.4–40.9ROR 30.3 · calibrated p 3e-4 ✓
28.1 EB05 21.9 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious n=45 · ♀ 100% (drug 48%)no trial arm names this drug
Retroperitoneal haematoma13630.0
25.2–35.6ROR 30.1 · calibrated p 3e-4 ✓
28.1 EB05 24.3 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=135no trial arm names this drug
Coagulation test abnormal4427.8
20.5–37.7ROR 27.9 · calibrated p 5e-4 ✓
26.0 EB05 20.2 · IC025 +3.9
3/3 methods agree
Reporting / coding artifactserious n=43no trial arm names this drug
Prothrombin time shortened7324.9
19.7–31.5ROR 24.9 · calibrated p 8e-4 ✓
23.5 EB05 19.3 · IC025 +4.0
3/3 methods agree
Lab value / disease markerserious n=54no trial arm names this drug
Cardioactive drug level increased6924.9
19.5–31.7ROR 24.9 · calibrated p 8e-4 ✓
23.5 EB05 19.2 · IC025 +3.9
3/3 methods agree
Lab value / disease markerserious n=67no trial arm names this drug
Retroperitoneal haemorrhage12323.8
19.8–28.5ROR 23.8 · calibrated p 9e-4 ✓
22.6 EB05 19.4 · IC025 +4.1
3/3 methods agree
Not in label — unassessedserious n=120 · 100% clinicianno trial arm names this drug
Intra-abdominal haematoma6023.0
17.8–29.8ROR 23.0 · calibrated p 0.001 ✓
21.8 EB05 17.6 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious n=60 · ♀ 25% (drug 48%) · 100% clinicianno trial arm names this drug
Blood phosphorus increased12521.8
18.2–26.1ROR 21.9 · calibrated p 0.001 ✓
20.8 EB05 17.9 · IC025 +4.0
3/3 methods agree
Lab value / disease markerserious n=124 · ♀ 17% (drug 48%) · 100% clinicianno trial arm names this drug
Prothrombin level decreased4321.5
15.8–29.1ROR 21.5 · calibrated p 0.002 ✓
20.4 EB05 15.7 · IC025 +3.6
3/3 methods agree
Lab value / disease markerserious n=38no trial arm names this drug
Haemorrhage intracranial65520.7
19.2–22.4ROR 21.0 · calibrated p 0.002 ✓
19.8 EB05 18.6 · IC025 +4.2
3/3 methods agree
Not in label — unassessedserious PRR 14.2 · 95% clinicianno trial arm names this drug
Muscle haemorrhage17220.4
17.5–23.7ROR 20.4 · calibrated p 0.002 ✓
19.5 EB05 17.2 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious n=171no trial arm names this drug
Sick sinus syndrome4618.7
13.9–25.1ROR 18.7 · calibrated p 0.003 ✓
17.8 EB05 13.9 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=46 · ♀ 0% (drug 48%) · 100% clinicianno trial arm names this drug
Activated partial thromboplastin time prolonged19718.3
15.9–21.1ROR 18.4 · calibrated p 0.003 ✓
17.6 EB05 15.6 · IC025 +3.8
3/3 methods agree
Lab value / disease markerserious n=187 · 94% clinicianno trial arm names this drug
Hyperphosphataemia8118.0
14.4–22.5ROR 18.1 · calibrated p 0.004 ✓
17.3 EB05 14.3 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=79 · ♀ 25% (drug 48%) · 100% clinicianno trial arm names this drug
Abdominal wall haematoma7317.7
14.0–22.3ROR 17.7 · calibrated p 0.004 ✓
17.0 EB05 13.9 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=72 · 100% clinicianno trial arm names this drug
Gastric haemorrhage42117.1
15.5–18.9ROR 17.3 · calibrated p 0.004 ✓
16.5 EB05 15.2 · IC025 +3.9
3/3 methods agree
Not in label — unassessedserious PRR 12.0 · ♀ 8% (drug 48%) · 96% clinicianno trial arm names this drug

Trial evidence (ClinicalTrials.gov)

No completed trial with posted adverse-event results was found on ClinicalTrials.gov for Warfarin Sodium (searched WARFARIN).

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
International normalised ratio increased5,08897.7
94.9–100.5ROR 109.6 · calibrated p 6e-8 ✓
80.3 EB05 78.5 · IC025 +6.3
3/3 methods agree
Labeled — boxed warning
synonym match
serious PRR 59.5no trial arm names this drug
Dyspnoea (shortness of breath)2,5352.0
2.0–2.1ROR 2.1 · calibrated p 0.999
2.0 EB05 2.0 · IC025 +1.0Not in label — unassessedserious PRR 1.8no trial arm names this drug
Drug interaction2,5117.3
7.0–7.6ROR 7.7 · calibrated p 0.076
7.2 EB05 7.0 · IC025 +2.8
3/3 methods agree
Reporting / coding artifactserious PRR 5.5no trial arm names this drug
Fatigue (tiredness)2,0951.2
1.2–1.3ROR 1.2 · calibrated p 0.466
1.2 EB05 1.2 · IC025 +0.2Not in label — unassessedserious PRR 1.2no trial arm names this drug
Nausea2,0821.2
1.2–1.3ROR 1.2 · calibrated p 0.447
1.2 EB05 1.2 · IC025 +0.2Labeled adverse reaction
exact term
serious PRR 1.3no trial arm names this drug
Diarrhoea (diarrhea)1,8861.3
1.3–1.4ROR 1.3 · calibrated p 0.541
1.3 EB05 1.3 · IC025 +0.3Labeled adverse reaction
exact term
serious PRR 1.2no trial arm names this drug
Dizziness1,8801.7
1.6–1.8ROR 1.8 · calibrated p 0.800
1.7 EB05 1.7 · IC025 +0.7Not in label — unassessedserious PRR 1.7no trial arm names this drug
Fall1,7002.3
2.2–2.4ROR 2.4 · calibrated p 0.865
2.3 EB05 2.2 · IC025 +1.1
3/3 methods agree
Not in label — unassessedserious PRR 1.9no trial arm names this drug
Asthenia (weakness)1,6932.1
2.0–2.2ROR 2.1 · calibrated p 0.993
2.0 EB05 2.0 · IC025 +1.0Not in label — unassessedserious PRR 1.8no trial arm names this drug
Anaemia (low red blood cells)1,6824.0
3.8–4.2ROR 4.1 · calibrated p 0.351
4.0 EB05 3.8 · IC025 +1.9
3/3 methods agree
Labeled — boxed warning
exact term
serious PRR 3.1no trial arm names this drug
Drug ineffective (drug did not work)1,6430.6
0.5–0.6ROR 0.6 · calibrated p 0.066
0.6 EB05 0.5 · IC025 -0.9
PRR-only: not supported by EBGM or IC
Reporting / coding artifactserious PRR 0.7no trial arm names this drug
Haemorrhage1,5726.9
6.6–7.3ROR 7.1 · calibrated p 0.093
6.8 EB05 6.5 · IC025 +2.7
3/3 methods agree
Labeled — boxed warning
exact term
serious PRR 5.5no trial arm names this drug
Headache1,5191.1
1.1–1.2ROR 1.1 · calibrated p 0.377
1.1 EB05 1.1 · IC025 +0.1Not in label — unassessedserious PRR 1.2no trial arm names this drug
Atrial fibrillation1,4767.0
6.6–7.3ROR 7.2 · calibrated p 0.092
6.9 EB05 6.6 · IC025 +2.7
3/3 methods agree
Likely indication confounding
term in indications
serious PRR 5.1no trial arm names this drug
Pain1,3971.0
1.0–1.1ROR 1.0 · calibrated p 0.329
1.0 EB05 1.0 · IC025 -0.0
PRR-only: not supported by EBGM or IC
Labeled adverse reaction
exact term
serious PRR 1.0no trial arm names this drug

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: Warfarin ↔ INR increased.

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 Warfarin Sodium?

In FDA FAERS, the most frequently co-reported reaction terms for Warfarin Sodium are international normalised ratio increased, dyspnoea, fatigue, nausea, diarrhoea, dizziness. 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 Warfarin Sodium have an FDA boxed warning?

Yes. The current FDA label carries a boxed warning: BLEEDING RISK Warfarin sodium can cause major or fatal bleeding [see Warnings and Precautions (5.1) ] . Perform regular monitoring of INR in all treated patients [see Dosage and Administration (2.1) ] . Drugs, dietary changes, and other factors affect INR levels achieved with warfarin sodium therapy [see Drug Interactions (7) ] .

Do FAERS signals prove that Warfarin Sodium 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.