Rivaroxaban side effects: what 206,900 FDA adverse event reports show
Drug class
Factor Xa Inhibitor
Brand names
Xarelto
Who reports
206,900 reports · 84% serious · 27,139 with death outcome · 50% female
Used for
XARELTO is a factor Xa inhibitor indicated: to reduce risk of stroke and systemic embolism in nonvalvular atrial fibrillation ( 1.1 ) for treatment of deep vein thrombosis (DVT) ( 1.2 ) for treatment of pulmonary embolism (PE) ( 1.3 ) for reduction in .
What it is
Rivaroxaban, a factor Xa (FXa) inhibitor, is the active ingredient in XARELTO ® Tablets and XARELTO ® for oral suspension with the chemical name 5-Chloro-N-({(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-1,3-oxazolidin-5-yl}methyl)-2-thiophenecarboxamide.
Boxed warning
(A) PREMATURE DISCONTINUATION OF XARELTO INCREASES THE RISK OF THROMBOTIC EVENTS, (B) SPINAL/EPIDURAL HEMATOMA A. Premature discontinuation of XARELTO increases the risk of thrombotic events Premature discontinuation of any oral anticoagulant, including XARELTO, increases the risk of thrombotic events.
Causality screen of the 40 strongest signals
What the badges mean
- Labeled adverse reaction The exact term appears in the label's warnings or adverse-reactions sections: a known, expected effect. The FAERS signal confirms the label rather than discovering anything.
- Labeled (related wording) The label describes this effect under different wording (e.g. 'neutropenia' for 'neutrophil count decreased'). Treated as known.
- Likely indication confounding The term appears in the label's indications: reports probably describe the disease being treated (or its progression), not a drug effect. Classic confounding by indication.
- 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). 1,208 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 |
|---|---|---|---|---|---|---|
| Haemorrhagic arteriovenous malformation | 816 | 690.4 568.8–838.0ROR 693.2 · calibrated p 3e-15 ✓ | 87.3 EB05 82.4 · IC025 +6.3 3/3 methods agree | Not in label — unassessed | serious n=816 · 85% consumer | no trial arm names this drug |
| Fractional exhaled nitric oxide increased | 122 | 246.5 176.9–343.3ROR 246.6 · calibrated p 2e-10 ✓ | 70.6 EB05 60.7 · IC025 +5.5 3/3 methods agree | Not in label — unassessed | serious n=122 · ♀ 0% (drug 50%) | no trial arm names this drug |
| Gastrointestinal vascular malformation haemorrhagic | 249 | 200.4 161.5–248.7ROR 200.6 · calibrated p 6e-10 ✓ | 66.6 EB05 59.9 · IC025 +5.7 3/3 methods agree | Labeled (related wording) related wording | serious n=249 | no trial arm names this drug |
| Gastrointestinal angiodysplasia haemorrhagic | 116 | 145.4 109.2–193.5ROR 145.4 · calibrated p 1e-8 ✓ | 58.9 EB05 50.5 · IC025 +5.3 3/3 methods agree | Labeled (related wording) related wording | serious n=116 · 100% consumer | no trial arm names this drug |
| Diverticulum intestinal haemorrhagic | 1,033 | 85.0 78.2–92.4ROR 85.4 · calibrated p 4e-7 ✓ | 46.2 EB05 43.8 · IC025 +5.4 3/3 methods agree | Labeled (related wording) related wording | serious n=1,033 · 77% consumer | no trial arm names this drug |
| Chronic gastrointestinal bleeding | 110 | 75.1 58.6–96.2ROR 75.1 · calibrated p 1e-6 ✓ | 42.8 EB05 36.5 · IC025 +4.9 3/3 methods agree | Labeled (related wording) related wording | serious n=110 · 100% consumer | no trial arm names this drug |
| Truncus arteriosus persistent | 82 | 69.4 52.3–92.0ROR 69.4 · calibrated p 2e-6 ✓ | 40.8 EB05 33.9 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=82 · 100% clinician | no trial arm names this drug |
| Haemorrhagic erosive gastritis | 114 | 53.0 42.2–66.5ROR 53.0 · calibrated p 1e-5 ✓ | 34.7 EB05 29.7 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious n=114 · 100% consumer | no trial arm names this drug |
| Basal ganglia haemorrhage | 263 | 47.9 41.4–55.6ROR 48.0 · calibrated p 2e-5 ✓ | 32.6 EB05 29.4 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=263 | no trial arm names this drug |
| Lower gastrointestinal haemorrhage | 2,378 | 47.6 45.3–50.0ROR 48.1 · calibrated p 2e-5 ✓ | 32.5 EB05 31.4 · IC025 +4.9 3/3 methods agree | Labeled (related wording) related wording | serious PRR 22.4 · 71% consumer | no trial arm names this drug |
| Internal haemorrhage | 3,653 | 47.3 45.5–49.2ROR 48.1 · calibrated p 2e-5 ✓ | 32.3 EB05 31.5 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | serious PRR 22.5 · 87% consumer | no trial arm names this drug |
| Gastrointestinal polyp haemorrhage | 178 | 42.4 35.5–50.5ROR 42.4 · calibrated p 4e-5 ✓ | 29.9 EB05 26.4 · IC025 +4.5 3/3 methods agree | Labeled (related wording) related wording | serious n=178 · 100% consumer | no trial arm names this drug |
| Anticoagulation drug level increased | 87 | 36.8 28.8–47.1ROR 36.8 · calibrated p 1e-4 ✓ | 27.0 EB05 22.5 · IC025 +4.2 3/3 methods agree | Lab value / disease marker | serious n=83 · ♀ 0% (drug 50%) · 100% clinician | no trial arm names this drug |
| Upper gastrointestinal haemorrhage | 4,502 | 36.7 35.4–37.9ROR 37.5 · calibrated p 8e-5 ✓ | 27.0 EB05 26.4 · IC025 +4.7 3/3 methods agree | Labeled (related wording) related wording | serious PRR 18.6 | no trial arm names this drug |
| Thalamus haemorrhage | 230 | 35.7 30.7–41.5ROR 35.7 · calibrated p 1e-4 ✓ | 26.4 EB05 23.7 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious n=230 | no trial arm names this drug |
| Gastrointestinal haemorrhage | 21,636 | 34.9 34.4–35.4ROR 38.9 · calibrated p 6e-5 ✓ | 26.1 EB05 25.8 · IC025 +4.7 3/3 methods agree | Labeled (related wording) related wording | age-adj. PRR 26.3 · serious PRR 18.1 | no trial arm names this drug |
| Embolic cerebral infarction | 163 | 32.6 27.3–38.9ROR 32.6 · calibrated p 2e-4 ✓ | 24.7 EB05 21.7 · IC025 +4.3 3/3 methods agree | Labeled (related wording) related wording | serious n=163 · 100% clinician | no trial arm names this drug |
| High frequency ablation | 98 | 31.7 25.3–39.8ROR 31.7 · calibrated p 2e-4 ✓ | 24.2 EB05 20.4 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=95 · ♀ 0% (drug 50%) | no trial arm names this drug |
| Pericardial haemorrhage | 519 | 31.3 28.3–34.5ROR 31.3 · calibrated p 2e-4 ✓ | 24.0 EB05 22.3 · IC025 +4.4 3/3 methods agree | Labeled (related wording) related wording | serious n=518 | no trial arm names this drug |
| Atrial thrombosis | 481 | 30.3 27.4–33.6ROR 30.4 · calibrated p 3e-4 ✓ | 23.4 EB05 21.7 · IC025 +4.4 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious n=481 · 100% clinician | no trial arm names this drug |
| Haemorrhagic stroke | 1,801 | 29.9 28.4–31.5ROR 30.2 · calibrated p 3e-4 ✓ | 23.2 EB05 22.3 · IC025 +4.5 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 15.9 | no trial arm names this drug |
| Adrenal haemorrhage | 122 | 27.8 22.7–33.9ROR 27.8 · calibrated p 4e-4 ✓ | 21.8 EB05 18.8 · IC025 +4.0 3/3 methods agree | Labeled (related wording) related wording | serious n=122 | no trial arm names this drug |
| Renal haemorrhage | 438 | 27.5 24.8–30.6ROR 27.6 · calibrated p 4e-4 ✓ | 21.7 EB05 20.1 · IC025 +4.3 3/3 methods agree | Labeled (related wording) related wording | serious n=438 · 77% consumer | no trial arm names this drug |
| Gastritis haemorrhagic | 319 | 27.1 23.9–30.7ROR 27.1 · calibrated p 5e-4 ✓ | 21.5 EB05 19.6 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious n=319 · 73% consumer | no trial arm names this drug |
| Blood loss anaemia | 449 | 25.4 22.9–28.1ROR 25.4 · calibrated p 6e-4 ✓ | 20.4 EB05 18.8 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious n=447 | no trial arm names this drug |
| Peptic ulcer haemorrhage | 133 | 23.9 19.8–28.9ROR 23.9 · calibrated p 9e-4 ✓ | 19.4 EB05 16.8 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious n=133 | no trial arm names this drug |
| Haemorrhagic transformation stroke | 284 | 23.4 20.6–26.7ROR 23.5 · calibrated p 1e-3 ✓ | 19.1 EB05 17.3 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious n=284 | no trial arm names this drug |
| Haemorrhoidal haemorrhage | 915 | 23.0 21.4–24.7ROR 23.1 · calibrated p 0.001 ✓ | 18.8 EB05 17.8 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=877 | no trial arm names this drug |
| Haemorrhagic anaemia | 829 | 23.0 21.3–24.8ROR 23.1 · calibrated p 0.001 ✓ | 18.8 EB05 17.8 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=829 | no trial arm names this drug |
| Cerebellar haemorrhage | 266 | 23.0 20.1–26.2ROR 23.0 · calibrated p 0.001 ✓ | 18.8 EB05 17.0 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious n=266 | no trial arm names this drug |
| Post procedural haematoma | 314 | 22.8 20.2–25.8ROR 22.9 · calibrated p 0.001 ✓ | 18.7 EB05 17.1 · IC025 +4.0 3/3 methods agree | Reporting / coding artifact | serious n=313 | no trial arm names this drug |
| Dysfunctional uterine bleeding | 227 | 22.8 19.7–26.3ROR 22.8 · calibrated p 0.001 ✓ | 18.7 EB05 16.7 · IC025 +4.0 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=225 · ♀ 100% (drug 50%) · 100% consumer | no trial arm names this drug |
| Splenic haemorrhage | 89 | 21.4 17.0–27.0ROR 21.4 · calibrated p 0.002 ✓ | 17.7 EB05 14.8 · IC025 +3.7 3/3 methods agree | Labeled (related wording) related wording | serious n=89 | no trial arm names this drug |
| Embolic stroke | 594 | 20.5 18.8–22.4ROR 20.6 · calibrated p 0.002 ✓ | 17.1 EB05 16.0 · IC025 +3.9 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious n=593 | no trial arm names this drug |
| Abdominal wall haematoma | 324 | 20.1 17.8–22.6ROR 20.1 · calibrated p 0.002 ✓ | 16.8 EB05 15.4 · IC025 +3.9 3/3 methods agree | Labeled (related wording) related wording | serious n=323 | no trial arm names this drug |
| Intraventricular haemorrhage | 400 | 19.2 17.2–21.4ROR 19.2 · calibrated p 0.002 ✓ | 16.2 EB05 14.9 · IC025 +3.8 3/3 methods agree | Labeled (related wording) related wording | serious n=400 | no trial arm names this drug |
| Small intestinal haemorrhage | 314 | 18.7 16.5–21.0ROR 18.7 · calibrated p 0.003 ✓ | 15.8 EB05 14.4 · IC025 +3.8 3/3 methods agree | Labeled (related wording) related wording | serious n=314 | no trial arm names this drug |
| Gastric ulcer haemorrhage | 867 | 18.5 17.2–19.9ROR 18.6 · calibrated p 0.003 ✓ | 15.7 EB05 14.9 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious n=867 · 72% consumer | no trial arm names this drug |
| Duodenal ulcer haemorrhage | 444 | 18.4 16.6–20.3ROR 18.4 · calibrated p 0.003 ✓ | 15.6 EB05 14.5 · IC025 +3.8 3/3 methods agree | Labeled (related wording) related wording | serious n=444 | no trial arm names this drug |
| Renal haematoma | 80 | 18.4 14.5–23.3ROR 18.4 · calibrated p 0.003 ✓ | 15.6 EB05 12.9 · IC025 +3.5 3/3 methods agree | Labeled (related wording) related wording | serious n=80 · ♀ 0% (drug 50%) · 100% consumer | 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 |
|---|---|---|---|
| Gi bleeding | 32,691 | 21.921.6–22.1 | signal |
| Venous thromboembolism | 14,942 | 7.47.3–7.6 | signal |
| Stroke | 14,143 | 6.05.9–6.1 | signal |
| Anaemia | 8,813 | 3.03.0–3.1 | signal |
| Arrhythmia / qt | 5,669 | 3.02.9–3.1 | signal |
| Kidney injury | 8,887 | 2.02.0–2.0 | raised |
| Heart failure | 3,194 | 1.81.8–1.9 | raised |
| Fall / fracture | 6,446 | 1.71.7–1.8 | raised |
| Thrombocytopenia | 2,613 | 1.21.2–1.3 | raised |
| Interstitial lung disease | 1,105 | 1.21.1–1.2 | raised |
| Myocardial infarction | 2,137 | 1.11.0–1.1 | raised |
| Hyponatraemia | 825 | 1.01.0–1.1 | no difference |
| Serious infection | 7,671 | 1.01.0–1.0 | no difference |
| Liver injury | 2,422 | 0.80.8–0.8 | lower than other drugs |
| Rhabdomyolysis / myopathy | 500 | 0.60.6–0.7 | lower than other drugs |
| Tendon disorder | 227 | 0.60.5–0.7 | lower than other drugs |
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 |
|---|---|---|---|---|---|---|
| Gastrointestinal haemorrhage | 21,636 | 34.9 34.4–35.4ROR 38.9 · calibrated p 6e-5 ✓ | 26.1 EB05 25.8 · IC025 +4.7 3/3 methods agree | Labeled (related wording) related wording | age-adj. PRR 26.3 · serious PRR 18.1 | no trial arm names this drug |
| Off label use (used outside approved label) | 7,977 | 0.9 0.9–1.0ROR 0.9 · calibrated p 0.260 | 0.9 EB05 0.9 · IC025 -0.1 PRR-only: not supported by EBGM or IC | Reporting / coding artifact | age-adj. PRR 0.9 · serious PRR 1.0 | no trial arm names this drug |
| Haemorrhage | 7,796 | 8.1 7.9–8.3ROR 8.4 · calibrated p 0.058 | 7.6 EB05 7.4 · IC025 +2.9 3/3 methods agree | Labeled — boxed warning synonym match | age-adj. PRR 5.1 · serious PRR 6.2 | no trial arm names this drug |
| Dyspnoea (shortness of breath) | 7,336 | 1.3 1.3–1.3ROR 1.3 · calibrated p 0.528 | 1.3 EB05 1.3 · IC025 +0.4 | Not in label — unassessed | age-adj. PRR 1.1 · serious PRR 1.1 | no trial arm names this drug |
| Epistaxis (nosebleed) | 6,774 | 10.0 9.7–10.2ROR 10.3 · calibrated p 0.029 ✓ | 9.2 EB05 9.0 · IC025 +3.2 3/3 methods agree | Labeled adverse reaction exact term | age-adj. PRR 8.4 · serious PRR 8.0 | no trial arm names this drug |
| Fatigue (tiredness) | 6,729 | 0.9 0.9–0.9ROR 0.9 · calibrated p 0.226 | 0.9 EB05 0.9 · IC025 -0.2 PRR-only: not supported by EBGM or IC | Labeled adverse reaction exact term | age-adj. PRR 0.8 · serious PRR 0.8 | no trial arm names this drug |
| Death | 6,146 | 0.7 0.7–0.7ROR 0.7 · calibrated p 0.137 | 0.7 EB05 0.7 · IC025 -0.5 PRR-only: not supported by EBGM or IC | Outcome field, not a reaction boxed warning mentions mortality | age-adj. PRR 0.4 · serious PRR 0.5 | no trial arm names this drug |
| Fall | 6,129 | 1.9 1.8–1.9ROR 1.9 · calibrated p 0.895 | 1.9 EB05 1.8 · IC025 +0.9 | Not in label — unassessed | age-adj. PRR 1.4 · serious PRR 1.5 | no trial arm names this drug |
| Pulmonary embolism (lung blood clot) | 6,021 | 6.8 6.6–6.9ROR 6.9 · calibrated p 0.101 | 6.4 EB05 6.3 · IC025 +2.6 3/3 methods agree | Likely indication confounding term in indications; also in warnings | age-adj. PRR 5.3 · serious PRR 4.4 | no trial arm names this drug |
| Drug ineffective (drug did not work) | 5,935 | 0.5 0.4–0.5ROR 0.4 · calibrated p 0.031 ✓ | 0.5 EB05 0.4 · IC025 -1.2 PRR-only: not supported by EBGM or IC | Reporting / coding artifact | age-adj. PRR 0.6 · serious PRR 0.7 | no trial arm names this drug |
| Diarrhoea (diarrhea) | 5,713 | 0.9 0.9–0.9ROR 0.9 · calibrated p 0.241 | 0.9 EB05 0.9 · IC025 -0.2 PRR-only: not supported by EBGM or IC | Not in label — unassessed | age-adj. PRR 0.8 · serious PRR 0.8 | no trial arm names this drug |
| Anaemia (low red blood cells) | 5,703 | 3.1 3.0–3.2ROR 3.2 · calibrated p 0.579 | 3.0 EB05 3.0 · IC025 +1.6 3/3 methods agree | Not in label — unassessed | age-adj. PRR 2.6 · serious PRR 2.2 | no trial arm names this drug |
| Cerebrovascular accident (stroke) | 5,619 | 3.4 3.3–3.5ROR 3.5 · calibrated p 0.485 | 3.3 EB05 3.3 · IC025 +1.7 3/3 methods agree | Labeled (related wording) related wording | age-adj. PRR 2.3 · serious PRR 2.3 | no trial arm names this drug |
| Dizziness | 5,520 | 1.1 1.1–1.2ROR 1.1 · calibrated p 0.392 | 1.1 EB05 1.1 · IC025 +0.1 | Labeled adverse reaction exact term | age-adj. PRR 1.0 · serious PRR 1.0 | no trial arm names this drug |
| Nausea | 5,410 | 0.7 0.7–0.7ROR 0.7 · calibrated p 0.123 | 0.7 EB05 0.7 · IC025 -0.6 PRR-only: not supported by EBGM or IC | Not in label — unassessed | age-adj. PRR 0.7 · serious PRR 0.7 | no 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.
- Haemorrhagic arteriovenous malformation — n=816, PRR 690.4
- Fractional exhaled nitric oxide increased — n=122, PRR 246.5
- Truncus arteriosus persistent — n=82, PRR 69.4
- Haemorrhagic erosive gastritis — n=114, PRR 53.0
- Basal ganglia haemorrhage — n=263, PRR 47.9
- Internal haemorrhage — n=3,653, PRR 47.3
- Thalamus haemorrhage — n=230, PRR 35.7
- High frequency ablation — n=98, PRR 31.7
- Gastritis haemorrhagic — n=319, PRR 27.1
- Blood loss anaemia — n=449, PRR 25.4
✓ A hand-written Bradford Hill causality assessment exists for this drug: Rivaroxaban ↔ Gastrointestinal bleeding.
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 Rivaroxaban?
In FDA FAERS, the most frequently co-reported reaction terms for Rivaroxaban are gastrointestinal haemorrhage, haemorrhage, dyspnoea, epistaxis, fatigue, fall. 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 Rivaroxaban have an FDA boxed warning?
Yes. The current FDA label carries a boxed warning: (A) PREMATURE DISCONTINUATION OF XARELTO INCREASES THE RISK OF THROMBOTIC EVENTS, (B) SPINAL/EPIDURAL HEMATOMA A. Premature discontinuation of XARELTO increases the risk of thrombotic events Premature discontinuation of any oral anticoagulant, including XARELTO, increases the risk of thrombotic events.
Do FAERS signals prove that Rivaroxaban 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 10db92f9-2300-4a80-836b-673e1ae91610, effective 20260910; matched on
openfda.generic_name.exact:"RIVAROXABAN" AND openfda.product_type:"HUMAN PRESCRIPTION DRUG") - 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, 1,248 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
RIVAROXABAN, 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.