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Drug · FAERS side-effect profile with label screen

Rivaroxaban side effects: what 206,900 FDA adverse event reports show

Rivaroxaban · Xarelto · 1,248 reaction terms · 554,666 drug–reaction co-reports · data 2026-09-14
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Drug class

Factor Xa Inhibitor

FDA label (Established Pharmacologic Class)

Brand names

Xarelto

openFDA label

Who reports

206,900 reports · 84% serious · 27,139 with death outcome · 50% female

openFDA FAERS counts, all years, deduplication not applied

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 .

FDA label, Indications and Usage

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.

FDA label, Description section

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.

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 adverse reaction 1Labeled (related wording) 18Likely indication confounding 3Reporting / coding artifact 1Lab value / disease marker 1Not in label — unassessed 16
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). 1,208 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
Haemorrhagic arteriovenous malformation816690.4
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 — unassessedserious n=816 · 85% consumerno trial arm names this drug
Fractional exhaled nitric oxide increased122246.5
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 — unassessedserious n=122 · ♀ 0% (drug 50%)no trial arm names this drug
Truncus arteriosus persistent8269.4
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 — unassessedserious n=82 · 100% clinicianno trial arm names this drug
Haemorrhagic erosive gastritis11453.0
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 — unassessedserious n=114 · 100% consumerno trial arm names this drug
Basal ganglia haemorrhage26347.9
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 — unassessedserious n=263no trial arm names this drug
Internal haemorrhage3,65347.3
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 — unassessedserious PRR 22.5 · 87% consumerno trial arm names this drug
Anticoagulation drug level increased8736.8
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 markerserious n=83 · ♀ 0% (drug 50%) · 100% clinicianno trial arm names this drug
Thalamus haemorrhage23035.7
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 — unassessedserious n=230no trial arm names this drug
High frequency ablation9831.7
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 — unassessedserious n=95 · ♀ 0% (drug 50%)no trial arm names this drug
Atrial thrombosis48130.3
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% clinicianno trial arm names this drug
Haemorrhagic stroke1,80129.9
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 15.9no trial arm names this drug
Gastritis haemorrhagic31927.1
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 — unassessedserious n=319 · 73% consumerno trial arm names this drug
Blood loss anaemia44925.4
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 — unassessedserious n=447no trial arm names this drug
Peptic ulcer haemorrhage13323.9
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 — unassessedserious n=133no trial arm names this drug
Haemorrhagic transformation stroke28423.4
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 — unassessedserious n=284no trial arm names this drug
Haemorrhoidal haemorrhage91523.0
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 — unassessedserious n=877no trial arm names this drug
Haemorrhagic anaemia82923.0
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 — unassessedserious n=829no trial arm names this drug
Cerebellar haemorrhage26623.0
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 — unassessedserious n=266no trial arm names this drug
Post procedural haematoma31422.8
20.2–25.8ROR 22.9 · calibrated p 0.001 ✓
18.7 EB05 17.1 · IC025 +4.0
3/3 methods agree
Reporting / coding artifactserious n=313no trial arm names this drug
Dysfunctional uterine bleeding22722.8
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% consumerno trial arm names this drug
Embolic stroke59420.5
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=593no trial arm names this drug
Gastric ulcer haemorrhage86718.5
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 — unassessedserious n=867 · 72% consumerno 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
Gi bleeding32,69121.921.6–22.1signal
Venous thromboembolism14,9427.47.3–7.6signal
Stroke14,1436.05.9–6.1signal
Anaemia8,8133.03.0–3.1signal
Arrhythmia / qt5,6693.02.9–3.1signal
Kidney injury8,8872.02.0–2.0raised
Heart failure3,1941.81.8–1.9raised
Fall / fracture6,4461.71.7–1.8raised
Thrombocytopenia2,6131.21.2–1.3raised
Interstitial lung disease1,1051.21.1–1.2raised
Myocardial infarction2,1371.11.0–1.1raised
Hyponatraemia8251.01.0–1.1no difference
Serious infection7,6711.01.0–1.0no difference
Liver injury2,4220.80.8–0.8lower than other drugs
Rhabdomyolysis / myopathy5000.60.6–0.7lower than other drugs
Tendon disorder2270.60.5–0.7lower than other drugs

Trial evidence (ClinicalTrials.gov)

No completed trial with posted adverse-event results was found on ClinicalTrials.gov for Rivaroxaban (searched RIVAROXABAN).

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
Off label use (used outside approved label)7,9770.9
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 artifactage-adj. PRR 0.9 · serious PRR 1.0no trial arm names this drug
Haemorrhage7,7968.1
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 6.2no trial arm names this drug
Dyspnoea (shortness of breath)7,3361.3
1.3–1.3ROR 1.3 · calibrated p 0.528
1.3 EB05 1.3 · IC025 +0.4Not in label — unassessedage-adj. PRR 1.1 · serious PRR 1.1no trial arm names this drug
Epistaxis (nosebleed)6,77410.0
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 8.0no trial arm names this drug
Fatigue (tiredness)6,7290.9
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 0.8no trial arm names this drug
Death6,1460.7
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 0.5no trial arm names this drug
Fall6,1291.9
1.8–1.9ROR 1.9 · calibrated p 0.895
1.9 EB05 1.8 · IC025 +0.9Not in label — unassessedage-adj. PRR 1.4 · serious PRR 1.5no trial arm names this drug
Pulmonary embolism (lung blood clot)6,0216.8
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 4.4no trial arm names this drug
Drug ineffective (drug did not work)5,9350.5
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 artifactage-adj. PRR 0.6 · serious PRR 0.7no trial arm names this drug
Diarrhoea (diarrhea)5,7130.9
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 — unassessedage-adj. PRR 0.8 · serious PRR 0.8no trial arm names this drug
Anaemia (low red blood cells)5,7033.1
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 — unassessedage-adj. PRR 2.6 · serious PRR 2.2no trial arm names this drug
Dizziness5,5201.1
1.1–1.2ROR 1.1 · calibrated p 0.392
1.1 EB05 1.1 · IC025 +0.1Labeled adverse reaction
exact term
age-adj. PRR 1.0 · serious PRR 1.0no trial arm names this drug
Nausea5,4100.7
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 — unassessedage-adj. PRR 0.7 · serious PRR 0.7no 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: 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

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.