Rivaroxaban: uses, dosing, side effects & brands
Rivaroxaban is a factor xa inhibitor sold in the U.S. under one brand, for pulmonary embolism and venous thrombosis. Below: what the FDA label says, every product that contains it, what the pills look like, and its recall record.
Key facts
- Drug class
- Factor Xa Inhibitor
- Treats (across its forms)
- Pulmonary Embolism and Venous Thrombosis
- Available as
- Powder · Tablet · Kit
- Sold as
- Xarelto
- Prescription?
- Prescription only
- Generic available?
- Not in our catalog
- Half-life
- about 5 to 9 hours (11 to 13 hours in older adults)
- What the pharmacy pays
- about $0.98 per ml — not your price
- Boxed warning
- Boxed warning
How rivaroxaban is dosed
From the FDA label for Xarelto (application NDA215859). Other rivaroxaban products — different forms, different strengths — are dosed differently. Follow the label for the one you were prescribed.
Nonvalvular Atrial Fibrillation : 15 or 20 mg, once daily with food ( 2.1 ) Treatment of DVT and/or PE : 15 mg orally twice daily with food for the first 21 days followed by 20 mg orally once daily with food for the remaining treatment ( 2.1 ) Reduction in the Risk of Recurrence of DVT and/or PE in patients at continued risk for DVT and/or PE : 10 mg once daily with or without food, after at least 6 months of standard anticoagulant treatment ( 2.1 ) Prophylaxis of DVT Following Hip or Knee Replacement Surgery : 10 mg orally once daily with or without food ( 2.1 ) Prophylaxis of VTE in Acutely Ill Medical Patients at Risk for Thromboembolic Complications Not at High Risk of Bleeding : 10 mg once daily, with or without food, in hospital and after hospital discharge for a total recommended duration of 31 to 39 days ( 2.1 ) CAD or PAD : 2.5 mg orally twice daily with or without food, in combination with aspirin (75–100 mg) once daily ( 2.1 ) Pediatric Patients: See dosing recommendations in the Full Prescribing Information ( 2.2 ) 2.1 Recommended Dosage in Adults Table 1: Recommended Dosage in Adults Indication Renal Considerations Calculate CrCl based on actual weight [see Warnings and Precautions (5.4) and Use in Specific Populations (8.6) ] . Dosage Food/Timing [See Clinical Pharmacology (12.3) ] . Reduction in Risk of Stroke in Nonvalvular Atrial Fibrillation CrCl >50 mL/min…
Rivaroxaban side effects
The following clinically significant adverse reactions are also discussed in other sections of the labeling: Increased Risk of Stroke After Discontinuation in Nonvalvular Atrial Fibrillation [see Boxed Warning and Warnings and Precautions (5.1) ] Bleeding Risk [see Warnings and Precautions (5.2 , 5.4 , 5.5 , 5.6 , 5.7) ] Spinal/Epidural Hematoma [see Boxed Warning and Warnings and Precautions (5.3) ] The most common adverse reaction (>5%) in adult patients was bleeding ( 6.1 ) The most common adverse reactions (>10%) in pediatric patients were bleeding, cough, vomiting, and gastroenteritis ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Janssen Pharmaceuticals, Inc. at 1-800-526-7736 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice. During clinical development for the approved indications, 34,947 adult patients were exposed to XARELTO. Hemorrhage The most common adverse reactions with XARELTO were bleeding complications [see Warnings and Precautions (5.2) ] . Nonvalvular Atrial Fibrillation In the ROCKET AF trial, the most frequent adverse reactions associated with…
Who shouldn’t take rivaroxaban
XARELTO is contraindicated in patients with: active pathological bleeding [see Warnings and Precautions (5.2) ] severe hypersensitivity reaction to XARELTO (e.g., anaphylactic reactions) [see Adverse Reactions (6.2) ] Active pathological bleeding ( 4 ) Severe hypersensitivity reaction to XARELTO ( 4 )
Rivaroxaban drug interactions
Avoid combined P-gp and strong CYP3A inhibitors and inducers ( 7.2 , 7.3 ) Anticoagulants: Avoid concomitant use ( 7.4 ) 7.1 General Inhibition and Induction Properties Rivaroxaban is a substrate of CYP3A4/5, CYP2J2, and the P-gp and ATP-binding cassette G2 (ABCG2) transporters, the latter also known as breast cancer resistance protein (BCRP). Combined P-gp and strong CYP3A inhibitors increase exposure to rivaroxaban and may increase the risk of bleeding. Combined P-gp and strong CYP3A inducers decrease exposure to rivaroxaban and may increase the risk of thromboembolic events. 7.2 Drugs that Inhibit Cytochrome P450 3A Enzymes and Drug Transport Systems Interaction with Combined P-gp and Strong CYP3A Inhibitors Avoid concomitant administration of XARELTO with known combined P-gp and strong CYP3A inhibitors (e.g., ketoconazole and ritonavir) [see Warnings and Precautions (5.6) and Clinical Pharmacology (12.3) ] . Although clarithromycin is a combined P-gp and strong CYP3A inhibitor, pharmacokinetic data suggests that no precautions are necessary with concomitant administration with XARELTO as the change in exposure is unlikely to affect the bleeding risk [see Clinical Pharmacology (12.3) ] . Interaction with Combined P-gp and Moderate CYP3A Inhibitors in Patients with Renal Impairment XARELTO should not be used in patients with CrCl 15 to <80 mL/min who are receiving concomitant combined P-gp and moderate CYP3A inhibitors (e.g., erythromycin) unless the potential benefit justifies the potential risk [see Warnings and Precautions (5.4) and Clinical Pharmacology (12.3) ] . 7.3 Drugs that Induce Cytochrome P450 3A Enzymes and Drug Transport Systems Avoid concomitant use of XARELTO with drugs that are combined P-gp and strong CYP3A inducers (e.g., carbamazepine, phenytoin, rifampin, St. John's wort) [see Warnings and Precautions (5.6) and Clinical Pharmacology (12.3) ] . 7.4 Anticoagulants and NSAIDs/Aspirin Coadministration of enoxaparin, warfarin, aspirin, clopidogrel and chronic NSAID use may increase the risk of bleeding [see Clinical Pharmacology (12.3) ]. Avoid concurrent use of XARELTO with other anticoagulants due to increased bleeding risk unless benefit outweighs risk. Promptly evaluate any signs or symptoms of blood loss if patients are treated concomitantly with aspirin, other platelet aggregation inhibitors, or NSAIDs [see Warnings and Precautions (5.2) ] .
Every rivaroxaban product we track (1)
Same active ingredient — different manufacturer, form, price and FDA recall record. That last one is what our independent score measures.
Only one: Xarelto.
What rivaroxaban pills look like
Imprint codes, colour and shape from the FDA’s labelling data. Match the imprint on your pill — or search any imprint.
Can you crush or split rivaroxaban?
At least one rivaroxabanproduct is labelled to be swallowed whole — crushing an extended-release tablet releases the whole day’s dose at once. Which applies depends on the form you were given.
What each rivaroxaban label says about crushing, splitting and chewingHow long rivaroxaban keeps
The date on a sealed pack is not the only one: some rivaroxaban labels start a second clock once the product is opened or mixed, as short as 60 days.
Does rivaroxaban expire? The in-use limits and storage rules from its labelsRivaroxaban and breastfeeding
From LactMed, the US National Library of Medicine’s Drugs and Lactation Database — quoted, not rewritten.
Full LactMed record for rivaroxaban: levels in milk, effects in breastfed infants, and the drugs it would consider insteadSeveral case reports, a thorough pharmacokinetic analysis, and a pharmacokinetic computer model consistently indicate that maternal doses of rivaroxaban of 15 to 30 mg daily produce low levels in milk that are considerably below doses (7% or less) required for anticoagulation in infants. Plasma rivaroxaban levels in two breastfed infants were undetectable. If the mother requires rivaroxaban, it is not a reason to discontinue breastfeeding.
National Institute of Child Health and Human Development, record revised May 15, 2026. LactMed states its information is not a substitute for professional judgement.
What people report to the FDA about rivaroxaban
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 27,527 reports naming rivaroxaban, and the FDA flagged 96% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:
- dyspnoea1,544 reports
- anaemia1,338 reports
- pulmonary embolism1,086 reports
- fatigue1,043 reports
- gastrointestinal haemorrhage973 reports
- atrial fibrillation959 reports
- dizziness926 reports
- fall881 reports
Read these as a signal, not a rate. A report does not mean rivaroxaban caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label section above.
Source: openFDA drug/event (FAERS), retrieved July 26, 2026.
How long rivaroxaban stays in your system
The elimination half-life of rivaroxaban is about 5 to 9 hours (11 to 13 hours in older adults). The FDA label gives a terminal elimination half-life of 5 to 9 hours in healthy adults aged 20-45, rising to 11 to 13 hours in elderly subjects (60-76). Rivaroxaban is NOT a prodrug and has no clinically relevant active circulating metabolite (the unchanged parent is the predominant form in plasma), so nothing outlasts the parent drug. Blood levels stay higher and clearance slows with older age, renal impairment, and moderate hepatic impairment, effectively lengthening how long the drug persists.
XARELTO (rivaroxaban) tablet, film coated — DailyMed FDA label, Clinical Pharmacology (Pharmacokinetics: Elimination) ↗Half-life is how long the body takes to clear half a dose. It is not the same as how long a drug test can detect it, and it varies with age, kidney and liver function.
Related calculators
Frequently asked questions
What is rivaroxaban?
Xarelto (Rivaroxaban) is a factor xa inhibitor used to treat Pulmonary Embolism, Venous Thrombosis.
What kind of drug is rivaroxaban?
The FDA classifies rivaroxaban as a factor xa inhibitor. If you are checking whether it is safe to combine with something else, the class is what matters — two drugs from the same class usually should not be stacked.
How long does rivaroxaban stay in your system?
The elimination half-life of rivaroxaban is about 5 to 9 hours (11 to 13 hours in older adults) — that is how long the body takes to clear half of a dose. The FDA label gives a terminal elimination half-life of 5 to 9 hours in healthy adults aged 20-45, rising to 11 to 13 hours in elderly subjects (60-76). Rivaroxaban is NOT a prodrug and has no clinically relevant active circulating metabolite (the unchanged parent is the predominant form in plasma), so nothing outlasts the parent drug. Blood levels stay higher and clearance slows with older age, renal impairment, and moderate hepatic impairment, effectively lengthening how long the drug persists. Half-life is not the same as how long a drug test can detect the drug, and it varies with age, kidney and liver function.
Can you take rivaroxaban with other medicines?
It depends on the medicine. We check it against the FDA labels rather than guessing: our interaction checker searches each drug's own label for the other and quotes what it says, naming the section it came from. Run rivaroxaban against whatever else you take — and remember that a label not naming a drug is not the same as that combination being safe.
What forms does rivaroxaban come in?
Across the brands we track, rivaroxaban is currently marketed as powder, tablet and kit, per the FDA's National Drug Code Directory. Each form is dosed differently — follow the label for the exact product you were prescribed.
Is there a generic rivaroxaban?
We do not currently list a generic-labelled rivaroxaban product. That does not always mean none exists — it means none appears under a generic name in the FDA data we track. Ask your pharmacist.
What are the most common side effects of rivaroxaban (Xarelto)?
Bleeding, which the label lists as the most common adverse reaction in adults — nosebleeds, easy bruising, bleeding gums, heavier periods, blood in urine, and cuts that keep oozing. These persist for as long as you take the drug rather than fading in a few weeks. Non-bleeding complaints reported with rivaroxaban include itching and wound drainage after joint-replacement surgery. In children the label also lists cough, vomiting, and gastroenteritis. Note that "more bruising than before" is expected; bleeding with no injury behind it, or bleeding that won't stop, is not.
Take rivaroxaban with food or not? This one actually matters.
The 15 mg and 20 mg tablets must be taken with food — for atrial fibrillation, with your evening meal. Rivaroxaban is poorly absorbed at those strengths on an empty stomach, so a skipped meal can mean an underdose and a preventable clot or stroke. The 10 mg and 2.5 mg strengths can be taken with or without food. Anchor the dose to a meal you never skip rather than to a clock alarm. If you miss a once-daily dose, take it as soon as you remember — but do not double the dose within the same day. On the twice-daily 15 mg phase used in the first 21 days of clot treatment, the label does allow taking two 15 mg tablets at once to reach 30 mg for that day; confirm with your prescriber or pharmacist.
What are rivaroxaban's boxed warnings, and when do I go to the ER?
Two boxed warnings. (A) Stopping rivaroxaban early increases the risk of clotting events — never stop on your own for a procedure, a dental visit, or bruising; the prescriber decides whether to bridge with another anticoagulant. (B) Spinal or epidural hematoma in anyone getting neuraxial anesthesia or a spinal puncture, which can cause long-term or permanent paralysis. Tell anesthesia before an epidural, spinal block, or spinal injection. Emergency signs: bleeding that won't stop, vomiting blood or coffee-ground material, black or bloody stools, coughing up blood, red or brown urine, sudden severe headache, one-sided weakness, confusion, or vision change. Any head injury or fall means an ER visit even if you feel fine.
Who should not be on rivaroxaban, and what sets the dose?
The label says rivaroxaban is not recommended in people with a prosthetic heart valve. That recommendation rests on the GALILEO study in patients who had undergone transcatheter aortic valve replacement (TAVR), where patients randomized to rivaroxaban had higher rates of death and of bleeding than those on an antiplatelet regimen; for other prosthetic valves and valve procedures, it simply has not been studied. It is also not recommended in triple-positive antiphospholipid syndrome, where direct oral anticoagulants have been associated with more recurrent clots than warfarin. Kidney function sets the dose: for atrial fibrillation the label gives 20 mg once daily with the evening meal when creatinine clearance is above 50 mL/min, and 15 mg once daily when it is 50 mL/min or below, and advises avoiding the drug below 15 mL/min. Ask which number your dose was based on and when it was last measured. If any of this applies and you're already taking it, don't stop — book an appointment. Also flag aspirin, NSAIDs, SSRI/SNRI antidepressants, and drugs like ketoconazole, ritonavir, or rifampin, all of which change your bleeding risk.
Cite this page
- APA
- pharmaranks. (2026, July 24). Rivaroxaban: uses, dosing, side effects & brands. https://pharmaranks.com/drugs/rivaroxaban
- MLA
- “Rivaroxaban: uses, dosing, side effects & brands.” pharmaranks, 24 July 2026, https://pharmaranks.com/drugs/rivaroxaban.
We summarise public FDA and NIH sources — for a clinical claim, cite the primary source we link to as well.
Sources: FDA openFDA drug label, National Drug Code Directory, and Enforcement (recall) database. This page reproduces public FDA data and is not medical advice. Dosing is set by your prescriber.
Read the full FDA label for rivaroxaban on DailyMed (NIH) ↗ — including its boxed warning in full.