Skip to main content

Two medicines, side by side

Edoxaban vs rivaroxaban

Edoxaban and rivaroxaban are both labeled for atrial fibrillation, blood clots (DVT and PE) and stroke prevention. Drugs@FDA records approvals of edoxaban since 2015 and of rivaroxaban since 2011. Pharmacies paid $15.51 per Savaysa 60 mg tablet and $0.650 per rivaroxaban 2.5 mg tablet (NADAC, October 7, 2026); the strengths differ and one is a brand and one a generic, so the two prices are not like for like. Rivaroxaban's other strengths are brand-only: $19.54 per Xarelto 20 mg tablet. How each works, in its label's words: Edoxaban, “Edoxaban is a selective inhibitor of FXa.”; Rivaroxaban, “XARELTO is a selective inhibitor of FXa.”

Check it at the source: the edoxaban FDA label on DailyMed (effective July 10, 2025); the rivaroxaban FDA label on DailyMed (effective September 10, 2026).

Highlights of the edoxaban record

Edoxaban (Savaysa) · label of July 10, 2025

Boxed warning

(A) REDUCED EFFICACY IN NONVALVULAR ATRIAL FIBRILLATION PATIENTS WITH CREATININE CLEARANCE (CRCL) > 95 ML/MIN (B) PREMATURE DISCONTINUATION OF SAVAYSA INCREASES THE RISK OF ISCHEMIC EVENTS (C) SPINAL/EPIDURAL HEMATOMA WARNING: (A) REDUCED EFFICACY IN NONVALVULAR ATRIAL FIBRILLATION PATIENTS WITH CREATININE CLEARANCE (CRCL) > 95 ML/MIN (B) PREMATURE DISCONTINUATION OF SAVAYSA INCREASES THE RISK OF ISCHEMIC EVENTS (C) SPINAL/EPIDURAL HEMATOMA See full prescribing information for complete boxed warning.

Used for

From the label: indications

SAVAYSA is a factor Xa inhibitor indicated: To reduce the risk of stroke and systemic embolism (SE) in patients with nonvalvular atrial fibrillation (NVAF) ( 1.1 ) Limitation of Use for NVAF SAVAYSA should not be used in patients with creatinine clearance (CrCL) > 95 mL/min because of increased risk of ischemic stroke compared to warfarin at the highest dose studied (60 mg) ( 1.1 ) SAVAYSA is indicated for the […]

On the market

Earliest approval on file
January 8, 2015
Generic labelers
none listed
Pharmacy cost
$15.51 per tablet

Supply and safety

Shortage
No current entry
Recalls
0

Highlights of the rivaroxaban record

Rivaroxaban (Xarelto) · label of September 10, 2026

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.

Used for

From the label: indications

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 the risk of recurrence of DVT or PE ( 1.4 ) for the prophylaxis of DVT, which may lead to PE in patients undergoing knee or hip replacement surgery ( 1.5 ) for […]

On the market

Earliest approval on file
July 1, 2011
Generic labelers
20 labelers
Pharmacy cost
$0.650 per tablet

Supply and safety

Shortage
A presentation being discontinued
Recalls
1

Source: FDA drug labels via openFDA (Edoxaban label of July 10, 2025, Rivaroxaban label of September 10, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do edoxaban and rivaroxaban differ on the record?

How each works, in its label's words: Edoxaban, “Edoxaban is a selective inhibitor of FXa.”; Rivaroxaban, “XARELTO is a selective inhibitor of FXa.”

Both are in FDA's class factor Xa inhibitors.

Half-life, in each label's words: Edoxaban, “The terminal elimination half-life of edoxaban following oral administration is 10 to 14 hours.”; Rivaroxaban, “The terminal elimination half-life of rivaroxaban is 5 to 9 hours in healthy subjects aged 20 to 45 years.”

Both labels carry a boxed warning; the records quote them.

Generics: edoxaban none approved; rivaroxaban since 2025 (Drugs@FDA).

EdoxabanRivaroxaban
Labeled forAtrial fibrillation, Stroke prevention, Blood clots (DVT and PE)Atrial fibrillation, Heart attack and coronary artery disease, Blood clots (DVT and PE), Stroke prevention
Pharmacologic classFactor Xa InhibitorFactor Xa Inhibitor
How it works (label)Edoxaban is a selective inhibitor of FXa. It does not require antithrombin III for antithrombotic activity. Edoxaban inhibits free FXa, and prothrombinase activity and inhibits thrombin-induced platelet aggregation.XARELTO is a selective inhibitor of FXa. It does not require a cofactor (such as Anti-thrombin III) for activity. Rivaroxaban inhibits free FXa and prothrombinase activity.
Half-life (label)The terminal elimination half-life of edoxaban following oral administration is 10 to 14 hours.The terminal elimination half-life of rivaroxaban is 5 to 9 hours in healthy subjects aged 20 to 45 years.
Earliest approval on file (Drugs@FDA)January 8, 2015July 1, 2011
First generic approvednoneMarch 3, 2025
Generic labelers (NDC)none listed20 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$15.51 per tablet (Savaysa 60 mg tablet)$0.650 per tablet (Rivaroxaban 2.5 mg tablet)
12-month price change+6%-81%
Boxed warningYesYes
Shortage nowNo current entryA presentation being discontinued
Recalls recorded01
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)6,591206,938
DEA schedulenonenone

Source: Drugs@FDA, FDA NDC Directory, CMS NADAC of October 7, 2026, FDA shortages and recalls, FAERS via openFDA (FDA files October 8, 2026)

What do the labels say about using others of their kind?

Edoxaban label, drug interactions

Long-term concomitant treatment with SAVAYSA and other anticoagulants is not recommended because of increased risk of bleeding [see Warnings and Precautions (5.3) ].

Rivaroxaban label, drug interactions

Avoid concurrent use of XARELTO with other anticoagulants due to increased bleeding risk unless benefit outweighs risk.

Source: FDA drug labels via openFDA

What next?

Alternatives to edoxaban
every medicine labeled for the same conditions