Consistent Protection after Knee Replacement Surgery, Evidenced in Clinical Studies,1,2 Reaffirmed in the Real-World3

Prevention of VTE after elective knee replacement surgery

The first approved indication4 for Xarelto® was for the prevention of venous thromboembolism in adults undergoing elective knee replacement surgery

Superior Protection for Your Elective Knee Surgery Patients1

Provide better protection against DVT , nonfatal PE and death from any cause vs enoxaparin

Xarelto significantly reduces DVT (either symptomatic or detected by bilateral venography if the patient was asymptomatic), nonfatal PE , or death from any cause by 9.2% ARR vs enoxaparin.1

RECORD 3 efficacy

Comparable Safety Profile1

Maintain a low major bleeding rate vs enoxaparin

Treatment with Xarelto results in a similar major bleeding rate as enoxaparin in elective knee replacement surgery patients.1

RECORD 3 efficacy

Effective Thromboprophylaxis Achieved with Less Medicinal Treatment2

Better protect your patients with less medicinal treatment vs enoxaparin

Treatment with Xarelto 10 mg OD for 1014 days significantly reduces DVT (either symptomatic or detected by bilateral venography if the patient was asymptomatic), nonfatal PE , or death from any cause up to day 17 after surgery by 3.2% ARR vs enoxaparin 30 mg BID.2

RECORD 4 efficacy

Consistent Protection Confirmed in the Real World3

Give your everyday patients the consistent protection they need

Xarelto has been associated with significantly lower symptomatic thromboembolic events vs standard of care (0.9% vs 1.4% [OR, 0.65; 95% CI, 0.49–0.87]) in elective hip and knee surgery patients.3

xamos

Standard of care included, but was not limited to, LMWHs, unfractionated heparins, fondaparinux, dabigatran etexilate, acetylsalicylic acid and vitamin K antagonists.

Major bleeding rates were similar in patients treated with either Xarelto or standard of care.3

XAMOS safety

* Standard of care included, but was not limited to, LMWHs, unfractionated heparins, fondaparinux, dabigatran etexilate, acetylsalicylic acid and vitamin K antagonists. † As defined in the RECORD studies clinically overt bleeding that was fatal, occurred in a critical organ, necessitated re-operation or was outside of the surgical site and was associated with a fall in haemoglobin of ≥2 g/dl or required a transfusion of ≥2 units of blood.

ARR, absolute risk reduction; CI, confidence interval; DVT , deep vein  thrombosis ITT , intention-to-treat;  LMWH , low-molecular-weight heparin; OD, once daily; OR, odds ratio;  PE , pulmonary embolism; RRR , relative risk reduction; VTE , venous thromboembolism.

 

PP-XAR-ALL-1794-1

References

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