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rivaroxaban

EMA’s human medicines committee (CHMP) September meeting highlights

20 September 2021 | By Anna Begley (European Pharmaceutical Review)

In its most recent meeting, the CHMP recommended nine new medicines and concluded its review of Vaxzevria’s thrombosis risk.

article

Summarising 2019: a year of firsts for the EMA

17 January 2020 | By Victoria Rees (European Pharmaceutical Review)

The EMA was a proactive force in 2019, granting marketing authorisation for a range of drugs. This article highlights some of the most important advancements made by the agency last year.

news

SMC accepts restricted use of rivaroxaban for CAD

13 February 2019 | By Iqra Farooq (European Pharmaceutical Review)

The SMC has approved a drug, called rivaroxaban, that targets Factor Xa to treat those with coronary artery disease (CAD)...

news

Rivaroxaban reduced blood clots and related death in cancer patients

4 December 2018 | By European Pharmaceutical Review

Through a clinical trial, Cleveland researchers have identified how rivaroxaban reduces blood clots in cancer patients and also decreases related deaths...

news

New anti-clotting drugs linked to lower risk of serious bleeding

5 July 2018 | By European Pharmaceutical Review

Direct oral anticoagulants (DOACs) used to treat serious blood clots are associated with reduced risks of major bleeding compared with the older anti-clotting drug, warfarin, finds a new study.

news

FDA approves new dosing for Xarelto to reduce the risk of VTE

30 October 2017 | By Dr Zara Kassam (European Pharmaceutical Review)

The FDA has approved the 10 mg once-daily dose of Xarelto, for reducing the continued risk of recurrent venous thromboembolism...

news

Anticoagulant drugs appear to reduce the risk of stroke in patients with AF

25 October 2017 | By Dr Zara Kassam (European Pharmaceutical Review)

Blood-thinning drugs not only reduce the risk of stroke in patients with AF but are also associated with a significant reduction in the risk of dementia...

news

FDA Advisory Committee recommends against approval of the use of oral anticoagulant XARELTO® to reduce the risk of thrombotic cardiovascular events in patients with Acute Coronary Syndrome

16 January 2014 | By Johnson & Johnson

Janssen is seeking approval of rivaroxaban at a proposed dose of 2.5 mg twice daily (BID) for a 90 day treatment duration...

news

Cost effectiveness and clinical efficacy of Pradaxa® (dabigatran etexilate) versus rivaroxaban analysed

24 August 2012 | By Boehringer Ingelheim

Indirect comparison based on the RE-LY® trial and the Rocket AF trial suggests advantages of Pradaxa® in stroke prevention in patients with atrial fibrillation...

news

Bayer’s Xarelto® approved in the EU for the prevention of stroke in patients

20 December 2011 | By Bayer HealthCare

The only new oral anticoagulant approved in three indications across all 27 EU member states...

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