Edoxaban vs warfarin in patients with nonvalvular atrial fibrillation in the US Food and Drug Administration approval population: An analysis from the Effective Anticoagulation with Factor Xa Next Generation in Atrial Fibrillation–Thrombolysis in Myocardial Infarction 48 (ENGAGE AF–TIMI 48) trial

2016 ◽  
Vol 172 ◽  
pp. 144-151 ◽  
Author(s):  
Alon Eisen ◽  
Robert P. Giugliano ◽  
Christian T. Ruff ◽  
Francesco Nordio ◽  
Harinder S. Gogia ◽  
...  
1987 ◽  
Vol 25 (5) ◽  
pp. 17-19

When we last reviewed the use of aspirin in vascular disorders we concluded that a preventive effect in coronary thrombosis was uncertain.1 In 1985 the US Food and Drug Administration accepted, after reviewing the evidence, that aspirin can reduce the likelihood of heart attacks for some patients.2 How strong is this evidence?


1966 ◽  
Vol 4 (12) ◽  
pp. 47-48

On February 28 the US Food and Drug Administration took the unprecedented step of seizing stocks of Peritrate SA (Warner-Chileott Labs), a sustained-action preparation of pentaerythritol tetranitrate. This was done because the FDA judged advertisements for the drug to be ‘false and misleading’. They implied that the drug increased survival after myocardial infarction by asking ‘Is Peritrate life - sustaining?’, clearly inviting the answer ‘yes’.


Circulation ◽  
2018 ◽  
Vol 137 (17) ◽  
pp. 1867-1869 ◽  
Author(s):  
Maria Rubini Gimenez ◽  
Patrick Badertscher ◽  
Raphael Twerenbold ◽  
Jasper Boeddinghaus ◽  
Thomas Nestelberger ◽  
...  

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