Модератор: Евгений Хоменко
A new study, reported to FDA on September 27, 2006 Following a September 21, 2006 discussion of the two published observational studies and other information at an FDA Cardiovascular and Renal Drugs Advisory Committee meeting, Bayer Pharmaceuticals informed FDA of another observational study they had performed using a contract research organization. Existing hospital data from 67,000 records of patients undergoing coronary artery bypass graft surgery were examined. 30,000 of the patients were treated with Trasylol and 37,000 were treated with alternate products. Using complex epidemiological and statistical methods, the report suggested that patients receiving Trasylol were at increased risk for death, kidney failure, congestive heart failure and stroke.
igor bulatov писал(а):На сколько актуален у вас апротинин?Или FDA информация-больше для самоуспокоения:не было-и не надо?
michail77 писал(а):Спасибо за ответы. буем переходить на транексам.
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