Drug Maker Issued FDA Warning for Failure to Report on 3,500 Deaths
by nm
In September the FDA issued a warning letter the the drug company Actelion Pharmaceuticals for failure to report on deaths of 3,500 patients who died while on the drugs Tracleer or Ventavis, used to treat pulmonary arterial hypertension. The letter follows a 2009 inspection of the company. “The inspection focused...



