The 250/50 Advair Diskus was approved in 2003 for maintenance treatment of airflow obstruction in COPD patients. The FDA questioned how Advair 500/50 ...
... government regulators rejected the company's request to allow a higher dose of its drug Advair Diskus for patients with a common respiratory disease. ...
AP 08.08.07, 12:06 PM ET Drug maker GlaxoSmithKline PLC said Wednesday government regulators rejected the company's request to allow its Advair Diskus drug ...
L: Quote, Profile, Research) said on Wednesday that US health regulators declined to approve a higher strength version of its inhaled Advair Diskus for the ...
Advair Diskus may increase this risk, therefore, bone mineral density assessment is recommended prior to starting Advair Diskus and periodically thereafter. ...
8/8/2007 1:38:13 PM British drug giant Glaxosmithkline plc's (GSK) hopes to expand the label for Advair Diskus appears to be a long shot at least for now ...
8 (Bloomberg) -- GlaxoSmithKline Plc failed to win US approval to market the strongest dose of the asthma inhaler Advair Diskus, the company's top-selling ...
... a not approvable letter for the supplemental drug application for the 500/50 strength of Advair Diskus (fluticasone propionate and salmeterol inhalation ...
... Respiratory Inflammatory Disease development programs, as well as contributing to both Advair Diskus and Advair HFA New Drug Application submissions. ...
(Reuters) GlaxoSmithKline has failed to win approval from the US Food and Drug Administration to market a higher-dose version of Advair Diskus, ...