Serevent Diskus should be stored inside the unopened moisture-protective foil pouch and only removed from the pouch immediately before initial use. Discard Serevent Diskus 6 weeks after opening the ...
Serevent Diskus does not replace fast-acting inhalers for sudden symptoms and should not be taken more than twice a day. In patients with asthma, medicines like Serevent may increase the chance of ...
Nov. 18, 2005 — The U.S. Food and Drug Administration (FDA) has warned healthcare professionals regarding the increased risk of severe asthma episodes and death associated with use of inhalation ...
The dye FD&C Blue No. 1 (Blue 1; triphenylmethane) is sometimes added to enteral feeding solutions of critically ill patients to detect pulmonary aspiration. However, serious outcomes have been ...
On November 18, 2005, FDA alerted health care professionals and patients that several long-acting bronchodilator medicines have been associated with possible increased risk of worsening wheezing ...
During a senate hearing, convened following the withdrawal of Merck & Co.'s COX-2 Vioxx (rofecoxib) in September, the FDA's David Graham commented that the safety profile of five other currently ...
GlaxoSmithKline plc (LSE/NYSE:GSK) today announced publication of results from the 'LABA' (long acting beta2-agonist) safety study, AUSTRI (SAS115359) in the New England Journal of Medicine (NEJM).
Dec. 1, 2004 -- The U.S. Food and Drug Administration (FDA) approved in September revisions to safety labeling to advise healthcare professionals of the following changes: use of nalidixic acid may be ...
WASHINGTON — Some patients using a popular asthma medication called salmeterol face a small, increased risk of severe, and occasionally fatal, asthma attacks, the Food and Drug Administration warned ...
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