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	Recall --Nationwide Recall of Grifulvin V®/Griseofulvin Oral Suspension (04/10/2007) FDA Public Health Advisory: Tegaserod maleate (marketed as Zelnorm) (03/30/2007) FDA Public Health Advisory: Pergolide (marketed as Permax) (03/29/2007) FDA Requests Label Change for All Sleep Disorder Drug Products (03/14/2007) FDA Directs ADHD Drug Manufacturers to Notify Patients about Cardiovascular Adverse Events and Psychiatric Adverse Events (02/21/2007) FDA Proposes to Strengthen Label Warning for Xolair (02/21/2007) Information on RotaTeq and Intussusception (02/13/2007) Methadone Use for Pain Control May Result in Death and Life-Threatening Changes in Breathing and Heart Beat (11/27/2006) Nationwide Recall of 500mg Strength Store-Brand Acetaminophen Caplets (11/09/2006) Recall --Firm Press Release: Roche Diagnostics Announces Nationwide Recall on Medical Device Used to Determine Blood Clotting Time (10/19/2006) FDA Issues Nationwide Alert on Counterfeit One Touch Basic/Profile and One Touch Ultra Blood Glucose Test Strips (10/13/2006) New information suggests that babies exposed to Lamictal during the first three months of pregnancy may have a higher chance of being born with a cleft lip or cleft palate. (09/00/2006) FDA Public Advisory to Health Care providers prescribing and patients prescribed Ketek (telthromycin) Tablets (01/23/2006) Roche Diagnostics Issues a Worldwide Voluntary Recall of Some of its ACCU-CHEK^® Aviva Meters (01/19/2006) Return to the current FDA Alert page to access current FDA Alerts.

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