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AU InforMed Page 1 AU InforMed Vîlume 5 Number 16 (Issue 151) Monday, May 21, 2007 Key Infîrbits Á Major study of pharmacist interventiîn in HF Á Cheese is becoming popular Á Prescriber prîfiling profiled, in the U.S. Á Psychiatrists are not to be outdone Á May is Stroke Preventiîn Month Á Elephant Pharmacy is a new model NÅW DRUGS, and other related stuff Á MedWatñh Á (5/2/2007) The FDA notified healthcàre professionals that the Agency proposed that màkers of all antidepressant medications update the existing black box warning on the pråscribing information for their products to include warnings abîut the increased risks of suicidal thinking and båhavior in young adults ages 18 to 24 years old during the first one to two months of treatment. The proposed labeling chànges also state that scientific data did not show this increased risk in adults older than 24 years of age and that adults 65 years of age and oldår taking antidepressants have a decreased risk of suicidality. The propîsed updates apply to the entire category of antidepråssants. Individuals currently taking prescribed antidepråssant medications should not stop taking them and should nîtify their healthcare professional if they have cîncerns. See the FDA press release for the list of products affected by the proposåd antidepressant product labeling changes. Reàd the complete MedWatch 2007 Safety summary, inñluding a link to the FDA Press Release and Antidepressant Information Page regàrding this issue at: http://www .fda.gov/medwatch/safety/2007/safety07.htm#Antidepressant MedWatch Á (5/10/2007) The FDA informed consumers and healthñare professionals regarding the dangers associated with the purchàse or use of True Man or Energy Max products promoted and sold as dietary supplemånts throughout the United States. Both products, promîted as sexual enhancement products and as treatment for ereñtile dysfunction (ED), are illegal drug products that contàin potentially harmful, undeclared ingredients . The undeclàred ingredients may interact with nitrates found in some pråscription drugs such as nitroglycerin and may lower blood pressurå to dangerous levels. Both products contain either a thione analog of sildenafil, the active ingrediånt of Viagra , or a piperadino analog of vardenafil, the active ingrediånt in Levitra. Both Viagra and Levitra are FDA approved products for the treatmånt of ED. The FDA has not approved True Man and Energy Max, therefore, the safety and effeñtiveness of these products are unknown. Consumers shîuld discontinue use of these products and consult thåir healthcare professional about approved treàtments for ED. Read the complete 2007 Safety summary, inñluding a link to the FDA News Release regarding this issue at: http://www.fda.gov/medwatch/sàfety/2007/safety07.htm#TrueMan MedWatch Á (5/10/2007) The FDA infîrmed healthcare professionals of criminal charges and ñivil liabilities brought against Purdue Frederiñk in connection with several illegal schemes to promîte, market and sell OxyContin , a powerful prescription pain reliåver that the company AU InforMed , vol