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Erectile Dysfunction News (Page 4)
Related terms: Erection Problems, Impotence, Sexual Dysfunction, Male, ED, Impotency
FDA Medwatch Alert: Best Enhancer: Recall - Undeclared Drug Ingredient
ISSUE: FDA lab analyses found that the products to contain Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used in the treatment of male Erectile Dysfunction (ED), making these...
FDA approves Staxyn (vardenafil HCl) orally disintegrating tablets for erectile dysfunction (ED)
Philadelphia, PA & Whitehouse Station, NJ June 18, 2010 – GlaxoSmithKline and Merck & Co., Inc. announced today the U.S. Food and Drug Administration (FDA) has approved Staxyn (vardenafil HCl), an o...
FDA Medwatch Alert: Viril-ity Power (VIP) Tablets
[Posted 05/30/2008] International Pharmaceuticals, Ltd. and FDA notified consumers and healthcare professionals that the company is recalling all supplement products sold under the brand name of...
FDA Medwatch Alert: Xiadafil VIP Tablets
[Posted 05/27/2008] FDA alerted consumers and healthcare professionals not to buy or use Xiadafil VIP Tablets sold in bottles of 8 tablets (Lot #6K029) or blister cards of 2 tablets (Lot# 6K029-SEI)....
FDA Medwatch Alert: Super Shangai, Strong Testis, Shangai Ultra, Shangai Ultra X, Lady Shangai, Shangai Regular (also known as Shangai Chaojimengnan)
[Posted 12/31/2007] FDA notified consumers and healthcare professionals not to buy or use Super Shangai, Strong Testis, Shangai Ultra, Shangai Ultra X, Lady Shangai, and Shangai Regular (also known...
FDA Medwatch Alert: Energy Max
[Posted 05/10/2007] FDA informed consumers and healthcare professionals regarding the dangers associated with the purchase or use of True Man or Energy Max products promoted and sold as dietary...
FDA Medwatch Alert: V.MAX supplement product
[Posted 03/19/2007] Barodon SF and FDA notified consumers and healthcare professionals of a voluntary nationwide recall of a supplement product sold under the name V.MAX. Lab analysis by FDA of...
FDA Medwatch Alert: Rhino Max (Rhino V Max) supplement product
[Posted 03/16/2007] Cosmos Trading, Inc. and FDA notified consumers and healthcare professionals of a voluntary nationwide recall of a supplement product sold under the name Rhino Max (Rhino V Max)...
FDA Medwatch Alert: Liviro3
[Posted 01/25/2007] FDA and Ebek, Inc. notified healthcare professionals and consumers of a voluntary nationwide recall of the company's dietary supplement because the product contains tadalafil, a...
FDA Medwatch Alert: Viagra (sildenafil)
[Posted 10/18/2007] FDA informed healthcare professionals of reports of sudden decreases or loss of hearing following the use of PDE5 inhibitors Viagra, Levitra, Cialis for the treatment of erectile...
FDA Medwatch Alert: Levitra (vardenafil)
[Posted 10/18/2007] FDA informed healthcare professionals of reports of sudden decreases or loss of hearing following the use of PDE5 inhibitors Viagra, Levitra, Cialis for the treatment of erectile...
FDA Medwatch Alert: Cialis (tadalafil) - Oct 18, 2007
[Posted 10/18/2007] FDA informed healthcare professionals of reports of sudden decreases or loss of hearing following the use of PDE5 inhibitors Viagra, Levitra, Cialis for the treatment of erectile...
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