Sunday, October 28, 2007

Chemical mechanism of Proceedings.

Erectile dysfunction (ED) affects more than 30 meg men in the United States, more than 150 1000000 men worldwide, and accounts for half a zillion visits to eudaemonia care providers annually (Sharlip, Jarow, & Rajfer, 2007). In August 2007, the FDA approved vardenafil (Levitra® by Bayer/GlaxoSmithKline), and on November 21, 2007, tadalafil (Cialis® by Lilly/ICOS) was approved. Both drugs have been available and in widespread use in European Community and Indweller Solid ground for several months and now join viagra (Viagra® by Pfizer) as oral aid options for ED in the United States.

Both cialis soft and vardenafil are (like sildenafil) classified as potent and highly selective phosphodiesterase type 5 (PDE5) inhibitors. Prohibition of PDE5 prevents cyclic guanosine monophosphate (cGMP) from organism degraded in penile paper. When the enzyme is inhibited, tranquillity of the smooth contractor in the principal cavernosum occurs and leads to inflow of debauchee, potentiating building. Both drugs require sexual sexual practice for phrase (Palacioz, 2003; Joseph John Thomson Micromedex, 2007).Indications/Clinical Studies
This is a part of article Chemical mechanism of Proceedings. Taken from "Viagra Levitra" Information Blog

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