About Cialis

Posted by Pharmaceutical-Stuff on Saturday 23 February 2008

How works:
When an goes limp, you have PDE5 to thank. Specialized tissue produces a substance called cyclic guanosine monophosphate (cGMP) in response to sexual stimulation. The more cGMP available, the more durable the . inhibits the PDE5 enzyme, preserving cGMP levels, therefore aiding viability and durability.

About Cialis

  • was developed by , a relatively small biotech company located in Washington State, in the United states. has formed a 50/50 joint venture with American Pharmaceutical Giant, Eli Lilly & company. The partnership is called Lilly .
  • is known as the ” 36 hour pill” or the “weekend pill” because unlike other similar drugs, has a long duration of action.
  • received approval for use in the United States November 21, 2003.
  • is a member of a family of drugs known as PDE5 enzyme inhibitors.
  • is a member of a family of drugs called PDE5 Inhibitors. is now marketed in approximately 40 countries and is available by prescription in pharmacies on five continents.
  • blocks an enzyme that causes an to go flaccid. Although is similar to and , its dose, onset of action, and duration of action is unique.

Some very smart scientists discovered that cyclic guanosine monophosphate (cGMP) was the key to sustaining an . They discovered that when a man gets stimulated, a chain reaction occurs in the tissue of the that in elevated levels of a substance called cyclic guanosine monophosphate (cGMP). As long as there are sufficient levels of cGMP, the can remain erect. The more cGMP, the more robust and durable the . If you inhibit the degradation of cGMP it stays around in the longer, producing a more durable . Another way you can think of (and all other similar medicines) is that it preserves the elevated levels of cGMP that are created when a man is stimulated for a stronger, more lasting .

That’s how works - blocks the enzyme phosphodiesterase-5 (PDE5) which is responsible for the neutralization of cGMP. (tadalafil) is a highly selective inhibitor of PDE5. (PDE5 is not the only phosphodiesterase involved in the erectile physiology but it appears to be the most important one). The nice thing about PDE5 blockers is that they shouldn’t cause erections at inappropriate times because they only block degradation of cGMP produced in reaction to sexual stimulation, such as thinking about something sexy. If you are not being stimulated, there is no cGMP to protect, so the drug remains in the background.

Dose:
is available 10mg and 20mg tablets. The recommended dose is 10mg taken prior to anticipated sexual activity and without regard to food. In those patients in whom tadalafil 10mg does not produce an adequate effect, 20mg might be tried. It can be taken from 30 minutes to 12 hours prior to sexual activity. The efficacy of tadalafil may persist up to 24 hours post-dose.
The maximum recommended dose is one pill per day.

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