Earlier this twelvemonth , we reportedon how the government health officials who advise the U.S.Food and Drug Administration(FDA ) had backed what is being address “ distaff Viagra , ” voting 18 - 6 in favor of the drug . It seems that the FDA has   take their advice on board , and finally give way it the dark-green - light . design to increase a womanhood ’s libido by alter chemicals in the brain , the newly approved drug   is expected to be   made available through health professionals and chemist’s shop by October this twelvemonth .

Because it crop in a different way to traditional Viagra , which simply relaxes muscle and increases profligate flow to certain regions of the body , the female version has to be taken day by day for alter the Libra of dopamine and serotonin in the learning ability . These hormones are known to play a role in sexual desire and motivation , and it ’s think that by alter these , it could help women brook from Hypoactive Sexual Desire Disorder .

It is this day-by-day dose that has been the Crux Australis of the FDA ’s emergence with the drug , called flibanserin , and is the reason   why it has   taken three attempts before the FDA would approve it . The organisation has   also previously adduce side effects such as vertigo , nausea , and broken line of descent pressure as real concerns . In plus to this , despite the manufacturer of the drug , Sprout Pharmaceuticals , claiming that between 46 and 60 % of women experienced “ good ” results , other scientistshave forestall that the real chassis is much lower , possibly in the part of 8–13 % .

To be marketed under the name Addyi , theFDA has   saidthat the drug should be taken daily for no more than eight weeks if there has been no melioration in the patient role ’s sexual libido . advocator of the birth control pill have arrogate that the only reason it has taken this long to produce a drug for intimate desire marketed at woman has been   an inherently sexist society , and orient to the fact that there are already six   separate drug propose at treating erectile dysfunction   but only   one sexual desire drug   for women .

But as the committee conclude in their June appraisal of the drug , as currently women have nothing on the market to aid them with low intimate desire , the tablet should be made uncommitted even if the benefits are moderate , furnish that it deport suitable warning and that patient are full cognizant of all side effects .