Since Pfizer’s male impotence wonder drug Viagra
first burst onto the scene an incredible 17 years ago, it was
subsequently joined by Eli Lily’s Cialis and Bayer’s Levitra by 2003.
Over the next 12 years the industry has witnessed variations on these such as the lower-strength Cialis Daily tablets
for the more ‘active’ male and Levitra orodispersible tablets –
especially suitable for men who aren’t comfortable with swallowing
pills, wanting to take it with some discretion and without the
requirement of a glass of water.
Men also have the options of the newer
erectile dysfunction treatment Spedra (Avanafil) or Vitaros cream –
ideal for men that have not experienced success with the aforementioned
PDE5 inhibitor tablets or cannot take PDE5s for medical reasons.
If all that wasn’t enough choice, men suffering with premature ejaculation have over-the-counter premature ejaculation treatments
such as Stud 100 Spray, condoms containing benzocaine like Durex
Performa (to prolong climax), whilst there is also prescription
medication such as Priligy, which is taken orally and works to prolong a
man’s sexual performance by an average of 200% to 300%.
Simply put, men are spoilt for choice when it comes to finding the
right treatment option for sexual dysfunction, whether this be for
persistent impotence or premature ejaculation problems.
So, what is there for women? If Medical Specialists® Pharmacy were to
quiz our thousands of patients to come up with the name of an existing
female sexual dysfunction treatment, we’d be surprised if anyone could
muster a reply.
In early 2014 Medical Specialists® reported
how British pharmaceutical company ORLIBID were developing a drug
tentatively titled ‘ORL101’, aimed at boosting a woman’s sex drive,
however no further information has been released about ORL101 since
then.
However, Medical Specialists® are delighted to announce that a new
pill to boost a woman’s libido could be one step closer after US experts
gave its endorsement. This will be fantastic news for those that have
fought for women’s sex drives to get a similar medical attention to deal
put into it as the male treatments.
A panel of Food and Drug Administration (FDA) advisers decided to
vote 18-6 in favour of recommending flibanserin, a daily pill nicknamed
the ‘female Viagra’ and manufactured by Sprout Pharmaceuticals, who
picked up the drug back in 2011 after its initial developer, Boehringer
Ingelheim, decided to drop it.
The vote came following a testimony from various women who vigorously
persuaded the agency to approve the drug and told of their fear of
never being able to have sex again. The final judgement of course will
have to come from the FDA themselves, with a verdict on suitability for
public use due later this year.
Coincidentally, flibanserin, just like the discovery of Viagra, was
an unintended find. The drug was firstly developed with the intention of
treating depression, but wasn’t as effective for this purpose as
expected.
Many of the 11,000 women involved in the trials did note that they
were experiencing some rather unexpected side effects from the
flibanserin. Increased sexual interest and overall, more satisfying
sexual experiences than previous, were being commonly reported.
North Carolina drug maker Sprout Pharmaceuticals, have claimed that
their clinical trials have demonstrated that women have experienced a
37% rise in sexual desire in comparison to a placebo. The women reported
an average of between 0.5 and one more sexually satisfying events each
month, compared to those women taking a placebo. In addition, they had
higher scores on questionnaires on desire and scored lower on questions
about stress.
The drug – which changes brain chemistry as opposed to Viagra
increasing blood flow – isn’t without a chequered history though, with
the FDA twice rejecting the drug since 2010, arguing flibanserin’s
benefits did not outweigh the risks, which can include low blood
pressure and fainting spells.
However, Susan Scanlan, chairwoman of Even The Score, hit back and
noted that Viagra can have varying side effects, arguing that the FDA
hasn’t approved flibanserin because of their discomfort with women
taking control over their sexuality. “The implication is that men can be
trusted to make a rational decision of risk versus reward and women
can’t,” she said.
The FDA has highlighted female sexual dysfunction as one of 20
priority areas of unmet medical need, and is obviously a major and
genuine health problem that needs to be addressed.
Keep checking the Medical Specialists® NHS Pharmacy website for
further updates about flibanserin or other female sexual dysfunction
products that may become available in the future, and we already have an
extension range of male impotence and premature ejaculation treatments,
some of which were mentioned earlier.
Showing posts with label vitaros. Show all posts
Showing posts with label vitaros. Show all posts
Thursday, 18 June 2015
Monday, 17 September 2012
New erectile dysfunction drug in the pipeline
Apricus Biosciences Inc. has entered into an exclusive license agreement with Takeda Pharmaceuticals International, to market Vitaros, a treatment for erectile dysfunction in the UK. The marketing authorization application for Vitaros, was accepted by the European Medicines Agency (EMA) for review in June 2011 and the license is anticipated in 2013.
European health regulators approved a marketing application for Vitaros last year. According to market researcher IMS Health, the erectile dysfunction (ED) market in the U.K. was valued at 202 million euros in 2011.
“We look forward to expanding the reach of our Vitaros product for erectile dysfunction in the U.K., the second largest ED market inEurope”, Apricus’ chief executive Bassam Damaj said in a statement.
Apricus say that, “Vitaros is a topically delivered formulation of alprostadil delivered with Dodecyl 2-N, N-(dimethylamino)-propionate hydrochloride (DDAIP HCl), Apricus’ proprietary NexACT delivery technology, for the treatment of erectile dysfunction.
When absorbed through the skin, alprostadil, a vasodilator, directly boosts blood flow, thereby causing an erection. The NexACT technology is designed to enhance the delivery of an active drug, to improve therapeutic outcomes and cut down systemic side effects, associated with oral and injectable medications.
Vitaros has received marketing authorization in Canada and is being marketed by Abbott Laboratories Ltd. In theUSA, commercial rights to Vitaros have been licensed to Warner Chilcott. Agreements have also been signed with Sandoz-Novartis in Germany, Bracco inItaly, Elis Pharmaceuticals in certain Middle East, and Neopharm inIsraelfor marketing the erectile dysfunction therapy.
This application for Vitaros to the EMA comes hot on the heels of Stendra (avanafil), which received approval inAmericafrom the Food and Drug Administration (FDA). Stendra is the latest in line to try and steal Viagra’s crown as the best selling erectile dysfunction drug, however whilst Stendra has been approved in America, it has yet to receive approval in the UK and Europe.
Currently in the UK we have available Viagra, Cialis and Levitra, which are approved for the treatment of erectile dysfunction. Here at Medical Specialists, we have helped many men suffering from erectile dysfunction through our discreet, online consultation process. One thing for sure is, if the likes of Stendra and Vitaros receive approval in the UK in the coming years, then we here at Medical Specialists will be stocking it, to provide our patients with the widest choice and range of erectile dysfunction drugs.
Subscribe to:
Posts (Atom)
