Calgary Herald

Boosting female sexuality

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U. S. federal health officials on Tuesday approved the first prescripti­on drug intended to treat women suffering from a lack of sexual desire, ending a vigorous debate over the drug’s fate. The daily pill, called Addyi, comes with warnings about risks of fainting if it is combined with certain other drugs or alcohol. Additional­ly, doctors won’t be able to prescribe it unless they complete an online certificat­ion test. Here’s a look at the new drug from Sprout Pharmaceut­icals Inc.

Q How does it work?

A Addyi, known genericall­y as flibanseri­n, acts on brain chemicals associated with mood and appetite, similar to antidepres­sant drugs. In fact, it was originally studied as a treatment for depression before being repurposed into a libido drug. It’s not entirely clear why the drug increases sexual desire but researcher­s point to its ability to increase dopamine — a brain chemical associated with appetite — while lowering serotonin — another chemical linked with feelings of satiation.

Q Who will take this drug?

A The U. S. Food and Drug Administra­tion approved Addyi for premenopau­sal women with hypoactive sexual desire disorder, described as a lack of sexual appetite that causes emotional distress.

Surveys estimate that between 5.5 million and 8.6 million U. S. women have the condition, or roughly eight to 14 per cent of women ages 20 to 49. Because so many other factors affect sexual appetite, there are a number of alternate causes doctors must rule out before diagnosing the condition, including relationsh­ip problems, medical conditions and mood issues caused by other medication­s like sleeping aids and painkiller­s.

The diagnosis is not universall­y accepted and many psychologi­sts argue that low sex drive should not be considered a medical condition.

Q I’ve heard this decision was controvers­ial. Why?

A The drug followed a long, contentiou­s path to approval, including two previous rejections by the FDA. For years, two opposing sides have argued over the fate of the drug.

On one hand, drugmakers and some medical experts argue that women need FDA- approved medication­s to treat sexual disorders, which they consider serious medical problems. On the other side, consumer- safety advocates have said the drug’s side- effects are too risky, and there are those who question whether low libido is a medical condition. On top of this debate, Sprout Pharmaceut­icals enlisted outside politician­s and women’s groups to lobby the FDA.

Q Does the drug work?

A Experts usually describe Addyi’s effect as “modest.” In company studies, women taking flibanseri­n reported a slight increase in sexually satisfying events each month. Their answers to separate questionna­ires indicated they experience­d a slight increase in desire and a slight decrease in stress. While FDA scientists describe these effects as “small,” they were significan­t enough to meet FDA effectiven­ess standards.

Q How much will it cost?

A Sprout says women who have health insurance will pay between US$ 30 and US$ 75 for a month’s supply.

Q What are the side- effects?

A About 10 per cent of patients in Sprout’s studies experience­d the most common problems: dizziness, fatigue and nausea. The drug will also bear a boxed warning that women should not drink or take certain types of other medication­s because of an interactio­n that can cause low blood pressure and fainting.

Q Why did the FDA approve Addyi this time around?

A When FDA regulators first rejected Addyi in 2010 they noted that the drug failed to achieve a key study goal — increasing desire based on patients’ daily journal entries. Because of that lack of effectiven­ess, they said, the drug’s negative side- effects outweighed its benefits.

Since then, Sprout conducted another study of sexual desire using a different method that achieved statistica­l significan­ce.

While the FDA is required to make all decisions based on science, critics say that the concerted lobbying effort by Sprout-funded supporters also played a role in Addyi’s approval.

Q When will it be available?

A Sprout plans to launch the drug in mid- October.

 ?? ALLEN G. BREED/ THE ASSOCIATED PRESS ?? After two rejections, the U. S. Food and Drug Administra­tion gave its OK Tuesday to a female sex- drive drug as a treatment for hypoactive sexual desire disorder, a first for women.
ALLEN G. BREED/ THE ASSOCIATED PRESS After two rejections, the U. S. Food and Drug Administra­tion gave its OK Tuesday to a female sex- drive drug as a treatment for hypoactive sexual desire disorder, a first for women.

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