Flibanserin, the drug that gives women one extra sexually satisfying experience every two months

Australia hasn’t followed suit, though flibanserin is available through internet pharmacies. However, its limited effectiveness and serious side-effects should cause potential users to rethink purchasing flibanserin online.

What does it ‘treat’?

Hypo-active sexual desire disorder HSDD was listed in the DSM-4, the previous edition of the Diagnostic and Statistical Manual of Mental Disorders. The disorder relates to persistently deficient (or absent) sexual fantasies and desire for sexual activity, which causes marked distress and relationship problems.

For a diagnosis, HSDD could not be due to the physiological effects of a substance or a general medical condition. Estimates of the prevalence of sexual desire problems vary widely depending on the criteria used – from 3% to 31% in one study. Others suggest up to 43% of women may experience low sexual desire.

However, there is fierce debate about the definition of disorders of sexual desire, with HSDD described as a “highly controversial diagnostic construct”.

The newer DSM-5, published in May 2013, combined features of HSDD and another condition known as female sexual arousal disorder, to form a new condition, female sexual interest/arousal disorder (FSIAD). This has stricter diagnostic criteria and as yet unknown prevalence.

Originally trialled as an antidepressant, flibanserin found new life as a treatment for low sexual desire in women.

After being rejected for approval by the FDA in 2010, developers Boehringer Ingelheim transferred the rights to Sprout Pharmaceuticals, which finally and controversially secured FDA approval in August 2015.

How it works

Flibanserin modulates neurotransmitters in the brain, increasing levels of dopamine and norepinephrine and decreasing serotonin.

As dopamine and norepinephrine promote sexual arousal, and serotonin reduces sexual arousal, flibanserin may increase libido by improving the balance between these neurotransmitter systems.

Problems and controversies

The US FDA approval process was mired in controversy, particularly in relation to the active role of Sprout Pharmaceuticals in lobbying. It funded a high-profile public advocacy campaign called Even the Score, which misleadingly claimed the drug was initially rejected because of FDA sexism.

Despite counter campaigns by scientists and doctors, the FDA scientific advisory committee voted 18 to six in favour of approving the drug, with the condition that risk-management options were put in place.

The committee members were concerned the drug had significant risks from side-effects, particularly if used off label or taken in combination with alcohol, and few benefits. The committee’s recommendation that the drug be approved therefore attracted widespread criticism that it allowed politics to trump clinical science.

Within hours of the FDA approval, Sprout Pharmaceuticals was acquired by Valeant for $US1 billion. Valeant set the price of Addyi at $US800 per month, leading to accusations of price gouging.

Sales flagged as insurers refused to cover the drug. With its stock value plummeting, Valeant reportedlydismissed the drug’s entire sales team and said it planned to reintroduce the drug at a later date. The company may be waiting until the 18-month restriction on direct-to-consumer marketing is over.

Safety and efficacy

A recent review of studies – including five published and three unpublished randomised clinical trials involving 5,914 women – concluded the overall quality of the evidence for both efficacy and safety outcomes was very low.

The published studies reported more favourable outcomes than unpublished studies. The authors’ attempts to gain further information from study leaders and sponsors were not successful.

Side-effects include dizziness (11.4% of users), drowsiness (11.2%), nausea (10.4%), fatigue (9.2%), insomnia (4.9%) and dry mouth (2.4%). The most serious problems – low blood pressure and a resulting loss of consciousness – are amplified by concurrent alcohol use.

Other serious adverse events were uncommon but flibanserin can’t be viewed as safe without further studies including a broader range of diverse women.

The FDA approved flibanserin on condition it carry a black-box warning not to drink alcohol while taking the medication.

The manufacturer is also required to undertake three additional studies to examine the side-effects among women using alcohol with the drug. Strangely, the evidence about alcohol interactions with flibanserin presented to the FDA included data on 25 healthy volunteers, of whom only two were women.

Side-effects are lessened if taken at night, but it has been reported about one out of every eight women will discontinue flibanserin because of adverse effects.

A rigorous meta-analysis showed that, on average, flibanserin led to one-half an additional sexually satisfying event per month. This is a less optimistic finding than the (still underwhelming) one extra sexually satisfying event per month frequently quoted by reports.

Availability and cost

Flibanserin is approved for prescription only in the US; it is not available in Australia. US doctors must be certified before prescribing it, and dispensing pharmacists must also complete training.

In the first month it was available, Addyi (the brand name of flibanserin) was prescribed just 227 times, compared with more than half a million for Viagra in its first month. Doctors had prescribed the drug fewer than 4,000 times as of February this year.

In the US, a one-month supply of flibanserin (one 100mg tablet per day, taken at bed time) costs between $US200 to $US830, depending on insurance coverage and means of acquisition. That’s a lot of money for an extra sexually satisfying experience every two months.

This article was originally published on The Conversation. Read the original article.