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Priligy is believed to increase the time it takes to ejaculate by increasing the amount of a neurotransmitter between the nerve cells. The grounds for the referral were concerns over the benefit-risk balance of the 60 mg tablet by some Member States, who considered its additional benefit compared with the 30 mg tablet to be too modest when weighed against the increased risk of severe cases of syncope fainting seen in studies with the medicine. Based on the evaluation of the currently available data and the scientific discussion within the Committee, the CHMP concluded that the benefits of Priligy 60 mg outweigh its risks, and that therefore the marketing authorisation for Priligy 30 mg and 60 mg should be granted in all concerned Member States. The CHMP also concluded that the potential increased risk for syncope has been proven to be manageable. Patients should not start treatment with 60 mg tablets, and may only be switched to 60 mg if they have not responded sufficiently to the 30 mg tablets and have not experienced moderate or severe adverse reactions or symptoms suggestive of syncope. Current status. European Commission final decision. Expand section Collapse section. Priligy is a medicine used to treat premature ejaculation in men aged 18 to 64 years old. The European Commission issued a decision on 20 January
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