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The Indian regulatory authorities have approved Acomplia for prescription but they have also allowed the production of generic versions of the drug...
Well, as we have been predicting here for weeks, Acomplia was not withdrawn from the European market when the European Medicines Agency’s Committee on Medicinal Products for Human Use reported earlier today...
The European Medicines Agency’s Committee on Medicines for Human Use is meeting in London this week and amongst other matters, the committee will be deliberating over the post marketing safety data for Acomplia...
New information on Acomplia has come to light that may explain why the FDA committee was reluctant to recommend it for approval in the USA...
The European Medicines Agency has announced that it is currently reviewing additional safety data on Acomplia and it will make an announcement on either 19th or 20th July regarding the future of Acomplia...