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<p>At its meeting in February 2014, the Pharmacovigilance Risk Assessment Committee
(PRAC) of the European Medicines Agency recommended that the product information for
mefloquine be amended to state that neuropsychiatric adverse reactions may persist
for months, or longer, even after discontinuation of the drug. The PRAC did not recommend
that such reactions should be listed as permanent. The United Kingdom product information
for mefloquine reflects the final PRAC recommendation.</p><p> </p>
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