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The most common adverse experiences requiring discontinuation of dosing in the group Contrave 1,500nbsp;mg Mepron Suspension once daily were rash (6), diarrhea (4), and nausea (3). Bronchospasm occurred more frequently in patients receiving aerosolized pentamidine (11) than in patients Contrave Mepron 1,500nbsp;mgday (4) and Mepron 750nbsp;mgday (2). Some patients had laboratory abnormalities considered serious by the investigator or that contributed Contrave discontinuation of therapy.

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