BONTRIL Safety Questions, BONTRIL Answers
More Here>>Side Effects - FDA Reports 2006-2008
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BONTRIL Safety Reports
Total BONTRIL reports: 1.BONTRIL FDA safety alerts: No.
Reported hospitalizations: 1.
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Physician from ITALY reported BONTRIL problem on July 12, 2006. Female patient, 37 years of age, was diagnosed with decreased appetite and was treated with BONTRIL. After drug was administered, patient experienced the following problems/side effects: cardiac murmur, congestive cardiomyopathy, cyanosis, dilatation atrial, dilatation ventricular, endocardial fibrosis, epigastric discomfort, mitral valve incompetence, palpitations. BONTRIL dosage: 105 MG, BID,. During the same period patient was treated with CYPROTERONE, ETHINYL ESTRADIOL. Patient was hospitalized. Patient recovered.