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Total Veregen reports: 3.Veregen FDA safety alerts: No.
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FDA Reported Veregen Side Effects: hepatic necrosis, hepatitis, blood albumin increased, muscular weakness, liver transplant, hepatic failure, encephalopathy, coagulopathy, cholestasis.
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Veregen Side Effects Report #5763758-5
Consumer or non-health professional from UNITED STATES reported VEREGEN problem on Apr 18, 2008. Male patient, 37 years of age, weighting 140.3 lb, was diagnosed with anogenital warts and was treated with VEREGEN. After drug was administered, patient experienced the following problems/side effects: blood glucose increased. VEREGEN dosage: unknown. Patient recovered.
Veregen Side Effects Report #5331700-7
VEREGEN problem was reported by a Consumer or non-health professional from UNITED STATES on May 08, 2007. Female patient, 44 years of age, was diagnosed with weight control and was treated with VEREGEN. After drug was administered, patient experienced the following problems/side effects: cholestasis, coagulopathy, encephalopathy, hepatic failure, hepatic necrosis, liver transplant, muscular weakness. VEREGEN dosage: 729 MG/DAY ORAL. During the same period patient was treated with PROGESTERONEECTIONS. Patient recovered.
Veregen Side Effects Report #5331701-9
Consumer or non-health professional from UNITED STATES reported VEREGEN problem on May 08, 2007. Female patient, 37 years of age, was diagnosed with weight control and was treated with VEREGEN. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, hepatic necrosis, hepatitis. VEREGEN dosage: 128 MG/CAPSULE ORAL 4 MONTHS IN 2005. Patient recovered.