Duricef and hepatic function abnormal Patient Reports February 13, 2012

Duricef Side Effects Report #5485977-8
Duricef side effect was reported by a Consumer or non-health professional from INDONESIA on Sept 28, 2007. Male patient, 51 years of age, was treated with Duricef. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, arthralgia, aspartate aminotransferase increased, blood alkaline phosphatase increased, dermatitis exfoliative, hepatic function abnormal, lymphocyte morphology abnormal, myalgia. Duricef dosage: 500 MG, BID. Patient was hospitalized. Patient recovered.

Duricef Side Effects Report #5423106-7
Duricef side effect was reported by a Consumer or non-health professional from JAPAN on Aug 09, 2007. Male patient, 29 years of age, was treated with Duricef. After drug was administered, patient experienced the following side effects: hepatic function abnormal, pancreatitis, toxic epidermal necrolysis. Duricef dosage: unknown. During the same period patient was treated with COLD REMEDY, STOMACHIC AND DIGESTIVES. Patient was hospitalized. Patient recovered.

Duricef Side Effects Report #5766951-0
Duricef side effect was reported by a Health Professional from JAPAN on May 23, 2008. Male patient, 29 years of age, was treated with Duricef. After drug was administered, patient experienced the following side effects: hepatic function abnormal, pancreatitis, toxic epidermal necrolysis. Duricef dosage: unknown. During the same period patient was treated with COLD REMEDY, STOMACHIC AND DIGESTIVES. Patient was hospitalized. Patient recovered.