Copegus and alanine aminotransferase increased Patient Reports February 12, 2012

Copegus Side Effects Report #4713430-5
Copegus side effect was reported by a Health Professional from UNITED STATES on July 13, 2004. Female patient, 53 years of age, weighting 177.0 lb, was diagnosed with hepatitis c  and was treated with Copegus. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, alpha 1 foetoprotein increased, aspartate aminotransferase increased, globulins increased, haematocrit decreased, haemoglobin decreased, lymphocyte count decreased, mean cell haemoglobin concentration decreased, neutrophil count decreased. Copegus dosage: unknown. During the same period patient was treated with PEGASYS. Patient recovered.

Copegus Side Effects Report #6082319-4
Copegus side effect was reported by a Health Professional from UNITED STATES on Jan 03, 2008. Male patient, 47 years of age, weighting 246.0 lb, was diagnosed with hepatitis c  and was treated with Copegus. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood albumin decreased, blood bilirubin increased, fatigue, haematocrit decreased, haemoglobin decreased, neutrophil count decreased, no therapeutic response. Copegus dosage: 1400 MG DAILY ORAL. During the same period patient was treated with INFERGEN, NADOLOL, FUROSEMIDE, OMEPRAZOLE, LISINOPRIL. Patient recovered.

Copegus Side Effects Report #5525290-3
Copegus side effect was reported by a Physician from GERMANY on Nov 12, 2007. Male patient, 30 years of age, was diagnosed with hepatitis c  and was treated with Copegus. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, gamma-glutamyltransferase increased, infectious mononucleosis . Copegus dosage: unknown. During the same period patient was treated with PEGASYS. Patient recovered.

Copegus Side Effects Report #5633492-0
Copegus side effect was reported by a Physician from JAPAN on Feb 13, 2008. Female patient, 59 years of age, weighting 83.78 lb, was treated with Copegus. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, pulmonary hypertension , right ventricular failure. Copegus dosage: unknown. During the same period patient was treated with PEGASYS, THYRADIN S, SOLON. Patient died on 11/10/2007.


Copegus Side Effects Report #5657442-6
Copegus side effect was reported by a Physician from JAPAN on Feb 27, 2008. Female patient, 59 years of age, weighting 83.78 lb, was treated with Copegus. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, anaemia, aspartate aminotransferase increased, pulmonary hypertension , right ventricular failure. Copegus dosage: unknown. During the same period patient was treated with PEGASYS, THYRADIN S, THYRADIN S, SOLON, TAKEPRON, CETAPRIL, ZYLORIC. Patient died on 11/10/2007.

Copegus Side Effects Report #5700059-5
Copegus side effect was reported by a Physician from JAPAN on Apr 01, 2008. Female patient, weighting 83.78 lb, was treated with Copegus. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, anaemia, aspartate aminotransferase increased, pulmonary hypertension , right ventricular failure. Copegus dosage: unknown. During the same period patient was treated with PEGASYS, THYRADIN S, THYRADIN S, SOLON, TAKEPRON, CETAPRIL, ZYLORIC. Patient died on 11/10/2007.