Copegus and fatigue Patient Reports February 10, 2010

Copegus Side Effects Report #5308026-0
Copegus side effect was reported by a Consumer or non-health professional from UNITED STATES on Jan 02, 2006. Male patient, 53 years of age, weighting 257.9 lb, was diagnosed with hepatitis c  and was treated with Copegus. After drug was administered, patient experienced the following side effects: fatigue, nausea , red blood cell count decreased. Copegus dosage: unknown. Patient recovered.

Copegus Side Effects Report #4896609-1
Copegus side effect was reported by a Consumer or non-health professional from UNITED STATES on Nov 30, 2005. Female patient, 53 years of age, was diagnosed with hepatitis c  and was treated with Copegus. After drug was administered, patient experienced the following side effects: anaemia, fatigue, rheumatoid arthritis . Copegus dosage: unknown. During the same period patient was treated with COMBIVENT INHALER, DEPAKOTE, FLONASE, KLONOPIN, SEROQUEL, SPIRONOLACTONE, ZANTAC. Patient recovered.

Copegus Side Effects Report #5164561-X
Copegus side effect was reported by a Health Professional from GERMANY on Sept 22, 2006. Male patient, 52 years of age, weighting 227.1 lb, was diagnosed with hepatitis c  and was treated with Copegus. After drug was administered, patient experienced the following side effects: depression , disturbance in attention, dry mouth, dyspnoea, emotional distress, fatigue, hypertrophic cardiomyopathy, influenza like illness, mental disorder. Copegus dosage: unknown. During the same period patient was treated with PEGASYS, INTERFERON NOS, AMANTADINE, ESCITALOPRAM OXALATE. 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 #5157779-3
Copegus side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 12, 2005. Female patient, 46 years of age, weighting 300.0 lb, was diagnosed with hepatitis c  and was treated with Copegus. After drug was administered, patient experienced the following side effects: anaemia, blood glucose decreased, dyspnoea, fatigue, haemoglobin decreased, loss of consciousness, refusal of treatment by patient, syncope. Copegus dosage: unknown. During the same period patient was treated with TYLENOL. Patient was hospitalized and became disabled. Patient recovered.

Copegus Side Effects Report #4805741-X
Copegus side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 12, 2005. Female patient, 46 years of age, weighting 300.0 lb, was diagnosed with hepatitis c  and was treated with Copegus. After drug was administered, patient experienced the following side effects: anaemia, blood glucose decreased, dyspnoea, fatigue, loss of consciousness, refusal of treatment by patient, syncope, vaginal haemorrhage. Copegus dosage: unknown. During the same period patient was treated with TYLENOL. Patient was hospitalized and became disabled. Patient recovered.

Copegus Side Effects Report #5157735-5
Copegus side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 12, 2005. Male patient, 40 years of age, weighting 216.1 lb, was diagnosed with hepatitis c  and was treated with Copegus. After drug was administered, patient experienced the following side effects: anaemia, anorexia, asthenia, blood glucose abnormal, convulsion, fatigue, hepatomegaly, loss of consciousness, platelet count decreased. Copegus dosage: unknown. During the same period patient was treated with PROZAC, SEROQUEL, TEGRETOL, TRAZODONE, TYLENOL W, ULTRAM. Patient recovered.

Copegus Side Effects Report #5061179-4
Copegus side effect was reported by a Consumer or non-health professional from UNITED STATES on June 29, 2006. Male patient, 33 years of age, was treated with Copegus. After drug was administered, patient experienced the following side effects: abortion spontaneous, anaemia, anger, dyspnoea, ear infection , fatigue, heart rate increased, impaired healing, irritability. Copegus dosage: unknown. During the same period patient was treated with PEGASYS. Patient recovered.