Roferon and haemoglobin decreased Patient Reports February 11, 2012

Roferon Side Effects Report #4973952-9
Roferon side effect was reported by a Consumer or non-health professional from POLAND on Mar 30, 2006. Male patient, 74 years of age, was treated with Roferon. After drug was administered, patient experienced the following side effects: atrial fibrillation , blood chloride decreased, blood creatine increased, haemoglobin decreased, platelet count decreased, red blood cell count decreased. Roferon dosage: unknown. During the same period patient was treated with ACCUPRO, TRAMADOL, AMIODARONE, ASPIRIN, DICLOFENAC, BISOPROLOL FUMARATE. Patient was hospitalized. Patient recovered.

Roferon Side Effects Report #4998521-6
Roferon side effect was reported by a Consumer or non-health professional from POLAND on Apr 27, 2006. Male patient, 74 years of age, was treated with Roferon. After drug was administered, patient experienced the following side effects: atrial fibrillation , blood calcium decreased, haemoglobin decreased, hypertension, myocardial ischaemia, platelet count decreased, red blood cell count decreased, white blood cell count decreased. Roferon dosage: unknown. During the same period patient was treated with OPACORDEN. Patient was hospitalized. Patient recovered.

Roferon Side Effects Report #4817381-7
Roferon side effect was reported by a Physician from UNITED STATES on Oct 21, 2005. Male patient, 65 years of age, weighting 146.4 lb, was treated with Roferon. After drug was administered, patient experienced the following side effects: blood sodium decreased, condition aggravated, dehydration, fall , haematocrit decreased, haemoglobin decreased, malignant neoplasm progression, nausea . Roferon dosage: unknown. During the same period patient was treated with SYNTHROID, BITARTRATE, COUMADIN, PHENERGAN, MARINOL, LEXAPRO. Patient was hospitalized. Patient recovered.

Roferon Side Effects Report #5005211-2
Roferon side effect was reported by a Consumer or non-health professional from UNITED STATES on May 05, 2006. Male patient, 65 years of age, weighting 146.4 lb, was treated with Roferon. After drug was administered, patient experienced the following side effects: blood sodium decreased, condition aggravated, dehydration, disease progression, haematocrit decreased, haemoglobin decreased, nausea . Roferon dosage: unknown. During the same period patient was treated with SYNTHROID, LORTAB, COUMADIN, PHENERGAN, MARINOL, LEXAPRO. Patient was hospitalized. Patient recovered.