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Imurel Safety Reports
Total Imurel reports: 4.Imurel FDA safety alerts: No.
Reported deaths: 2 Reported hospitalizations: 2.
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Reported Imurel Side Effects: blood creatine phosphokinase increased, hypoxia, hyperkalaemia, dyspnoea, cytomegalovirus infection, cough, bradycardia, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, vomiting, transaminases increased.
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Imurel Side Effects Report #5207208-6
Consumer or non-health professional from FRANCE reported IMUREL problem on Jan 08, 2007. Female patient, 26 years of age, weighting 132.3 lb, was diagnosed with mixed connective tissue disease, pericarditis, autoimmune thyroiditis and was treated with IMUREL. After drug was administered, patient experienced the following problems/side effects: aldolase increased, blood creatine phosphokinase increased, blood immunoglobulin a increased, blood immunoglobulin g increased, blood thyroid stimulating hormone increased, cholestasis, gamma-glutamyltransferase increased, hepatic failure, hepatocellular damage. IMUREL dosage: 100MG PER DAY. During the same period patient was treated with CLAMOXYL, ASPEGIC, COLCHIMAX, LEVOTHYROXINE, RULID. Patient was hospitalized. Patient recovered.
Imurel Side Effects Report #5123854-2
IMUREL problem was reported by a Consumer or non-health professional from FRANCE on Sept 28, 2006. Female patient, 40 years of age, was diagnosed with prophylaxis against transplant rejection and was treated with IMUREL. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, blood lactate dehydrogenase increased, bradycardia, cough, cytomegalovirus infection, dyspnoea, hyperkalaemia, hypoxia, multi-organ failure. IMUREL dosage: unknown. During the same period patient was treated with WELLVONE, BACTRIM, CYMEVAN, PROGRAF, XIGRIS. Patient died on 07/24/2006.
Imurel Side Effects Report #5129687-5
Consumer or non-health professional from FRANCE reported IMUREL problem on Sept 28, 2006. Female patient, 40 years of age, was diagnosed with prophylaxis against transplant rejection and was treated with IMUREL. After drug was administered, patient experienced the following problems/side effects: asthenia, blood creatine phosphokinase increased, blood lactate dehydrogenase increased, bradycardia, cough, cytomegalovirus infection, dyspnoea, hyperkalaemia, hypoxia. IMUREL dosage: unknown. During the same period patient was treated with WELLVONE, BACTRIM, CYMEVAN, PROGRAF, XIGRIS. Patient died on 07/24/2006.
Imurel Side Effects Report #5142371-7
IMUREL problem was reported by a Consumer or non-health professional from FRANCE on Oct 25, 2006. Male patient, 72 years of age, was diagnosed with polyarthritis, bronchitis and was treated with IMUREL. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, anorexia, blood alkaline phosphatase increased, diarrhoea, gamma-glutamyltransferase increased, hepatitis, transaminases increased, vomiting. IMUREL dosage: unknown. During the same period patient was treated with CLAMOXYL, CORTICOID. Patient was hospitalized. Patient recovered.