Tahor and blood lactate dehydrogenase increased Patient Reports February 12, 2012

Tahor Side Effects Report #4596828-8
Tahor side effect was reported by a Physician from on Feb 16, 2005. Male patient, 81 years of age, was diagnosed with ill-defined disorder and was treated with Tahor. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood creatine phosphokinase increased, blood lactate dehydrogenase increased, bronchial infection, myalgia, renal failure. Tahor dosage: 10 MG (1 IN 1 D), ORAL. During the same period patient was treated with ACETYLSALICYLIC ACID SRT, ATENOLOL, AMLODIPINE BESYLATE. Patient was hospitalized. Patient recovered.

Tahor Side Effects Report #4648621-5
Tahor side effect was reported by a Physician from on Apr 18, 2005. Female patient, 75 years of age, was diagnosed with ill-defined disorder and was treated with Tahor. After drug was administered, patient experienced the following side effects: blood bilirubin increased, blood lactate dehydrogenase increased, coombs test positive, haemolytic anaemia, jaundice , pituitary tumour benign. Tahor dosage: 10 MG (1 D), ORAL. During the same period patient was treated with DOSTINEX, VALPROMIDE, CLONAZEPAM. Patient was hospitalized. Patient recovered.

Tahor Side Effects Report #4672760-6
Tahor side effect was reported by a Physician from on May 16, 2005. Female patient, 70 years of age, was diagnosed with ill-defined disorder, bronchitis  and was treated with Tahor. After drug was administered, patient experienced the following side effects: aspartate aminotransferase increased, asthenia, biopsy muscle abnormal, blood creatine phosphokinase increased, blood lactate dehydrogenase increased, bronchitis , c-reactive protein increased, dermatomyositis, dilatation ventricular. Tahor dosage: unknown. During the same period patient was treated with KETEK, ACTONEL. Patient was hospitalized and became disabled. Patient recovered.

Tahor Side Effects Report #4676991-0
Tahor side effect was reported by a Physician from on May 16, 2005. Female patient, 70 years of age, was diagnosed with ill-defined disorder, bronchitis  and was treated with Tahor. After drug was administered, patient experienced the following side effects: asthenia, blood creatine phosphokinase increased, blood lactate dehydrogenase increased, bronchitis , dermatomyositis, dyspnoea exertional, mobility decreased, motor dysfunction, muscle disorder . Tahor dosage: unknown. During the same period patient was treated with KETEK, ACTONEL. Patient was hospitalized. Patient recovered.


Tahor Side Effects Report #5036574-X
Tahor side effect was reported by a Physician from FRANCE on June 13, 2006. Female patient, 57 years of age, was diagnosed with ill-defined disorder and was treated with Tahor. After drug was administered, patient experienced the following side effects: blood lactate dehydrogenase increased, cholestasis, gamma-glutamyltransferase increased. Tahor dosage: (40 MG), ORAL. During the same period patient was treated with ACETAMINOPHEN W, FLUINDIONE, OMEPRAZOLE, RAMIPRIL, BISOPROLOL FUMARATE, TINZAPARIN. Patient was hospitalized. Patient recovered.

Tahor Side Effects Report #4559544-4
Tahor side effect was reported by a Physician from on Jan 10, 2005. Male patient, 77 years of age, was diagnosed with hypercholesterolaemia and was treated with Tahor. After drug was administered, patient experienced the following side effects: abdominal pain , blood creatine phosphokinase increased, blood lactate dehydrogenase increased, c-reactive protein increased, diverticulitis, electrocardiogram abnormal, myoglobin blood increased, pyrexia, rhabdomyolysis. Tahor dosage: 10 MG (1 IN 1 D), ORAL. During the same period patient was treated with ACARBOSE, LACTOBACILLUS BIFIDUS, OMEPRAZOLE, HEXAQUINE, DILTIAZEM HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Tahor Side Effects Report #5044316-7
Tahor side effect was reported by a Physician from FRANCE on June 19, 2006. Male patient, 65 years of age, weighting 165.3 lb, was diagnosed with hypercholesterolaemia and was treated with Tahor. After drug was administered, patient experienced the following side effects: abdominal pain upper, acute pulmonary oedema, alanine aminotransferase increased, anxiety , arrhythmia , aspartate aminotransferase increased, blood calcium decreased, blood lactate dehydrogenase increased, blood pressure systolic increased. Tahor dosage: 10 MG (10 MG, 1 IN 1 D). During the same period patient was treated with DISOPYRAMIDE, VALPROATE, LOSARTAN POTASSIUM. Patient was hospitalized. Patient recovered.

Tahor Side Effects Report #4618546-X
Tahor side effect was reported by a Physician from on Mar 17, 2005. Female patient, 54 years of age, was diagnosed with hypercholesterolaemia and was treated with Tahor. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood amylase increased, blood lactate dehydrogenase increased, blood triglycerides increased, cholelithiasis, gamma-glutamyltransferase increased. Tahor dosage: 20 MG (20 MG, 1 IN 1 D). Patient was hospitalized. Patient recovered.

Tahor Side Effects Report #5093356-0
Tahor side effect was reported by a Physician from FRANCE on Aug 16, 2006. Male patient, 51 years of age, was treated with Tahor. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood creatine phosphokinase increased, blood creatinine increased, blood lactate dehydrogenase increased, blood triglycerides increased, cholestasis. Tahor dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with DALACIN, PLAVIX, RAMIPRIL, SECTRAL, OMEPRAZOLE, LEXOMIL, BACTRIM, ACENOCOUMAROL. Patient was hospitalized. Patient recovered.