Tahor and aspartate aminotransferase increased Patient Reports February 12, 2012

Tahor Side Effects Report #5070340-4
Tahor side effect was reported by a Physician from FRANCE on July 26, 2006. Male patient, 65 years of age, was diagnosed with prophylaxis and was treated with Tahor. After drug was administered, patient experienced the following side effects: acute pulmonary oedema, alanine aminotransferase increased, aspartate aminotransferase increased, dialysis , duodenal ulcer, haemodialysis, mallory-weiss syndrome, metabolic acidosis, renal failure acute. Tahor dosage: 10 MG (1 D); ORAL. During the same period patient was treated with DISOPYRAMIDE. Patient was hospitalized. Patient recovered.

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 #4927933-1
Tahor side effect was reported by a Physician from FRANCE on Feb 17, 2006. Male patient, 71 years of age, weighting 174.2 lb, was diagnosed with ill-defined disorder, back pain , bone pain 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, gamma-glutamyltransferase increased. Tahor dosage: 10 MG (1 D), ORAL. During the same period patient was treated with FLOCTAFENINE, ACETAMINOPHEN W, FLUINDIONE, COVERSYL, ALENDRONIC ACID, BROMAZEPAM, BUDESONIDE. 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 #5295399-0
Tahor side effect was reported by a Health Professional from FRANCE on Apr 02, 2007. Female patient, 57 years of age, was diagnosed with hyperlipidaemia and was treated with Tahor. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, eosinophilia, gamma-glutamyltransferase increased. Tahor dosage: unknown. During the same period patient was treated with EZETIMIBE. Patient was hospitalized. Patient recovered.

Tahor Side Effects Report #4634597-3
Tahor side effect was reported by a Physician from on Apr 06, 2005. Male patient, 44 years of age, was diagnosed with hyperlipidaemia and was treated with Tahor. After drug was administered, patient experienced the following side effects: amyotrophy, anuria, ascites, aspartate aminotransferase increased, blood creatine phosphokinase increased, dialysis , hepatic cirrhosis, hepatorenal syndrome, hyperkalaemia. Tahor dosage: 40 MG (40 MG, 1 IN 1 D), ORAL. During the same period patient was treated with SUCRALFATE, TAUROURSODESOXYCHOLIC ACID, PROPRANOLOL HYDROCHLORIDE. Patient was hospitalized. Patient died on 02/10/2005.

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 #4563979-3
Tahor side effect was reported by a Physician from on Jan 11, 2005. Male patient, 60 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 cholesterol increased, blood iron increased, gamma-glutamyltransferase increased, nausea , transaminases increased. Tahor dosage: 80 MG. 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 #5296875-7
Tahor side effect was reported by a Physician from FRANCE on Apr 03, 2007. Male patient, 44 years of age, was diagnosed with cardiac disorder and was treated with Tahor. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, chest pain , gamma-glutamyltransferase increased, gastritis, helicobacter infection, liver function test abnormal. Tahor dosage: unknown. During the same period patient was treated with ASPIRIN, CLOPIDOGREL, ACEBUTOLOL, PERINDOPRIL ERBUMINE, ESOMEPRAZOLE MAGNESIUM, PANTOPRAZOLE. Patient died.

Tahor Side Effects Report #5296610-2
Tahor side effect was reported by a Health Professional from FRANCE on Apr 04, 2007. Female patient, 83 years of age, was diagnosed with deep vein thrombosis  and was treated with Tahor. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, cytolytic hepatitis, lung disorder. Tahor dosage: unknown. During the same period patient was treated with ACARBOSE, MOGADON, FUROSEMIDE, PREVISCAN, FLECAINIDE ACETATE, ALLOPURINOL, TRIATEC. 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.