Tahor and blood alkaline phosphatase increased Patient Reports February 10, 2010

Tahor Side Effects Report #5635544-8
Tahor side effect was reported by a Physician from FRANCE on Feb 12, 2008. Female patient, weighting 135.4 lb, was diagnosed with ischaemic stroke, depression , bone pain and was treated with Tahor. After drug was administered, patient experienced the following side effects: blood alkaline phosphatase increased, transaminases increased. Tahor dosage: unknown. During the same period patient was treated with ZOLOFT, PARACETAMOL, EFFERALGAN CODEINE. 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 #4563923-9
Tahor side effect was reported by a Physician from on Jan 10, 2005. Female patient, 51 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, antinuclear antibody positive, arthralgia, autoantibody positive, blood alkaline phosphatase increased, pericarditis, peripheral ischaemia, raynaud's phenomenon. Tahor dosage: unknown. 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 #4583834-2
Tahor side effect was reported by a Physician from on Feb 02, 2005. Male patient, 31 years of age, was diagnosed with hypercholesterolaemia, ill-defined disorder, chronic myeloid leukaemia and was treated with Tahor. After drug was administered, patient experienced the following side effects: blood alkaline phosphatase increased, blood creatine increased, gamma-glutamyltransferase increased, hypercalcaemia, hyperuricaemia. Tahor dosage: 10 MG (INTERVAL: EVERY DAY), ORAL. During the same period patient was treated with CYCLOSPORINE, MYCOPHENOLATE MOFETIL, IMATINIB MESILATE, PAROXETINE. Patient was hospitalized. Patient recovered.

Tahor Side Effects Report #4589430-5
Tahor side effect was reported by a Physician from on Feb 08, 2005. Male patient, 31 years of age, was diagnosed with hypercholesterolaemia, ill-defined disorder, chronic myeloid leukaemia and was treated with Tahor. After drug was administered, patient experienced the following side effects: blood alkaline phosphatase increased, blood creatinine increased, hyperuricaemia. Tahor dosage: 10 MG (1 IN 1 D), ORAL. During the same period patient was treated with CYCLOSPORINE, MYCOPHENOLATE MOFETIL, IMATINIB MESILATE, PAROXETINE. Patient was hospitalized. Patient recovered.

Tahor Side Effects Report #5197529-8
Tahor side effect was reported by a Physician from FRANCE on Dec 27, 2006. Female patient, weighting 141.1 lb, was diagnosed with blood cholesterol increased, low density lipoprotein increased and was treated with Tahor. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, blood alkaline phosphatase increased, gamma-glutamyltransferase increased, hip arthroplasty. Tahor dosage: unknown. During the same period patient was treated with PLAVIX, ART. Patient recovered.

Tahor Side Effects Report #5342800-X
Tahor side effect was reported by a Health Professional from FRANCE on May 23, 2007. Female patient, 73 years of age, was diagnosed with diabetes mellitus, essential hypertension and was treated with Tahor. After drug was administered, patient experienced the following side effects: blood alkaline phosphatase increased, hepatic enzyme increased, hypoglycaemic coma. Tahor dosage: unknown. During the same period patient was treated with AMARYL, COTAREG, RIVOTRIL, ZYPREXA, LEVOTHYROXINE. 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.