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

Zaditen Side Effects Report #4784335-9
Zaditen side effect was reported by a Physician from JAPAN on Sept 22, 2005. Male patient, 56 years of age, was diagnosed with urticaria and was treated with Zaditen. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, liver disorder. Zaditen dosage: 2 MG/DAY. During the same period patient was treated with OXAROL. Patient was hospitalized. Patient recovered.

Zaditen Side Effects Report #4806420-5
Zaditen side effect was reported by a Physician from JAPAN on Sept 22, 2005. Male patient, 56 years of age, was diagnosed with urticaria and was treated with Zaditen. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, hepatitis b , liver disorder. Zaditen dosage: 2 MG/DAY. During the same period patient was treated with OXAROL. Patient was hospitalized. Patient recovered.

Zaditen Side Effects Report #5317612-3
Zaditen side effect was reported by a Physician from JAPAN on Apr 26, 2007. Female patient, 60 years of age, weighting 154.3 lb, was diagnosed with nasopharyngitis, angina pectoris, hypertension, hyperuricaemia, gastritis and was treated with Zaditen. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood immunoglobulin e increased, blood lactate dehydrogenase increased, eosinophil count increased, gamma-glutamyltransferase increased, liver disorder. Zaditen dosage: unknown. During the same period patient was treated with LOXONIN, FLOMOX, BUFFERIN, DIOVAN, TOWAMIN, ADALAT, ALLOPURINOL, SELBEX. Patient was hospitalized. Patient recovered.

Zaditen Side Effects Report #4802102-4
Zaditen side effect was reported by a Physician from MEXICO on Oct 07, 2005. Female patient, 57 years of age, was diagnosed with hypersensitivity and was treated with Zaditen. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, anti-hbc igg antibody positive, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood lactate dehydrogenase increased, c-reactive protein increased, chills, erythema, gamma-glutamyltransferase increased. Zaditen dosage: 1 MG/DAY. Patient recovered.


Zaditen Side Effects Report #4560229-9
Zaditen side effect was reported by a Physician from on Nov 18, 2004. Female patient, child 11 years of age, weighting 72.75 lb, was diagnosed with eczema , wound infection, diarrhoea and was treated with Zaditen. After drug was administered, patient experienced the following side effects: blood alkaline phosphatase increased, blood immunoglobulin e increased, blood lactate dehydrogenase increased, eosinophil count increased, erythema multiforme, pruritus. Zaditen dosage: 2 MG/DAY. During the same period patient was treated with CEFZON, BIOFERMIN R. Patient recovered.

Zaditen Side Effects Report #5810879-4
Zaditen side effect was reported by a Physician from JAPAN on June 25, 2008. Female patient, weighting 63.93 lb, was diagnosed with eczema , loss of consciousness, constipation , hypertension and was treated with Zaditen. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood glucose increased, blood lactate dehydrogenase increased, blood pressure decreased, blood pressure increased, electroencephalogram abnormal. Zaditen dosage: 2 MG, UNK. During the same period patient was treated with ALEVIATIN, MAGNESIUM OXIDE, CORINAE L, DIOVAN, VALPROATE, LEXIN. Patient was hospitalized. Patient recovered.

Zaditen Side Effects Report #5821582-9
Zaditen side effect was reported by a Physician from JAPAN on July 18, 2008. Female patient, weighting 63.93 lb, was diagnosed with eczema , loss of consciousness, constipation , hypertension and was treated with Zaditen. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood glucose increased, blood lactate dehydrogenase increased, blood pressure decreased, blood pressure increased, electroencephalogram abnormal. Zaditen dosage: 2 MG, UNK. During the same period patient was treated with ALEVIATIN, MAGNESIUM OXIDE, CORINAE L, DIOVAN, VALPROATE, LEXIN. Patient was hospitalized. Patient recovered.

Zaditen Side Effects Report #5465255-3
Zaditen side effect was reported by a Physician from JAPAN on Sept 13, 2007. Male patient, 75 years of age, was diagnosed with dermatitis and was treated with Zaditen. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood cholesterol increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, haematuria, hepatic function abnormal. Zaditen dosage: 20 MG, QD. During the same period patient was treated with ATELEC, MICARDIS. Patient recovered.

Zaditen Side Effects Report #5518968-9
Zaditen side effect was reported by a Physician from JAPAN on Nov 09, 2007. Male patient, 75 years of age, was diagnosed with dermatitis and was treated with Zaditen. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood cholesterol increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, haematuria, hepatic function abnormal. Zaditen dosage: 20 MG, QD. During the same period patient was treated with ATELEC, MICARDIS. Patient recovered.