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CARNITINE DECREASED side effect

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Cerezyme Side Effects Report #5369941-5
Physician from JAPAN reported CEREZYME problem on June 11, 2007. Female patient, child 2 years of age, weighting 22.05 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: carnitine decreased, condition aggravated, gaucher's disease, . CEREZYME dosage: unknown. During the same period patient was treated with DIAZEPAM, MIDAZOLAM, CHLORAL HYDRATE, PHENOBARBITOL, POTASSIUM BROMIDE, VALPROATE, LEVODOPA. Patient died on 04/17/2006.

Depakote Side Effects Report #5588943-7
DEPAKOTE ER problem was reported by a Physician from UNITED STATES on Jan 03, 2008. Male patient, weighting 6.69 lb, was treated with DEPAKOTE ER. After drug was administered, patient experienced the following problems/side effects: anaemia, carnitine decreased, cyanosis, heart rate decreased, metabolic acidosis, pallor, sluggishness, small for dates baby, thrombocytopenia, . DEPAKOTE ER dosage: unknown. During the same period patient was treated with ZONISAMIDE, SERTRALINE. Patient was hospitalized. Patient died on 11/30/2007.

Carbamazepine Side Effects Report #5694463-1
Health Professional from PORTUGAL reported CARBAMAZEPINE problem on Mar 26, 2008. Male patient, weighting 6.97 lb, was treated with CARBAMAZEPINE. After drug was administered, patient experienced the following problems/side effects: arachnoid cyst, carnitine decreased, cerebral disorder, congenital carnitine deficiency, nuclear magnetic resonance imaging brain abnormal, . CARBAMAZEPINE dosage: MATERNAL DOSE: 600 MG/D. During the same period patient was treated with FOLIC ACID. Patient recovered.

Meiact Side Effects Report #5698236-5
MEIACT problem was reported by a Consumer or non-health professional from on Mar 25, 2008. Female patient was treated with MEIACT. After drug was administered, patient experienced the following problems/side effects: ammonia increased, carnitine decreased, coma, . MEIACT dosage: unknown. Patient recovered.


Altace Side Effects Report #5662695-4
Health Professional from UNITED STATES reported ALTACE problem on Mar 03, 2008. Female patient was diagnosed with dialysis and was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: aplastic anaemia, cardio-respiratory arrest, carnitine decreased, diabetic complication, impaired healing, leg amputation, leukopenia, therapeutic response decreased, thrombocytopenia, . ALTACE dosage: unknown. During the same period patient was treated with EPOGEN, CLOPIDOGREL BISULPHATE, QUININE, ASPIRIN, HEPARIN, ZOLPIDEM TARTRATE. Patient was hospitalized and became disabled. Patient recovered.