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BASOPHIL PERCENTAGE INCREASED side effect

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Natalizumab Side Effects Report #5510863-4
Health Professional from UNITED STATES reported NATALIZUMAB problem on Oct 29, 2007. Female patient, 43 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: basophil percentage increased, blood creatinine decreased, blood lactate dehydrogenase increased, blood urea decreased, cardiac failure congestive, cholesterol granuloma, condition aggravated, depression, low density lipoprotein increased, . NATALIZUMAB dosage: 300 MG; QM; IV. During the same period patient was treated with BIRTH CONTROL S, EFFEXOR, AMBIEN, HYDROCODONE W, ZANAFLEX, PROVIGIL, LASIX, VITAMIN E. Patient died on 10/11/2007.

Natalizumab Side Effects Report #5498377-1
NATALIZUMAB problem was reported by a Health Professional from UNITED STATES on Oct 11, 2007. Female patient, 43 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: basophil percentage increased, cardiac disorder, cardiac failure congestive, cholesterol granuloma, condition aggravated, depression, intervertebral disc protrusion, low density lipoprotein increased, . NATALIZUMAB dosage: 300 MG; QW; IV. During the same period patient was treated with BIRTH CONTROL S, EFFEXOR, AMBIEN, HYDROCONE W, ZANAFLEX, PROVIGIL, LASIX, VITAMIN E. Patient died on 10/11/2007.

Natalizumab Side Effects Report #5519611-5
Health Professional from UNITED STATES reported NATALIZUMAB problem on Nov 05, 2007. Female patient, 43 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: abasia, basophil percentage increased, blood creatine decreased, blood urea decreased, cardiac failure congestive, cholesterol granuloma, depression, mean cell haemoglobin increased, . NATALIZUMAB dosage: 300 MG;QM;IV. During the same period patient was treated with BIRTH CONTROL S, EFFEXOR, AMBIEN, HYDROCODONE W, ZANAFLEX, PROVIGIL, LASIX, VITAMIN E. Patient died on 10/11/2007.

Thalidomide Side Effects Report #5324212-8
THALIDOMIDE problem was reported by a Physician from UNITED KINGDOM on Apr 12, 2007. Male patient, 60 years of age, was diagnosed with multiple myeloma and was treated with THALIDOMIDE. After drug was administered, patient experienced the following problems/side effects: arteriosclerosis, basophil percentage increased, eosinophil percentage increased, haematocrit decreased, haematocrit increased, haemoglobin decreased, haemoglobin increased, lymphocyte percentage decreased, mean cell haemoglobin decreased, . THALIDOMIDE dosage: 100 MG, ORAL. During the same period patient was treated with ASPIRIN, METOPROLOL TARTRATE, IMIDAPRIL, ISOSORBIDE MONONITRATE, VITAMIN, LACTULOSE, DULCOLAX, MELOXICAM. Patient recovered.


Litalir Side Effects Report #5677428-5
Physician from GERMANY reported LITALIR CAPS problem on Mar 19, 2008. Female patient, 80 years of age, weighting 99.21 lb, was diagnosed with polycythaemia vera and was treated with LITALIR CAPS. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, basophil percentage increased, blood bilirubin increased, granulocyte count increased, haematocrit increased, hepatic enzyme increased, leukopenia, lymphocyte count decreased, . LITALIR CAPS dosage: unknown. Patient recovered.