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Gleevec Side Effects Report #5573294-7
Physician from JAPAN reported GLEEVEC problem on Dec 21, 2007. Male patient, 74 years of age, was diagnosed with chronic myeloid leukaemia and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: basophil count increased, blast cell count increased, blood creatinine increased, bone pain, brain oedema, dyslalia, eosinophil count increased, haematocrit decreased, haemoglobin decreased, . GLEEVEC dosage: 100 MG, QD. Patient was hospitalized and became disabled. Patient died on 09/21/2005.

Gleevec Side Effects Report #5575997-7
GLEEVEC problem was reported by a Physician from CANADA on Dec 21, 2007. Male patient, 68 years of age, was diagnosed with chronic myeloid leukaemia and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: basophil count increased, blast cell count increased, haematocrit decreased, haemoglobin decreased, lymphocyte count decreased, myelocyte count increased, platelet count decreased, . GLEEVEC dosage: 600 MG, QD. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5501780-4
Physician from JAPAN reported GLEEVEC problem on Oct 26, 2007. Male patient, 74 years of age, was diagnosed with chronic myeloid leukaemia and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: basophil count increased, blast cell count increased, blood creatinine increased, bone pain, brain oedema, dyslalia, eosinophil count increased, haematocrit decreased, haemoglobin decreased, . GLEEVEC dosage: 100 MG, QD. Patient was hospitalized and became disabled. Patient died on 09/21/2005.

Gleevec Side Effects Report #5502556-4
GLEEVEC problem was reported by a Physician from JAPAN on Oct 26, 2007. Male patient, 74 years of age, was diagnosed with chronic myeloid leukaemia and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: basophil count increased, blast cell count increased, blood creatinine increased, bone pain, brain oedema, dyslalia, eosinophil count increased, haematocrit decreased, haemoglobin decreased, . GLEEVEC dosage: 100 MG, QD. Patient was hospitalized and became disabled. Patient died on 09/21/2005.


Zometa Side Effects Report #5447189-3
Physician from JAPAN reported ZOMETA problem on Aug 31, 2007. Female patient, 64 years of age, was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: basophil count increased, blood glucose increased, c-reactive protein increased, eosinophil count decreased, granulocyte count increased, haematocrit decreased, haemoglobin decreased, joint swelling, lymphocyte count decreased, . ZOMETA dosage: 4 MG, UNK. During the same period patient was treated with AREDIA, NAVELBINE. Patient recovered.

Zometa Side Effects Report #5463969-2
ZOMETA problem was reported by a Physician from JAPAN on Sept 13, 2007. Female patient, 64 years of age, was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: basophil count increased, blood glucose increased, c-reactive protein increased, eosinophil count decreased, granulocyte count increased, haematocrit decreased, haemoglobin decreased, joint swelling, lymphocyte count decreased, . ZOMETA dosage: 4 MG, UNK. During the same period patient was treated with AREDIA, NAVELBINE. Patient recovered.

Diovan Side Effects Report #5382562-3
Physician from JAPAN reported DIOVAN problem on July 04, 2007. Male patient, 80 years of age, weighting 114.6 lb, was diagnosed with hypertension, pyrexia, oedema and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: basophil count increased, blood creatinine increased, blood potassium decreased, blood sodium decreased, blood urea increased, bone marrow failure, eosinophil count increased, fracture, haematocrit decreased, . DIOVAN dosage: 20 MG/DAY. During the same period patient was treated with VANCOMYCIN, LASIX. Patient was hospitalized. Patient recovered.

Diovan Side Effects Report #5382562-3
DIOVAN problem was reported by a Physician from JAPAN on July 04, 2007. Male patient, 80 years of age, weighting 114.6 lb, was diagnosed with hypertension, pyrexia, oedema and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: basophil count increased, blood creatinine increased, blood potassium decreased, blood sodium decreased, blood urea increased, bone marrow failure, eosinophil count increased, fracture, haematocrit decreased, . DIOVAN dosage: 20 MG/DAY. During the same period patient was treated with VANCOMYCIN, LASIX. Patient was hospitalized. Patient recovered.

Nexavar Side Effects Report #5756488-7
Physician from JAPAN reported NEXAVAR problem on May 23, 2008. Female patient, 60 years of age, weighting 127.9 lb, was diagnosed with renal cell carcinoma and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: basophil count increased, blood creatinine increased, blood lactate dehydrogenase increased, c-reactive protein increased, erythema, flushing, gamma-glutamyltransferase increased, oedema peripheral, skin exfoliation, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG UNIT DOSE: 200 MG. Patient recovered.


Taxotere Side Effects Report #5713971-8
TAXOTERE problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 22, 2008. Male patient, weighting 229.5 lb, was treated with TAXOTERE. After drug was administered, patient experienced the following problems/side effects: basophil count increased, blood albumin decreased, blood creatine phosphokinase decreased, blood creatine phosphokinase mb increased, blood glucose increased, blood urea increased, bundle branch block right, carbon dioxide decreased, dilatation ventricular, . TAXOTERE dosage: 165 MG. Patient was hospitalized. Patient recovered.

Diovan Side Effects Report #5352049-2
Physician from JAPAN reported DIOVAN problem on June 05, 2007. Male patient, 80 years of age, weighting 114.6 lb, was diagnosed with hypertension, pyrexia, oedema, nephrogenic anaemia, diabetes mellitus and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: basophil count increased, blood creatinine increased, blood potassium decreased, blood sodium decreased, blood urea increased, bone marrow failure, eosinophil count increased, fracture, haematocrit decreased, . DIOVAN dosage: 20 MG/DAY. During the same period patient was treated with VANCOMYCIN, LASIX, LEVOFLOXACIN, FOSMICIN, EPOGEN, HUMULIN, OMEGACIN. Patient was hospitalized. Patient recovered.

Betaseron Side Effects Report #5357623-5
BETASERON problem was reported by a Physician from UNITED STATES on May 31, 2007. Female patient, 51 years of age, weighting 192.0 lb, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: basophil count increased, blast cell count increased, chronic myeloid leukaemia, eosinophil count increased, haematocrit decreased, hypersensitivity, injection site pain, monocyte count increased, multiple sclerosis, . BETASERON dosage: unknown. During the same period patient was treated with BACLOFEN, WELLBUTRIN, ATIVAN, GLEEVEC. Patient recovered.

Diovan Side Effects Report #5373257-0
Physician from JAPAN reported DIOVAN problem on June 26, 2007. Male patient, 80 years of age, weighting 114.6 lb, was diagnosed with hypertension, pyrexia, oedema and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: basophil count increased, blood creatinine increased, blood potassium decreased, blood sodium decreased, blood urea increased, bone marrow failure, eosinophil count increased, fracture, haematocrit decreased, . DIOVAN dosage: 20 MG/DAY. During the same period patient was treated with VANCOMYCIN, LASIX. Patient was hospitalized. Patient recovered.

Valtrex Side Effects Report #5403984-8
VALTREX problem was reported by a Physician from JAPAN on July 27, 2007. Female patient, 87 years of age, weighting 94.80 lb, was diagnosed with facial palsy, hypothyroidism, hypertension, insomnia, gastritis and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: albumin globulin ratio decreased, basophil count increased, blood albumin decreased, blood alkaline phosphatase increased, blood calcium increased, blood cholinesterase decreased, blood creatinine increased, blood lactate dehydrogenase increased, blood phosphorus, . VALTREX dosage: 500MG PER DAY. During the same period patient was treated with THYRADIN, ENALAPRIL MALEATE, OLMESARTAN MEDOXOMIL, ATELEC, NITRAZEPAM, METHYCOBAL, SELBEX, ALFAROL. Patient was hospitalized. Patient recovered.


Valtrex Side Effects Report #5386580-0
Physician from JAPAN reported VALTREX problem on July 09, 2007. Female patient, 87 years of age, weighting 94.80 lb, was diagnosed with facial palsy, hypothyroidism, hypertension, insomnia, gastritis and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: albumin globulin ratio decreased, basophil count increased, blood albumin decreased, blood alkaline phosphatase increased, blood calcium increased, blood cholinesterase decreased, blood creatinine increased, blood lactate dehydrogenase increased, blood phosphorus, . VALTREX dosage: 500MG PER DAY. During the same period patient was treated with THYRADIN, RENIVACE, OLMESARTAN MEDOXOMIL, ATELEC, NITRAZEPAM, CYANOCOBALAMIN, SELBEX, ALFAROL. Patient was hospitalized. Patient recovered.

Valtrex Side Effects Report #5386580-0
VALTREX problem was reported by a Physician from JAPAN on July 09, 2007. Female patient, 87 years of age, weighting 94.80 lb, was diagnosed with facial palsy, hypothyroidism, hypertension, insomnia, gastritis and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: albumin globulin ratio decreased, basophil count increased, blood albumin decreased, blood alkaline phosphatase increased, blood calcium increased, blood cholinesterase decreased, blood creatinine increased, blood lactate dehydrogenase increased, blood phosphorus, . VALTREX dosage: 500MG PER DAY. During the same period patient was treated with THYRADIN, RENIVACE, OLMESARTAN MEDOXOMIL, ATELEC, NITRAZEPAM, CYANOCOBALAMIN, SELBEX, ALFAROL. Patient was hospitalized. Patient recovered.

Tegretol Side Effects Report #5657383-4
Consumer or non-health professional from JAPAN reported TEGRETOL problem on Mar 03, 2008. Female patient, 17 years of age, was diagnosed with obsessive-compulsive disorder and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, basophil count increased, blood lactate dehydrogenase increased, c-reactive protein increased, emotional disorder, erythema, gamma-glutamyltransferase increased, . TEGRETOL dosage: 400 MG/DAY. During the same period patient was treated with FLUVOXAMINE MALEATE, ZYPREXA, DESYREL, SEROQUEL, PROMETHAZINE. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5581322-8
GLEEVEC problem was reported by a Consumer or non-health professional from JAPAN on Dec 26, 2007. Female patient, 33 years of age, weighting 132.3 lb, was diagnosed with chronic myeloid leukaemia and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: abortion induced, alanine aminotransferase increased, basophil count increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, haematocrit decreased, haemoglobin decreased, lymphocyte count decreased, . GLEEVEC dosage: 400 MG, QD. Patient recovered.

Natalizumab Side Effects Report #5533578-5
Health Professional from UNITED STATES reported NATALIZUMAB problem on Nov 20, 2007. Female patient, 43 years of age, weighting 225.0 lb, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: abasia, alcohol use, basophil count increased, blood creatinine decreased, blood urea decreased, cardiac failure congestive, cholesterol granuloma, condition aggravated, depression, . NATALIZUMAB dosage: 300 MG;QM;IV. During the same period patient was treated with AVONEX, EFFEXOR, AMBIEN, HYDROCODONE W, ZANAFLEX, PROVIGIL, LASIX, VITAMIN E. Patient died on 10/11/2007.