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Buminate Side Effects Report #5505091-2
Consumer or non-health professional from UNITED STATES reported BUMINATE problem on Oct 29, 2007. Male patient, 73 years of age, was diagnosed with blood product transfusion and was treated with BUMINATE. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, pseudomonas infection, sepsis, . BUMINATE dosage: unknown. Patient recovered.

Lioresal Side Effects Report #5476052-7
LIORESAL problem was reported by a Physician from SPAIN on Oct 01, 2007. Female patient, weighting 121.3 lb, was diagnosed with hiccups, depression, anaemia, anorexia, gastritis, pain, gastric cancer and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, empyema, neutropenia, pleural effusion, . LIORESAL dosage: unknown. During the same period patient was treated with REXER, ORAL FERRUM, BOREA, RABEPRAZOL, IBUPROFEN, DOCETAXEL, OXALIPLATIN, FLUOROURACIL. Patient was hospitalized. Patient died on 09/19/2007.

Buminate Side Effects Report #5493478-6
Consumer or non-health professional from UNITED STATES reported BUMINATE problem on Oct 12, 2007. Male patient, 73 years of age, was diagnosed with blood product transfusion and was treated with BUMINATE. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, pseudomonas infection, sepsis, . BUMINATE dosage: unknown. Patient recovered.

Lamotrigine Side Effects Report #5455120-X
LAMOTRIGINE problem was reported by a Consumer or non-health professional from BULGARIA on Sept 03, 2007. Male patient, 32 years of age, was diagnosed with convulsion and was treated with LAMOTRIGINE. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, blood pressure decreased, corneal epithelium defect, eosinophilia, escherichia infection, hepatic enzyme increased, hepatosplenomegaly, lymphadenopathy, onychomadesis, . LAMOTRIGINE dosage: unknown. During the same period patient was treated with VALPROATE. Patient was hospitalized and became disabled. Patient recovered.


Hydroxychloroqui Side Effects Report #5416454-8
Physician from NETHERLANDS reported HYDROXYCHLOROQUINE SULPHATE problem on Aug 02, 2007. Female patient, 65 years of age, was treated with HYDROXYCHLOROQUINE SULPHATE. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, beta haemolytic streptococcal infection, gastrointestinal perforation, multi-organ failure, sepsis, stomatitis, toxic epidermal necrolysis, wound infection pseudomonas, . HYDROXYCHLOROQUINE SULPHATE dosage: unknown. Patient died.

Fluorouracil Side Effects Report #5394108-4
FLUOROURACIL problem was reported by a Consumer or non-health professional from UNITED STATES on July 20, 2007. Male patient, weighting 242.5 lb, was treated with FLUOROURACIL. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, catheter related infection, haemoglobin decreased, neutrophil count increased, platelet count increased, pyrexia, staphylococcal identification test positive, white blood cell count increased, . FLUOROURACIL dosage: 5600 MG. During the same period patient was treated with ELOXATIN. Patient was hospitalized. Patient recovered.

Fluorouracil Side Effects Report #5394108-4
Consumer or non-health professional from UNITED STATES reported FLUOROURACIL problem on July 20, 2007. Male patient, weighting 242.5 lb, was treated with FLUOROURACIL. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, catheter related infection, haemoglobin decreased, neutrophil count increased, platelet count increased, pyrexia, staphylococcal identification test positive, white blood cell count increased, . FLUOROURACIL dosage: 5600 MG. During the same period patient was treated with ELOXATIN. Patient was hospitalized. Patient recovered.

Mirena Side Effects Report #5778193-3
MIRENA problem was reported by a Physician from UNITED STATES on May 19, 2008. Female patient, 19 years of age, weighting 149.9 lb, was diagnosed with contraception and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, pelvic pain, . MIRENA dosage: unknown. Patient recovered.

Exjade Side Effects Report #5735141-X
Physician from ITALY reported EXJADE problem on May 05, 2008. Female patient, 18 years of age, was diagnosed with iron overload and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, diarrhoea, polymerase chain reaction, pyrexia, vomiting, yersinia infection, . EXJADE dosage: 30 MG/KG DAILY. During the same period patient was treated with ORAL REHYDRATION SALT, BRUFEN, CIPROFLOXACIN. Patient recovered.


Erlotinib Side Effects Report #5744909-5
ERLOTINIB problem was reported by a Health Professional from FINLAND on May 02, 2008. Female patient, 88 years of age, was diagnosed with non-small cell lung cancer and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, fall, limb injury, post procedural haemorrhage, skin graft, skin ulcer, wound infection staphylococcal, . ERLOTINIB dosage: 150 MG, QD, ORAL. During the same period patient was treated with EMGESAN, EMCONCOR, ISOSORBIDE MONONITRATE, PANTOPRAZOLE, DANAZOL, ASPIRIN, CITALOPRAM HYDROBROMIDE, FUROSEMIDE. Patient was hospitalized. Patient recovered.

Antithymocyte Side Effects Report #5691389-4
Consumer or non-health professional from JAPAN reported ANTITHYMOCYTE IMMUNOGLOBULIN problem on Mar 27, 2008. Female patient, child 4 years of age, was diagnosed with graft versus host disease and was treated with ANTITHYMOCYTE IMMUNOGLOBULIN. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, biopsy skin abnormal, graft versus host disease, lymph node pain, lymphadenopathy, mycobacterium chelonei infection, rash, subcutaneous abscess, subcutaneous nodule, . ANTITHYMOCYTE IMMUNOGLOBULIN dosage: 10 MG/KG/DAY. During the same period patient was treated with CYCLOSPORINE, METHYLPREDNISOLONE, MYCOPHENOLATE MOFETIL. Patient recovered.

Metformin Side Effects Report #5692864-9
METFORMIN HYDROCHLORIDE problem was reported by a Consumer or non-health professional from on Mar 15, 2008. Female patient, 55 years of age, was diagnosed with type 2 diabetes mellitus and was treated with METFORMIN HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, coma, confusional state, dehydration, haemodialysis, lactic acidosis, lower respiratory tract infection, malaise, . METFORMIN HYDROCHLORIDE dosage: 1000MG, DAILY; PO. During the same period patient was treated with METFORMIN HYDROCHLORIDE, AMITRIPTYLINE, DICLOFENAC, LEVOTHYROXINE, LUMIRACOXIB, TRAMADOL. Patient was hospitalized and became disabled. Patient recovered.

Cetuximab Side Effects Report #5695110-5
Health Professional from GERMANY reported CETUXIMAB problem on Mar 27, 2008. Female patient, 64 years of age, weighting 165.3 lb, was diagnosed with colorectal cancer metastatic and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, biliary fistula, debridement, impaired healing, purulence, staphylococcal infection, surgical procedure repeated, suture related complication, . CETUXIMAB dosage: unknown. During the same period patient was treated with FLUOROURACIL, FOLINIC ACID, IRINOTECAN. Patient was hospitalized. Patient recovered.

Hematopoetic Side Effects Report #5705749-6
HEMATOPOETIC PROGENITOR CELLS problem was reported by a Health Professional from UNITED STATES on Apr 11, 2008. Male patient, 64 years of age, weighting 216.1 lb, was diagnosed with multiple myeloma and was treated with HEMATOPOETIC PROGENITOR CELLS. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, therapeutic product contamination, . HEMATOPOETIC PROGENITOR CELLS dosage: unknown. Patient recovered.


Betamethasone Side Effects Report #5710493-5
Consumer or non-health professional from JAPAN reported BETAMETHASONE PHOSPHATE problem on Apr 02, 2008. Male patient, 23 years of age, was diagnosed with pemphigus and was treated with BETAMETHASONE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, bacterial infection, blister, blood lactate dehydrogenase increased, fall, fungal infection, immune system disorder, injury, purulence, . BETAMETHASONE PHOSPHATE dosage: 30 G;QD; 20 MG;QD; 40 MG;QD; 25 MG;QD. During the same period patient was treated with PREDNISOLONE, CYCLOSPORINE, METHYLPREDNISOLONE SUCCINATE, MINOCYCLINE HYDROCHLORIDE. Patient recovered.

Bevacizumab Side Effects Report #5713660-X
BEVACIZUMAB problem was reported by a Physician from UNITED STATES on Apr 14, 2008. Female patient was diagnosed with glioblastoma multiforme and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, blood creatine phosphokinase increased, cellulitis, necrotising fasciitis, . BEVACIZUMAB dosage: 10 MG/KG, UNK. During the same period patient was treated with IRINOTECAN, TRAZODONE, DAYPRO, SENOKOT, DOCUSATE, METHOCARBAMOL, POTASSIUM CHLORIDE, NORCO. Patient was hospitalized. Patient recovered.

Phenytoin Side Effects Report #5714526-1
Health Professional from SPAIN reported PHENYTOIN problem on Apr 08, 2008. Female patient, 76 years of age, was diagnosed with convulsion and was treated with PHENYTOIN. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, blood culture positive, hypoalbuminaemia, pseudomonas infection, superinfection, toxic epidermal necrolysis, . PHENYTOIN dosage: 300 MG' QD. During the same period patient was treated with DEXAMETHASONE, OMEPRAZOLE. Patient was hospitalized. Patient recovered.

Exjade Side Effects Report #5719439-7
EXJADE problem was reported by a Physician from ITALY on Apr 18, 2008. Female patient was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, yersinia infection, . EXJADE dosage: 30 MG/KG. Patient recovered.

Hematopoetic Side Effects Report #5335523-4
Physician from UNITED STATES reported HEMATOPOETIC PROGENITOR CELLS problem on Apr 16, 2007. Male patient, weighting 205.0 lb, was diagnosed with amyloidosis and was treated with HEMATOPOETIC PROGENITOR CELLS. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, complications of transplant surgery, micrococcus infection, . HEMATOPOETIC PROGENITOR CELLS dosage: 111ML IV. 6.2E6 CD34+. During the same period patient was treated with MELPHALAN, NEUPOGEN, VORICONAZOLE. Patient recovered.


Valtrex Side Effects Report #5337205-1
VALTREX problem was reported by a Consumer or non-health professional from UNITED STATES on May 24, 2007. Female patient, 55 years of age, was diagnosed with genital herpes and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, fungal infection, fungus culture positive, hypersensitivity, pruritus, rash, ulcer, vulval ulceration, . VALTREX dosage: unknown. During the same period patient was treated with ACYCLOVIR, FENTANYL, ZOFRAN, BENADRYL, MS CONTIN, ELAVIL. Patient was hospitalized and became disabled. Patient recovered.

Remicade Side Effects Report #5339833-6
Physician from UNITED KINGDOM reported REMICADE problem on May 21, 2007. Male patient, weighting 127.9 lb, was diagnosed with colitis ulcerative, angina pectoris, cardiovascular disorder, hypertension, anxiety and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, pneumonia, . REMICADE dosage: unknown. During the same period patient was treated with PREDNISOLONE, AZATHIOPRINE, TILDIEM, DIPYRIDAMOLE, NITROGLYCERIN, PERINDOPRIL, CITALOPRAM HYDROBROMIDE. Patient died on 05/06/2006.

Carboplatin Side Effects Report #5286198-4
CARBOPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 03, 2007. Female patient, weighting 164.3 lb, was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, bacterial infection, chills, culture urine positive, enterococcal infection, neutrophil count decreased, vomiting, . CARBOPLATIN dosage: 978 MG. During the same period patient was treated with TAXOL. Patient was hospitalized. Patient recovered.

Allogeneic Side Effects Report #5301788-8
Physician from UNITED STATES reported ALLOGENEIC PERIPHERAL BLOOD problem on Apr 16, 2007. Male patient, 66 years of age, weighting 175.5 lb, was diagnosed with acute myeloid leukaemia and was treated with ALLOGENEIC PERIPHERAL BLOOD. After drug was administered, patient experienced the following problems/side effects: bacterial culture positive, . ALLOGENEIC PERIPHERAL BLOOD dosage: unknown. Patient recovered.

Sch Side Effects Report #5664321-7
SCH problem was reported by a Physician from UNITED STATES on Mar 04, 2008. Female patient, 44 years of age, weighting 127.3 lb, was diagnosed with hepatitis c and was treated with SCH. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, bacterial culture positive, blood glucose increased, confusional state, dehydration, diarrhoea, dysarthria, dystonia, enterococcal infection, . SCH dosage: 800 MG; TID; PO. During the same period patient was treated with RIBAVIRIN, LEVOTHYROXINE, ESCITALOPRAM OXALATE, ALPRAZOLAM, PHENERGAN, LAXATIVES, ULTRAM. Patient was hospitalized. Patient recovered.

Naprosyn Side Effects Report #5684731-1
Consumer or non-health professional from UNITED STATES reported NAPROSYN problem on Feb 04, 1986. Male patient, 72 years of age, was treated with NAPROSYN. After drug was administered, patient experienced the following problems/side effects: arteriosclerosis, bacterial culture positive, blood creatinine increased, blood urea increased, cardiomegaly, chest pain, cholelithiasis, coronary artery disease, . NAPROSYN dosage: unknown. During the same period patient was treated with ZANTAC, TAGAMET. Patient was hospitalized. Patient died on 08/30/1984.

Cephalexin Side Effects Report #5603804-2
CEPHALEXIN problem was reported by a Physician from UNITED STATES on Jan 11, 2008. Male patient was diagnosed with purulent discharge and was treated with CEPHALEXIN. After drug was administered, patient experienced the following problems/side effects: alpha haemolytic streptococcal infection, bacterial culture positive, erysipelas, swelling, . CEPHALEXIN dosage: 500 MG; QID; PO. Patient was hospitalized. Patient recovered.

Zelnorm Side Effects Report #5500992-3
Consumer or non-health professional from UNITED STATES reported ZELNORM problem on Oct 19, 2007. Female patient, weighting 164.5 lb, was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: angina pectoris, bacterial culture positive, chest pain, hernia, . ZELNORM dosage: unknown. During the same period patient was treated with ESTRATEST. Patient recovered.

Zelnorm Side Effects Report #5501017-6
ZELNORM problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 19, 2007. Female patient, weighting 164.5 lb, was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: angina pectoris, bacterial culture positive, chest pain, hernia, . ZELNORM dosage: unknown. During the same period patient was treated with ESTRATEST. Patient recovered.

Lipitor Side Effects Report #5411593-X
Physician from JAPAN reported LIPITOR problem on July 27, 2007. Male patient, weighting 149.9 lb, was diagnosed with hypercholesterolaemia and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: anorexia, bacterial culture positive, malaise, pyrexia, . LIPITOR dosage: unknown. During the same period patient was treated with TICLOPIDINE, TOCOPHERYL NICOTINATE, MICARDIS, ADALAT, DOXAZOSIN MESYLATE, ASPIRIN, SELBEX, ZANTAC. Patient was hospitalized. Patient recovered.

Lipitor Side Effects Report #5428041-6
LIPITOR problem was reported by a Physician from JAPAN on Aug 20, 2007. Male patient, weighting 149.9 lb, was diagnosed with hypercholesterolaemia and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: anorexia, bacterial culture positive, malaise, pyrexia, . LIPITOR dosage: unknown. During the same period patient was treated with TICLOPIDINE, TOCOPHEROL CONCENTRATE CAP, MICARDIS, ADALAT, DOXAZOSIN MESYLATE, ASPIRIN, SELBEX, ZANTAC. Patient was hospitalized. Patient recovered.

Exjade Side Effects Report #5737366-6
Physician from ITALY reported EXJADE problem on May 05, 2008. Female patient, 18 years of age, was diagnosed with iron overload and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: back pain, bacterial culture positive, diarrhoea, polymerase chain reaction, pyrexia, vomiting, yersinia infection, . EXJADE dosage: 30 MG/KG DAILY. Patient recovered.

Thalidomide Side Effects Report #5740372-9
THALIDOMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on May 06, 2008. Female 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: alpha haemolytic streptococcal infection, bacterial culture positive, bone debridement, bone disorder, bone erosion, brain abscess, breath odour, cerebral decompression, craniotomy, . THALIDOMIDE dosage: 200 MG, QD. During the same period patient was treated with DEXAMETHASONE, ZOMETA. Patient recovered.

Antithymocyte Side Effects Report #5693239-9
Consumer or non-health professional from JAPAN reported ANTITHYMOCYTE IMMUNOGLOBULIN problem on Mar 27, 2008. Female patient, child 4 years of age, was diagnosed with graft versus host disease and was treated with ANTITHYMOCYTE IMMUNOGLOBULIN. After drug was administered, patient experienced the following problems/side effects: acute graft versus host disease in skin, bacterial culture positive, biopsy skin abnormal, lymph node pain, lymphadenopathy, mycobacterium chelonei infection, purulent discharge, rash, . ANTITHYMOCYTE IMMUNOGLOBULIN dosage: 10 MG/KG/DAY. During the same period patient was treated with CYCLOSPORINE, METHYLPREDNISOLONE, MYCOPHENOLATE MOFETIL, BUSULFAN, CYCLOPHOSPHAMIDE, ETOPOSIDE, METHOTREXATE. Patient recovered.

Buminate Side Effects Report #5697840-8
BUMINATE problem was reported by a Pharmacist from UNITED STATES on Apr 04, 2008. Male patient, 53 years of age, weighting 224.9 lb, was diagnosed with hypovolaemia and was treated with BUMINATE. After drug was administered, patient experienced the following problems/side effects: bacteria blood identified, bacterial culture positive, blood lactic acid abnormal, heart rate increased, hypotension, infusion related reaction, tachypnoea, . BUMINATE dosage: 500ML IV ONCE. Patient was hospitalized. Patient recovered.

Thalidomide Side Effects Report #5703220-9
Consumer or non-health professional from UNITED STATES reported THALIDOMIDE problem on Mar 31, 2008. Female 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: alpha haemolytic streptococcal infection, bacterial culture positive, bone debridement, bone erosion, brain abscess, breath odour, cerebral decompression, craniotomy, cyst, . THALIDOMIDE dosage: 200 MG, QD. During the same period patient was treated with DEXAMETHASONE, ZOMETA. Patient recovered.

Decadron Side Effects Report #5317364-7
DECADRON problem was reported by a Physician from JAPAN on Mar 20, 2007. Female patient, child 12 years of age, was treated with DECADRON. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, bacterial culture positive, hyperlipidaemia, lung infiltration, multi-organ failure, neutrophil count decreased, streptococcal bacteraemia, . DECADRON dosage: unknown. During the same period patient was treated with AMIKACINA, CYTARABINE, METHOTREXATE, ONCOVIN, ADRIAMYCIN PFS, LEUNASE, SULFAMETHOXAZOLE AND TRIMETHOPRIM, FLORID. Patient died.

Decadron Side Effects Report #5289653-6
Physician from JAPAN reported DECADRON problem on Mar 28, 2007. Female patient, child 12 years of age, was treated with DECADRON. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, bacterial culture positive, hyperlipidaemia, lung infiltration, multi-organ failure, neutrophil count decreased, streptococcal bacteraemia, . DECADRON dosage: unknown. During the same period patient was treated with AMIKACINA, CYTARABINE, METHOTREXATE, ONCOVIN, ADRIAMYCIN PFS, LEUNASE, SULFAMETHOXAZOLE AND TRIMETHOPRIM, FLORID. Patient died.

Decadron Side Effects Report #5282040-6
DECADRON problem was reported by a Physician from JAPAN on Mar 20, 2007. Female patient, child 12 years of age, was treated with DECADRON. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, bacterial culture positive, hyperlipidaemia, lung infiltration, multi-organ failure, neutrophil count decreased, streptococcal bacteraemia, . DECADRON dosage: unknown. During the same period patient was treated with AMIKACINA, CYTARABINE, METHOTREXATE, ONCOVIN, ADRIAMYCIN PFS, LEUNASE, SULFAMETHOXAZOLE AND TRIMETHOPRIM, FLORID. Patient died.

Zometa Side Effects Report #5629892-5
Consumer or non-health professional from UNITED STATES reported ZOMETA problem on Feb 11, 2008. Female patient, 93 years of age, weighting 126.0 lb, was diagnosed with multiple myeloma, anaemia and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, anxiety, bacterial culture positive, biopsy bone abnormal, bone debridement, bone disorder, epistaxis, gingival bleeding, impaired healing, . ZOMETA dosage: unknown. During the same period patient was treated with PROCRIT. Patient was hospitalized. Patient recovered.