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Duragesic Side Effects Report #5670793-4
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Mar 10, 2008. Female patient, weighting 140.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: bacteria blood identified, depression, headache, hypoaesthesia, vomiting, . DURAGESIC dosage: unknown. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5637833-X
PROGRAF problem was reported by a Health Professional from UNITED STATES on Feb 11, 2008. Male patient, 57 years of age, was diagnosed with liver transplant rejection and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: bacteria blood identified, corynebacterium infection, cytomegalovirus colitis, . PROGRAF dosage: 1.5 MG, BID, ORAL; 0.5 MG, QOD, ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, MYCOPHENOLATE MOFETIL, MYCOPHENOLATE MOFETIL, PREDNISOLONE ACETATE, PREDNISOLONE ACETATE, METOPROLOL TARTRATE, PROTONIX. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5643915-9
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Feb 13, 2008. Female patient was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: bacteria blood identified, condition aggravated, fall, gout, memory impairment, multiple sclerosis, pelvic fracture, pharyngitis streptococcal, pneumonia, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Tekturna Side Effects Report #5634878-0
TEKTURNA problem was reported by a Physician from UNITED STATES on Oct 15, 2007. Male patient, 77 years of age, was diagnosed with hypertension and was treated with TEKTURNA. After drug was administered, patient experienced the following problems/side effects: bacteria blood identified, blood pressure decreased, dizziness, . TEKTURNA dosage: 150 MG, QD, ORAL. During the same period patient was treated with PREVACID, ATENOLOL, ZETIA, ZOCOR, DIOVAN, ZANTAC, FLONASE, CLONIDINE. Patient recovered.


Prednisone Side Effects Report #5526070-5
Physician from DENMARK reported PREDNISONE problem on Nov 05, 2007. Female patient, 68 years of age, was diagnosed with polymyalgia rheumatica and was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: bacteria blood identified, pneumonia, . PREDNISONE dosage: unknown. During the same period patient was treated with ORAPRED. Patient recovered.

Ethyol Side Effects Report #5527707-7
ETHYOL problem was reported by a Health Professional from FRANCE on Nov 09, 2007. Female patient, 65 years of age, weighting 158.7 lb, was diagnosed with neoplasm malignant and was treated with ETHYOL. After drug was administered, patient experienced the following problems/side effects: bacteria blood identified, dermatitis, erythema, face oedema, hyperthermia, radiation skin injury, skin exfoliation, skin fissures, . ETHYOL dosage: 200 MG/M2, INTRAVENOUS (NOT OTHERWISE SPECIFIED) ; 200 MG/M2, INTRAVENOUS (NOT OTHERWISE SPECIFIED). During the same period patient was treated with ERBITUX, CARBOPLATIN, INSULIN. Patient was hospitalized. Patient recovered.

Tekturna Side Effects Report #5574595-9
Physician from UNITED STATES reported TEKTURNA problem on Oct 15, 2007. Male patient, 77 years of age, was diagnosed with hypertension and was treated with TEKTURNA. After drug was administered, patient experienced the following problems/side effects: bacteria blood identified, blood pressure decreased, dizziness, . TEKTURNA dosage: 150 MG, QD, ORAL. During the same period patient was treated with PREVACID, ATENOLOL, ZETIA, ZOCOR, DIOVAN, ZANTAC, FLONASE, CLONIDINE. Patient recovered.

Infliximab Side Effects Report #5475484-0
INFLIXIMAB problem was reported by a Health Professional from UNITED KINGDOM on Sept 21, 2007. Male patient, 46 years of age, was diagnosed with psoriasis and was treated with INFLIXIMAB. After drug was administered, patient experienced the following problems/side effects: bacteria blood identified, dermatitis atopic, impetigo, psoriasis, . INFLIXIMAB dosage: unknown. During the same period patient was treated with CYCLOSPORINE, METHOTREXATE. Patient was hospitalized. Patient recovered.

Neoral Side Effects Report #5409234-0
Physician from UNITED STATES reported NEORAL problem on July 27, 2007. Female patient, 62 years of age, was diagnosed with psoriasis and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: bacteria blood identified, blood carbon monoxide increased, blood glucose increased, blood uric acid increased, cd4 lymphocytes increased, cd8 lymphocytes decreased, dermatitis psoriasiform, lymphocyte percentage increased, monocyte percentage decreased, . NEORAL dosage: unknown. Patient recovered.


Heparin Side Effects Report #5726135-9
HEPARIN problem was reported by a Consumer or non-health professional from UNITED STATES on May 02, 2008. Female patient, 65 years of age, was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: bacteria blood identified, escherichia infection, . HEPARIN dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Buminate Side Effects Report #5697840-8
Pharmacist from UNITED STATES reported BUMINATE problem 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.

Levofloxacin Side Effects Report #5713821-X
LEVOFLOXACIN problem was reported by a Health Professional from SPAIN on Apr 11, 2008. Female patient was diagnosed with pneumonia and was treated with LEVOFLOXACIN. After drug was administered, patient experienced the following problems/side effects: bacteria blood identified, hypotension, tachycardia, treatment failure, . LEVOFLOXACIN dosage: 500 MG, QD. During the same period patient was treated with AMOXICILLIN. Patient died.

Clofarabine Side Effects Report #5368303-4
Physician from UNITED KINGDOM reported CLOFARABINE problem on June 07, 2007. Female patient, 51 years of age, was diagnosed with acute myeloid leukaemia, disease recurrence and was treated with CLOFARABINE. After drug was administered, patient experienced the following problems/side effects: bacteria blood identified, blood culture positive, central line infection, embolism infective, enterococcal infection, fungal infection, neutropenia, rash, staphylococcal infection, . CLOFARABINE dosage: unknown. Patient recovered.

Avastin Side Effects Report #5301522-1
AVASTIN problem was reported by a Health Professional from AUSTRALIA on Mar 30, 2007. Male patient, 67 years of age, weighting 177.9 lb, was diagnosed with colon cancer and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: bacteria blood identified, chills, device related infection, pyrexia, . AVASTIN dosage: 578 MG, Q3W, INTRAVENOUS. During the same period patient was treated with CAPECITABINE, OXALIPLATIN, IRBESARTAN, VALPROATE, NEXIUM, VANCOMYCIN HYDROCHLORIDE, TIMENTIN. Patient was hospitalized. Patient recovered.


Avastin Side Effects Report #5271768-X
Health Professional from AUSTRALIA reported AVASTIN problem on Feb 28, 2007. Male patient, 67 years of age, weighting 177.9 lb, was diagnosed with colon cancer and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: bacteria blood identified, chills, device related infection, . AVASTIN dosage: 578 MG, Q3W, INTRAVENOUS. During the same period patient was treated with CAPECITABINE, OXALIPLATIN, IRBESARTAN, VALPROATE, NEXIUM, VANCOMYCIN HYDROCHLORIDE, TIMENTIN. Patient was hospitalized. Patient recovered.

Levofloxacin Side Effects Report #5650462-7
LEVOFLOXACIN problem was reported by a Pharmacist from UNITED STATES on Mar 04, 2008. Male patient, 86 years of age, was diagnosed with urinary tract infection, atrial fibrillation and was treated with LEVOFLOXACIN. After drug was administered, patient experienced the following problems/side effects: asthenia, bacteria blood identified, blood creatinine increased, catheter related infection, diarrhoea haemorrhagic, faeces discoloured, heart rate irregular, international normalised ratio increased, malaise, . LEVOFLOXACIN dosage: 250 MG EVERY OTHER DAY PO. During the same period patient was treated with WARFARIN, LASIX, LANOXIN, COUMADIN, FLUOXETINE, GEMFIBROZIL, ARICEPT, LISINOPRIL. Patient was hospitalized. Patient recovered.

Cyclophosphamide Side Effects Report #5394114-X
Consumer or non-health professional from UNITED STATES reported CYCLOPHOSPHAMIDE problem on July 20, 2007. Female patient, weighting 145.5 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: bacillus infection, bacteria blood identified, balance disorder, blood pressure diastolic decreased, dizziness, febrile neutropenia, headache, heart rate increased, respiratory rate increased, . CYCLOPHOSPHAMIDE dosage: 1700 MG. During the same period patient was treated with CYTARABINE, ELSPAR, METHOTREXATE. Patient was hospitalized. Patient recovered.

Cyclophosphamide Side Effects Report #5394114-X
CYCLOPHOSPHAMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on July 20, 2007. Female patient, weighting 145.5 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: bacillus infection, bacteria blood identified, balance disorder, blood pressure diastolic decreased, dizziness, febrile neutropenia, headache, heart rate increased, respiratory rate increased, . CYCLOPHOSPHAMIDE dosage: 1700 MG. During the same period patient was treated with CYTARABINE, ELSPAR, METHOTREXATE. Patient was hospitalized. Patient recovered.

Vancomycin Side Effects Report #5272427-X
Consumer or non-health professional from UNITED STATES reported VANCOMYCIN problem on Mar 20, 2007. Female patient, 57 years of age, weighting 279.0 lb, was diagnosed with arthritis infective, post procedural infection and was treated with VANCOMYCIN. After drug was administered, patient experienced the following problems/side effects: alopecia, bacteria blood identified, blood pressure decreased, dehydration, erythrodermic psoriasis, infection, malnutrition, nail discolouration, . VANCOMYCIN dosage: unknown. During the same period patient was treated with CIPRO. Patient was hospitalized and became disabled. Patient recovered.


Albuterol Side Effects Report #5752616-8
ALBUTEROL problem was reported by a Pharmacist from UNITED STATES on May 27, 2008. Female patient, 81 years of age, was diagnosed with bronchospasm and was treated with ALBUTEROL. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, atrial flutter, bacteria blood identified, culture urine positive, hypovolaemia, klebsiella infection, productive cough, pulmonary embolism, pyrexia, . ALBUTEROL dosage: 5ML Q4H PO. During the same period patient was treated with IPRATROPIUM BROMIDE, ACETYLCYSTEINE, LEVAQUIN, ZOSYN, VANCOMYCIN. Patient was hospitalized. Patient recovered.

Daunorubicin Side Effects Report #5725915-3
Physician from UNITED STATES reported DAUNORUBICIN HYDROCHLORIDE problem on Apr 14, 2008. Male patient, 17 years of age, was diagnosed with acute lymphocytic leukaemia and was treated with DAUNORUBICIN HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, aspergillosis, bacteria blood identified, fungal infection, lung infection, mucosal inflammation, myalgia, neutropenia, . DAUNORUBICIN HYDROCHLORIDE dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient was hospitalized. Patient died.