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Remicade Side Effects Report #5654539-1
Physician from JAPAN reported REMICADE problem on Feb 27, 2008. Male patient, weighting 141.1 lb, was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, pneumonia primary atypical, staphylococcal sepsis, . REMICADE dosage: unknown. Patient was hospitalized. Patient recovered.

Subutex Side Effects Report #5678078-7
SUBUTEX problem was reported by a Consumer or non-health professional from FRANCE on Mar 05, 2008. Male patient, 34 years of age, was treated with SUBUTEX. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, bacteraemia, myalgia, purpura, pyrexia, staphylococcal infection, substance abuse, . SUBUTEX dosage: SUBLINGUAL TABLET 6 MG QD INTRAVENOUS (NOT OTHERWISE SPECIFIED). Patient was hospitalized. Patient recovered.

Clofarabine Side Effects Report #5637702-5
Physician from UNITED STATES reported CLOFARABINE problem on Feb 14, 2008. Male patient, 24 years of age, weighting 137.6 lb, was diagnosed with acute myeloid leukaemia, bone marrow conditioning regimen and was treated with CLOFARABINE. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, bacterial infection, blood creatinine increased, blood culture positive, convulsion, enterococcal infection, fungal infection, grand mal convulsion, headache, . CLOFARABINE dosage: 40 MG/M2, QD, INTRAVENOUS. During the same period patient was treated with CYTARABINE, THYMOGLOBULIN, PREDNISOLONE ACETATE. Patient was hospitalized. Patient died on 02/13/2008.

Cubicin Side Effects Report #5638269-8
CUBICIN problem was reported by a Consumer or non-health professional from SPAIN on Feb 06, 2008. Female patient, 57 years of age, was diagnosed with cardiac disorder and was treated with CUBICIN. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, acute pulmonary oedema, arrhythmia, cardiac arrest, cardiogenic shock, catheter sepsis, colitis ischaemic, encephalopathy, endocarditis, . CUBICIN dosage: 350 MG; Q24H; IV. During the same period patient was treated with MEROPENEM, ENALAPRIL MALEATE, TORASEMIDE SINTROM, LANACORDIN, OXYGEN, LAMOTRIGINE, VANCOMYCIN. Patient was hospitalized. Patient recovered.


Tigecycline Side Effects Report #5641691-7
Physician from UNITED STATES reported TIGECYCLINE problem on Feb 15, 2008. Male patient, 51 years of age, was diagnosed with acinetobacter infection, mediastinitis, bacteraemia and was treated with TIGECYCLINE. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, . TIGECYCLINE dosage: 100MG LOADING DOSE THEN 50MG EVERY 12 HOURS. During the same period patient was treated with TOBRAMYCIN. Patient died.

Tigecycline Side Effects Report #5641692-9
TIGECYCLINE problem was reported by a Physician from UNITED STATES on Feb 15, 2008. Male patient, 80 years of age, was diagnosed with acinetobacter infection, pneumonia and was treated with TIGECYCLINE. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, . TIGECYCLINE dosage: 100MG LOADING DOSE THEN 50MG EVERY 12 HOURS. During the same period patient was treated with CEFEPIME. Patient died.

Tigecycline Side Effects Report #5641693-0
Physician from UNITED STATES reported TIGECYCLINE problem on Feb 15, 2008. Female patient, 59 years of age, was diagnosed with acinetobacter infection, pneumonia and was treated with TIGECYCLINE. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, . TIGECYCLINE dosage: 100 MG LOADING DOSE THEN 50MG EVERY 12 HOURS. During the same period patient was treated with COLISTIN SULPHATE, AMIKACIN. Patient died.

Tigecycline Side Effects Report #5641696-6
TIGECYCLINE problem was reported by a Physician from UNITED STATES on Feb 15, 2008. Female patient, 64 years of age, was diagnosed with acinetobacter infection, pneumonia, empyema and was treated with TIGECYCLINE. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, . TIGECYCLINE dosage: 100MG LOADING DOSE THEN 50MG EVERY 12 HOURS. During the same period patient was treated with COLISTIN SULPHATE. Patient died.

Busulfan Side Effects Report #5586034-2
Consumer or non-health professional from JAPAN reported BUSULFAN problem on Dec 21, 2007. Female patient, 40 years of age, was diagnosed with stem cell transplant and was treated with BUSULFAN. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, acute graft versus host disease, bacterial sepsis, cystitis haemorrhagic, cytomegalovirus viraemia, liver disorder, pseudomembranous colitis, staphylococcal sepsis, stomatitis, . BUSULFAN dosage: 31.2 ML; X1; IV. During the same period patient was treated with FLUDARABINE PHOSPHATE, PHENYTOIN. Patient was hospitalized and became disabled. Patient recovered.


Ambisome Side Effects Report #5613191-1
AMBISOME problem was reported by a Health Professional from FRANCE on Jan 11, 2008. Female patient, 33 years of age, was diagnosed with cerebral aspergillosis and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, biliary cirrhosis primary, caesarean section, cerebral aspergillosis, cytolytic hepatitis, haemolysis, hepatic encephalopathy, . AMBISOME dosage: unknown. During the same period patient was treated with VFEND, BACTRIM, KETAMINE, MEROPEN, COLISTIN SULPHATE. Patient was hospitalized. Patient died.

Prograf Side Effects Report #5506353-5
Physician from UNITED STATES reported PROGRAF problem on Oct 22, 2007. Female patient, 52 years of age, weighting 166.4 lb, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, pneumocystis jiroveci pneumonia, respiratory failure, sepsis, . PROGRAF dosage: unknown. During the same period patient was treated with PREDNISONE. Patient was hospitalized. Patient died on 11/25/2006.

Myozyme Side Effects Report #5510571-X
MYOZYME problem was reported by a Physician from UNITED STATES on Oct 23, 2007. Female patient, weighting 29.98 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, bacteria urine identified, blood ph increased, blood pressure diastolic decreased, diarrhoea, enterococcal infection, escherichia infection, heart rate increased, hydronephrosis, . MYOZYME dosage: 20 MG/KG Q2WKS IV. During the same period patient was treated with ALPHA, PREVACID, ENALAPRIL MALEATE, DIGOXIN, MIRALAX, LASIX. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5512664-X
Physician from CHINA reported MYOZYME problem on Oct 22, 2007. Female patient, child 2 years of age, weighting 13.87 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, alpha haemolytic streptococcal infection, blood immunoglobulin g increased, blood sodium decreased, cardiac failure, condition aggravated, electrolyte imbalance, fluid retention, gene mutation identification test positive, . MYOZYME dosage: 20 MG/KG Q2WKS IV. During the same period patient was treated with MILRINONE. Patient was hospitalized. Patient recovered.

Cubicin Side Effects Report #5520546-2
CUBICIN problem was reported by a Physician from UNITED STATES on Nov 01, 2007. Male patient, 48 years of age, weighting 99.30 lb, was diagnosed with bacteraemia and was treated with CUBICIN. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, bacterial infection, klebsiella infection, pneumonia aspiration, . CUBICIN dosage: 6 MG/KG; Q48H; IV. During the same period patient was treated with VANCOMYCIN, CEFEPIME, PHENYTOIN, COLISTIN SULPHATE. Patient died.


Enbrel Side Effects Report #5490774-3
Physician from FRANCE reported ENBREL problem on Oct 08, 2007. Female patient was diagnosed with rheumatoid arthritis, sicca syndrome and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, acute myelomonocytic leukaemia, eosinophil count increased, gastroenteritis, hot flush, pruritus, . ENBREL dosage: 50 MG TOTAL WEEKLY. During the same period patient was treated with NOVATREX, SULFARLEM, ESTREVA, UTROGESTAN. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5493148-4
TACROLIMUS problem was reported by a Physician from MALAYSIA on Oct 11, 2007. Female patient, 42 years of age, was diagnosed with stem cell transplant and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, acute graft versus host disease in skin, enterococcal infection, pneumonia klebsiella, proteus infection, pseudomonas infection, sepsis, stenotrophomonas infection, . TACROLIMUS dosage: unknown. Patient was hospitalized. Patient died.

Nitric Side Effects Report #5500107-1
Physician from GERMANY reported NITRIC OXIDE problem on Oct 19, 2007. Female patient, weighting 2.18 lb, was diagnosed with lung disorder, prophylaxis and was treated with NITRIC OXIDE. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, apnoea, bradycardia, necrotising colitis, pneumatosis intestinalis, . NITRIC OXIDE dosage: unknown. During the same period patient was treated with NITRIC OXIDE, MEROPENEM, TEICOPLANIN, PHENOBARBITAL, MIDAZOLAM, NYSTATIN, CHLORAL HYDRATE. Patient recovered.

Fluconazole Side Effects Report #5470865-3
FLUCONAZOLE problem was reported by a Consumer or non-health professional from ITALY on Sept 10, 2007. Male patient, 55 years of age, was diagnosed with non-hodgkin's lymphoma and was treated with FLUCONAZOLE. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, blood culture positive, culture wound positive, staphylococcal infection, toxic epidermal necrolysis, . FLUCONAZOLE dosage: unknown. During the same period patient was treated with ACYCLOVIR, SULFAMETHOXAZOLE AND TRIMETHOPRIM, ALLOPURINOL. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5474817-9
Physician from CHINA reported MYOZYME problem on Sept 13, 2007. Female patient, child 2 years of age, weighting 13.23 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, alpha haemolytic streptococcal infection, aspiration tracheal abnormal, blood creatinine increased, blood sodium decreased, cardiac failure, disease recurrence, electrolyte imbalance, fluid retention, . MYOZYME dosage: 20 MG/KG Q2WKS IV. During the same period patient was treated with MILRINONE. Patient was hospitalized. Patient recovered.


Sandoglobulin Side Effects Report #5368437-4
SANDOGLOBULIN problem was reported by a Health Professional from FRANCE on June 04, 2007. Male patient, 61 years of age, was diagnosed with neuropathy peripheral and was treated with SANDOGLOBULIN. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, blood pressure increased, catheter sepsis, dizziness, enterobacter infection, heart rate increased, livedo reticularis, oxygen saturation decreased, serratia infection, . SANDOGLOBULIN dosage: unknown. During the same period patient was treated with DIANTALVIC, IMOVANE, DIFFU K. Patient recovered.

Ortho Side Effects Report #5382226-6
Consumer or non-health professional from UNITED STATES reported ORTHO EVRA problem on June 27, 2007. Female patient, weighting 345.5 lb, was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, brain natriuretic peptide increased, cardiac arrest, cardiac failure congestive, cardiomegaly, deep vein thrombosis, diastolic dysfunction, fibrin d dimer increased, hypoxia, . ORTHO EVRA dosage: unknown. During the same period patient was treated with ACIPHEX, DIOVAN, VALPROIC ACID, LITHIUM CARBONATE, LITHIUM CARBONATE. Patient was hospitalized. Patient died on 12/27/2004.

Remodulin Side Effects Report #5385468-9
REMODULIN problem was reported by a Physician from UNITED STATES on July 06, 2007. Female patient, weighting 103.0 lb, was diagnosed with pulmonary hypertension and was treated with REMODULIN. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, blood culture positive, catheter site infection, condition aggravated, pneumonia klebsiella, pseudomonas infection, pulmonary hypertension, shock, stenotrophomonas infection, . REMODULIN dosage: unknown. Patient was hospitalized. Patient recovered.

Acyclovir Side Effects Report #5402010-4
Consumer or non-health professional from ITALY reported ACYCLOVIR problem on July 16, 2007. Male patient, 55 years of age, was diagnosed with non-hodgkin's lymphoma and was treated with ACYCLOVIR. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, bacterial infection, blood culture positive, central line infection, culture wound positive, pyrexia, staphylococcal infection, toxic epidermal necrolysis, . ACYCLOVIR dosage: unknown. During the same period patient was treated with ALLOPURINOL, FLUCONAZOLE. Patient was hospitalized. Patient recovered.

Sandoglobulin Side Effects Report #5368437-4
SANDOGLOBULIN problem was reported by a Health Professional from FRANCE on June 04, 2007. Male patient, 61 years of age, was diagnosed with neuropathy peripheral and was treated with SANDOGLOBULIN. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, blood pressure increased, catheter sepsis, dizziness, enterobacter infection, heart rate increased, livedo reticularis, oxygen saturation decreased, serratia infection, . SANDOGLOBULIN dosage: unknown. During the same period patient was treated with DIANTALVIC, IMOVANE, DIFFU K. Patient recovered.

Ortho Side Effects Report #5382226-6
Consumer or non-health professional from UNITED STATES reported ORTHO EVRA problem on June 27, 2007. Female patient, weighting 345.5 lb, was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, brain natriuretic peptide increased, cardiac arrest, cardiac failure congestive, cardiomegaly, deep vein thrombosis, diastolic dysfunction, fibrin d dimer increased, hypoxia, . ORTHO EVRA dosage: unknown. During the same period patient was treated with ACIPHEX, DIOVAN, VALPROIC ACID, LITHIUM CARBONATE, LITHIUM CARBONATE. Patient was hospitalized. Patient died on 12/27/2004.

Remodulin Side Effects Report #5385468-9
REMODULIN problem was reported by a Physician from UNITED STATES on July 06, 2007. Female patient, weighting 103.0 lb, was diagnosed with pulmonary hypertension and was treated with REMODULIN. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, blood culture positive, catheter site infection, condition aggravated, pneumonia klebsiella, pseudomonas infection, pulmonary hypertension, shock, stenotrophomonas infection, . REMODULIN dosage: unknown. Patient was hospitalized. Patient recovered.

Acyclovir Side Effects Report #5402010-4
Consumer or non-health professional from ITALY reported ACYCLOVIR problem on July 16, 2007. Male patient, 55 years of age, was diagnosed with non-hodgkin's lymphoma and was treated with ACYCLOVIR. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, bacterial infection, blood culture positive, central line infection, culture wound positive, pyrexia, staphylococcal infection, toxic epidermal necrolysis, . ACYCLOVIR dosage: unknown. During the same period patient was treated with ALLOPURINOL, FLUCONAZOLE. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5766175-7
VELCADE problem was reported by a Physician from UNITED STATES on May 27, 2008. Male patient, 60 years of age, was diagnosed with myelofibrosis and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, catheter related infection, fungal infection, glucose tolerance impaired, graft versus host disease, stevens-johnson syndrome, toxic epidermal necrolysis, . VELCADE dosage: 1.3 MG/M2, INTRAVENOUS. During the same period patient was treated with TACROLIMUS, METHOTREXATE, ACTOS, ACYCLOVIR, BACTRIM, CELLCEPT, CLOBETASOL PROPIONATE, DIOVAN HCT. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5766220-9
Physician from UNITED STATES reported PROGRAF problem on May 29, 2008. Female patient, 53 years of age, weighting 117.1 lb, was diagnosed with lung transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, anuria, aspergillosis, blood alkaline phosphatase increased, blood glucose increased, blood pressure decreased, bronchiolitis, bronchitis fungal, bronchopulmonary aspergillosis, . PROGRAF dosage: unknown. During the same period patient was treated with VALCYTE, CELLCEPT, PREDNISOLONE ACETATE, FLUCONAZOLE, BACTRIM, VORICONAZOLE, ANTIBIOTICS. Patient died on 04/21/2008.

Cerezyme Side Effects Report #5775743-8
CEREZYME problem was reported by a Physician from JAPAN on June 06, 2008. Female patient, 19 years of age, weighting 66.14 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, infusion site infection, sepsis, staphylococcal infection, . CEREZYME dosage: unknown. Patient was hospitalized. Patient recovered.

Clofarabine Side Effects Report #5780880-8
Physician from UNITED STATES reported CLOFARABINE problem on Feb 14, 2008. Male patient, 24 years of age, weighting 137.6 lb, was diagnosed with acute myeloid leukaemia, bone marrow conditioning regimen and was treated with CLOFARABINE. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, blood culture positive, cerebral haemorrhage, enterococcal infection, fungal infection, grand mal convulsion, headache, hemianopia, hypotension, . CLOFARABINE dosage: 40 MG/M2, QD, INTRAVENOUS. During the same period patient was treated with CYTARABINE, PREDNISONE, THYMOGLOBULIN. Patient was hospitalized. Patient died on 02/13/2008.

Alemtuzumab Side Effects Report #5749064-3
ALEMTUZUMAB problem was reported by a Consumer or non-health professional from UNITED STATES on May 07, 2008. Female patient was diagnosed with chronic lymphocytic leukaemia, prophylaxis, infection prophylaxis, antiviral prophylaxis and was treated with ALEMTUZUMAB. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, anaemia, angina pectoris, aspergillosis, bacterial infection, cardiac failure congestive, chills, corynebacterium infection, cytokine release syndrome, . ALEMTUZUMAB dosage: TOTAL DAILY DOSE: 3 MG. During the same period patient was treated with DIPHENHYDRAMINE, ACETAMINOPHEN, SULFAMETHOXAZOLE AND TRIMETHOPRIM, VALACYCLOVIR. Patient died.

Busulfex Side Effects Report #5698170-0
Consumer or non-health professional from JAPAN reported BUSULFEX problem on Mar 21, 2008. Female patient, 40 years of age, was diagnosed with stem cell transplant and was treated with BUSULFEX. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, acute graft versus host disease, anorexia, cystitis haemorrhagic, cytomegalovirus antigen positive, liver disorder, malaise, mucous membrane disorder, nausea, . BUSULFEX dosage: 31.2 ML, INTRAVENOUS. During the same period patient was treated with FLUDARABINE PHOSPHATE, METHOTREXATE, ITRACONAZOLE, GANCICLOVIR. Patient was hospitalized and became disabled. Patient recovered.

Velcade Side Effects Report #5706373-1
VELCADE problem was reported by a Physician from FRANCE on Dec 13, 2007. Female patient, 64 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, dehydration, disease progression, mucous membrane disorder, pharyngeal inflammation, pruritus, sepsis, . VELCADE dosage: 2.00 MG. During the same period patient was treated with DEXAMETHASONE, CYCLOPHOSPHAMIDE, ETOPOSIDE, CISPLATIN, MELPHALAN. Patient was hospitalized. Patient recovered.

Metronidazole Side Effects Report #5363349-4
Consumer or non-health professional from ITALY reported METRONIDAZOLE problem on June 04, 2007. Female patient, 44 years of age, was diagnosed with lung infection and was treated with METRONIDAZOLE. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, sepsis, toxic epidermal necrolysis, . METRONIDAZOLE dosage: unknown. During the same period patient was treated with PIPERACILLIN. Patient died.

Sandoglobulin Side Effects Report #5368437-4
SANDOGLOBULIN LYO problem was reported by a Consumer or non-health professional from FRANCE on June 04, 2007. Male patient, 61 years of age, was diagnosed with neuropathy peripheral and was treated with SANDOGLOBULIN LYO. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, blood pressure increased, catheter sepsis, dizziness, enterobacter infection, heart rate increased, livedo reticularis, oxygen saturation decreased, serratia infection, . SANDOGLOBULIN LYO dosage: unknown. During the same period patient was treated with SANDOGLOBULIN LYO, SANDOGLOBULIN LYO, SANDOGLOBULIN LYO, SANDOGLOBULIN LYO, SANDOGLOBULIN LYO, DIANTALVIC, IMOVANE, DIFFU K. Patient recovered.

Clofarabine Side Effects Report #5337709-1
Health Professional from UNITED STATES reported CLOFARABINE problem on Mar 22, 2007. Female patient, 24 years of age, weighting 223.5 lb, was diagnosed with acute lymphocytic leukaemia and was treated with CLOFARABINE. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, pleural effusion, pulmonary haemorrhage, pulmonary oedema, serratia sepsis, . CLOFARABINE dosage: 82.8 MG DAILY IV. During the same period patient was treated with CYTARABINE. Patient was hospitalized. Patient died on 03/26/2007.

Daclizumab Side Effects Report #5293398-6
DACLIZUMAB problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 31, 2007. Female patient, 33 years of age, weighting 242.5 lb, was diagnosed with multiple sclerosis and was treated with DACLIZUMAB. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, alopecia, blood triglycerides increased, cardio-respiratory arrest, dysphagia, dysphonia, enterococcal infection, haematocrit decreased, haemoglobin decreased, . DACLIZUMAB dosage: unknown. During the same period patient was treated with INTERFERON BETA, CLORAZEPATE, MICRODIOL, ORLISTAT. Patient was hospitalized. Patient recovered.

Myfortic Side Effects Report #5298937-7
Physician from POLAND reported MYFORTIC problem on Apr 04, 2007. Male patient, 52 years of age, weighting 124.8 lb, was diagnosed with renal transplant and was treated with MYFORTIC. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, impaired healing, wound infection bacterial, . MYFORTIC dosage: 720MG/DAY. During the same period patient was treated with CELLCEPT, ENCORTON, PROGRAF, NEORAL. Patient was hospitalized. Patient recovered.

Daclizumab Side Effects Report #5307601-7
DACLIZUMAB problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 13, 2007. Female patient, 33 years of age, weighting 242.5 lb, was diagnosed with multiple sclerosis and was treated with DACLIZUMAB. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, anaemia, blood calcium decreased, blood phosphorus decreased, blood triglycerides increased, cardio-respiratory arrest, dysphagia, dysphonia, enterococcal infection, . DACLIZUMAB dosage: unknown. During the same period patient was treated with INTERFERON BETA, CLORAZEPATE, MICRODIOL, ORLISTAT. Patient was hospitalized. Patient recovered.

Busulfan Side Effects Report #5308978-9
Consumer or non-health professional from JAPAN reported BUSULFAN problem on Apr 06, 2007. Female patient, 54 years of age, was diagnosed with stem cell transplant and was treated with BUSULFAN. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, anorexia, depressed level of consciousness, graft versus host disease, inappropriate antidiuretic hormone secretion, malaise, nausea, sepsis, thrombotic microangiopathy, . BUSULFAN dosage: unknown. During the same period patient was treated with NEUPOGEN, NEUTROGIN, IMATINIB MESYLATE, VALPROATE, CYCLOPHOSPHAMIDE, METHOTREXATE. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5276689-4
REMICADE problem was reported by a Physician from UNITED STATES on Mar 15, 2007. Male patient, weighting 115.0 lb, was diagnosed with crohn's disease, pain and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, acute respiratory distress syndrome, chest pain, disseminated tuberculosis, fatigue, lymphohistiocytosis, myalgia, nausea, pancytopenia, . REMICADE dosage: unknown. During the same period patient was treated with PENTASA, IMURAN, PERCOCET. Patient was hospitalized. Patient died on 12/30/2004.

Clolar Side Effects Report #5283028-1
Consumer or non-health professional from UNITED STATES reported CLOLAR problem on Mar 28, 2007. Female patient, weighting 223.5 lb, was treated with CLOLAR. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, acute respiratory distress syndrome, bacterial sepsis, haemorrhage, pulmonary oedema, serratia sepsis, . CLOLAR dosage: 82.8 MG. During the same period patient was treated with CYTARABINE. Patient was hospitalized. Patient recovered.

Betamethasone Side Effects Report #5284395-5
BETAMETHASONE problem was reported by a Physician from JAPAN on Sept 06, 2006. Male patient, 59 years of age, was diagnosed with benign familial pemphigus and was treated with BETAMETHASONE. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, benign familial pemphigus, blood cortisol decreased, candidiasis, disease recurrence, dry mouth, erythema, hyperuricaemia, . BETAMETHASONE dosage: 1.5 MG; QD; PO. During the same period patient was treated with MINOCYCLINE. Patient was hospitalized. Patient recovered.

Diclofenac Side Effects Report #5616694-9
Health Professional from SAUDI ARABIA reported DICLOFENAC problem on Jan 30, 2008. Female patient, 43 years of age, was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: acanthosis, acinetobacter infection, arthritis, biopsy skin abnormal, blood culture positive, blood glucose increased, blood urea increased, citrobacter infection, . DICLOFENAC dosage: unknown. Patient was hospitalized. Patient recovered.

Risperdal Side Effects Report #5320515-1
RISPERDAL problem was reported by a Health Professional from FRANCE on May 03, 2007. Female patient, 89 years of age, weighting 110.2 lb, was diagnosed with abnormal behaviour, cardiac flutter, atrial fibrillation, diabetes mellitus and was treated with RISPERDAL. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, acinetobacter infection, eczema, escherichia infection, staphylococcal infection, toxic skin eruption, . RISPERDAL dosage: unknown. During the same period patient was treated with PREVISCAN, INSULATARD. Patient was hospitalized. Patient recovered.