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Revlimid Side Effects Report #5656172-4
Health Professional from GERMANY reported REVLIMID problem on Feb 25, 2008. Male patient, 39 years of age, weighting 196.2 lb, was diagnosed with hodgkin's disease and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, cardiovascular insufficiency, diarrhoea, emphysema, hepatic failure, hepatomegaly, jaundice, lymphadenopathy, neutropenia, . REVLIMID dosage: 25 MG, DAILY, ORAL; 25 MG, ORAL. During the same period patient was treated with PANTAZOL, DIFLUCAN, PREDNISOLONE, LINEZOLID. Patient was hospitalized. Patient died on 02/16/2008.

Rituximab Side Effects Report #5675385-9
RITUXIMAB problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 12, 2008. Female patient was diagnosed with b-cell lymphoma, prophylaxis and was treated with RITUXIMAB. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, . RITUXIMAB dosage: 375 MG/M2, 1/MONTH. During the same period patient was treated with FLUDARABINE, HYDROCHLOROTHIAZIDE, METOPROLOL TARTRATE, PRILOSEC, ACYCLOVIR, LEXAPRO, ASPIRIN. Patient was hospitalized. Patient died on 03/11/2008.

Rituximab Side Effects Report #5683403-7
Consumer or non-health professional from UNITED STATES reported RITUXIMAB problem on Mar 21, 2008. Female patient was diagnosed with b-cell lymphoma, prophylaxis and was treated with RITUXIMAB. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, . RITUXIMAB dosage: 375 MG/M2, 1/MONTH. During the same period patient was treated with FLUDARABINE, HYDROCHLOROTHIAZIDE, METOPROLOL TARTRATE, PRILOSEC, ACYCLOVIR, LEXAPRO, ASPIRIN. Patient was hospitalized. Patient died on 03/11/2008.

Methotrexate Side Effects Report #5688198-9
METHOTREXATE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 18, 2008. Female patient, 60 years of age, weighting 176.4 lb, was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, haemodialysis, multi-organ failure, . METHOTREXATE dosage: 7.5 MG WEEKLY. During the same period patient was treated with ENBREL, PREDNISOLONE, ASPIRIN, ATENOLOL, FUROSEMIDE, GLICLAZIDE, MELOXICAM, OMEPRAZOLE. Patient recovered.


Carboplatin Side Effects Report #5611094-X
Health Professional from KOREA, REPUBLIC OF reported CARBOPLATIN problem on Jan 31, 2008. Male patient, 59 years of age, was diagnosed with non-small cell lung cancer and was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, cardiac arrest, haemolysis, liver abscess, neutropenia, . CARBOPLATIN dosage: unknown. During the same period patient was treated with PACLITAXEL. Patient died.

Fluorouracil Side Effects Report #5616342-8
FLUOROURACIL problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 06, 2008. Male patient, weighting 151.9 lb, was treated with FLUOROURACIL. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, diarrhoea, gastrointestinal haemorrhage, haemoglobin decreased, loss of consciousness, oesophageal mass, oesophageal ulcer, open wound, septic shock, . FLUOROURACIL dosage: 5240 MG. During the same period patient was treated with ERBITUX, LEUCOVORIN CALCIUM, ELOXATIN. Patient was hospitalized. Patient recovered.

Doxorubicin Side Effects Report #5626747-7
Consumer or non-health professional from reported DOXORUBICIN problem on Feb 05, 2008. Male patient, weighting 172.0 lb, was diagnosed with hodgkin's disease and was treated with DOXORUBICIN. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, chills, convulsion, diarrhoea, fall, myoclonus, neutropenia, pancytopenia, pyrexia, . DOXORUBICIN dosage: DAILY DOSE:35MG/M2. During the same period patient was treated with ETOPOSIDE, ENDOXAN, VINCRISTINE, BLEOMYCIN, PROCARBAZINE HYDROCHLORIDE, NEUPOGEN, DECORTIN. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5633327-6
REMICADE problem was reported by a Physician from UNITED STATES on Feb 12, 2008. Male patient was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, coccidioidomycosis, idiopathic thrombocytopenic purpura, . REMICADE dosage: unknown. Patient was hospitalized. Patient died.

Etoposide Side Effects Report #5634210-2
Health Professional from GERMANY reported ETOPOSIDE problem on Feb 11, 2008. Male patient, 22 years of age, was diagnosed with hodgkin's disease and was treated with ETOPOSIDE. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, chills, diarrhoea, escherichia infection, fall, klebsiella infection, myoclonic epilepsy, pancytopenia, pyrexia, . ETOPOSIDE dosage: 200 MG/M2 FREQ. During the same period patient was treated with VINCRISTINE, BLEOMYCIN, DOXORUBICIN, CYCLOPHOSPHAMIDE, PROCARBAZINE, NEUPOGEN, PREDNISONE. Patient was hospitalized. Patient recovered.


Remicade Side Effects Report #5638450-8
REMICADE problem was reported by a Physician from UNITED STATES on Feb 15, 2008. Male patient, 60 years of age, was diagnosed with crohn's disease, pulmonary embolism and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, hepatic cancer metastatic, hepatic failure, pulmonary embolism, . REMICADE dosage: unknown. During the same period patient was treated with IMURAN, COUMADIN. Patient died.

Endoxan Side Effects Report #5600266-6
Consumer or non-health professional from UNITED STATES reported ENDOXAN problem on Jan 09, 2008. Male patient, 22 years of age, was diagnosed with hodgkin's disease and was treated with ENDOXAN. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, chills, convulsion, diarrhoea, fall, myoclonus, pancytopenia, pyrexia, renal failure acute, . ENDOXAN dosage: unknown. During the same period patient was treated with ETOPOSIDE, VINCRISTINE SULPHATE, DOXORUBICIN, BLEOMYCIN, PROCARBAZINE, NEUPOGEN, DECORTIN. Patient was hospitalized. Patient recovered.

Carboplatin Side Effects Report #5606105-1
CARBOPLATIN problem was reported by a Health Professional from KOREA, REPUBLIC OF on Jan 28, 2008. Male patient, 59 years of age, was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, cardiac arrest, haemolysis, liver abscess, neutropenia, . CARBOPLATIN dosage: unknown. During the same period patient was treated with PACLITAXEL. Patient died.

Enbrel Side Effects Report #5607724-9
Physician from GERMANY reported ENBREL problem on Jan 16, 2008. Male patient, weighting 138.9 lb, was diagnosed with polyarthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, multi-organ failure, pneumonia, septic shock, . ENBREL dosage: 50 MG WEEKLY. During the same period patient was treated with CORTISONE, LANTAREL. Patient was hospitalized. Patient recovered.

Carboplatin Side Effects Report #5615451-7
CARBOPLATIN problem was reported by a Physician from KOREA, REPUBLIC OF on Jan 21, 2008. Male patient, 59 years of age, was diagnosed with non-small cell lung cancer stage iiia and was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, cardiac arrest, chills, chromaturia, haemolytic anaemia, hypoxia, jaundice, lethargy, liver abscess, . CARBOPLATIN dosage: unknown. During the same period patient was treated with PACLITAXEL. Patient died.


Pegasys Side Effects Report #5534277-6
Health Professional from UNITED STATES reported PEGASYS problem on Nov 29, 2007. Male patient, 52 years of age, was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, cryoglobulinaemia, vasculitis gastrointestinal, . PEGASYS dosage: unknown. During the same period patient was treated with COPEGUS. Patient died on 07/05/2007.

Neoral Side Effects Report #5521666-9
NEORAL problem was reported by a Physician from ITALY on Nov 15, 2007. Male patient, 58 years of age, weighting 224.9 lb, was diagnosed with liver transplant and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, cerebral haemorrhage, concomitant disease progression, fungal sepsis, graft ischaemia, multi-organ failure, renal failure acute, . NEORAL dosage: 790 MG/DAILY. During the same period patient was treated with METHYLPREDNISOLONE. Patient was hospitalized. Patient died on 09/10/2007.

Cancidas Side Effects Report #5526089-4
Physician from FRANCE reported CANCIDAS problem on Nov 12, 2007. Female patient, 44 years of age, was diagnosed with pyrexia and was treated with CANCIDAS. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, bronchopulmonary aspergillosis, graft versus host disease, leukaemia recurrent, zygomycosis, . CANCIDAS dosage: unknown. Patient died.

Cosmegen Side Effects Report #5527386-9
COSMEGEN problem was reported by a Physician from UNITED STATES on Nov 09, 2007. Female patient was diagnosed with ewing's sarcoma metastatic and was treated with COSMEGEN. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, . COSMEGEN dosage: 1.25 MG/M**2; ; IV. During the same period patient was treated with VINCRISTINE, IFOSFAMIDE, ADRIAMYCIN PFS, ETOPOSIDE, CYCLOPHOSPHAMIDE. Patient died.

Rituximab Side Effects Report #5489482-4
Physician from GERMANY reported RITUXIMAB problem on Oct 10, 2007. Female patient was diagnosed with diffuse large b-cell lymphoma and was treated with RITUXIMAB. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, neutropenia, . RITUXIMAB dosage: 375 MG/M2, UNK. During the same period patient was treated with CISPLATIN, CYTOSINE ARABINOSIDE, DEXAMETHASONE, LENOGRASTIM. Patient was hospitalized. Patient died on 12/29/2004.


Neoral Side Effects Report #5491502-8
NEORAL problem was reported by a Physician from ITALY on Oct 16, 2007. Male patient, 58 years of age, weighting 224.9 lb, was diagnosed with liver transplant and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, cerebral haemorrhage, concomitant disease progression, fungal sepsis, graft ischaemia, renal failure acute, . NEORAL dosage: 790 MG/DAILY. During the same period patient was treated with METHYLPREDNISOLONE. Patient was hospitalized. Patient died on 09/10/2007.

Cancidas Side Effects Report #5495332-2
Physician from FRANCE reported CANCIDAS problem on Oct 17, 2007. Female patient, 44 years of age, was diagnosed with pyrexia and was treated with CANCIDAS. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, bronchopulmonary aspergillosis, graft versus host disease, leukaemia recurrent, zygomycosis, . CANCIDAS dosage: unknown. Patient died.

Myfortic Side Effects Report #5443001-7
MYFORTIC VS CELLCEPT problem was reported by a Pharmacist from UNITED STATES on Aug 27, 2007. Female patient, 50 years of age, weighting 119.0 lb, was diagnosed with renal transplant and was treated with MYFORTIC VS CELLCEPT. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, blood creatinine increased, diarrhoea, haemoglobin decreased, hypotension, urinary tract infection, ventricular tachycardia, . MYFORTIC VS CELLCEPT dosage: 360 MG, BID. Patient was hospitalized. Patient recovered.

Gemcitabine Side Effects Report #5449730-3
Consumer or non-health professional from UNITED STATES reported GEMCITABINE problem on Sept 10, 2007. Male patient, 67 years of age, weighting 134.5 lb, was diagnosed with pancreatic carcinoma metastatic and was treated with GEMCITABINE. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, disease progression, intestinal obstruction, obstruction gastric, . GEMCITABINE dosage: 1000MG/M2 IV BOLUS. During the same period patient was treated with BEVACIZUMAB, ERLOTINIB, AMBIEN, CALCIUM, COMPAZINE, CREON, GLYCOLAX, LIPITOR. Patient was hospitalized. Patient recovered.

Myfortic Side Effects Report #5450845-4
MYFORTIC VS CELLCEPT problem was reported by a Pharmacist from UNITED STATES on Sept 04, 2007. Female patient, 50 years of age, weighting 119.0 lb, was diagnosed with renal transplant and was treated with MYFORTIC VS CELLCEPT. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, blood creatinine increased, diarrhoea, haemoglobin decreased, hypotension, urinary tract infection, ventricular tachycardia, . MYFORTIC VS CELLCEPT dosage: 360 MG, BID. Patient was hospitalized. Patient recovered.

Myfortic Side Effects Report #5461116-4
Pharmacist from UNITED STATES reported MYFORTIC VS CELLCEPT problem on Sept 10, 2007. Female patient, 50 years of age, weighting 119.0 lb, was diagnosed with renal transplant and was treated with MYFORTIC VS CELLCEPT. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, blood creatinine increased, diarrhoea, haemoglobin decreased, hypotension, urinary tract infection, ventricular tachycardia, . MYFORTIC VS CELLCEPT dosage: 360 MG, BID. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5462350-X
CISPLATIN problem was reported by a Health Professional from UNITED STATES on Sept 18, 2007. Male patient, weighting 163.1 lb, was diagnosed with tonsil cancer and was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, band neutrophil percentage increased, diarrhoea, febrile neutropenia, neutrophil percentage decreased, respiratory failure, staphylococcal infection, white blood cell count decreased, . CISPLATIN dosage: 100MG/M2 IV Q4WKS. During the same period patient was treated with CETUXIMAB. Patient was hospitalized. Patient recovered.

Cardyl Side Effects Report #5464924-9
Consumer or non-health professional from SPAIN reported CARDYL problem on Sept 13, 2007. Female patient, 72 years of age, was diagnosed with blood triglycerides increased, blood cholesterol increased, blood uric acid increased and was treated with CARDYL. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, multi-organ failure, toxic epidermal necrolysis, . CARDYL dosage: unknown. During the same period patient was treated with ALLOPURINOL. Patient was hospitalized. Patient died.

Cymbalta Side Effects Report #5468285-0
CYMBALTA problem was reported by a Physician from UNITED STATES on Sept 12, 2007. Female patient, 55 years of age, weighting 175.3 lb, was diagnosed with neuralgia and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, herpes zoster, hypotension, pain, rash, skin exfoliation, stevens-johnson syndrome, thrombocytopenia, toxic epidermal necrolysis, . CYMBALTA dosage: unknown. During the same period patient was treated with LYRICA, HUMALOG, LANTUS, PREDNISONE, LOPID, AVAPRO, SYNTHROID, IMDUR. Patient was hospitalized. Patient recovered.

Propofol Side Effects Report #5470515-6
Consumer or non-health professional from UNITED STATES reported PROPOFOL problem on Sept 27, 2007. Male patient, weighting 210.0 lb, was treated with PROPOFOL. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, body temperature increased, chest discomfort, chills, cough, dysphonia, influenza, malaise, pain, . PROPOFOL dosage: unknown. Patient recovered.

Humira Side Effects Report #5411499-6
HUMIRA problem was reported by a Physician from SOUTH AFRICA on Aug 03, 2007. Male patient, weighting 187.4 lb, was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, fungal sepsis, lung disorder, multi-organ failure, pericardial effusion, pericarditis constrictive, pleural effusion, pneumonia, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, FOLIC ACID, PREDNISONE, DICLOFENAC, SULFASALAZINE. Patient was hospitalized. Patient died on 06/27/2007.

Bevacizumab Side Effects Report #5412684-X
Physician from UNITED STATES reported BEVACIZUMAB problem on Aug 01, 2007. Female patient, 50 years of age, weighting 171.3 lb, was diagnosed with breast cancer and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, blood creatinine increased, blood urea increased, cardiac valve disease, encephalitis herpes, fungus serology test, haemorrhage intracranial, hepatic function abnormal, hydrocephalus, . BEVACIZUMAB dosage: 15 MG/KG, UNK. During the same period patient was treated with TRASTUZUMAB, DOCETAXEL, CARBOPLATIN, ENTEX LA, FISH OIL, VITAMIN CAP, PROTONIX. Patient was hospitalized. Patient died on 07/26/2007.

Ranitidine Side Effects Report #5428625-5
RANITIDINE problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 14, 2007. Female patient was diagnosed with feeding disorder neonatal and was treated with RANITIDINE. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, sepsis neonatal, staphylococcal infection, . RANITIDINE dosage: unknown. Patient was hospitalized. Patient recovered.

Raptiva Side Effects Report #5379206-3
Physician from SWITZERLAND reported RAPTIVA problem on June 26, 2007. Male patient was diagnosed with psoriasis and was treated with RAPTIVA. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, chronic myeloid leukaemia, diverticular perforation, multi-organ failure, pneumonia, . RAPTIVA dosage: unknown. During the same period patient was treated with ALENDRONATE. Patient was hospitalized. Patient died on 02/07/2007.

Humira Side Effects Report #5391802-6
HUMIRA problem was reported by a Physician from SOUTH AFRICA on July 12, 2007. Male patient, 29 years of age, was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, fungal sepsis, lung disorder, multi-organ failure, pericardial effusion, pericarditis, pleural effusion, pneumonia, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, FOLIC ACID, PREDNISONE, DICLOFENAC, SULFASALAZINE. Patient was hospitalized. Patient died on 06/27/2007.

Remodulin Side Effects Report #5403902-2
Physician from UNITED STATES reported REMODULIN problem on Oct 11, 2006. Female patient, 36 years of age, was diagnosed with pulmonary hypertension and was treated with REMODULIN. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, delusion, diarrhoea, dyspnoea, haematocrit decreased, international normalised ratio increased, oxygen saturation decreased, pyrexia, septic embolus, . REMODULIN dosage: unknown. During the same period patient was treated with CARDIZEM CD, FUROSEMIDE, WARFARIN, POTASSIUM CHLORIDE, DIGOXIN, SOTALOL HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Remodulin Side Effects Report #5404783-3
REMODULIN problem was reported by a Health Professional from UNITED STATES on Jan 24, 2007. Female patient, child 9 years of age, was diagnosed with pulmonary hypertension and was treated with REMODULIN. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, central line infection, . REMODULIN dosage: unknown. During the same period patient was treated with BUDESONIDE, FUROSEMIDE, LEVALBUTEROL, SPIRONOLACTONE, BOSENTAN. Patient was hospitalized. Patient recovered.

Raptiva Side Effects Report #5379206-3
Physician from SWITZERLAND reported RAPTIVA problem on June 26, 2007. Male patient was diagnosed with psoriasis and was treated with RAPTIVA. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, chronic myeloid leukaemia, diverticular perforation, multi-organ failure, pneumonia, . RAPTIVA dosage: unknown. During the same period patient was treated with ALENDRONATE. Patient was hospitalized. Patient died on 02/07/2007.

Humira Side Effects Report #5391802-6
HUMIRA problem was reported by a Physician from SOUTH AFRICA on July 12, 2007. Male patient, 29 years of age, was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, fungal sepsis, lung disorder, multi-organ failure, pericardial effusion, pericarditis, pleural effusion, pneumonia, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, FOLIC ACID, PREDNISONE, DICLOFENAC, SULFASALAZINE. Patient was hospitalized. Patient died on 06/27/2007.

Remodulin Side Effects Report #5403902-2
Physician from UNITED STATES reported REMODULIN problem on Oct 11, 2006. Female patient, 36 years of age, was diagnosed with pulmonary hypertension and was treated with REMODULIN. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, delusion, diarrhoea, dyspnoea, haematocrit decreased, international normalised ratio increased, oxygen saturation decreased, pyrexia, septic embolus, . REMODULIN dosage: unknown. During the same period patient was treated with CARDIZEM CD, FUROSEMIDE, WARFARIN, POTASSIUM CHLORIDE, DIGOXIN, SOTALOL HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Remodulin Side Effects Report #5404783-3
REMODULIN problem was reported by a Health Professional from UNITED STATES on Jan 24, 2007. Female patient, child 9 years of age, was diagnosed with pulmonary hypertension and was treated with REMODULIN. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, central line infection, . REMODULIN dosage: unknown. During the same period patient was treated with BUDESONIDE, FUROSEMIDE, LEVALBUTEROL, SPIRONOLACTONE, BOSENTAN. Patient was hospitalized. Patient recovered.

Mabthera Side Effects Report #5757594-3
Consumer or non-health professional from UNITED KINGDOM reported MABTHERA problem on May 19, 2008. Female patient was diagnosed with non-hodgkin's lymphoma, b-cell lymphoma and was treated with MABTHERA. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, . MABTHERA dosage: 375 MG/M2, UNK. During the same period patient was treated with DOXORUBICIN, VINCRISTINE, PREDNISONE, ETOPOSIDE, CYCLOPHOSPHAMIDE, MITOXANTRONE, MELPHALAN, NEUPOGEN. Patient died.

Temozolomide Side Effects Report #5758162-X
TEMOZOLOMIDE problem was reported by a Consumer or non-health professional from CANADA on June 02, 2008. Male patient, weighting 156.3 lb, was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, enterocolitis, gastrointestinal ischaemia, mental status changes, performance status decreased, pneumonia, . TEMOZOLOMIDE dosage: 3640 MG. Patient was hospitalized. Patient recovered.

Rituximab Side Effects Report #5761351-1
Consumer or non-health professional from UNITED KINGDOM reported RITUXIMAB problem on May 27, 2008. Male patient was diagnosed with mantle cell lymphoma and was treated with RITUXIMAB. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, febrile bone marrow aplasia, hyperthermia, . RITUXIMAB dosage: 450 MG, UNK. During the same period patient was treated with CYCLOPHOSPHAMIDE, DOXORUBICIN, VINCRISTINE, PREDNISONE. Patient was hospitalized. Patient recovered.

Mabthera Side Effects Report #5761524-8
MABTHERA problem was reported by a Physician from UNITED KINGDOM on June 04, 2008. Female patient was diagnosed with b-cell lymphoma and was treated with MABTHERA. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, . MABTHERA dosage: 4375 MG/M2, UNK. During the same period patient was treated with CYCLOPHOSPHAMIDE, DOXORUBICIN, VINCRISTINE, PREDNISONE. Patient died.

Humira Side Effects Report #5770905-8
Physician from UNITED STATES reported HUMIRA problem on May 30, 2008. Female patient, weighting 118.1 lb, was diagnosed with crohn's disease, diarrhoea, mineral supplementation, vitamin supplementation, osteoporosis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, weight increased, white blood cell count increased, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISONE, OPIUM DROPS, COLESTYRAMINE, POTASSIUM, ERGOCALCIFEROL, CALCIUM MAGNESIUM ZINC. Patient was hospitalized. Patient recovered.

Rituximab Side Effects Report #5774542-0
RITUXIMAB problem was reported by a Consumer or non-health professional from UNITED STATES on June 02, 2008. Female patient was diagnosed with b-cell lymphoma, prophylaxis and was treated with RITUXIMAB. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, . RITUXIMAB dosage: 375 MG/M2, 1/MONTH. During the same period patient was treated with FLUDARABINE PHOSPHATE, HYDROCHLOROTHIAZIDE, METOPROLOL, PRILOSEC, ACYCLOVIR, LEXAPRO, ASPIRIN. Patient was hospitalized. Patient died on 03/12/2008.

Bevacizumab Side Effects Report #5779708-1
Physician from UNITED KINGDOM reported BEVACIZUMAB problem on June 05, 2008. Male patient was diagnosed with colorectal cancer and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, dehydration, oesophagitis, . BEVACIZUMAB dosage: 5 MG/KG, Q2W. During the same period patient was treated with CAPECITABINE, OXALIPLATIN, ONDANSETRON, CIPRO, NYSTATIN, OPIUM, TRAZODONE, COZAAR. Patient was hospitalized. Patient recovered.

Propofol Side Effects Report #5784248-X
PROPOFOL problem was reported by a Pharmacist from UNITED STATES on June 19, 2008. Male patient, weighting 34.79 lb, was diagnosed with sedation and was treated with PROPOFOL. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, chills, pain, pyrexia, . PROPOFOL dosage: unknown. Patient recovered.

Velcade Side Effects Report #5788254-0
Health Professional from UNITED STATES reported VELCADE problem on June 13, 2008. Male patient, 79 years of age, weighting 132.9 lb, was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, fall, hypotension, muscular weakness, skin laceration, thrombocytopenia, . VELCADE dosage: 3.4 MG, UNK, INTRAVENOUS. During the same period patient was treated with ALIMTA, VITAMINS, KELP, ASPIRIN, PERCOCET, DEXAMETHASONE, FOLIC ACID, COMPAZINE. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5792549-4
VELCADE problem was reported by a Physician from FRANCE on June 13, 2008. Male 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: bacterial sepsis, catheter related infection, stenotrophomonas infection, . VELCADE dosage: 2.60 MG, INTRAVENOUS. During the same period patient was treated with VINCRISTINE, DOXORUBICIN, DEXAMETHASONE. Patient was hospitalized. Patient recovered.

Treprostinil Side Effects Report #5726057-3
Pharmacist from UNITED STATES reported TREPROSTINIL problem on May 01, 2008. Female patient, weighting 145.0 lb, was diagnosed with pulmonary hypertension and was treated with TREPROSTINIL. After drug was administered, patient experienced the following problems/side effects: bacterial sepsis, infusion related reaction, . TREPROSTINIL dosage: unknown. During the same period patient was treated with SPIRONOLACTONE, OXYCODONE, ESTRADIOL, SILDENAFIL CITRATE, WARFARIN, BOSENTAN. Patient died on 04/23/2008.