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Cyclophosphamide Side Effects Report #5648536-X
Consumer or non-health professional from UNITED STATES reported CYCLOPHOSPHAMIDE problem on Mar 03, 2008. Female patient, weighting 140.2 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: acidosis, acute respiratory distress syndrome, blood culture positive, deep vein thrombosis, dilatation ventricular, dyspnoea, enterovesical fistula, escherichia infection, . CYCLOPHOSPHAMIDE dosage: 820 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE. Patient was hospitalized. Patient died on 08/13/2007.

Acetazolamide Side Effects Report #5648853-3
ACETAZOLAMIDE problem was reported by a Pharmacist from UNITED STATES on Mar 03, 2008. Male patient, 73 years of age, was diagnosed with glaucoma, iris neovascularisation and was treated with ACETAZOLAMIDE. After drug was administered, patient experienced the following problems/side effects: acidosis, azotaemia, blood creatinine increased, blood urea increased, confusional state, dehydration, hyperglycaemia, mental status changes, renal tubular acidosis, . ACETAZOLAMIDE dosage: 250MG BID PO. Patient was hospitalized. Patient recovered.

Glucophage Side Effects Report #5650378-6
Health Professional from GERMANY reported GLUCOPHAGE problem on Feb 27, 2008. Female patient, 58 years of age, was treated with GLUCOPHAGE. After drug was administered, patient experienced the following problems/side effects: acidosis, . GLUCOPHAGE dosage: unknown. Patient recovered.

Sirolimus Side Effects Report #5650458-5
SIROLIMUS problem was reported by a Pharmacist from UNITED STATES on Mar 04, 2008. Male patient, 72 years of age, weighting 198.6 lb, was diagnosed with heart transplant, immune system disorder and was treated with SIROLIMUS. After drug was administered, patient experienced the following problems/side effects: acidosis, cardio-respiratory arrest, hypersensitivity, hypotension, hypoxia, lactic acidosis, lung injury, no therapeutic response, pleural effusion, . SIROLIMUS dosage: 2MG DAILY PO. During the same period patient was treated with MYCOPHENOLATE MOFETIL, FENOFIBRATE, QUININE SULPHATE, LEVOTHYROXINE, OMEPRAZOLE, POTASSIUM CHLORIDE, AMLODIPINE. Patient was hospitalized. Patient died on 04/28/2007.


Lapatinib Side Effects Report #5651039-X
Physician from UNITED STATES reported LAPATINIB problem on Feb 28, 2008. Female patient, 65 years of age, was diagnosed with pancreatic carcinoma metastatic and was treated with LAPATINIB. After drug was administered, patient experienced the following problems/side effects: acidosis, anal ulcer, aspiration, blood creatinine abnormal, cholangitis, decubitus ulcer, hypotension, infection, sepsis, . LAPATINIB dosage: 1500MG PER DAY. During the same period patient was treated with GEMCITABINE. Patient died on 02/27/2008.

Ribavirin Side Effects Report #5652225-5
RIBAVIRIN problem was reported by a Physician from POLAND on Feb 19, 2008. Male patient, 21 years of age, was diagnosed with hepatitis c virus and was treated with RIBAVIRIN. After drug was administered, patient experienced the following problems/side effects: acidosis, altered state of consciousness, anaemia, brain oedema, carbohydrate metabolism disorder, cholestasis, hyperammonaemia, liver transplant rejection, . RIBAVIRIN dosage: unknown. During the same period patient was treated with TACROLIMUS, MYCOPHENOLATE MOFETIL. Patient recovered.

Zyprexa Side Effects Report #5653210-X
Physician from UNITED STATES reported ZYPREXA problem on Feb 25, 2008. Male patient, 22 years of age, was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: acidosis, decubitus ulcer, depressed level of consciousness, dysarthria, miosis, mucous membrane disorder, overdose, somnolence, . ZYPREXA dosage: unknown. During the same period patient was treated with TRIHEXYPHENIDYL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5657364-0
SUTENT problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 27, 2008. Male patient, 56 years of age, weighting 224.9 lb, was diagnosed with bladder transitional cell carcinoma and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: acidosis, anorexia, dehydration, fatigue, gastrointestinal necrosis, hypotension, intestinal ischaemia, intussusception, . SUTENT dosage: unknown. During the same period patient was treated with BEVACIZUMAB, NORVASC, TOPROL, PRINIVIL, OXYCODONE, CELEXA, NASONEX. Patient was hospitalized. Patient died on 10/21/2007.

Atarax Side Effects Report #5657527-4
Health Professional from FRANCE reported ATARAX problem on Mar 03, 2008. Male patient, 55 years of age, was diagnosed with schizophrenia and was treated with ATARAX. After drug was administered, patient experienced the following problems/side effects: acidosis, acute respiratory distress syndrome, intestinal ischaemia, intestinal obstruction, pneumonia aspiration, septic shock, . ATARAX dosage: DAILY DOSE:150MG-FREQ:DAILY. During the same period patient was treated with NOZINAN, TRANXENE, PARKINANE, MEPRONIZINE, ZYPREXA, COZAAR, SULFARLEM, CORVASAL. Patient was hospitalized. Patient recovered.


Methylene Side Effects Report #5657656-5
METHYLENE BLUE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Feb 21, 2008. Male patient, 65 years of age, weighting 176.4 lb, was diagnosed with scan parathyroid and was treated with METHYLENE BLUE. After drug was administered, patient experienced the following problems/side effects: acidosis, agitation, blood potassium increased, bundle branch block left, cardiac disorder, depressed level of consciousness, disorientation, electrocardiogram st-t segment depression, . METHYLENE BLUE dosage: 650 MG DAILY IV. During the same period patient was treated with METHYLENE BLUE, INSULIN, QUININE SULPHATE, OMEPRAZOLE, CLOPIDOGREL, ATORVASTATIN CALCIUM, ALFACALCIDOL, CITALOPRAM HYDROBROMIDE. Patient was hospitalized. Patient recovered.

Citalopram Side Effects Report #5660280-1
Health Professional from UNITED KINGDOM reported CITALOPRAM HYDROBROMIDE problem on Feb 22, 2008. Male patient, 65 years of age, was diagnosed with parathyroid disorder and was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: acidosis, blood potassium increased, bundle branch block left, calcium ionised decreased, cardiac output decreased, continuous haemodiafiltration, depressed level of consciousness, disorientation, . CITALOPRAM HYDROBROMIDE dosage: unknown. During the same period patient was treated with METHYLENE BLUE, METHYLENE BLUE, ALFACALCIDOL, ALUMINUM HYDROXIDE GEL, ATORVASTATIN CALCIUM, CLOPIDOGREL, INSULIN, OMEPRAZOLE. Patient was hospitalized. Patient recovered.

Prinivil Side Effects Report #5661672-7
PRINIVIL problem was reported by a Health Professional from UNITED STATES on Mar 11, 2008. Male patient, 56 years of age, was diagnosed with bladder transitional cell carcinoma and was treated with PRINIVIL. After drug was administered, patient experienced the following problems/side effects: acidosis, anorexia, dehydration, fatigue, gastrointestinal necrosis, hypotension, intussusception, . PRINIVIL dosage: unknown. During the same period patient was treated with SUTENT, BEVACIZUMAB, NORVASC, TOPROL, CELEXA, NASONEX, OXYCODONE. Patient was hospitalized. Patient died on 10/21/2007.

Metformin Side Effects Report #5663897-3
Consumer or non-health professional from reported METFORMIN HYDROCHLORIDE problem on Mar 03, 2008. Male patient, 68 years of age, weighting 156.5 lb, was treated with METFORMIN HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: acidosis, diarrhoea, renal failure, vomiting, . METFORMIN HYDROCHLORIDE dosage: unknown. During the same period patient was treated with ASPIRIN, ATORVASTATIN CALCIUM, ROSIGLITAZONE, SPIRONOLACTONE, IRBESARTAN AND HCTZ. Patient was hospitalized. Patient recovered.

Cytarabine Side Effects Report #5669731-X
CYTARABINE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 13, 2008. Male patient, weighting 31.75 lb, was treated with CYTARABINE. After drug was administered, patient experienced the following problems/side effects: acidosis, blood culture positive, clostridial infection, hepatitis, ileus, micrococcus infection, multi-organ failure, pancreatitis, respiratory distress, . CYTARABINE dosage: 14400 MG. Patient was hospitalized. Patient recovered.


Toprol Side Effects Report #5675657-8
Consumer or non-health professional from UNITED STATES reported TOPROL problem on Mar 18, 2008. Male patient, 56 years of age, weighting 224.9 lb, was diagnosed with bladder transitional cell carcinoma and was treated with TOPROL. After drug was administered, patient experienced the following problems/side effects: acidosis, anorexia, dehydration, fatigue, gastrointestinal necrosis, hypotension, intussusception, respiratory failure, . TOPROL dosage: unknown. During the same period patient was treated with SUNITINIB, BEVACIZUMAB, PRINIVIL, NORVASC, OXYCODONE, CELEXA, NASONEX. Patient was hospitalized. Patient died on 10/21/2007.

Paxil Side Effects Report #5675882-6
PAXIL problem was reported by a Health Professional from UNITED STATES on Mar 07, 2008. Male patient, weighting 4.85 lb, was diagnosed with panic attack, anxiety, constipation and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: acidosis, atrial septal defect, bronchial hyperreactivity, cardiac disorder, cardiac failure congestive, cerebral haemorrhage, cholestasis, congenital anomaly, congenital pulmonary hypertension, . PAXIL dosage: 20MG PER DAY. During the same period patient was treated with PAROXETINE, VITAMIN CAP, FERROUS SULPHATE, CHLOROTHIAZIDE, DIGOXIN, PHENOBARBITAL, POLYVISOL, COLACE. Patient was hospitalized. Patient recovered.

Clolar Side Effects Report #5675998-4
Physician from UNITED STATES reported CLOLAR problem on Mar 11, 2008. Female patient, 74 years of age, was diagnosed with myeloid leukaemia and was treated with CLOLAR. After drug was administered, patient experienced the following problems/side effects: acidosis, acute respiratory distress syndrome, aspergillosis, bone marrow failure, electromechanical dissociation, febrile neutropenia, haemoptysis, haemorrhage, pneumonia necrotising, . CLOLAR dosage: 43 MG, QDX3, INTRAVENOUS; 87 MG, QDX3, INTRAVENOUS. During the same period patient was treated with ZOLPIDEM TARTRATE, ACYCLOVIR, CEFEPIME, FLUCONAZOLE, FUROSEMIDE. Patient died on 03/05/2008.

Citalopram Side Effects Report #5676560-X
CITALOPRAM HYDROBROMIDE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 10, 2008. Male patient, 65 years of age, was diagnosed with scan parathyroid and was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: acidosis, blood calcium decreased, blood potassium increased, bundle branch block left, confusional state, electrocardiogram st segment depression, hypercapnia, . CITALOPRAM HYDROBROMIDE dosage: unknown. During the same period patient was treated with METHYLENE BLUE, METHYLENE BLUE, ALFACALCIDOL, ALUMINUM HYDROXIDE GEL, ATORVASTATIN CALCIUM, CLOPIDOGREL, INSULIN, OMEPRAZOLE. Patient was hospitalized. Patient recovered.

Paxil Side Effects Report #5678989-2
Consumer or non-health professional from UNITED STATES reported PAXIL CR problem on Mar 11, 2008. Male patient was diagnosed with anxiety and was treated with PAXIL CR. After drug was administered, patient experienced the following problems/side effects: acidosis, atelectasis, atrial septal defect, blepharospasm, blood pressure increased, brain hypoxia, cardiac failure congestive, cardiac murmur, cardiac output decreased, . PAXIL CR dosage: 25MG PER DAY. During the same period patient was treated with VITAMIN. Patient was hospitalized. Patient recovered.


Zolinza Side Effects Report #5684455-0
ZOLINZA problem was reported by a Physician from UNITED STATES on Mar 17, 2008. Male patient, 55 years of age, was diagnosed with mycosis fungoides stage ii and was treated with ZOLINZA. After drug was administered, patient experienced the following problems/side effects: acidosis, anorexia, chills, cough, dehydration, dysuria, fatigue, feeling abnormal, headache, . ZOLINZA dosage: unknown. Patient was hospitalized. Patient recovered.

Bevacizumab Side Effects Report #5685070-5
Consumer or non-health professional from UNITED KINGDOM reported BEVACIZUMAB problem on Mar 13, 2008. Male patient was diagnosed with rectal cancer and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: acidosis, alanine aminotransferase abnormal, anorexia, aspartate aminotransferase abnormal, blood bilirubin abnormal, blood potassium increased, condition aggravated, disease progression, . BEVACIZUMAB dosage: 10 MG/KG, Q2W. During the same period patient was treated with FLUOROURACIL, ISOVORIN, OXALIPLATIN, CYTOTEC, DICLOFENAC, LOXONIN, MORPHINE ELIXIR, NORVASC. Patient died on 11/10/2007.

Paxil Side Effects Report #5612578-0
PAXIL CR problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 24, 2008. Male patient was diagnosed with anxiety and was treated with PAXIL CR. After drug was administered, patient experienced the following problems/side effects: acidosis, atelectasis, atrial septal defect, blepharospasm, blood pressure increased, brain hypoxia, cardiac failure congestive, cardiac murmur, cardiac output decreased, . PAXIL CR dosage: 25MG PER DAY. During the same period patient was treated with PRENATAL VITAMINS. Patient was hospitalized. Patient recovered.

Mercaptopurine Side Effects Report #5612663-3
Consumer or non-health professional from UNITED STATES reported MERCAPTOPURINE problem on Feb 01, 2008. Female patient, weighting 37.26 lb, was treated with MERCAPTOPURINE. After drug was administered, patient experienced the following problems/side effects: acidosis, acute prerenal failure, blood bilirubin increased, blood culture positive, culture stool positive, dehydration, dialysis, diarrhoea haemorrhagic, fungus stool identified, . MERCAPTOPURINE dosage: 1700 MG. During the same period patient was treated with METHOTREXATE, VINCRISTINE SULPHATE, DEXAMETHASONE, DIFLUCAN, FLAGYL, GANCICLOVIR, PROTONIX, VANCOMYCIN. Patient was hospitalized. Patient recovered.

Cymbalta Side Effects Report #5615835-7
CYMBALTA problem was reported by a Physician from GERMANY on Jan 25, 2008. Female patient, weighting 176.4 lb, was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: acidosis, cyanosis, intentional overdose, somnolence, suicide attempt, tachycardia, . CYMBALTA dosage: 2040 MG, ONCE. During the same period patient was treated with CARBAMAZEPINE, ALCOHOL. Patient recovered.

Temozolomide Side Effects Report #5616652-4
Physician from MEXICO reported TEMOZOLOMIDE problem on Jan 28, 2008. Female patient, 67 years of age, weighting 114.6 lb, was diagnosed with colorectal cancer and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: acidosis, asthenia, haemoglobin decreased, hepatic encephalopathy, hypotension, leukopenia, miosis, neutropenia, . TEMOZOLOMIDE dosage: 215 MG; QD;. During the same period patient was treated with LOMOTIL. Patient was hospitalized. Patient died on 01/23/2008.

Novoseven Side Effects Report #5621528-2
NOVOSEVEN problem was reported by a Physician from AUSTRALIA on Feb 05, 2008. Female patient was diagnosed with haemorrhage and was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: acidosis, anaemia, atrial fibrillation, bradycardia, cellulitis, coagulopathy, colostomy, diarrhoea, hypotension, . NOVOSEVEN dosage: 9.6 MG, SINGLE. During the same period patient was treated with ASPIRIN, PARACETAMOL, HEPARIN, ESOMEPRAZOLE MAGNESIUM, AVAPRO, CARTIA, ATENOLOL. Patient died on 09/30/2007.

Olmesartan Side Effects Report #5622214-5
Consumer or non-health professional from SPAIN reported OLMESARTAN MEDOXOMIL problem on Jan 25, 2008. Male patient, 77 years of age, was diagnosed with hypertension and was treated with OLMESARTAN MEDOXOMIL. After drug was administered, patient experienced the following problems/side effects: acidosis, electrolyte imbalance, metabolic disorder, renal failure acute, . OLMESARTAN MEDOXOMIL dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with ANAGASTRA, ISCOVER, SPIRIVA. Patient was hospitalized. Patient recovered.

Irinotecan Side Effects Report #5622531-9
IRINOTECAN problem was reported by a Consumer or non-health professional from on Feb 04, 2008. Male patient, 69 years of age, was treated with IRINOTECAN. After drug was administered, patient experienced the following problems/side effects: acidosis, gastrointestinal toxicity, neutropenia, pneumatosis intestinalis, portal venous gas, . IRINOTECAN dosage: unknown. During the same period patient was treated with CISPLATIN. Patient was hospitalized. Patient recovered.

Voltaren Side Effects Report #5624214-8
Consumer or non-health professional from JAPAN reported VOLTAREN problem on Feb 08, 2008. Male patient, 55 years of age, weighting 176.4 lb, was diagnosed with abdominal pain, shock and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: acidosis, adrenal insufficiency, anuria, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood creatinine increased, blood urea increased, c-reactive protein increased, dehydration, . VOLTAREN dosage: 25 MG, QD. During the same period patient was treated with BOSMIN, INOVAN. Patient was hospitalized. Patient recovered.

Avastin Side Effects Report #5624749-8
AVASTIN problem was reported by a Physician from UNITED STATES on Feb 04, 2008. Male patient, 56 years of age, was diagnosed with bladder cancer and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: acidosis, intussusception, . AVASTIN dosage: 5 MG/KG, D1,15,29. During the same period patient was treated with SUNITINIB MALATE, OXYCODONE, NORVASC, CELEXA, PRINIVIL, TOPROL, NASONEX. Patient died on 10/21/2007.

Nisis Side Effects Report #5626006-2
Consumer or non-health professional from FRANCE reported NISIS problem on Feb 05, 2008. Female patient, 80 years of age, was diagnosed with hypertensive cardiomyopathy, infection, insomnia, dyslipidaemia, depression, gastrooesophageal reflux disease, hypothyroidism and was treated with NISIS. After drug was administered, patient experienced the following problems/side effects: acidosis, anaemia, blood creatinine increased, blood folate decreased, c-reactive protein increased, creatinine renal clearance decreased, fall, haemoconcentration, . NISIS dosage: unknown. During the same period patient was treated with BACTRIM, HAVLANE, ALDALIX, LIPANTHYL, ATHYMIL, INIPOMP, LEVOTHYROX. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5628401-4
SUTENT problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 04, 2008. Male patient, 56 years of age, weighting 224.9 lb, was diagnosed with bladder transitional cell carcinoma and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: acidosis, anorexia, dehydration, fatigue, gastrointestinal necrosis, hypotension, intussusception, . SUTENT dosage: unknown. During the same period patient was treated with BEVACIZUMAB, NORVASC, TOPROL, PRINIVIL, OXYCODONE, CELEXA, NASONEX. Patient was hospitalized. Patient died on 10/21/2007.

Exjade Side Effects Report #5629913-X
Consumer or non-health professional from FRANCE reported EXJADE problem on Feb 08, 2008. Female patient, 18 years of age, weighting 121.3 lb, was diagnosed with iron overload and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: acidosis, blood phosphorus decreased, blood sodium decreased, condition aggravated, constipation, dizziness, glycosuria, hypokalaemia, paraesthesia, . EXJADE dosage: 1250 MG, QD. Patient was hospitalized. Patient recovered.

Zyloric Side Effects Report #5632095-1
ZYLORIC problem was reported by a Consumer or non-health professional from FRANCE on Feb 12, 2008. Female patient, 84 years of age, was treated with ZYLORIC. After drug was administered, patient experienced the following problems/side effects: acidosis, asthenia, bradycardia, coma, dehydration, hyperkalaemia, hyperlactacidaemia, lymphoedema, malaise, . ZYLORIC dosage: 200MG PER DAY. During the same period patient was treated with SERETIDE DISKUS, ALDACTONE, RAMIPRIL, LASILIX, ACEBUTOLOL, AMLOR, PLAVIX, KARDEGIC. Patient was hospitalized. Patient recovered.

Clofarabine Side Effects Report #5632633-9
Physician from UNITED STATES reported CLOFARABINE problem on Feb 12, 2008. Female patient, 24 years of age, weighting 172.4 lb, was diagnosed with acute myeloid leukaemia and was treated with CLOFARABINE. After drug was administered, patient experienced the following problems/side effects: acidosis, anaemia, asthenia, bacterial infection, blood culture positive, cough, diarrhoea, dyspnoea, fatigue, . CLOFARABINE dosage: 75 MG, QDX5, INTRAVENOUS. During the same period patient was treated with CYTARABINE. Patient was hospitalized. Patient recovered.

Zyvox Side Effects Report #5633441-5
ZYVOX problem was reported by a Pharmacist from UNITED STATES on Feb 09, 2008. Male patient, weighting 102.2 lb, was diagnosed with osteomyelitis, diabetes mellitus and was treated with ZYVOX. After drug was administered, patient experienced the following problems/side effects: acidosis, atrial fibrillation, lactic acidosis, renal failure acute, . ZYVOX dosage: unknown. During the same period patient was treated with INSULIN. Patient was hospitalized. Patient died on 11/21/2007.

Toprol Side Effects Report #5634727-0
Consumer or non-health professional from UNITED STATES reported TOPROL problem on Feb 20, 2008. Male patient, 56 years of age, weighting 224.9 lb, was diagnosed with bladder transitional cell carcinoma and was treated with TOPROL. After drug was administered, patient experienced the following problems/side effects: acidosis, anorexia, dehydration, fatigue, gastrointestinal necrosis, hypotension, intussusception, respiratory failure, . TOPROL dosage: unknown. During the same period patient was treated with SUNITINIB, BEVACIZUMAB, PRINIVIL, NORVASC, OXYCODONE, CELEXA, NASONEX. Patient was hospitalized. Patient died on 10/21/2007.

Heparin Side Effects Report #5636314-7
HEPARIN problem was reported by a Pharmacist from UNITED STATES on Feb 25, 2008. Male patient, 30 years of age, weighting 309.0 lb, was diagnosed with mitral valve replacement and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: acidosis, hypotension, pyrexia, . HEPARIN dosage: unknown. Patient died on 12/22/2007.

Xeloda Side Effects Report #5637123-5
Consumer or non-health professional from AUSTRALIA reported XELODA problem on Feb 11, 2008. Male patient, 78 years of age, weighting 149.9 lb, was treated with XELODA. After drug was administered, patient experienced the following problems/side effects: acidosis, dehydration, diarrhoea, hepatic failure, hypokalaemia, . XELODA dosage: unknown. Patient was hospitalized. Patient died on 12/31/2007.

Clofarabine Side Effects Report #5637705-0
CLOFARABINE problem was reported by a Physician from UNITED STATES on Feb 15, 2008. Female patient, 24 years of age, weighting 172.4 lb, was diagnosed with myeloid leukaemia and was treated with CLOFARABINE. After drug was administered, patient experienced the following problems/side effects: acidosis, anaemia, asthenia, bacterial infection, cough, diarrhoea, fatigue, fluid overload, headache, . CLOFARABINE dosage: 75 MG, QDX5, INTRAVENOUS. During the same period patient was treated with CYTARABINE. Patient was hospitalized. Patient recovered.

Warfarin Side Effects Report #5638009-2
Pharmacist from UNITED STATES reported WARFARIN problem on Feb 22, 2008. Male patient, 89 years of age, weighting 172.0 lb, was diagnosed with pulmonary embolism and was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: acidosis, blood lactic acid increased, colon cancer metastatic, gastrointestinal haemorrhage, haemoglobin decreased, international normalised ratio increased, metastases to liver, sepsis, . WARFARIN dosage: unknown. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5638024-9
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 07, 2008. Female patient, 60 years of age, weighting 110.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: acidosis, blood pressure decreased, convulsion, deafness bilateral, diabetes mellitus, dialysis, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Heparin Side Effects Report #5640707-1
Pharmacist from UNITED STATES reported HEPARIN problem on Feb 20, 2008. Male patient, 30 years of age, weighting 308.6 lb, was diagnosed with atrial fibrillation, cardiac disorder, medical diet, pulmonary hypertension and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: acidosis, blood ph decreased, blood potassium increased, hypotension, . HEPARIN dosage: unknown. During the same period patient was treated with COUMADIN, CARDIZEM, FEOSOL, PROTONIX, LASIX, VIAGRA, VASOTEC, LOPRESSOR. Patient died on 12/22/2007.

Prinivil Side Effects Report #5643086-9
PRINIVIL problem was reported by a Physician from UNITED STATES on Feb 20, 2008. Male patient, 56 years of age, was diagnosed with bladder transitional cell carcinoma and was treated with PRINIVIL. After drug was administered, patient experienced the following problems/side effects: acidosis, alanine aminotransferase increased, anorexia, aspartate aminotransferase increased, blood bilirubin increased, dehydration, fatigue, gastrointestinal necrosis, hyperkalaemia, . PRINIVIL dosage: unknown. During the same period patient was treated with TOPROL, SUNITINIB MALATE, BEVACIZUMAB, NORVASC, OXYCODONE, CELEXA, NASONEX. Patient was hospitalized. Patient died on 10/21/2007.

Certican Side Effects Report #5644324-9
Physician from UNITED STATES reported CERTICAN problem on Feb 20, 2008. Female patient, 49 years of age, weighting 153.9 lb, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: acidosis, blood creatinine increased, hyperkalaemia, hypotension, mental status changes, overdose, renal failure acute, respiratory depression, somnolence, . CERTICAN dosage: 1 MG, BID. During the same period patient was treated with NEORAL, PREDNISONE, OXYCODONE, MS CONTIN, CHI. Patient was hospitalized. Patient recovered.

Metformin Side Effects Report #5645273-2
METFORMIN problem was reported by a Physician from UNITED KINGDOM on Feb 22, 2008. Male patient, 53 years of age, was diagnosed with type 2 diabetes mellitus, colon cancer, hypercholesterolaemia and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: acidosis, anorexia, blood potassium decreased, dehydration, dyspnoea, lethargy, nausea, polyuria, renal tubular acidosis, . METFORMIN dosage: unknown. During the same period patient was treated with CAPECITABINE, OXALIPLATIN, SIMVASTATIN. Patient was hospitalized. Patient recovered.

Altace Side Effects Report #5645546-3
Consumer or non-health professional from FRANCE reported ALTACE problem on Feb 20, 2008. Female patient was diagnosed with hypertension, urinary tract infection, prostate cancer, prostatic adenoma and was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: acidosis, anorexia, blood creatinine increased, blood sodium decreased, cardiovascular disorder, creatinine renal clearance decreased, gamma-glutamyltransferase increased, haemoglobin decreased, . ALTACE dosage: 1.25 MG, QD. During the same period patient was treated with GENTAMICINE, ROCEPHIN, BACTRIM, OFLOCET, ZOLADEX, PROSCAR, XATRAL. Patient was hospitalized. Patient recovered.

Gemcitabine Side Effects Report #5646487-8
GEMCITABINE problem was reported by a Health Professional from UNITED STATES on Feb 28, 2008. Female patient, 65 years of age, was diagnosed with pancreatic carcinoma metastatic and was treated with GEMCITABINE. After drug was administered, patient experienced the following problems/side effects: acidosis, anal ulcer, blood creatinine increased, cholangitis, decubitus ulcer, hypotension, infection, sepsis, . GEMCITABINE dosage: unknown. During the same period patient was treated with LAPATINIB. Patient died on 02/27/2008.

Campath Side Effects Report #5578919-8
Physician from UNITED STATES reported CAMPATH problem on Dec 21, 2007. Female patient, 65 years of age, weighting 97.00 lb, was diagnosed with antifungal prophylaxis and was treated with CAMPATH. After drug was administered, patient experienced the following problems/side effects: acidosis, anaemia, catheter thrombosis, cerebral toxoplasmosis, chondrocalcinosis pyrophosphate, escherichia infection, febrile neutropenia, gingival bleeding, headache, . CAMPATH dosage: unknown. During the same period patient was treated with ETOPOSIDE, ONCOVIN, HYDROXYDAUNORUBICIN, CYCLOPHOSPHAMIDE, PREDNISONE, NEUPOGEN, PENTAMIDINE ISETHIONATE, ACYCLOVIR. Patient was hospitalized. Patient died on 05/10/2007.

Gemzar Side Effects Report #5580435-4
GEMZAR problem was reported by a Physician from CANADA on Dec 24, 2007. Female patient was diagnosed with neoplasm malignant and was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: acidosis, . GEMZAR dosage: 1700MG WITHIN 2 WEEKS. During the same period patient was treated with CARBOPLATIN. Patient was hospitalized. Patient died on 11/04/2007.

Carboplatin Side Effects Report #5585832-9
Pharmacist from CANADA reported CARBOPLATIN problem on Dec 24, 2007. Female patient, 63 years of age, was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: acidosis, sepsis, shock, . CARBOPLATIN dosage: unknown. During the same period patient was treated with GEMCITABINE. Patient died.