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Humira Side Effects Report #5666919-9
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Jan 04, 2008. Female patient, weighting 120.1 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, diarrhoea, . HUMIRA dosage: unknown. During the same period patient was treated with MESALAMINE. Patient recovered.

Kaletra Side Effects Report #5602952-0
KALETRA problem was reported by a Consumer or non-health professional from BELGIUM on Jan 17, 2008. Male patient was diagnosed with hiv infection, prophylaxis and was treated with KALETRA. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, diffuse large b-cell lymphoma, necrotising colitis, post procedural haemorrhage, renal impairment, septic shock, thrombocytopenia, . KALETRA dosage: 400MG, 2 IN 1 D. During the same period patient was treated with TENOFOVIR DISOPROXIL FUMARATE, LAMIVUDINE, BACTRIM, ACYCLOVIR, AZITHROMYCIN, OMEPRAZOLE, ALLOPURINOL, TRAMADOL. Patient died on 12/05/2007.

Bactrim Side Effects Report #5549811-X
Pharmacist from UNITED STATES reported BACTRIM problem on Dec 07, 2007. Female patient, 69 years of age, weighting 158.5 lb, was treated with BACTRIM. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, electrolyte imbalance, hypovolaemia, nausea, vomiting, . BACTRIM dosage: unknown. Patient was hospitalized. Patient recovered.

Fluorouracil Side Effects Report #5564360-0
FLUOROURACIL problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 14, 2007. Male patient, weighting 125.0 lb, was treated with FLUOROURACIL. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, body temperature increased, dizziness, fall, gait disturbance, head injury, hyponatraemia, hypotension, joint injury, . FLUOROURACIL dosage: 5040 MG. During the same period patient was treated with ERBITUX, LEUCOVORIN CALCIUM, ELOXATIN. Patient was hospitalized. Patient recovered.


Myozyme Side Effects Report #5566507-9
Health Professional from UNITED STATES reported MYOZYME problem on Nov 30, 2007. Male patient, weighting 11.68 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: bacteria stool identified, bronchial hyperreactivity, central line infection, condition aggravated, enterobacter bacteraemia, eyelid function disorder, haemoglobin decreased, lobar pneumonia, nystagmus, . MYOZYME dosage: 20 MG/KG Q2WKS IV. During the same period patient was treated with BACTRIM, RITUXIMAB, METHOTREXATE, BENADRYL, TYLENOL. Patient was hospitalized. Patient recovered.

Ceftriaxone Side Effects Report #5572473-2
CEFTRIAXONE problem was reported by a Physician from UNITED KINGDOM on Dec 10, 2007. Female patient was diagnosed with meningococcal sepsis and was treated with CEFTRIAXONE. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, escherichia infection, haemolytic uraemic syndrome, . CEFTRIAXONE dosage: unknown. Patient recovered.

Certican Side Effects Report #5505512-5
Physician from SWITZERLAND reported CERTICAN problem on Oct 25, 2007. Male patient, 58 years of age, weighting 148.2 lb, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, blood creatinine increased, hepatic cyst infection, incision site haematoma, liver operation, lymphocele, lymphocele marsupialisation, nephrectomy, nephropathy toxic, . CERTICAN dosage: unknown. During the same period patient was treated with MYFORTIC, NEORAL. Patient was hospitalized. Patient recovered.

Loperamide Side Effects Report #5517638-0
LOPERAMIDE problem was reported by a Consumer or non-health professional from on Nov 08, 2007. Male patient, 48 years of age, was diagnosed with diarrhoea, bacteria stool identified and was treated with LOPERAMIDE. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, large intestine perforation, megacolon, . LOPERAMIDE dosage: unknown. During the same period patient was treated with DICYCLOMINE, STEROIDS, FLAGYL, CIPROFLOXACIN. Patient recovered.

Velcade Side Effects Report #5491280-2
Physician from GERMANY reported VELCADE problem on Oct 11, 2007. Female patient, 58 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, clostridial infection, diarrhoea, pyrexia, renal failure acute, vomiting, . VELCADE dosage: unknown. During the same period patient was treated with DOXORUBICIN, DEXAMETHASONE, MELPHALAN, PANTOZOL, COTRIMTE, METOPROLOL TARTRATE. Patient was hospitalized. Patient recovered.


Oxaliplatin Side Effects Report #5409240-6
OXALIPLATIN problem was reported by a Health Professional from UNITED STATES on Aug 08, 2007. Male patient, weighting 175.5 lb, was diagnosed with hepatic neoplasm malignant and was treated with OXALIPLATIN. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, clostridium difficile colitis, diverticulum, haematocrit decreased, haemoglobin decreased, . OXALIPLATIN dosage: 50MG/M2 D1 AND 8 Q21DAYS IV. During the same period patient was treated with XELODA. Patient was hospitalized. Patient recovered.

Natalizumab Side Effects Report #5420398-5
Consumer or non-health professional from UNITED STATES reported NATALIZUMAB problem on Aug 07, 2007. Female patient, 41 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, diarrhoea, fatigue, feeling abnormal, headache, influenza like illness, neck pain, pneumonia, upper respiratory tract infection, . NATALIZUMAB dosage: 300 MG; QM; IV. Patient was hospitalized. Patient recovered.

Paroxetine Side Effects Report #5387346-8
PAROXETINE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on June 29, 2007. Female patient, 36 years of age, was treated with PAROXETINE. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, diarrhoea, . PAROXETINE dosage: 25 MG;QD. During the same period patient was treated with CLOZARIL, FLUOXETINE, LEVOTHYROXINE, LITHIUM CARBONATE, OMEPRAZOLE, ZOPICLONE. Patient died.

Paroxetine Side Effects Report #5387346-8
Consumer or non-health professional from UNITED KINGDOM reported PAROXETINE problem on June 29, 2007. Female patient, 36 years of age, was treated with PAROXETINE. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, diarrhoea, . PAROXETINE dosage: 25 MG;QD. During the same period patient was treated with CLOZARIL, FLUOXETINE, LEVOTHYROXINE, LITHIUM CARBONATE, OMEPRAZOLE, ZOPICLONE. Patient died.

Augmentin Side Effects Report #5726442-X
AUGMENTIN problem was reported by a Consumer or non-health professional from FRANCE on Apr 22, 2008. Female patient, 98 years of age, was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, culture stool negative, diarrhoea, . AUGMENTIN dosage: unknown. During the same period patient was treated with CLAMOXYL, CORDARONE, LASILIX, CHRONOADALATE, HEMIGOXINE, CALCIUM D, DAFALGAN, FONZYLANE. Patient was hospitalized. Patient recovered.


Augmentin Side Effects Report #5704412-5
Consumer or non-health professional from FRANCE reported AUGMENTIN problem on Mar 31, 2008. Female patient, 98 years of age, was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, culture stool negative, diarrhoea, . AUGMENTIN dosage: unknown. During the same period patient was treated with CLAMOXYL, CORDARONE, LASILIX, CHRONOADALATE, HEMIGOXINE, CALCIUM D, DAFALGAN, FONZYLANE. Patient was hospitalized. Patient recovered.

Clamoxyl Side Effects Report #5355622-0
CLAMOXYL problem was reported by a Consumer or non-health professional from FRANCE on June 12, 2007. Female patient, 83 years of age, weighting 130.1 lb, was treated with CLAMOXYL. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, diarrhoea, . CLAMOXYL dosage: unknown. During the same period patient was treated with AUGMENTIN, CLAFORAN, OFLOCET, LASIX, PREVISCAN. Patient was hospitalized. Patient recovered.

Imatinib Side Effects Report #5377109-1
Consumer or non-health professional from UNITED STATES reported IMATINIB MESYLATE problem on June 28, 2007. Male patient, weighting 251.3 lb, was diagnosed with malignant glioma and was treated with IMATINIB MESYLATE. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, blood culture positive, cellulitis, clostridial infection, embolism, erythema, furuncle, muscular weakness, . IMATINIB MESYLATE dosage: 500 MG BID FOR 8 DAYS PO. During the same period patient was treated with IMATINIB MESYLATE, TEMOZOLOMIDE, FENTANYL TRANSDERMAL SYSTEM, LANTUS, PROVIGIL, TEMAZEPAM, METFORMIN. Patient was hospitalized. Patient recovered.

Tegretol Side Effects Report #5304757-7
TEGRETOL problem was reported by a Physician from JAPAN on Apr 11, 2007. Female patient, 16 years of age, was diagnosed with epilepsy and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, enterocolitis infectious, haematochezia, . TEGRETOL dosage: 400 MG/DAY. Patient was hospitalized. Patient recovered.

Tegretol Side Effects Report #5305294-6
Physician from JAPAN reported TEGRETOL problem on Apr 11, 2007. Female patient, 16 years of age, was diagnosed with epilepsy and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, enterocolitis infectious, haematochezia, . TEGRETOL dosage: 400 MG/DAY. Patient was hospitalized. Patient recovered.


Tegretol Side Effects Report #5305586-0
TEGRETOL problem was reported by a Physician from JAPAN on Apr 11, 2007. Female patient, 16 years of age, was diagnosed with epilepsy and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, enterocolitis infectious, haematochezia, . TEGRETOL dosage: 400 MG/DAY. Patient was hospitalized. Patient recovered.

Temozolomide Side Effects Report #5257280-2
Physician from FRANCE reported TEMOZOLOMIDE problem on Feb 27, 2007. Male patient, 76 years of age, was diagnosed with glioma and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: bacteria stool identified, cardiac flutter, confusional state, dehydration, dry skin, epilepsy, fall, grand mal convulsion, malaise, . TEMOZOLOMIDE dosage: unknown. During the same period patient was treated with ZOPHREN, MEDROL, CIPROFLOXACIN, FLAGYL, DIANTALVIC, NEURONTIN. Patient was hospitalized. Patient recovered.

Augmentin Side Effects Report #5612617-7
AUGMENTIN problem was reported by a Consumer or non-health professional from FRANCE on Jan 22, 2008. Female patient, 83 years of age, was diagnosed with lung disorder and was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, bacteria stool identified, diverticulum, lung disorder, neutrophil count increased, rectal haemorrhage, tachycardia, white blood cell count increased, . AUGMENTIN dosage: 2MG PER DAY. During the same period patient was treated with COUMADIN, ENOXAPARIN, CORDARONE, DIGITALINE NATIVELLE, LANSOPRAZOLE, FORLAX, CACIT VITAMINE D3, PROTELOS. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5592442-6
Physician from GERMANY reported VELCADE problem on Jan 08, 2008. Male patient was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, bacteria stool identified, bacterial sepsis, candidiasis, cheyne-stokes respiration, cyanosis, deep vein thrombosis, encephalitis herpes, enterococcal infection, . VELCADE dosage: 1.30 MG/M2, INTRAVENOUS. During the same period patient was treated with CYCLOPHOSPHAMIDE, DEXAMETHASONE. Patient was hospitalized. Patient recovered.

Methotrexate Side Effects Report #5598688-5
METHOTREXATE problem was reported by a Physician from GERMANY on Jan 08, 2008. Female patient, child 5 years of age, was diagnosed with prophylaxis against graft versus host disease, bone marrow conditioning regimen and was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: acute graft versus host disease in skin, bacteria stool identified, enterococcal infection, mucosal inflammation, pyrexia, . METHOTREXATE dosage: unknown. During the same period patient was treated with CYCLOPHOSPHAMIDE, CYCLOSPORINE. Patient recovered.

Clofarabine Side Effects Report #5526441-7
Health Professional from UNITED STATES reported CLOFARABINE GENZYME problem on Nov 21, 2007. Female patient, 38 years of age, weighting 163.8 lb, was diagnosed with acute lymphocytic leukaemia and was treated with CLOFARABINE GENZYME. After drug was administered, patient experienced the following problems/side effects: anuria, bacteria stool identified, blood culture positive, caecitis, dialysis, hypotension, mental status changes, mucosal inflammation, neutropenic colitis, . CLOFARABINE GENZYME dosage: 30 MG/M2 1XQD/5DAYS IV. During the same period patient was treated with MELPHALAN. Patient died on 11/17/2007.

Rocephin Side Effects Report #5442110-6
ROCEPHIN problem was reported by a Health Professional from FRANCE on Aug 21, 2007. Male patient, 17 years of age, was diagnosed with meningitis, miller fisher syndrome and was treated with ROCEPHIN. After drug was administered, patient experienced the following problems/side effects: agranulocytosis, bacteria stool identified, cholelithiasis, cytolytic hepatitis, . ROCEPHIN dosage: unknown. During the same period patient was treated with TEGELINE. Patient was hospitalized. Patient recovered.

Zevalin Side Effects Report #5466955-1
Health Professional from FRANCE reported ZEVALIN problem on Sept 04, 2007. Male patient, 57 years of age, was diagnosed with bone marrow conditioning regimen and was treated with ZEVALIN. After drug was administered, patient experienced the following problems/side effects: aspergillosis, bacteria stool identified, cholestasis, culture stool positive, escherichia infection, febrile neutropenia, haemoglobin decreased, hepatosplenomegaly, lung neoplasm, . ZEVALIN dosage: unknown. During the same period patient was treated with TAZOCILLINE, FORTUM, RITUXAN, ETOPOSIDE, CYTARABINE, BICNU, ALKERAN. Patient recovered.

Rocephin Side Effects Report #5437595-5
ROCEPHIN problem was reported by a Health Professional from FRANCE on Aug 21, 2007. Male patient, 17 years of age, was diagnosed with meningitis, miller fisher syndrome and was treated with ROCEPHIN. After drug was administered, patient experienced the following problems/side effects: agranulocytosis, bacteria stool identified, cholelithiasis, cytolytic hepatitis, . ROCEPHIN dosage: unknown. During the same period patient was treated with TEGELINE. Patient was hospitalized. Patient recovered.

Augmentin Side Effects Report #5730598-2
Consumer or non-health professional from FRANCE reported AUGMENTIN problem on Apr 28, 2008. Female patient, 85 years of age, was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: abdominal pain, bacteria stool identified, c-reactive protein increased, diarrhoea, hypokalaemia, inflammation, leukocytosis, pyrexia, . AUGMENTIN dosage: unknown. During the same period patient was treated with ASPIRIN, DEXERYL, OGAST, CARDENSIEL, MOTILIUM, LASILIX RETARD, MORPHINE SUL. Patient was hospitalized. Patient recovered.

Augmentin Side Effects Report #5730599-4
AUGMENTIN problem was reported by a Consumer or non-health professional from FRANCE on Apr 28, 2008. Female patient, 87 years of age, was diagnosed with erysipelas, pain and was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: abdominal distension, bacteria stool identified, c-reactive protein increased, culture stool negative, diarrhoea, flatulence, hypokalaemia, pyrexia, . AUGMENTIN dosage: unknown. During the same period patient was treated with PAROXETINE, ARICEPT, ENDOTELON, TRIMETAZIDINE, OMEPRAZOLE, DOLIPRANE, TARDYFERON. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5706625-5
Health Professional from UNITED STATES reported MYOZYME problem on Apr 02, 2008. Male patient, weighting 11.68 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: bacteraemia, bacteria stool identified, bronchial hyperreactivity, catheter related infection, central line infection, clostridial infection, enterobacter infection, eyelid disorder, lobar pneumonia, . MYOZYME dosage: 20 MG/KG, Q2W, INTRAVENOUS. During the same period patient was treated with BACTRIM, RITUXIMAB, METHOTREXATE, BENADRYL, ACETAMINOPHEN. Patient was hospitalized. Patient recovered.

Carboplatin Side Effects Report #5320891-X
CARBOPLATIN problem was reported by a Consumer or non-health professional from JAPAN on Apr 24, 2007. Male patient, 46 years of age, weighting 144.8 lb, was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: bacteraemia, bacteria stool identified, helicobacter infection, white blood cell count decreased, . CARBOPLATIN dosage: 540 MG ON DAY 1. During the same period patient was treated with ETOPOSIDE. Patient recovered.

Neupogen Side Effects Report #5326398-8
Physician from UNITED STATES reported NEUPOGEN problem on May 04, 2007. Female patient, weighting 109.1 lb, was treated with NEUPOGEN. After drug was administered, patient experienced the following problems/side effects: asthenia, bacteria stool identified, breast cancer metastatic, dehydration, eating disorder, hypokalaemia, hypoxia, lethargy, neutropenia, . NEUPOGEN dosage: unknown. During the same period patient was treated with FEMARA, TAXOTERE, FUROSEMIDE, HEPARIN. Patient was hospitalized. Patient died on 05/03/2006.

Pemetrexed Side Effects Report #5290726-2
PEMETREXED problem was reported by a Health Professional from UNITED STATES on Apr 05, 2007. Female patient, 65 years of age, was diagnosed with non-small cell lung cancer and was treated with PEMETREXED. After drug was administered, patient experienced the following problems/side effects: abdominal pain, bacteria stool identified, colitis, diarrhoea, nausea, white blood cell count increased, . PEMETREXED dosage: 250MG/M2, IV. During the same period patient was treated with SORAFENIB, VICODIN, DEXAMETHASONE. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5297732-2
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on Apr 12, 2007. Female patient, weighting 206.0 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: bacteraemia, bacteria stool identified, cystitis klebsiella, febrile neutropenia, . CISPLATIN dosage: 100 MG. During the same period patient was treated with NAVELBINE. Patient was hospitalized. Patient recovered.

Abraxane Side Effects Report #5307797-7
ABRAXANE problem was reported by a Health Professional from UNITED STATES on Apr 03, 2007. Female patient, 53 years of age, weighting 137.0 lb, was diagnosed with breast cancer, colony stimulating factor prophylaxis and was treated with ABRAXANE. After drug was administered, patient experienced the following problems/side effects: abscess intestinal, bacteria stool identified, candidiasis, enterocolitis infectious, haemoglobin decreased, large intestine perforation, lung consolidation, platelet count decreased, pleural effusion, . ABRAXANE dosage: 292MG TOTAL DOSE/LAST DOSE PRIOR TO SAE 01-FEB-2007(175MG/M2); INTRAVENOUS. During the same period patient was treated with GEMCITABINE, EPIRUBICIN, NEULASTA, EMEND, COMPAZINE, DARVOCET, MIRALAX, DICYCLOMINE. Patient was hospitalized. Patient recovered.

Carboplatin Side Effects Report #5314722-1
Consumer or non-health professional from JAPAN reported CARBOPLATIN problem on Apr 12, 2007. Male patient, 46 years of age, was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: bacteraemia, bacteria stool identified, helicobacter infection, white blood cell count decreased, . CARBOPLATIN dosage: 540 MG ON DAY 1. During the same period patient was treated with ETOPOSIDE. Patient recovered.

Thalomid Side Effects Report #5285871-1
THALOMID problem was reported by a Physician from UNITED STATES on Mar 20, 2007. Male patient, 67 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: acidosis, bacteria stool identified, blood calcium increased, blood urea increased, clostridial infection, colitis ischaemic, diarrhoea, hypotension, mesenteric artery thrombosis, . THALOMID dosage: 200 MG, 1 IN 1 D, ORAL. During the same period patient was treated with DECADRON, AREDIA, UNIRECTIC, PROMETHAZINE, RANITIDINE. Patient was hospitalized. Patient died on 12/30/2006.

Cisplatin Side Effects Report #5678496-7
Health Professional from UNITED STATES reported CISPLATIN problem on Mar 21, 2008. Male patient, 60 years of age, was diagnosed with metastatic gastric cancer, diarrhoea and was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: aeromona infection, anaemia, bacteria stool identified, bacterial infection, blood glucose increased, dehydration, diverticulum intestinal, febrile neutropenia, gastroenteritis, . CISPLATIN dosage: unknown. During the same period patient was treated with IMODIUM, CENTRUM, PROTONIX, EMEND, LOMOTIL, ZYRTEC. Patient was hospitalized. Patient recovered.

Trisenox Side Effects Report #5515366-9
TRISENOX problem was reported by a Physician from UNITED STATES on Oct 26, 2007. Female patient, weighting 85.76 lb, was diagnosed with multiple myeloma and was treated with TRISENOX. After drug was administered, patient experienced the following problems/side effects: angina pectoris, bacteraemia, bacteria stool identified, bence jones protein urine present, chest pain, culture urine positive, dialysis, disease progression, . TRISENOX dosage: 11.5 MG DAILY FOR 7 DAYS INTRAVENOUS DRIP. During the same period patient was treated with ASCORBIC ACID, MELPHALAN, PROPOXYPHENE HC, ESTRADIOL, VALGANCICLOVIR HC, CALCIUM CARBONATE W, ISOSORBIDE MONONITRATE, HYDRALAZINE. Patient was hospitalized. Patient died on 05/11/2007.

Clofarabine Side Effects Report #5525056-4
Health Professional from UNITED STATES reported CLOFARABINE problem on Nov 01, 2007. Female patient, 13 years of age, weighting 81.57 lb, was diagnosed with acute lymphocytic leukaemia and was treated with CLOFARABINE. After drug was administered, patient experienced the following problems/side effects: alpha haemolytic streptococcal infection, aspergillosis, bacteria stool identified, blood amylase increased, blood creatine phosphokinase increased, blood culture positive, brain oedema, capillary leak syndrome, cardio-respiratory arrest, . CLOFARABINE dosage: 48 MG QD IV. During the same period patient was treated with ETOPOSIDE, CYCLOPHOSPHAMIDE. Patient died on 11/13/2007.

Prograf Side Effects Report #5710529-1
PROGRAF problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 03, 2008. Male patient, 59 years of age, was diagnosed with liver transplant rejection, liver abscess and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: amyotrophy, anastomotic stenosis, bacteria stool identified, bile duct necrosis, cholangitis, clostridium difficile colitis, hepatic artery occlusion, hepatic artery thrombosis, liver abscess, . PROGRAF dosage: 2 MG, BID; 3 MG, BID. During the same period patient was treated with MYCOPHENOLATE MOFETIL, MYCOPHENOLATE MOFETIL, SIROLIMUS, ANTIBIOTICS, ACYCLOVIR. Patient was hospitalized. Patient recovered.

Azathioprine Side Effects Report #5717170-5
Physician from UNITED STATES reported AZATHIOPRINE problem on Apr 11, 2008. Male patient, 45 years of age, was diagnosed with immunosuppression and was treated with AZATHIOPRINE. After drug was administered, patient experienced the following problems/side effects: ascites, bacteraemia, bacteria stool identified, cryptococcosis, diarrhoea, dysarthria, gait disturbance, haemodialysis, hydrocephalus, . AZATHIOPRINE dosage: 100 MG/DAY,. During the same period patient was treated with METHYLPREDNISOLONE, CYCLOSPORINE, MYCOPHENOLATE MOFETIL, PREDNISONE, TACROLIMUS, PROPRANOLOL, CLOTRIMAZOLE, OMEPRAZOLE. Patient died.

Zantac Side Effects Report #5257186-9
ZANTAC problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 05, 2007. Male patient, weighting 10.58 lb, was treated with ZANTAC. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, bacteria stool identified, diarrhoea, discomfort, eructation, faeces discoloured, frequent bowel movements, haematochezia, . ZANTAC dosage: unknown. During the same period patient was treated with PRILOSEC, ACIDOPHILUS, BIFIDUS. Patient recovered.

Abraxane Side Effects Report #5272409-8
Health Professional from UNITED STATES reported ABRAXANE problem on Mar 02, 2007. Female patient, 53 years of age, weighting 137.0 lb, was diagnosed with breast cancer, colony stimulating factor prophylaxis and was treated with ABRAXANE. After drug was administered, patient experienced the following problems/side effects: abscess bacterial, abscess intestinal, bacteria stool identified, clostridial infection, enterocolitis infectious, escherichia infection, haemoglobin decreased, lung consolidation, pelvic abscess, . ABRAXANE dosage: 292MG TOTAL DOSE / LAST DOSE PRIOR TO SAE 01-FEB-2007 (175 MG/M2), INTRAVENOUS. During the same period patient was treated with GEMCITABINE, EPIRUBICIN, NEULASTA, EMEND, COMPAZINE, DARVOCET, MIRALAX, DICYCLOMINE. Patient was hospitalized. Patient recovered.

Thalomid Side Effects Report #5285430-0
THALOMID problem was reported by a Physician from UNITED STATES on Mar 20, 2007. Male patient, 67 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: acidosis, asthenia, bacteria stool identified, blood calcium increased, blood urea increased, colitis ischaemic, hypotension, mesenteric artery thrombosis, multi-organ failure, . THALOMID dosage: 200 MG, 1 IN 1 D, ORAL. During the same period patient was treated with DECADRON, AREDIA, UNIRECTIC, PROMETHAZINE, RANITIDINE. Patient was hospitalized. Patient died on 12/30/2006.