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Zyvox Side Effects Report #5661387-5
Physician from CHINA reported ZYVOX problem on Feb 28, 2008. Female patient, 45 years of age, was diagnosed with prophylaxis and was treated with ZYVOX. After drug was administered, patient experienced the following problems/side effects: coma hepatic, hepatic failure, liver function test abnormal, . ZYVOX dosage: unknown. Patient died.

Crestor Side Effects Report #5674837-5
CRESTOR problem was reported by a Health Professional from UNITED STATES on Mar 19, 2008. Female patient, 56 years of age, weighting 180.0 lb, was diagnosed with hyperlipidaemia and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: coma hepatic, impaired work ability, neuropathy peripheral, paralysis, . CRESTOR dosage: 10MG DAILY PO. Patient was hospitalized and became disabled. Patient recovered.

Cerezyme Side Effects Report #5679176-4
Physician from POLAND reported CEREZYME problem on Mar 10, 2008. Male patient, 51 years of age, weighting 149.9 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: coma hepatic, hepatic failure, hepatic neoplasm malignant, hepatomegaly, osteoarthritis, thrombocytopenia, varices oesophageal, . CEREZYME dosage: unknown. Patient died on 11/12/2007.

Arava Side Effects Report #5682450-9
ARAVA problem was reported by a Physician from UNITED STATES on Mar 26, 2008. Female patient, 54 years of age, weighting 175.0 lb, was diagnosed with psoriatic arthropathy, psoriasis and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: coma hepatic, hepatic failure, . ARAVA dosage: 20 MG DAILY PO. During the same period patient was treated with REMICADE. Patient recovered.


Xalatan Side Effects Report #5590293-X
Physician from ITALY reported XALATAN problem on Jan 09, 2008. Female patient was diagnosed with vertigo, epilepsy, cerebrovascular accident and was treated with XALATAN. After drug was administered, patient experienced the following problems/side effects: coma hepatic, hepatic failure, hepatitis acute, . XALATAN dosage: unknown. During the same period patient was treated with COSOPT, EUTIROX, ENAPREN, VERTISERC, TEGRETOL, PLAVIX. Patient died on 11/09/2007.

Adefovir Side Effects Report #5602926-X
ADEFOVIR DIPIVOXIL problem was reported by a Physician from KOREA, REPUBLIC OF on Jan 22, 2008. Female patient was diagnosed with hepatitis b and was treated with ADEFOVIR DIPIVOXIL. After drug was administered, patient experienced the following problems/side effects: coma hepatic, peritonitis, . ADEFOVIR DIPIVOXIL dosage: 10MG PER DAY. Patient died on 08/17/2007.

Xalatan Side Effects Report #5576465-9
Physician from ITALY reported XALATAN problem on Dec 18, 2007. Female patient was diagnosed with vertigo, epilepsy, cerebrovascular accident and was treated with XALATAN. After drug was administered, patient experienced the following problems/side effects: coma hepatic, hepatic failure, hepatitis acute, . XALATAN dosage: unknown. During the same period patient was treated with COSOPT, EUTIROX, ENAPREN, VERTISERC, TEGRETOL, PLAVIX. Patient died on 11/09/2007.

Celebrex Side Effects Report #5486073-6
CELEBREX problem was reported by a Physician from UNITED STATES on Oct 03, 2007. Female patient, 48 years of age, was diagnosed with anaesthesia and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: coma hepatic, hepatitis, joint swelling, . CELEBREX dosage: unknown. Patient was hospitalized. Patient recovered.

Panaldine Side Effects Report #5455059-X
Consumer or non-health professional from JAPAN reported PANALDINE problem on Aug 30, 2007. Female patient, 74 years of age, weighting 99.21 lb, was diagnosed with ruptured cerebral aneurysm, hypertension and was treated with PANALDINE. After drug was administered, patient experienced the following problems/side effects: coma hepatic, convulsion, escherichia sepsis, gastric ulcer haemorrhage, gastrointestinal haemorrhage, haematemesis, hepatic failure, hepatitis fulminant, hepatorenal syndrome, . PANALDINE dosage: 200 MG (100 MG, 2 IN 1 D), PER ORAL. During the same period patient was treated with OLMESARTAN MEDOXOMIL, MUCOSTA, NORVASC. Patient was hospitalized. Patient died on 08/11/2007.


Herceptin Side Effects Report #5463013-7
HERCEPTIN problem was reported by a Physician from UNITED KINGDOM on Sept 05, 2007. Female patient, 45 years of age, was diagnosed with breast cancer metastatic and was treated with HERCEPTIN. After drug was administered, patient experienced the following problems/side effects: coma hepatic, disease progression, hepatic failure, . HERCEPTIN dosage: unknown. Patient died on 08/01/2007.

Humalog Side Effects Report #5377177-7
Physician from SLOVAKIA (Slovak Republic) reported HUMALOG problem on June 26, 2007. Male patient, 51 years of age, weighting 132.3 lb, was diagnosed with type 1 diabetes mellitus and was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: coma hepatic, gastrointestinal haemorrhage, hyperglycaemia, malignant neoplasm progression, . HUMALOG dosage: unknown. During the same period patient was treated with HUMULIN N, HUMULIN N, TRAMADOL, FUROSEMIDE, ETHAMSYLATE. Patient died on 01/30/2007.

Prograf Side Effects Report #5383236-5
PROGRAF problem was reported by a Physician from JAPAN on June 22, 2007. Male patient, 58 years of age, weighting 147.7 lb, was diagnosed with bone marrow transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: coma hepatic, complications of transplant surgery, dialysis, graft versus host disease, hepatitis fulminant, pyrexia, renal impairment, tremor, . PROGRAF dosage: unknown. During the same period patient was treated with PREDNISOLONE, MUCOSTA, LAC B, DEPAS, DIFLUCAN. Patient died on 10/24/2004.

Humalog Side Effects Report #5392502-9
Physician from SLOVAKIA (Slovak Republic) reported HUMALOG problem on July 11, 2007. Male patient, 51 years of age, weighting 132.3 lb, was diagnosed with type 1 diabetes mellitus and was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: coma hepatic, gastrointestinal haemorrhage, hyperglycaemia, malignant neoplasm progression, . HUMALOG dosage: unknown. During the same period patient was treated with HUMULIN N, HUMULIN N, HUMULIN N, TRAMADOL, FUROSEMIDE, ETHAMSYLATE. Patient died on 01/30/2007.

Humalog Side Effects Report #5377177-7
HUMALOG problem was reported by a Physician from SLOVAKIA (Slovak Republic) on June 26, 2007. Male patient, 51 years of age, weighting 132.3 lb, was diagnosed with type 1 diabetes mellitus and was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: coma hepatic, gastrointestinal haemorrhage, hyperglycaemia, malignant neoplasm progression, . HUMALOG dosage: unknown. During the same period patient was treated with HUMULIN N, HUMULIN N, TRAMADOL, FUROSEMIDE, ETHAMSYLATE. Patient died on 01/30/2007.


Prograf Side Effects Report #5383236-5
Physician from JAPAN reported PROGRAF problem on June 22, 2007. Male patient, 58 years of age, weighting 147.7 lb, was diagnosed with bone marrow transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: coma hepatic, complications of transplant surgery, dialysis, graft versus host disease, hepatitis fulminant, pyrexia, renal impairment, tremor, . PROGRAF dosage: unknown. During the same period patient was treated with PREDNISOLONE, MUCOSTA, LAC B, DEPAS, DIFLUCAN. Patient died on 10/24/2004.

Humalog Side Effects Report #5392502-9
HUMALOG problem was reported by a Physician from SLOVAKIA (Slovak Republic) on July 11, 2007. Male patient, 51 years of age, weighting 132.3 lb, was diagnosed with type 1 diabetes mellitus and was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: coma hepatic, gastrointestinal haemorrhage, hyperglycaemia, malignant neoplasm progression, . HUMALOG dosage: unknown. During the same period patient was treated with HUMULIN N, HUMULIN N, HUMULIN N, TRAMADOL, FUROSEMIDE, ETHAMSYLATE. Patient died on 01/30/2007.

Artist Side Effects Report #5725220-5
Health Professional from JAPAN reported ARTIST problem on Apr 25, 2008. Male patient, 70 years of age, was treated with ARTIST. After drug was administered, patient experienced the following problems/side effects: coma hepatic, condition aggravated, hepatic enzyme increased, hepatitis fulminant, nausea, renal failure acute, . ARTIST dosage: unknown. During the same period patient was treated with LOSARTAN POTASSIUM, FUROSEMIDE, ALLOPURINOL, WARFARIN POTASSIUM, EPLERENONE, AMIODARONE. Patient was hospitalized. Patient recovered.

Hyzaar Side Effects Report #5708787-2
HYZAAR problem was reported by a Physician from JAPAN on Apr 11, 2008. Male patient, 70 years of age, was treated with HYZAAR. After drug was administered, patient experienced the following problems/side effects: coma hepatic, haemodialysis, hepatitis fulminant, renal failure acute, . HYZAAR dosage: unknown. During the same period patient was treated with AMIODARONE HYDROCHLORIDE, EPLERENONE, PLETAL, ALOSITOL, LASIX, ARTIST, WARFARIN. Patient was hospitalized. Patient recovered.

Hepsera Side Effects Report #5711590-0
Physician from KOREA, REPUBLIC OF reported HEPSERA problem on Apr 11, 2008. Female patient was treated with HEPSERA. After drug was administered, patient experienced the following problems/side effects: coma hepatic, hepatorenal syndrome, peritonitis bacterial, renal failure acute, sepsis, . HEPSERA dosage: 10MG PER DAY. During the same period patient was treated with LASIX, ALDACTONE, GANATON. Patient was hospitalized. Patient died on 08/17/2007.


Hepsera Side Effects Report #5720246-X
HEPSERA problem was reported by a Physician from KOREA, REPUBLIC OF on Apr 16, 2008. Female patient was diagnosed with hepatitis b, ascites and was treated with HEPSERA. After drug was administered, patient experienced the following problems/side effects: coma hepatic, hepatorenal syndrome, peritonitis bacterial, renal failure acute, sepsis, . HEPSERA dosage: 10MG PER DAY. During the same period patient was treated with LASIX, ALDACTONE, GANATON, URSODESOXYCHOLIC ACID. Patient was hospitalized. Patient died on 08/17/2007.

Taxotere Side Effects Report #5721207-7
Consumer or non-health professional from CHINA reported TAXOTERE problem on Apr 21, 2008. Female patient, 43 years of age, weighting 143.3 lb, was diagnosed with breast cancer and was treated with TAXOTERE. After drug was administered, patient experienced the following problems/side effects: coma hepatic, hepatic failure, hepatic function abnormal, hepatic necrosis, hyperbilirubinaemia, hypotension, neutropenia, pyrexia, . TAXOTERE dosage: unknown. During the same period patient was treated with PHARMORUBICIN. Patient recovered.

Humalog Side Effects Report #5370117-6
HUMALOG problem was reported by a Physician from SLOVAKIA (Slovak Republic) on June 14, 2007. Male patient, 51 years of age, weighting 132.3 lb, was diagnosed with diabetes mellitus insulin-dependent and was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: coma hepatic, gastrointestinal haemorrhage, pancreatic carcinoma, . HUMALOG dosage: unknown. During the same period patient was treated with HUMULIN N, TRAMADOL, FUROSEMIDE, ETHAMSYLATE. Patient died on 01/30/2007.

Aptivus Side Effects Report #5327926-9
Physician from reported APTIVUS problem on Dec 12, 2006. Female patient, weighting 105.8 lb, was diagnosed with acquired immunodeficiency syndrome and was treated with APTIVUS. After drug was administered, patient experienced the following problems/side effects: coma hepatic, hepatic function abnormal, . APTIVUS dosage: unknown. During the same period patient was treated with RITONAVIR, TRUVADA. Patient died on 07/25/2006.

Lispro Side Effects Report #5298162-X
LISPRO problem was reported by a Physician from KOREA, DEMOCRATIC PEOPLE'S REPUBLIC OF on Apr 06, 2007. Male patient, 64 years of age, weighting 121.3 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with LISPRO. After drug was administered, patient experienced the following problems/side effects: coma hepatic, . LISPRO dosage: unknown. Patient was hospitalized. Patient recovered.

Lispro Side Effects Report #5312745-X
Physician from KOREA, DEMOCRATIC PEOPLE'S REPUBLIC OF reported LISPRO problem on Apr 18, 2007. Male patient, 64 years of age, weighting 121.3 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with LISPRO. After drug was administered, patient experienced the following problems/side effects: coma hepatic, . LISPRO dosage: unknown. During the same period patient was treated with FUROSEMIDE, SPIRONOLACTONE, ALLICIN, BIPHENYL DICARBOXYLATE, ALUMINIUM HYDROXIDE GEL, GASMOTIN. Patient was hospitalized. Patient recovered.

Lipitor Side Effects Report #5254552-2
LIPITOR problem was reported by a Physician from JAPAN on Feb 20, 2007. Female patient, weighting 88.18 lb, was diagnosed with hypercholesterolaemia, gastritis, gastric disorder, pruritus, back pain and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: coma hepatic, hepatitis fulminant, . LIPITOR dosage: DAILY DOSE:5MG. During the same period patient was treated with SELBEX, TIMEPIDIUM BROMIDE, TIMEPIDIUM BROMIDE, MEQUITAZINE, LOXOPROFEN, ZYRTEC, MAGNESIUM OXIDE. Patient was hospitalized. Patient died on 01/30/2007.

Lipitor Side Effects Report #5266534-5
Physician from JAPAN reported LIPITOR problem on Mar 05, 2007. Female patient, weighting 88.18 lb, was diagnosed with hypercholesterolaemia, gastritis, gastric disorder, pruritus, back pain and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: coma hepatic, hepatic failure, hepatitis fulminant, . LIPITOR dosage: DAILY DOSE:5MG. During the same period patient was treated with SELBEX, TIMEPIDIUM BROMIDE, TIMEPIDIUM BROMIDE, MEQUITAZINE, LOXOPROFEN, ZYRTEC, MAGNESIUM OXIDE. Patient was hospitalized. Patient died on 01/30/2007.

Lipitor Side Effects Report #5274394-1
LIPITOR problem was reported by a Physician from JAPAN on Mar 13, 2007. Female patient, weighting 88.18 lb, was diagnosed with hypercholesterolaemia, gastritis, gastric disorder, pruritus, back pain and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: coma hepatic, hepatic cyst, hepatic failure, hepatitis fulminant, . LIPITOR dosage: DAILY DOSE:5MG. During the same period patient was treated with SELBEX, TIMEPIDIUM BROMIDE, TIMEPIDIUM BROMIDE, MEQUITAZINE, LOXOPROFEN, ZYRTEC, MAGNESIUM OXIDE. Patient was hospitalized. Patient died on 01/30/2007.

Avelox Side Effects Report #5278355-8
Physician from CHINA reported AVELOX problem on Mar 22, 2007. Male patient was diagnosed with pneumonia and was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: coma hepatic, jaundice, . AVELOX dosage: TOTAL DAILY DOSE: 400 MG UNIT DOSE: 400 MG. Patient died on 11/01/2006.

Taxotere Side Effects Report #5682354-1
TAXOTERE problem was reported by a Health Professional from VIET NAM on Mar 19, 2008. Female patient, 60 years of age, weighting 112.4 lb, was diagnosed with breast cancer and was treated with TAXOTERE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, coma hepatic, jaundice, oedema, . TAXOTERE dosage: unknown. During the same period patient was treated with FLUOROURACIL, EPIRUBICIN, CYCLOPHOSPHAMIDE. Patient was hospitalized. Patient died on 01/22/2008.

Amiodarone Side Effects Report #5643243-1
Pharmacist from TAIWAN, PROVINCE OF CHINA reported AMIODARONE problem on Feb 15, 2008. Female patient, 72 years of age, weighting 160.9 lb, was diagnosed with atrial fibrillation and was treated with AMIODARONE. After drug was administered, patient experienced the following problems/side effects: ascites, coma hepatic, hepatic enzyme increased, hepatocellular injury, jaundice, liver disorder, oliguria, renal failure acute, . AMIODARONE dosage: TOTAL DOSE 2.55 G, INTRAVENOUS; 1MG/MIN, INTRAVENOUS. During the same period patient was treated with ACETYLSALICYLIC ACID SRT, PENTOXIFYLLINE, INSULIN. Patient died.

Vfend Side Effects Report #5604895-5
VFEND problem was reported by a Health Professional from GERMANY on Jan 17, 2008. Female patient, weighting 28.66 lb, was diagnosed with infection prophylaxis, colitis ulcerative and was treated with VFEND. After drug was administered, patient experienced the following problems/side effects: coagulopathy, coma hepatic, hepatic failure, intra-abdominal haemorrhage, renal failure acute, . VFEND dosage: unknown. During the same period patient was treated with SANDIMMUNE, COTRIM, CORTISONE. Patient was hospitalized. Patient died on 01/01/2007.

Truvada Side Effects Report #5532492-9
Consumer or non-health professional from GERMANY reported TRUVADA problem on Nov 22, 2007. Male patient, weighting 100.5 lb, was diagnosed with hiv infection, oral candidiasis, pneumocystis jiroveci pneumonia, anaemia, atypical mycobacterial infection, blood uric acid increased and was treated with TRUVADA. After drug was administered, patient experienced the following problems/side effects: b-cell lymphoma, coma hepatic, kaposi's sarcoma, . TRUVADA dosage: unknown. During the same period patient was treated with SUSTIVA, DIFLUCAN, PENTACARINAT, NEUPOGEN, MYCOBUTIN, ZYLORIC, KLACID, CYCLOPHOSPHAMIDE DOXORUBICIN. Patient died on 02/05/2006.

Nexavar Side Effects Report #5497864-X
NEXAVAR problem was reported by a Physician from CHINA on Oct 19, 2007. Male patient, 56 years of age, was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, coma hepatic, diarrhoea, hepatitis, jaundice, rash, transaminases increased, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG. Patient recovered.

Gleevec Side Effects Report #5405648-3
Health Professional from JAPAN reported GLEEVEC problem on July 30, 2007. Male patient, 54 years of age, weighting 149.9 lb, was diagnosed with chronic myeloid leukaemia and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, coma hepatic, depressed level of consciousness, dyspepsia, fatigue, haemoglobin decreased, hepatic encephalopathy, hepatitis, hepatitis b, . GLEEVEC dosage: 300 MG/DAY. During the same period patient was treated with ADALAT, ALLOPURINOL. Patient was hospitalized. Patient died on 06/21/2004.

Gemcitabine Side Effects Report #5409683-0
GEMCITABINE problem was reported by a Physician from UNITED STATES on July 31, 2007. Female patient, 45 years of age, was diagnosed with breast cancer recurrent, back pain and was treated with GEMCITABINE. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, coma hepatic, hypercalcaemia, hypokalaemia, hyponatraemia, metastases to bone, metastases to liver, nausea, . GEMCITABINE dosage: 1300 MG, OTHER. During the same period patient was treated with CARBOPLATIN, ARIMIDEX, MS CONTIN, METYLPREDNISOLON SOLUBILE, VITAMIN K, PROMETHAZINE, ESOMEPRAZOLE MAGNESIUM, OXYCODONE. Patient died on 01/12/2002.

Capecitabine Side Effects Report #5372082-4
Physician from UNITED STATES reported CAPECITABINE problem on June 08, 2007. Female patient, 47 years of age, weighting 110.9 lb, was treated with CAPECITABINE. After drug was administered, patient experienced the following problems/side effects: cholestasis, coma hepatic, hepatic failure, hepatic fibrosis, metastases to liver, tumour necrosis, . CAPECITABINE dosage: unknown. During the same period patient was treated with BEVACIZUMAB, ABRAXANE. Patient was hospitalized. Patient died on 04/18/2007.

Flagyl Side Effects Report #5273721-9
FLAGYL problem was reported by a Physician from SWITZERLAND on Aug 11, 2005. Male patient, 85 years of age, was treated with FLAGYL. After drug was administered, patient experienced the following problems/side effects: anuria, coma hepatic, coma uraemic, hepatitis fulminant, inflammation, pyrexia, renal failure acute, . FLAGYL dosage: unknown. During the same period patient was treated with RIFATER, MAXIPIME. Patient was hospitalized. Patient died on 03/18/2005.

Amiodarone Side Effects Report #5631728-3
Consumer or non-health professional from TAIWAN, PROVINCE OF CHINA reported AMIODARONE problem on Feb 08, 2008. Female patient, 72 years of age, was diagnosed with atrial fibrillation and was treated with AMIODARONE. After drug was administered, patient experienced the following problems/side effects: ascites, cerebral infarction, coma hepatic, hepatotoxicity, loss of consciousness, pyelonephritis acute, renal failure acute, . AMIODARONE dosage: unknown. During the same period patient was treated with VERA. Patient was hospitalized. Patient died.

Hydrocortisone Side Effects Report #5595147-0
HYDROCORTISONE problem was reported by a Consumer or non-health professional from on Jan 10, 2008. Female patient, 33 years of age, was treated with HYDROCORTISONE. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, anuria, coma hepatic, hepatic encephalopathy, hepatic failure, hepatitis fulminant, herpes simplex, liver transplant rejection, metabolic acidosis, . HYDROCORTISONE dosage: unknown. During the same period patient was treated with PREDNISONE, TACROLIMUS, MYCOPHENOLIC ACID. Patient was hospitalized. Patient recovered.

Versed Side Effects Report #5565275-4
Consumer or non-health professional from UNITED STATES reported VERSED problem on Nov 26, 2001. Male patient was treated with VERSED. After drug was administered, patient experienced the following problems/side effects: chronic hepatic failure, collapse of lung, coma hepatic, lung disorder, multi-organ failure, overdose, respiratory failure, . VERSED dosage: THE PATIENT RECEIVED 2 MG, THEN 2 MG AND 1 MG.. During the same period patient was treated with METHAMPHETAMINE HYDROCHLORIDE, HEROIN, VALIUM. Patient died.

Kivexa Side Effects Report #5450158-0
KIVEXA problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Aug 31, 2007. Female patient, 40 years of age, was treated with KIVEXA. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, coma hepatic, hepatic failure, . KIVEXA dosage: unknown. During the same period patient was treated with VIRAMUNE, CHINESE HERBAL MEDICINE. Patient was hospitalized. Patient recovered.

Sertraline Side Effects Report #5759251-6
Consumer or non-health professional from DENMARK reported SERTRALINE problem on May 23, 2008. Female patient, 51 years of age, was diagnosed with relapsing-remitting multiple sclerosis, lipids increased and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: acute hepatic failure, autoimmune hepatitis, coma hepatic, hepatic encephalopathy, . SERTRALINE dosage: unknown. During the same period patient was treated with IBUROFEN, INTERFERON BETA, SIMVASTATIN, LORAZEPAM. Patient was hospitalized. Patient recovered.

Sertraline Side Effects Report #5792594-9
SERTRALINE problem was reported by a Consumer or non-health professional from DENMARK on June 16, 2008. Female patient, 51 years of age, was diagnosed with relapsing-remitting multiple sclerosis, lipids increased and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: acute hepatic failure, autoimmune hepatitis, coma hepatic, hepatic encephalopathy, . SERTRALINE dosage: unknown. During the same period patient was treated with IBUROFEN, INTERFERON BETA, SIMVASTATIN, LORAZEPAM. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5316299-3
Consumer or non-health professional from BRAZIL reported HUMIRA problem on Apr 24, 2007. Male patient, weighting 154.3 lb, was diagnosed with rheumatoid arthritis, pain, prophylaxis against gastrointestinal ulcer, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: arthralgia, bursitis infective, coma hepatic, diarrhoea, hepatic encephalopathy, hepatitis, localised oedema, malaise, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, PREDNISONE, DICLOFENAC, OMEPRAZOLE, ATENOLOL, NIFEDIPINE, ERGOCALCIFEROL, CORTICOID. Patient was hospitalized. Patient died on 12/21/2006.

Methotrexate Side Effects Report #5332768-4
METHOTREXATE problem was reported by a Consumer or non-health professional from SWITZERLAND on May 07, 2007. Male patient, 69 years of age, was diagnosed with acute lymphocytic leukaemia, aspergillosis and was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: bronchopulmonary aspergillosis, cholestasis, coma hepatic, gastrointestinal haemorrhage, hepatic encephalopathy, hepatic steatosis, liver injury, multi-organ failure, . METHOTREXATE dosage: unknown. During the same period patient was treated with VINCRISTINE, DAUNORUBICIN HYDROCHLORIDE, AMPHOTERICIN B, ASPARAGINASE, CYCLOPHOSPHAMIDE, VORICONAZOLE, VALACYCLOVIR. Patient was hospitalized. Patient died on 03/30/2005.