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HEPATORENAL SYNDROME side effect

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Nexavar Side Effects Report #5672528-8
Physician from CANADA reported NEXAVAR problem on Mar 13, 2008. Male patient, 66 years of age, was diagnosed with hepatic neoplasm malignant and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, . NEXAVAR dosage: TOTAL DAILY DOSE: 400 MG UNIT DOSE: 200 MG. During the same period patient was treated with TENORMIN, ADALAT, MONOPRIL, ATARAX, STATIN. Patient died on 10/25/2007.

Nexavar Side Effects Report #5674112-9
NEXAVAR problem was reported by a Physician from CANADA on Mar 13, 2008. Male patient, 66 years of age, was diagnosed with hepatic neoplasm malignant and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, . NEXAVAR dosage: TOTAL DAILY DOSE: 400 MG UNIT DOSE: 200 MG. During the same period patient was treated with TENORMIN, ADALAT, MONOPRIL, ATARAX, STATIN. Patient died on 10/25/2007.

Bevacizumab Side Effects Report #5624968-0
Physician from UNITED KINGDOM reported BEVACIZUMAB problem on Jan 29, 2008. Female patient, weighting 127.9 lb, was diagnosed with non-small cell lung cancer and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, . BEVACIZUMAB dosage: 870 MG, Q3W. During the same period patient was treated with CARBOPLATIN, DOCETAXEL, VERAPAMIL, METFORMIN. Patient was hospitalized. Patient recovered.

Hepsera Side Effects Report #5635094-9
HEPSERA problem was reported by a Physician from AUSTRIA on Feb 14, 2008. Male patient, weighting 172.0 lb, was diagnosed with hepatitis b, type 2 diabetes mellitus and was treated with HEPSERA. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, hypertension, renal failure acute, renal tubular necrosis, . HEPSERA dosage: unknown. During the same period patient was treated with PANTOPRAZOLE, KONAKION, SPIROBENE, ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE, INSULIN. Patient was hospitalized. Patient recovered.


Emtricitabine Side Effects Report #5643840-3
Consumer or non-health professional from UNITED STATES reported EMTRICITABINE problem on Feb 20, 2008. Male patient, weighting 154.1 lb, was diagnosed with hepatitis b, vitamin supplementation, peritonitis bacterial, ascites, nausea and was treated with EMTRICITABINE. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, peritonitis bacterial, . EMTRICITABINE dosage: unknown. During the same period patient was treated with VITAMIN CAP, CIPROFLOXACIN, LASIX, ALDACTONE, FOLIC ACID, REGLAN. Patient was hospitalized. Patient recovered.

Bevacizumab Side Effects Report #5646104-7
BEVACIZUMAB problem was reported by a Physician from UNITED KINGDOM on Feb 14, 2008. Female patient, weighting 127.9 lb, was diagnosed with non-small cell lung cancer and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, . BEVACIZUMAB dosage: 870 MG, Q3W. During the same period patient was treated with CARBOPLATIN, DOCETAXEL, VERAPAMIL, METFORMIN. Patient was hospitalized. Patient recovered.

Visipaque Side Effects Report #5483193-7
Health Professional from NORWAY reported VISIPAQUE problem on Oct 05, 2007. Male patient, 68 years of age, was diagnosed with prostate cancer and was treated with VISIPAQUE. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, . VISIPAQUE dosage: 120 ML, SINGLE DOSE, I.V.. During the same period patient was treated with SERENOA REPENS, IBUPROFEN, HESPERIDINE, FLUOCINOLONE ACETONIDE, MEGLUMINE AMIDOTRIZOATE AND SOLDIUM AMIDOTRIZOATE. Patient was hospitalized. Patient recovered.

Faslodex Side Effects Report #5382503-9
FASLODEX problem was reported by a Consumer or non-health professional from UNITED STATES on July 05, 2007. Female patient, 51 years of age, was diagnosed with breast cancer and was treated with FASLODEX. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, metastases to central nervous system, . FASLODEX dosage: unknown. During the same period patient was treated with SPIRONOLACTONE, LORTAB, NADOLOL, ZOFRAN, VITAMIN B6. Patient died on 04/02/2007.

Faslodex Side Effects Report #5401138-2
Consumer or non-health professional from UNITED STATES reported FASLODEX problem on Apr 24, 2007. Female patient, 51 years of age, was diagnosed with breast cancer and was treated with FASLODEX. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, metastases to central nervous system, . FASLODEX dosage: unknown. During the same period patient was treated with SPIRONOLACTONE, LORTAB, NADOLOL, ZOFRAN, VITAMIN B6. Patient died on 04/02/2007.


Faslodex Side Effects Report #5382503-9
FASLODEX problem was reported by a Consumer or non-health professional from UNITED STATES on July 05, 2007. Female patient, 51 years of age, was diagnosed with breast cancer and was treated with FASLODEX. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, metastases to central nervous system, . FASLODEX dosage: unknown. During the same period patient was treated with SPIRONOLACTONE, LORTAB, NADOLOL, ZOFRAN, VITAMIN B6. Patient died on 04/02/2007.

Faslodex Side Effects Report #5401138-2
Consumer or non-health professional from UNITED STATES reported FASLODEX problem on Apr 24, 2007. Female patient, 51 years of age, was diagnosed with breast cancer and was treated with FASLODEX. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, metastases to central nervous system, . FASLODEX dosage: unknown. During the same period patient was treated with SPIRONOLACTONE, LORTAB, NADOLOL, ZOFRAN, VITAMIN B6. Patient died on 04/02/2007.

Nexavar Side Effects Report #5759508-9
NEXAVAR problem was reported by a Physician from CANADA on May 23, 2008. Male patient, 66 years of age, was diagnosed with hepatic neoplasm malignant and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, . NEXAVAR dosage: TOTAL DAILY DOSE: 400 MG UNIT DOSE: 200 MG. During the same period patient was treated with TENORMIN, ADALAT, MONOPRIL, ATARAX, STATIN, PANTOPRAZOLE. Patient died on 10/25/2007.

Tygacil Side Effects Report #5724689-X
Health Professional from BELGIUM reported TYGACIL problem on Apr 30, 2008. Male patient was diagnosed with wound infection staphylococcal and was treated with TYGACIL. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, . TYGACIL dosage: unknown. Patient was hospitalized. Patient died.

Nexavar Side Effects Report #5749121-1
NEXAVAR problem was reported by a Physician from CANADA on May 16, 2008. Male patient, 66 years of age, was diagnosed with hepatic neoplasm malignant and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, . NEXAVAR dosage: TOTAL DAILY DOSE: 400 MG UNIT DOSE: 200 MG. During the same period patient was treated with TENORMIN, ADALAT, MONOPRIL, ATARAX, STATIN. Patient died on 10/25/2007.


Vivitrol Side Effects Report #5353865-3
Physician from UNITED STATES reported VIVITROL problem on May 24, 2007. Male patient, 36 years of age, was diagnosed with alcoholism and was treated with VIVITROL. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, pancreatitis, renal failure, treatment noncompliance, . VIVITROL dosage: (380 MG 1X/MONTH INTRAMUSCULAR). During the same period patient was treated with ANTABUSE, CAMPRAL. Patient was hospitalized. Patient died on 01/01/2007.

Augmentin Side Effects Report #5373559-8
AUGMENTIN problem was reported by a Physician from CAMEROON on June 22, 2007. Female patient, 75 years of age, was diagnosed with lobar pneumonia and was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, hypoglycaemic coma, jaundice, liver function test abnormal, liver tenderness, renal impairment, . AUGMENTIN dosage: unknown. Patient died on 06/14/2007.

Tacrolimus Side Effects Report #5336445-5
Health Professional from UNITED KINGDOM reported TACROLIMUS problem on May 11, 2007. Female patient, 46 years of age, was diagnosed with liver transplant and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, . TACROLIMUS dosage: unknown. During the same period patient was treated with METHYLPREDNISOLONE, TRIMETHOPRIM. Patient recovered.

Ciprofloxacin Side Effects Report #5294416-1
CIPROFLOXACIN problem was reported by a Pharmacist from UNITED KINGDOM on Apr 02, 2007. Female patient, 58 years of age, was diagnosed with gastroenteritis and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, . CIPROFLOXACIN dosage: TOTAL DAILY DOSE: 500 MG. During the same period patient was treated with PROCHLORPERAZINE, MEBEVERINE, BENDROFLUAZIDE, ZOLPIDEM TARTRATE, ATENOLOL, LORAZEPAM. Patient was hospitalized. Patient recovered.

Ciprofloxacin Side Effects Report #5263493-6
Pharmacist from UNITED KINGDOM reported CIPROFLOXACIN problem on Feb 27, 2007. Female patient, 58 years of age, was diagnosed with gastroenteritis and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: hepatorenal syndrome, . CIPROFLOXACIN dosage: TOTAL DAILY DOSE: 500 MG. During the same period patient was treated with PROCHLORPERAZINE, MEBEVERINE, BENDROFLUAZIDE, ZOLPIDEM TARTRATE, ATENOLOL, LORAZEPAM. Patient was hospitalized. Patient recovered.


Tacrolimus Side Effects Report #5574136-6
TACROLIMUS problem was reported by a Physician from JAPAN on Dec 05, 2007. Female patient, 66 years of age, weighting 108.0 lb, was diagnosed with rheumatoid arthritis and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: beta-n-acetyl-d-glucosaminidase increased, hepatorenal syndrome, lymphocyte count decreased, . TACROLIMUS dosage: 1.5 MG/D, ORAL; 3 MG, ORAL. During the same period patient was treated with PREDNISOLONE, METHOTREXATE, ENBREL, HYPEN, VOLTAREN, ISCOTIN. Patient died on 05/03/2007.

Visipaque Side Effects Report #5477637-4
Health Professional from NORWAY reported VISIPAQUE problem on Sept 28, 2007. Female patient, 54 years of age, was diagnosed with colon cancer and was treated with VISIPAQUE. After drug was administered, patient experienced the following problems/side effects: dyspnoea, hepatorenal syndrome, malaise, myalgia, oral herpes, pyrexia, vomiting, . VISIPAQUE dosage: 120 ML, SINGLE DOSE, I.V.. During the same period patient was treated with MEGLUMINE AMIDOTRIZOATE AND AMIDOTRIZOATE, VESIPAQUE. Patient was hospitalized. Patient recovered.

Visipaque Side Effects Report #5477780-X
VISIPAQUE problem was reported by a Health Professional from NORWAY on Sept 28, 2007. Male patient, 68 years of age, was diagnosed with prostate cancer and was treated with VISIPAQUE. After drug was administered, patient experienced the following problems/side effects: chills, hepatorenal syndrome, malaise, myalgia, pyrexia, vomiting, . VISIPAQUE dosage: 50 MG, SINGLE DOSE, I.V.. During the same period patient was treated with SERENOA REPENS, IBUPROFEN, HESPERIDINE. Patient was hospitalized. Patient recovered.

Isoflurane Side Effects Report #5485486-6
Pharmacist from UNITED STATES reported ISOFLURANE problem on Oct 10, 2007. Male patient, 45 years of age, was diagnosed with anaesthesia and was treated with ISOFLURANE. After drug was administered, patient experienced the following problems/side effects: hepatic failure, hepatorenal syndrome, . ISOFLURANE dosage: unknown. Patient recovered.

Capecitabine Side Effects Report #5499783-1
CAPECITABINE problem was reported by a Physician from SWITZERLAND on Oct 17, 2007. Male patient, 58 years of age, was diagnosed with pancreatic carcinoma and was treated with CAPECITABINE. After drug was administered, patient experienced the following problems/side effects: diarrhoea, hepatorenal syndrome, sepsis, . CAPECITABINE dosage: unknown. During the same period patient was treated with GEMCITABINE, OXALIPLATIN, ASPIRIN. Patient died on 10/15/2007.

Vancomycin Side Effects Report #5503176-8
Pharmacist from UNITED STATES reported VANCOMYCIN problem on Oct 29, 2007. Male patient, 68 years of age, was diagnosed with urinary tract infection staphylococcal and was treated with VANCOMYCIN. After drug was administered, patient experienced the following problems/side effects: antibiotic level above therapeutic, hepatorenal syndrome, renal failure acute, . VANCOMYCIN dosage: 1500MG BID IV. Patient recovered.

Plavix Side Effects Report #5404386-0
PLAVIX problem was reported by a Pharmacist from CANADA on July 25, 2007. Male patient, 73 years of age, weighting 172.4 lb, was diagnosed with coronary artery disease, stomach discomfort, cardiac disorder, hypercholesterolaemia, pain, neuralgia and was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: hepatitis acute, hepatorenal syndrome, hyperbilirubinaemia, . PLAVIX dosage: unknown. During the same period patient was treated with LOSEC, BETALOC, LESCOL, TYLENOL, GABAPENTIN, PANTOPRAZOLE. Patient was hospitalized. Patient died on 06/01/2007.

Sustiva Side Effects Report #5379139-2
Physician from SPAIN reported SUSTIVA problem on June 29, 2007. Male patient, 47 years of age, weighting 176.4 lb, was diagnosed with hiv infection and was treated with SUSTIVA. After drug was administered, patient experienced the following problems/side effects: hepatitis, hepatorenal syndrome, renal impairment, . SUSTIVA dosage: unknown. During the same period patient was treated with TRUVADA, CIALIS, ANTIDEPRESSANT NOS. Patient died on 01/04/2006.

Sustiva Side Effects Report #5379139-2
SUSTIVA problem was reported by a Physician from SPAIN on June 29, 2007. Male patient, 47 years of age, weighting 176.4 lb, was diagnosed with hiv infection and was treated with SUSTIVA. After drug was administered, patient experienced the following problems/side effects: hepatitis, hepatorenal syndrome, renal impairment, . SUSTIVA dosage: unknown. During the same period patient was treated with TRUVADA, CIALIS, ANTIDEPRESSANT NOS. Patient died on 01/04/2006.

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.

Cetuximab Side Effects Report #5325235-5
Health Professional from GERMANY reported CETUXIMAB problem on May 10, 2007. Male patient, 61 years of age, was diagnosed with colorectal cancer metastatic and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: disease progression, hepatorenal syndrome, ileus, . CETUXIMAB dosage: unknown. During the same period patient was treated with OXALIPLATIN, FLUOROURACIL, FOLINIC ACID, METOCLOPRAMIDE, FUROSEMIDE. Patient was hospitalized. Patient died on 06/17/2006.

Enbrel Side Effects Report #5287990-2
ENBREL problem was reported by a Physician from JAPAN on Mar 23, 2007. Female patient, weighting 132.3 lb, was diagnosed with rheumatoid arthritis, hypertension and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: hepatitis b, hepatorenal syndrome, . ENBREL dosage: unknown. During the same period patient was treated with PROGRAF, METHOTREXATE, PREDONINE, FOLIAMIN, VOLTAREN, HYPEN, KOLANTYL, DIOVAN. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5626496-5
Physician from JAPAN reported PROGRAF problem on Dec 05, 2007. Female patient, weighting 132.3 lb, was diagnosed with rheumatoid arthritis and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: dyspnoea, hepatitis b, hepatorenal syndrome, malaise, oedema peripheral, urine output decreased, weight increased, . PROGRAF dosage: 3 MG, UID/QD, ORAL. During the same period patient was treated with ENBREL, PREDNISOLONE, VOLTAREN, ETODOLAC, METHOTREXATE, ISCOTIN, FOLIC ACID, KOLANTYL. Patient was hospitalized. Patient recovered.

Tegretol Side Effects Report #5510953-6
TEGRETOL problem was reported by a Physician from JAPAN on Nov 05, 2007. Female patient, 94 years of age, was diagnosed with intercostal neuralgia and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: bradycardia, dizziness, hepatorenal syndrome, . TEGRETOL dosage: 200 MG, BID. Patient recovered.

Visipaque Side Effects Report #5477781-1
Health Professional from NORWAY reported VISIPAQUE problem on Sept 27, 2007. Female patient, 69 years of age, was diagnosed with vulval cancer and was treated with VISIPAQUE. After drug was administered, patient experienced the following problems/side effects: chills, diarrhoea, hepatorenal syndrome, malaise, pyrexia, vomiting, . VISIPAQUE dosage: 120 ML, SINGLE DOSE, I.V.. During the same period patient was treated with MEGLUMIN AMIDOTRIZOATE AND AMIDOTRIZOATE. Patient was hospitalized. Patient recovered.

Enbrel Side Effects Report #5402929-4
ENBREL problem was reported by a Physician from JAPAN on July 25, 2007. Female patient, weighting 132.3 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, hepatitis b, hepatorenal syndrome, . ENBREL dosage: unknown. During the same period patient was treated with PROGRAF, PREDNISOLONE, VOLTAREN, HYPEN, METHOTREXATE, ISCOTIN, FOLIAMIN, KOLANTYL. Patient was hospitalized. Patient died on 05/03/2007.

Vepesid Side Effects Report #5395173-0
Health Professional from PORTUGAL reported VEPESID problem on July 23, 2007. Male patient, 77 years of age, weighting 176.4 lb, was diagnosed with chronic myelomonocytic leukaemia, hypertension, hypercholesterolaemia, hyperuricaemia, benign prostatic hyperplasia and was treated with VEPESID. After drug was administered, patient experienced the following problems/side effects: acute hepatic failure, haematemesis, hepatorenal syndrome, hypotension, nausea, tachycardia, urine output decreased, vomiting, . VEPESID dosage: unknown. During the same period patient was treated with LOSARTAN POTASSIUM, ATORVASTATIN CALCIUM, ALLOPURINOL, SERENOA REPENS, DARBEPOETIN ALFA. Patient died on 07/14/2006.

Enbrel Side Effects Report #5400145-3
ENBREL problem was reported by a Physician from JAPAN on July 25, 2007. Female patient, weighting 132.3 lb, was diagnosed with rheumatoid arthritis, hypertension, osteoporosis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, hepatitis b, hepatorenal syndrome, . ENBREL dosage: unknown. During the same period patient was treated with PROGRAF, PREDONINE, FOLIAMIN, VOLTAREN, HYPEN, KOLANTYL, DIOVAN. Patient was hospitalized. Patient died on 05/03/2007.

Vepesid Side Effects Report #5395173-0
Health Professional from PORTUGAL reported VEPESID problem on July 23, 2007. Male patient, 77 years of age, weighting 176.4 lb, was diagnosed with chronic myelomonocytic leukaemia, hypertension, hypercholesterolaemia, hyperuricaemia, benign prostatic hyperplasia and was treated with VEPESID. After drug was administered, patient experienced the following problems/side effects: acute hepatic failure, haematemesis, hepatorenal syndrome, hypotension, nausea, tachycardia, urine output decreased, vomiting, . VEPESID dosage: unknown. During the same period patient was treated with LOSARTAN POTASSIUM, ATORVASTATIN CALCIUM, ALLOPURINOL, SERENOA REPENS, DARBEPOETIN ALFA. Patient died on 07/14/2006.

Enbrel Side Effects Report #5400145-3
ENBREL problem was reported by a Physician from JAPAN on July 25, 2007. Female patient, weighting 132.3 lb, was diagnosed with rheumatoid arthritis, hypertension, osteoporosis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, hepatitis b, hepatorenal syndrome, . ENBREL dosage: unknown. During the same period patient was treated with PROGRAF, PREDONINE, FOLIAMIN, VOLTAREN, HYPEN, KOLANTYL, DIOVAN. Patient was hospitalized. Patient died on 05/03/2007.

Coaprovel Side Effects Report #5740182-2
Health Professional from FRANCE reported COAPROVEL problem on May 13, 2008. Male patient, 60 years of age, was diagnosed with hypertension and was treated with COAPROVEL. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, hepatorenal syndrome, multi-organ failure, renal failure acute, shock, . COAPROVEL dosage: unknown. During the same period patient was treated with ZANTAC, MOPRAL, LORAZEPAM, ZOPICLONE, SERETIDE. Patient was hospitalized. Patient died.

Voltaren Side Effects Report #5341945-8
VOLTAREN problem was reported by a Health Professional from UNITED STATES on May 23, 2007. Female patient, 67 years of age, weighting 132.3 lb, was diagnosed with rheumatoid arthritis and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: dyspnoea, hepatitis b, hepatorenal syndrome, jaundice, malaise, oedema, urine output decreased, weight increased, . VOLTAREN dosage: 25 MG, QD. During the same period patient was treated with ISCOTIN, ETANERCEPT, PROGRAF, PREDONINE, HYPEN, METHOTREXATE, FOLIAMIN, KOLANTYL. Patient was hospitalized. Patient recovered.

Enbrel Side Effects Report #5360707-9
Physician from JAPAN reported ENBREL problem on June 15, 2007. Female patient, weighting 132.3 lb, was diagnosed with rheumatoid arthritis, hypertension, osteoporosis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, hepatitis b, hepatorenal syndrome, . ENBREL dosage: unknown. During the same period patient was treated with PROGRAF, PREDONINE, FOLIAMIN, VOLTAREN, HYPEN, KOLANTYL, DIOVAN. Patient was hospitalized. Patient died on 05/03/2007.

Enbrel Side Effects Report #5365647-7
ENBREL problem was reported by a Physician from JAPAN on June 15, 2007. Female patient, weighting 132.3 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, hepatitis b, hepatorenal syndrome, . ENBREL dosage: unknown. During the same period patient was treated with PROGRAF, PREDONINE, VOLTAREN, HYPEN, METHOTREXATE, ISCOTIN, FOLIAMIN, KOLANTYL. Patient was hospitalized. Patient died on 05/03/2007.

Enbrel Side Effects Report #5323526-5
Physician from JAPAN reported ENBREL problem on May 07, 2007. Female patient, weighting 132.3 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: hepatitis b, hepatorenal syndrome, . ENBREL dosage: unknown. During the same period patient was treated with PROGRAF, PREDONINE, VOLTAREN, HYPEN, METHOTREXATE, ISCOTIN, FOLIAMIN, KOLANTYL. Patient was hospitalized. Patient died on 01/01/2007.

Vepesid Side Effects Report #5326104-7
VEPESID problem was reported by a Health Professional from PORTUGAL on May 14, 2007. Male patient, 77 years of age, weighting 176.4 lb, was diagnosed with chronic myelomonocytic leukaemia, hypertension, hypercholesterolaemia, hyperuricaemia, benign prostatic hyperplasia and was treated with VEPESID. After drug was administered, patient experienced the following problems/side effects: acute hepatic failure, haematemesis, hepatorenal syndrome, hypotension, nausea, tachycardia, urine output decreased, vomiting, . VEPESID dosage: unknown. During the same period patient was treated with LOSARTAN POTASSIUM, ATORVASTATIN CALCIUM, ALLOPURINOL, SERENOA REPENS, DARBEPOETIN ALFA. Patient died on 07/14/2006.

Enbrel Side Effects Report #5295060-2
Physician from JAPAN reported ENBREL problem on Apr 06, 2007. Female patient, weighting 132.3 lb, was diagnosed with rheumatoid arthritis, hypertension, osteoporosis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, hepatitis b, hepatorenal syndrome, . ENBREL dosage: unknown. During the same period patient was treated with PROGRAF, PREDONINE, FOLIAMIN, VOLTAREN, HYPEN, KOLANTYL, DIOVAN. Patient was hospitalized. Patient recovered.

Enbrel Side Effects Report #5301121-1
ENBREL problem was reported by a Physician from JAPAN on Apr 06, 2007. Female patient, weighting 132.3 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, hepatitis b, hepatorenal syndrome, . ENBREL dosage: unknown. During the same period patient was treated with PROGRAF, PREDONINE, VOLTAREN, HYPEN, METHOTREXATE, ISCOTIN, FOLIAMIN, KOLANTYL. Patient was hospitalized. Patient recovered.

Flolan Side Effects Report #5272433-5
Consumer or non-health professional from UNITED STATES reported FLOLAN problem on Mar 02, 2007. Male patient, 58 years of age, was diagnosed with pulmonary hypertension and was treated with FLOLAN. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, haemodialysis, hepatorenal syndrome, pulmonary oedema, . FLOLAN dosage: unknown. Patient recovered.