HEPATIC HAEMORRHAGE side effect
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Drugs associated with HEPATIC HAEMORRHAGE
ADDERALL ANDRODERM ARIXTRA AVONEX BEVACIZUMAB BYETTA INDOMETHACIN NEOPROFEN NEXAVAR REMICADE VELCADE VIANIRemicade Side Effects Report #5582986-5
Health Professional from FRANCE reported REMICADE problem on Dec 28, 2007. Female patient, 50 years of age, weighting 145.5 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: hepatic haemorrhage, hepatitis fulminant, lupus hepatitis, peritoneal haemorrhage, sepsis, venous thrombosis, . REMICADE dosage: unknown. During the same period patient was treated with ARAVA, STAGID. Patient was hospitalized. Patient recovered.
Arixtra Side Effects Report #5507696-1
ARIXTRA problem was reported by a Pharmacist from JAPAN on Nov 01, 2007. Male patient, 38 years of age, weighting 114.6 lb, was diagnosed with nausea, abdominal pain and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: hepatic haemorrhage, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, KENTAN, MUCOSTA, DASEN, PRIMPERAN, FAMOTIDINE, BUSCOPAN, PENTAZOCINE LACTATE. Patient recovered.
Avonex Side Effects Report #5490172-2
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Oct 04, 2007. Female patient, 74 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: hepatic haemorrhage, liver disorder, urinary tract infection, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Velcade Side Effects Report #5775306-4
VELCADE problem was reported by a Physician from JAPAN on June 04, 2008. Female patient was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: hepatic haemorrhage, procedural complication, . VELCADE dosage: unknown. Patient died on 04/22/2008.
Velcade Side Effects Report #5731265-1
Physician from JAPAN reported VELCADE problem on Apr 30, 2008. Female patient was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: hepatic haemorrhage, hepatic neoplasm, post procedural haemorrhage, . VELCADE dosage: unknown. Patient died on 04/22/2008.
Bevacizumab Side Effects Report #5334813-9
BEVACIZUMAB problem was reported by a Health Professional from UNITED STATES on May 16, 2007. Female patient, 61 years of age, weighting 116.8 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: hepatic haemorrhage, hyperbilirubinaemia, respiratory distress, . BEVACIZUMAB dosage: 15 MG/KG, Q3W. During the same period patient was treated with GEMCITABINE, CARBOPLATIN, FENTANYL, MORPHINE SULPHATE, NEURONTIN, COMPAZINE, DULCOLAX. Patient was hospitalized. Patient recovered.
Nexavar Side Effects Report #5295838-5
Physician from CHINA reported NEXAVAR problem on Apr 09, 2007. Male patient was diagnosed with hepatic neoplasm malignant and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: hepatic haemorrhage, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG. Patient recovered.
Nexavar Side Effects Report #5299130-4
NEXAVAR problem was reported by a Physician from CHINA on Apr 09, 2007. Male patient was diagnosed with hepatic neoplasm malignant and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: hepatic haemorrhage, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG. Patient recovered.
Androderm Side Effects Report #5580998-9
Health Professional from AUSTRALIA reported ANDRODERM problem on Dec 19, 2007. Male patient, 31 years of age, was treated with ANDRODERM. After drug was administered, patient experienced the following problems/side effects: hepatic adenoma, hepatic haemorrhage, . ANDRODERM dosage: unknown. Patient was hospitalized. Patient recovered.
Avonex Side Effects Report #5510880-4
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 30, 2007. Female patient, 74 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: hepatic adenoma, hepatic haemorrhage, urinary tract infection, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Avonex Side Effects Report #5374065-7
Physician from UNITED STATES reported AVONEX problem on June 21, 2007. Female patient, 23 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: hepatic haemorrhage, hydronephrosis, pleural effusion, pregnancy, premature labour, rash, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Neoprofen Side Effects Report #5302925-1
NEOPROFEN problem was reported by a Physician from UNITED STATES on Apr 02, 2007. Male patient was diagnosed with patent ductus arteriosus and was treated with NEOPROFEN. After drug was administered, patient experienced the following problems/side effects: haemorrhage neonatal, hepatic haemorrhage, neonatal disorder, skin haemorrhage, . NEOPROFEN dosage: 5 MG/KG; QD; IV. Patient was hospitalized. Patient recovered.
Neoprofen Side Effects Report #5302936-6
Physician from UNITED STATES reported NEOPROFEN problem on Apr 02, 2007. Male patient was diagnosed with patent ductus arteriosus and was treated with NEOPROFEN. After drug was administered, patient experienced the following problems/side effects: haemorrhage neonatal, hepatic haemorrhage, skin haemorrhage, . NEOPROFEN dosage: 5 MG/KG; QD; IV. Patient was hospitalized. Patient recovered.
Viani Side Effects Report #5262813-6
VIANI problem was reported by a Physician from GERMANY on Mar 07, 2007. Male patient, 67 years of age, weighting 149.9 lb, was treated with VIANI. After drug was administered, patient experienced the following problems/side effects: hepatic cirrhosis, hepatic haemorrhage, . VIANI dosage: unknown. Patient was hospitalized. Patient recovered.
Avonex Side Effects Report #5679052-7
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Mar 11, 2008. Female patient, 36 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: cholelithiasis, hepatic enzyme increased, hepatic haemorrhage, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Arixtra Side Effects Report #5564945-1
ARIXTRA problem was reported by a Pharmacist from JAPAN on Dec 14, 2007. Male patient, 38 years of age, weighting 114.6 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, fall, hepatic haemorrhage, pyrexia, shock, vomiting, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, KENTAN, MUCOSTA, DASEN. Patient recovered.
Arixtra Side Effects Report #5571757-1
Pharmacist from JAPAN reported ARIXTRA problem on Dec 18, 2007. Male patient, 38 years of age, weighting 114.6 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, fall, hepatic haemorrhage, pyrexia, shock, vomiting, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, KENTAN, MUCOSTA, DASEN. Patient recovered.
Arixtra Side Effects Report #5520864-8
ARIXTRA problem was reported by a Pharmacist from JAPAN on Nov 16, 2007. Male patient, 38 years of age, weighting 114.6 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, fall, hepatic haemorrhage, shock, vomiting, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, KENTAN, MUCOSTA, DASEN. Patient recovered.
Arixtra Side Effects Report #5527311-0
Pharmacist from JAPAN reported ARIXTRA problem on Nov 22, 2007. Male patient, 38 years of age, weighting 114.6 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, fall, hepatic haemorrhage, shock, vomiting, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, KENTAN, MUCOSTA, DASEN. Patient recovered.
Adderall Side Effects Report #5424577-2
ADDERALL problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 17, 2007. Male patient, weighting 209.9 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with ADDERALL. After drug was administered, patient experienced the following problems/side effects: contusion, hepatic haemorrhage, hepatitis c, homicidal ideation, psychotic disorder, self-injurious ideation, . ADDERALL dosage: 20 MG, QID, ORAL, 20 MG, TID, ORAL. During the same period patient was treated with INSULIN, METFORMIN, GLIPIZIDE, LITHIUM CARBONATE. Patient was hospitalized. Patient recovered.
Nexavar Side Effects Report #5397911-X
Physician from BRAZIL reported NEXAVAR problem on July 20, 2007. Male patient was diagnosed with hepatic neoplasm malignant and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: encephalopathy, hepatic failure, hepatic haemorrhage, . NEXAVAR dosage: UNIT DOSE: 200 MG. Patient died on 07/01/2007.
Nexavar Side Effects Report #5399393-0
NEXAVAR problem was reported by a Physician from BRAZIL on July 20, 2007. Male patient was diagnosed with hepatic neoplasm malignant and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: encephalopathy, hepatic failure, hepatic haemorrhage, . NEXAVAR dosage: UNIT DOSE: 200 MG. Patient died on 07/01/2007.
Nexavar Side Effects Report #5397911-X
Physician from BRAZIL reported NEXAVAR problem on July 20, 2007. Male patient was diagnosed with hepatic neoplasm malignant and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: encephalopathy, hepatic failure, hepatic haemorrhage, . NEXAVAR dosage: UNIT DOSE: 200 MG. Patient died on 07/01/2007.
Nexavar Side Effects Report #5399393-0
NEXAVAR problem was reported by a Physician from BRAZIL on July 20, 2007. Male patient was diagnosed with hepatic neoplasm malignant and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: encephalopathy, hepatic failure, hepatic haemorrhage, . NEXAVAR dosage: UNIT DOSE: 200 MG. Patient died on 07/01/2007.
Byetta Side Effects Report #5354226-3
Consumer or non-health professional from UNITED STATES reported BYETTA problem on May 31, 2007. Female patient, 51 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: cholecystectomy, gastric operation, hepatic haemorrhage, liver disorder, liver operation, . BYETTA dosage: unknown. During the same period patient was treated with METOPROLOL. Patient was hospitalized. Patient recovered.
Indomethacin Side Effects Report #5304435-4
INDOMETHACIN problem was reported by a Health Professional from JAPAN on Apr 04, 2007. Male patient was diagnosed with patent ductus arteriosus and was treated with INDOMETHACIN. After drug was administered, patient experienced the following problems/side effects: anaemia neonatal, disseminated intravascular coagulation, hepatic haemorrhage, hydrocephalus, infantile spasms, intraventricular haemorrhage neonatal, neonatal disorder, thrombocytopenia neonatal, . INDOMETHACIN dosage: 0.1 MG;QD;IV. Patient recovered.
Indomethacin Side Effects Report #5304436-6
Health Professional from JAPAN reported INDOMETHACIN problem on Apr 04, 2007. Female patient was diagnosed with patent ductus arteriosus and was treated with INDOMETHACIN. After drug was administered, patient experienced the following problems/side effects: haemorrhage intracranial, haemorrhagic diathesis, hepatic haemorrhage, neonatal disorder, peritoneal haemorrhage, shock, thrombocytopenia neonatal, . INDOMETHACIN dosage: 0.7 MG;QD;IV. Patient died on 03/18/2005.