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BILIRUBIN CONJUGATED INCREASED side effect

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Mercaptopurine Side Effects Report #5648022-7
Consumer or non-health professional from UNITED STATES reported MERCAPTOPURINE problem on Feb 29, 2008. Male patient, weighting 249.6 lb, was treated with MERCAPTOPURINE. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, hepatic cirrhosis, ill-defined disorder, iron overload, transaminases increased, . MERCAPTOPURINE dosage: 5800 MG. During the same period patient was treated with VINCRISTINE SULPHATE, DEXAMETHASONE. Patient was hospitalized. Patient recovered.

Atazanavir Side Effects Report #5584372-0
ATAZANAVIR SULPHATE problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 04, 2008. Female patient, 14 years of age, weighting 61.73 lb, was diagnosed with hiv infection and was treated with ATAZANAVIR SULPHATE. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin unconjugated increased, hyperbilirubinaemia, jaundice, . ATAZANAVIR SULPHATE dosage: unknown. During the same period patient was treated with STAVUDINE, LAMIVUDINE, BACTRIM, LASIX, ALDACTONE, LOSEC I. Patient recovered.

Atazanavir Side Effects Report #5598845-8
Health Professional from UNITED STATES reported ATAZANAVIR SULPHATE problem on Jan 14, 2008. Female patient, 14 years of age, weighting 108.0 lb, was diagnosed with hiv infection and was treated with ATAZANAVIR SULPHATE. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, hyperbilirubinaemia, . ATAZANAVIR SULPHATE dosage: unknown. During the same period patient was treated with STAVUDINE, LAMIVUDINE, BACTRIM. Patient recovered.

Avidart Side Effects Report #5602516-9
AVIDART problem was reported by a Physician from SPAIN on Jan 21, 2008. Male patient, 62 years of age, was treated with AVIDART. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, blood bilirubin unconjugated increased, . AVIDART dosage: unknown. During the same period patient was treated with LIPEMOL, ALLOPURINOL. Patient recovered.


Sebivo Side Effects Report #5504045-X
Consumer or non-health professional from CHINA reported SEBIVO problem on Oct 24, 2007. Female patient was diagnosed with hepatitis b and was treated with SEBIVO. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, blood bilirubin unconjugated increased, cholelithiasis, mobility decreased, pain, poor quality sleep, protein total decreased, pruritus, . SEBIVO dosage: 600 MG, QD. During the same period patient was treated with HUGANNING, URSO FALK, ORYZANOL. Patient recovered.

Sebivo Side Effects Report #5504693-7
SEBIVO problem was reported by a Consumer or non-health professional from CHINA on Oct 24, 2007. Female patient was diagnosed with hepatitis b and was treated with SEBIVO. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, blood bilirubin unconjugated increased, cholelithiasis, mobility decreased, pain, poor quality sleep, protein total decreased, pruritus, . SEBIVO dosage: 600 MG, QD. During the same period patient was treated with HUGANNING, URSO FALK, ORYZANOL. Patient recovered.

Avodart Side Effects Report #5508787-1
Consumer or non-health professional from FRANCE reported AVODART problem on Nov 02, 2007. Male patient, 91 years of age, was diagnosed with prostatic adenoma and was treated with AVODART. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased, hepatitis cholestatic, jaundice cholestatic, . AVODART dosage: .5MG PER DAY. Patient was hospitalized. Patient recovered.

Calcium Side Effects Report #5512584-0
CALCIUM problem was reported by a Physician from GERMANY on Nov 02, 2007. Female patient, 54 years of age, weighting 130.1 lb, was diagnosed with hyperparathyroidism, gastrointestinal stromal tumour and was treated with CALCIUM. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood creatinine increased, bone pain, fatigue, hypercalcaemia, malignant neoplasm progression, nausea, renal failure acute, vomiting, . CALCIUM dosage: unknown. During the same period patient was treated with ROCALTROL. Patient recovered.

Malarone Side Effects Report #5520856-9
Physician from FRANCE reported MALARONE problem on Nov 12, 2007. Male patient, 24 years of age, was diagnosed with malaria prophylaxis and was treated with MALARONE. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, c-reactive protein increased, chills, eosinophil count increased, haemoglobin decreased, influenza like illness, lymphocyte count decreased, . MALARONE dosage: unknown. Patient was hospitalized. Patient recovered.


Tavanic Side Effects Report #5524598-5
TAVANIC problem was reported by a Health Professional from FRANCE on Nov 12, 2007. Male patient, 42 years of age, was diagnosed with sepsis and was treated with TAVANIC. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, blood bilirubin unconjugated increased, blood lactate dehydrogenase increased, c-reactive protein increased, glucose-6-phosphate dehydrogenase deficiency, glycogen storage disease type i, haemolytic anaemia, platelet count increased, . TAVANIC dosage: unknown. During the same period patient was treated with GENTAMICIN. Patient was hospitalized. Patient recovered.

Cancidas Side Effects Report #5492923-X
Consumer or non-health professional from SPAIN reported CANCIDAS problem on Sept 14, 2007. Female patient, 50 years of age, was diagnosed with lower respiratory tract infection fungal, aplastic anaemia and was treated with CANCIDAS. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, jaundice, respiratory failure, . CANCIDAS dosage: 70 MG/DAILY IV. During the same period patient was treated with CYCLOSPORINE, SULFAMETHOXAZOLE TRIMETHOPRIM, MYOLASTAN, NAPROXEN. Patient was hospitalized. Patient died.

Sorafenib Side Effects Report #5492931-9
SORAFENIB problem was reported by a Physician from UNITED STATES on Oct 16, 2007. Male patient, 67 years of age, weighting 160.9 lb, was diagnosed with non-small cell lung cancer, chronic obstructive pulmonary disease, obsessive-compulsive disorder and was treated with SORAFENIB. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood alkaline phosphatase increased, blood calcium decreased, blood phosphorus increased, blood urea nitrogen/creatinine ratio increased, condition aggravated, effusion, haematocrit decreased, haemoglobin decreased, . SORAFENIB dosage: TOTAL DAILY DOSE: 800 MG UNIT DOSE: 200 MG. During the same period patient was treated with CARBOPLATIN, PACLITAXEL, NASAL OXYGEN, NASAL OXYGEN, NASAL OXYGEN, ZOLOFT. Patient was hospitalized. Patient died on 10/13/2007.

Seroquel Side Effects Report #5460338-6
Health Professional from UNITED STATES reported SEROQUEL problem on June 29, 2007. Male patient, 46 years of age, was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, . SEROQUEL dosage: unknown. During the same period patient was treated with HYDROCHLOROTHIAZIDE, ACCUPRIL, GABAPENTIN, LAMICTAL, NEXIUM. Patient recovered.

Cancidas Side Effects Report #5468674-4
CANCIDAS problem was reported by a Consumer or non-health professional from SPAIN on Sept 14, 2007. Female patient, 50 years of age, was diagnosed with lower respiratory tract infection fungal, aplastic anaemia and was treated with CANCIDAS. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, jaundice, respiratory failure, . CANCIDAS dosage: 70 MG/DAILY IV. During the same period patient was treated with CYCLOSPORINE, SULFAMETHOXAZOLE TRIMETHOPRIM, MYOLASTAN, NAPROXEN. Patient was hospitalized. Patient died.


Amoclav Side Effects Report #5406076-7
Physician from GERMANY reported AMOCLAV problem on Aug 01, 2007. Male patient, 55 years of age, was treated with AMOCLAV. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood alkaline phosphatase increased, blood cholesterol increased, blood lactate dehydrogenase increased, diarrhoea, gamma-glutamyltransferase increased, hepatic enzyme increased, hyperbilirubinaemia, jaundice, . AMOCLAV dosage: 1000MG TWICE PER DAY. Patient recovered.

Diovan Side Effects Report #5408066-7
DIOVAN problem was reported by a Physician from CHINA on Aug 01, 2007. Male patient, 76 years of age, weighting 114.6 lb, was diagnosed with hypertension and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, blood bilirubin unconjugated increased, . DIOVAN dosage: 80 MG, QD. Patient was hospitalized. Patient recovered.

Oxaliplatin Side Effects Report #5415369-9
Health Professional from UNITED STATES reported OXALIPLATIN problem on Aug 14, 2007. Female patient, 70 years of age, weighting 112.0 lb, was diagnosed with carcinoid tumour of the appendix and was treated with OXALIPLATIN. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, culture positive, enterococcal infection, escherichia infection, granulocytes abnormal, haematoma infection, haemoglobin decreased, jaundice, . OXALIPLATIN dosage: 365MG INTRAPERITONEAL. During the same period patient was treated with LISINOPRIL, FOSAMAX, CENTRUM, ASPIRIN, FOLIC ACID. Patient was hospitalized. Patient recovered.

Clarithromycin Side Effects Report #5425375-6
CLARITHROMYCIN problem was reported by a Pharmacist from UNITED KINGDOM on Aug 14, 2007. Male patient, weighting 92.15 lb, was diagnosed with lower respiratory tract infection, sickle cell anaemia with crisis, pain, constipation and was treated with CLARITHROMYCIN. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, jaundice, . CLARITHROMYCIN dosage: unknown. During the same period patient was treated with MORPHINE, PARACETAMOL, CEFUROXIME, IBUPROFEN, LACTULOSE. Patient was hospitalized. Patient recovered.

Diovan Side Effects Report #5426292-8
Physician from CHINA reported DIOVAN problem on Aug 20, 2007. Male patient, 76 years of age, weighting 114.6 lb, was diagnosed with hypertension and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, blood bilirubin unconjugated increased, gamma-glutamyltransferase increased, jaundice, . DIOVAN dosage: 80 MG, QD. During the same period patient was treated with ISOSORBIDE DINITRATE, DIURETICS. Patient was hospitalized. Patient recovered.


Zantac Side Effects Report #5436021-X
ZANTAC problem was reported by a Pharmacist from JAPAN on Aug 28, 2007. Male patient, 55 years of age, weighting 154.5 lb, was diagnosed with gastritis and was treated with ZANTAC. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin unconjugated increased, hepatitis, liver disorder, . ZANTAC dosage: unknown. During the same period patient was treated with FLUMARIN, NEOLAMIN, SOLDEM. Patient was hospitalized. Patient recovered.

Thymoglobulin Side Effects Report #5423755-6
Health Professional from UNITED STATES reported THYMOGLOBULIN problem on July 15, 2004. Male patient, 13 years of age, was treated with THYMOGLOBULIN. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, graft versus host disease, obliterative bronchiolitis, obstructive airways disorder, . THYMOGLOBULIN dosage: unknown. Patient died on 07/06/2004.

Thymoglobulin Side Effects Report #5423755-6
THYMOGLOBULIN problem was reported by a Health Professional from UNITED STATES on July 15, 2004. Male patient, 13 years of age, was treated with THYMOGLOBULIN. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, graft versus host disease, obliterative bronchiolitis, obstructive airways disorder, . THYMOGLOBULIN dosage: unknown. Patient died on 07/06/2004.

Tolep Side Effects Report #5713081-X
Consumer or non-health professional from ITALY reported TOLEP problem on Apr 15, 2008. Male patient, 77 years of age, was diagnosed with epilepsy and was treated with TOLEP. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, jaundice, . TOLEP dosage: 300 MG/DAY. Patient was hospitalized. Patient recovered.

Tolep Side Effects Report #5714478-4
TOLEP problem was reported by a Consumer or non-health professional from ITALY on Apr 15, 2008. Male patient, 77 years of age, was diagnosed with epilepsy and was treated with TOLEP. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, jaundice, . TOLEP dosage: 300 MG/DAY. Patient was hospitalized. Patient recovered.

Tolep Side Effects Report #5719398-7
Consumer or non-health professional from ITALY reported TOLEP problem on Apr 21, 2008. Male patient, 77 years of age, was diagnosed with epilepsy and was treated with TOLEP. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, jaundice, . TOLEP dosage: 300 MG/DAY. Patient was hospitalized. Patient recovered.

Advil Side Effects Report #5365326-6
ADVIL problem was reported by a Health Professional from FRANCE on June 18, 2007. Female patient, 15 years of age, was treated with ADVIL. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased, gamma-glutamyltransferase increased, pneumonia pneumococcal, pyelonephritis, transaminases increased, . ADVIL dosage: unknown. During the same period patient was treated with DOLIPRANE. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5367805-4
Physician from GERMANY reported AVONEX problem on June 07, 2007. Female patient, 27 years of age, weighting 172.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, gamma-glutamyltransferase abnormal, influenza like illness, transaminases increased, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Advil Side Effects Report #5370026-2
ADVIL problem was reported by a Health Professional from FRANCE on June 18, 2007. Female patient, 15 years of age, was treated with ADVIL. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased, gamma-glutamyltransferase increased, pleurisy, pneumonia pneumococcal, pyelonephritis, transaminases increased, . ADVIL dosage: unknown. During the same period patient was treated with DOLIPRANE. Patient was hospitalized. Patient recovered.

Trileptal Side Effects Report #5317985-1
Physician from UNITED STATES reported TRILEPTAL problem on Apr 27, 2007. Male patient, 75 years of age, was diagnosed with convulsion and was treated with TRILEPTAL. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, blood lactate dehydrogenase increased, blood smear test abnormal, chromaturia, haematocrit decreased, haemoglobin decreased, haemolytic anaemia, haptoglobin decreased, . TRILEPTAL dosage: unknown. Patient was hospitalized. Patient recovered.

Lipitor Side Effects Report #5322794-3
LIPITOR problem was reported by a Pharmacist from UNITED STATES on May 02, 2007. Male patient, weighting 203.7 lb, was diagnosed with dyslipidaemia and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, jaundice cholestatic, streptococcal sepsis, . LIPITOR dosage: unknown. Patient was hospitalized. Patient recovered.

Temozolomide Side Effects Report #5328301-3
Consumer or non-health professional from UNITED STATES reported TEMOZOLOMIDE problem on May 16, 2007. Female patient, weighting 183.0 lb, was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, . TEMOZOLOMIDE dosage: 5800 MG. During the same period patient was treated with ACTOS, DARVOCET, GEMFIBROZIL, GLIPIZIDE, HYZAAR, LIPITOR, METOPROLOL SUCCINATE, POTASSIUM REPLACEMENT. Patient was hospitalized. Patient recovered.

Depakote Side Effects Report #5346252-5
DEPAKOTE problem was reported by a Health Professional from UNITED STATES on Mar 17, 2006. Female patient, 23 years of age, was diagnosed with epilepsy, hiv infection and was treated with DEPAKOTE. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, hepatic function abnormal, jaundice, pruritus, . DEPAKOTE dosage: unknown. During the same period patient was treated with REYATAZ, TRILEPTAL. Patient was hospitalized. Patient recovered.

Exjade Side Effects Report #5228022-1
Physician from UNITED STATES reported EXJADE problem on Sept 11, 2006. Male patient, child 5 years of age, was diagnosed with iron overload and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: bilirubin conjugated increased, blood bilirubin increased, cholecystectomy, cholelithiasis, endoscopic retrograde cholangiopancreatography, . EXJADE dosage: 500MG, QD, ORAL. During the same period patient was treated with AMOXICILLIN. Patient was hospitalized. Patient recovered.

Infergen Side Effects Report #5642248-4
INFERGEN problem was reported by a Health Professional from UNITED STATES on Jan 28, 2008. Male patient, weighting 226.0 lb, was diagnosed with hepatitis c and was treated with INFERGEN. After drug was administered, patient experienced the following problems/side effects: aspartate aminotransferase increased, bilirubin conjugated increased, blood chloride increased, blood creatinine increased, blood glucose increased, blood iron increased, blood triglycerides increased, blood urea increased, blood uric acid increased, . INFERGEN dosage: unknown. During the same period patient was treated with RIBAVIRIN, ASPIRIN, TOPROL, LISINOPRIL, ZOLOFT, PLAVIX. Patient recovered.

Vincristine Side Effects Report #5615476-1
Consumer or non-health professional from FRANCE reported VINCRISTINE problem on Jan 25, 2008. Male patient, 17 years of age, was treated with VINCRISTINE. After drug was administered, patient experienced the following problems/side effects: aplasia, bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased, cholestasis, gamma-glutamyltransferase increased, hepatosplenic candidiasis, immune reconstitution syndrome, pyrexia, . VINCRISTINE dosage: unknown. During the same period patient was treated with DOXORUBICIN, METHOTREXATE, ETOPOSIDE, CYCLOPHOSPHAMIDE, CYTARABINE, PREDNISONE. Patient was hospitalized. Patient recovered.

Zolpidem Side Effects Report #5534678-6
ZOLPIDEM TARTRATE problem was reported by a Health Professional from FRANCE on Nov 23, 2007. Female patient, 79 years of age, was treated with ZOLPIDEM TARTRATE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, bilirubin conjugated increased, blood bilirubin increased, cholelithiasis, jaundice cholestatic, . ZOLPIDEM TARTRATE dosage: unknown. During the same period patient was treated with ACARBOSE, FORLAX, LOVENOX, OGAST, LEVOTHYROX, NITRIDERM, DIFFU K, DEROXAT. Patient was hospitalized. Patient recovered.

Tykerb Side Effects Report #5563046-6
Health Professional from UNITED STATES reported TYKERB problem on Dec 07, 2007. Female patient, 52 years of age, weighting 145.3 lb, was diagnosed with breast cancer, back pain and was treated with TYKERB. After drug was administered, patient experienced the following problems/side effects: abdominal pain, bilirubin conjugated increased, blood bilirubin increased, dyspepsia, jaundice, nausea, . TYKERB dosage: 1250MG PER DAY. During the same period patient was treated with XELODA, IBUPROFEN, ENZYMES, GLUCOSAMINE, CALCIUM, ACIDOPHILUS, OMEGA. Patient recovered.

Lovenox Side Effects Report #5576628-2
LOVENOX problem was reported by a Health Professional from UNITED STATES on Dec 14, 2007. Male patient, 74 years of age, was diagnosed with asthma, hypertension, coronary artery disease and was treated with LOVENOX. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, bilirubin conjugated increased, hepatic enzyme increased, . LOVENOX dosage: unknown. During the same period patient was treated with ADVAIR DISKUS, LOTREL, HYDROCHLOROTHIAZIDE, GLYBERIDE, SIMVASTATIN, FLOMAX, PLAVIX, ASPIRIN. Patient recovered.

Lamisil Side Effects Report #5551676-7
Physician from UNITED STATES reported LAMISIL problem on Nov 14, 2006. Female patient, 54 years of age, was diagnosed with nail tinea and was treated with LAMISIL. After drug was administered, patient experienced the following problems/side effects: aspartate aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased, chromaturia, hepatic enzyme increased, pruritus, . LAMISIL dosage: 250 MG, QD, ORAL. Patient recovered.

Fortum Side Effects Report #5443395-2
FORTUM problem was reported by a Pharmacist from FRANCE on Sept 04, 2007. Male patient, weighting 7.72 lb, was diagnosed with sepsis, pain, antifungal prophylaxis and was treated with FORTUM. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase decreased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, hepatic enzyme abnormal, transaminases increased, . FORTUM dosage: 60MG THREE TIMES PER DAY. During the same period patient was treated with AMOXICILLIN, CLAFORAN, GENTAMICIN, AMIKLIN, PARACETAMOL, VITAMINS, FUNGIZONE, CIFLOX. Patient was hospitalized. Patient recovered.

Exjade Side Effects Report #5467758-4
Pharmacist from FRANCE reported EXJADE problem on Sept 19, 2007. Male patient, 28 years of age, weighting 119.0 lb, was diagnosed with iron overload and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: anaemia, bilirubin conjugated increased, blood bilirubin increased, blood cholesterol decreased, cytolytic hepatitis, dyspnoea exertional, folate deficiency, haemoglobin decreased, headache, . EXJADE dosage: 1000 MG, QD. Patient was hospitalized. Patient recovered.

Nelarabine Side Effects Report #5470544-2
NELARABINE problem was reported by a Pharmacist from UNITED STATES on Sept 27, 2007. Male patient, weighting 187.4 lb, was diagnosed with t-cell lymphoma refractory and was treated with NELARABINE. After drug was administered, patient experienced the following problems/side effects: aggression, bilirubin conjugated increased, blood bilirubin increased, cerebellar infarction, confusional state, csf white blood cell count positive, disorientation, hepatic enzyme increased, international normalised ratio increased, . NELARABINE dosage: 1275 MG DAILY X 5 DAYS IV. During the same period patient was treated with BACTRIM DS, LOVENOX, AMLODIPINE, GRANISETRON, ESOMEPRAZOLE MAGNESIUM, DIPHENHYDRAMINE, MORPHINE, NIFEDIPINE. Patient was hospitalized. Patient recovered.

Exjade Side Effects Report #5403589-9
Pharmacist from FRANCE reported EXJADE problem on July 27, 2007. Male patient, 28 years of age, weighting 119.0 lb, was diagnosed with iron overload and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: anaemia, bilirubin conjugated increased, blood bilirubin increased, blood cholesterol decreased, cytolytic hepatitis, dyspnoea exertional, folate deficiency, haemoglobin decreased, headache, . EXJADE dosage: 1000 MG, QD. Patient recovered.

Exjade Side Effects Report #5404819-X
EXJADE problem was reported by a Pharmacist from FRANCE on July 27, 2007. Male patient, 28 years of age, weighting 119.0 lb, was diagnosed with iron overload and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: anaemia, bilirubin conjugated increased, blood bilirubin increased, blood cholesterol decreased, cytolytic hepatitis, dyspnoea exertional, folate deficiency, haemoglobin decreased, headache, . EXJADE dosage: 1000 MG, QD. Patient recovered.

Ketek Side Effects Report #5430700-6
Consumer or non-health professional from UNITED STATES reported KETEK problem on Aug 23, 2007. Male patient was treated with KETEK. After drug was administered, patient experienced the following problems/side effects: ascites, bilirubin conjugated increased, gamma-glutamyltransferase increased, hepatotoxicity, jaundice, liver disorder, portal hypertension, splenomegaly, . KETEK dosage: unknown. Patient recovered.

Oxaliplatin Side Effects Report #5431691-4
OXALIPLATIN problem was reported by a Physician from UNITED STATES on Aug 23, 2007. Female patient, 70 years of age, weighting 112.0 lb, was diagnosed with carcinoid tumour of the appendix and was treated with OXALIPLATIN. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, bilirubin conjugated increased, central line infection, haemoglobin decreased, intestinal obstruction, leukocytosis, neutropenia, pelvic haematoma, pelvic infection, . OXALIPLATIN dosage: unknown. During the same period patient was treated with FOLIC ACID, ASPIRIN, CENTRUM, FOSAMAX, LISINOPRIL. Patient was hospitalized. Patient died on 08/13/2007.

Fortum Side Effects Report #5386597-6
Pharmacist from FRANCE reported FORTUM problem on July 12, 2007. Female patient, weighting 7.72 lb, was diagnosed with sepsis and was treated with FORTUM. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase decreased, . FORTUM dosage: 60MG THREE TIMES PER DAY. During the same period patient was treated with AMOXICILLIN, CLAFORAN, GENTAMICIN, AMIKLIN, VITAMIN. Patient was hospitalized. Patient recovered.

Cyclosporine Side Effects Report #5393812-1
CYCLOSPORINE problem was reported by a Consumer or non-health professional from JAPAN on July 13, 2007. Male patient was diagnosed with histiocytosis haematophagic and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: ascites, bilirubin conjugated increased, blood bilirubin increased, blood creatinine increased, blood pressure increased, blood urea increased, cardiac failure congestive, cardiomegaly, . CYCLOSPORINE dosage: 3 MG/KG/D. During the same period patient was treated with PREDONINE, ACYCLOVIR. Patient was hospitalized. Patient recovered.

Cyclosporine Side Effects Report #5394178-3
Consumer or non-health professional from JAPAN reported CYCLOSPORINE problem on July 13, 2007. Male patient was diagnosed with histiocytosis haematophagic and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: ascites, bilirubin conjugated increased, blood bilirubin increased, blood creatinine increased, blood pressure increased, blood urea increased, cardiac failure congestive, cardiomegaly, . CYCLOSPORINE dosage: 3 MG/KG/D. During the same period patient was treated with PREDONINE, ACYCLOVIR. Patient was hospitalized. Patient recovered.

Fortum Side Effects Report #5386597-6
FORTUM problem was reported by a Pharmacist from FRANCE on July 12, 2007. Female patient, weighting 7.72 lb, was diagnosed with sepsis and was treated with FORTUM. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase decreased, . FORTUM dosage: 60MG THREE TIMES PER DAY. During the same period patient was treated with AMOXICILLIN, CLAFORAN, GENTAMICIN, AMIKLIN, VITAMIN. Patient was hospitalized. Patient recovered.

Cyclosporine Side Effects Report #5393812-1
Consumer or non-health professional from JAPAN reported CYCLOSPORINE problem on July 13, 2007. Male patient was diagnosed with histiocytosis haematophagic and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: ascites, bilirubin conjugated increased, blood bilirubin increased, blood creatinine increased, blood pressure increased, blood urea increased, cardiac failure congestive, cardiomegaly, . CYCLOSPORINE dosage: 3 MG/KG/D. During the same period patient was treated with PREDONINE, ACYCLOVIR. Patient was hospitalized. Patient recovered.