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BLOOD BILIRUBIN INCREASED side effect

What is BLOOD BILIRUBIN INCREASED ?
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Drugs associated with BLOOD BILIRUBIN INCREASED

ABACAVIR  ABRAXANE  ACCUPRIL  ACCUTANE  ACETAMINOPHEN  ACTOS  ACYCLOVIR  ADVIL  ALDACTONE  ALDURAZYME  ALEVE  ALIMTA  ALKERAN  ALLOPURINOL  AMBISOME  AMEVIVE  AMIODARONE  AMNESTEEM  AMOKSIKLAV  AMOXICILLIN  AMPHOTERICIN  ANGIOMAX  ANTILYMPHOCYTE  AOTAL  APTIVUS  ARAVA  AREDIA  ARGATROBAN  ARIMIDEX  ARIXTRA  AROMASIN  ARRANON  ASACOL  ASPIRIN  ATAZANAVIR  AUGMENTIN  AUGMENTINE  AVANDAMET  AVANDIA  AVASTIN  AVELOX  AVIDART  AVODART  AVONEX  AZATHIOPRINE  BACLOFEN  BACTRIM  BARACLUDE  BENICAR  BENZACLIN  BETAFERON  BETAMETHASONE  BEVACIZUMAB  BRIPLATIN  BRISERIN  BUSULFAN  BUSULFEX  BYETTA  CADUET  CAMPATH  CAMPTO  CANCIDAS  CAP  CAPASTAT  CARBAMAZEPINE  CARBOPLATIN  CEFEPIME  CEFTRIAXONE  CEFUROXIME  CELLCEPT  CEPHADOL  CEPHALEXIN  CEREZYME  CETUXIMAB  CHAMPIX  CHANTIX  CILOSTAZOL  CISPLATIN  CITALOPRAM  CLARAVIS  CLAVURION  CLEMASTINE  CLOFARABINE  CLOLAR  CLONAZEPAM  CLOPIDOGREL  CLOZAPINE  CLOZARIL  COMBIVIR  COPEGUS  COSMEGEN  COZAAR  CRANOC  CRESTOR  CRIXIVAN  CVS  CYCLOSPORINE  CYMBALTA  CYMEVENE  CYTARABINE  DACARBAZINE  DACOGEN  DAUNORUBICIN  DECITABINE  DEPAKENE  DEPAKOTE  DEPAS  DEROXAT  DEXAMETHASONE  DICLOFENAC  DIFLUCAN  DIGOXIN  DIOVAN  DOCETAXEL  DOXEPIN  DULOXETINE  EFFEXOR  EFUDEX  ELSPAR  EMTRICITABINE  ENALAPRIL  ENBREL  ENOXAPARIN  ENTECAVIR  EPILIM  EPOETIN  ERLOTINIB  ESCITALOPRAM  ETOPOSIDE  ETRAVIRINE  EXJADE  FELDENE  FEMARA  FLUDARABINE  FLUOROURACIL  FLURAZEPAM  FOSRENOL  FUNGUARD  FUROSEMIDE  GAMUNEX  GEMCITABINE  GEMTUZUMAB  GEMZAR  GLEEVEC  GLIPIZIDE  GLIVEC  HEPTODIN  HERCEPTIN  HUMALOG  HUMIRA  HYCAMTIN  HYDRALAZINE  HYDROCODONE  HYDROXYCHLOROQUI HYDROXYUREA  IBUPROFEN  IDAMYCIN  IMATINIB  IMMUCYST  IMMUNE  INVANZ  INVEGA  IRINOTECAN  ISENTRESS  ISONIAZID  ISOTRETINOIN  ISOVORIN  ITRIZOLE  IXEMPRA  IZILOX  JANUVIA  KETEK  KIVEXA  KLACID  LAMICTAL  LAMISIL  LAMIVUDINE  LANSAP  LANTUS  LAPATINIB  LAPATINIBLET  LESCOL  LETROZOLE  LEUPROLIDE  LEVAQUIN  LEVOFLOXACIN  LINEZOLID  LIPITOR  LOTENSIN  LOTREL  LOVENOX  LUNESTA  LYRICA  MALARONE  MELPHALAN  MEMANTINE  MERCAPTOPURINE  METHADONE  METHOTREXATE  METHYLDOPA  METHYLPHENIDATE  METHYLPREDNISOLO METOCLOPRAMIDE  MICONAZOLE  MIGLITOLLET  MIRENA  MIRTAZAPINE  MOXIFLOXACIN  MYCOPHENOLATE  MYLOTARG  NAPROXEN  NATALIZUMAB  NAVELBINE  NECON  NEFAZODONE  NELARABINE  NEORAL  NEXAVAR  NIASPAN  NITROFURANTOIN  NOGITECAN  NOROXIN  NORVASC  NORVIR  NOXAFIL  OLMETEC  OMEPRAZOLE  OMNIPAQUE  OMNISCAN  ONDANSETRON  OPANA  OXALIPLATIN  OXCARBAZEPINE  OXYCONTIN  PANALDINE  PANITUMUMAB  PANTOPRAZOLE  PANTOZOL  PARACETAMOL  PARAPLATIN  PAXIL  PAZOPANIB  PEGASYS  PEGINTERFERON  PEGVISOMANT  PEMETREXED  PEPCID  PERCOCET  PHENYTOIN  PHOTOFRIN  PRAVACHOL  PRECEDEX  PREDNISOLONE  PROGRAF  PROLEUKIN  PROPAFENONE  PROPECIA  QUININE  RALTEGRAVIR  RAMIPRIL  RAPAMUNE  RAPTIVA  REBIF  RECLAST  RELENZA  REMICADE  RENIVACE  REQUIP  REVATIO  REVLIMID  REYATAZ  RIBAPAK  RIBASPHERE  RIBAVIRIN  RIFADIN  RIFAMPICIN  RILUTEK  RINDERON  RISPERDAL  RITALIN  RITONAVIR  RITUXAN  RITUXIMAB  ROACCUTANE  ROACUTAN  RYTHMOL  SANDIMMUNE  SANDOSTATIN  SAWACILLIN  SEBIVO  SEMPERA  SEROQUEL  SIMVASTATIN  SIMVISTATIN  SORAFENIB  SPEKTRAMOX  SPORANOX  SPRYCEL  STEROIDS  STRATTERA  SULPERAZON  SUNITINIB  SUTENT  SYMLIN  SYNAGIS  TAB  TACROLIMUS  TAMIFLU  TARCEVA  TASIGNA  TASMAR  TAVANIC  TAXOTERE  TAZOCILLINE  TAZOCIN  TEGRETAL  TEGRETOL  TELBIVUDINE  TELITHROMYCIN  TELZIR  TEMODAL  TEMODAR  TEMOZOLOMIDE  THYMOGLOBULIN  TICLOPIDINE  TIKOSYN  TOLEP  TORISEL  TRACLEER  TRAMADOL  TRASTUZUMAB  TRELSTAR  TRIDIOL  TRILEPTAL  TRISENOX  TRUVADA  TYGACIL  TYKERB  TYSABRI  ULTRAVIST  UROMITEXAN  URSO  VALPROIC  VALTREX  VELCADE  VENTAVIS  VESANOID  VFEND  VIRAFERONPEG  VIRAMUNE  VIREAD  VOLTAREN  VYTORIN  WARFARIN  WINRHO  XELODA  XIGRIS  ZANTAC  ZEFFIX  ZEFIX  ZELDOX  ZETIA  ZIAGEN  ZOCOR  ZOLINZA  ZOLPIDEM  ZOMETA  ZOSYN  ZOVIRAX  ZYBAN  ZYFLO  ZYPREXA  ZYVOX  


Exjade Side Effects Report #5646619-1
Physician from GERMANY reported EXJADE problem on Feb 22, 2008. Female patient was diagnosed with haemosiderosis and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, enteritis, . EXJADE dosage: 20 MG/KG, UNK. Patient was hospitalized. Patient recovered.

Kivexa Side Effects Report #5653455-9
KIVEXA problem was reported by a Physician from ISRAEL on Mar 03, 2008. Male patient, 40 years of age, was treated with KIVEXA. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, hepatic function abnormal, transaminases increased, . KIVEXA dosage: unknown. During the same period patient was treated with EPIVIR, ZIAGEN, KALETRA. Patient was hospitalized. Patient recovered.

Rilutek Side Effects Report #5654769-9
Physician from JAPAN reported RILUTEK problem on Feb 26, 2008. Female patient, 65 years of age, weighting 99.21 lb, was diagnosed with amyotrophic lateral sclerosis and was treated with RILUTEK. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, interstitial lung disease, . RILUTEK dosage: unknown. Patient recovered.

Strattera Side Effects Report #5657498-0
STRATTERA problem was reported by a Physician from GERMANY on Feb 25, 2008. Male patient was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, . STRATTERA dosage: 40 MG, DAILY (1/D). Patient recovered.


Exjade Side Effects Report #5657671-1
Physician from GERMANY reported EXJADE problem on Feb 28, 2008. Female patient was diagnosed with haemosiderosis and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, gastroenteritis norovirus, . EXJADE dosage: 20 MG/KG, UNK. Patient was hospitalized. Patient recovered.

Aleve Side Effects Report #5658957-7
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on May 17, 2007. Female patient was diagnosed with arthralgia and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, . ALEVE dosage: UNIT DOSE: 220 MG. Patient recovered.

Mylotarg Side Effects Report #5661546-1
Physician from JAPAN reported MYLOTARG problem on Feb 29, 2008. Male patient, weighting 123.5 lb, was diagnosed with acute myeloid leukaemia recurrent, prophylaxis and was treated with MYLOTARG. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, neutrophil count decreased, pseudomonas infection, sepsis, . MYLOTARG dosage: unknown. During the same period patient was treated with BAKTAR, OMEPRAL, PROGRAF, UNIPHYL, BEZATOL, PREDONINE. Patient was hospitalized. Patient recovered.

Lamisil Side Effects Report #5662019-2
LAMISIL AT problem was reported by a Pharmacist from JAPAN on Feb 19, 2008. Male patient was diagnosed with tinea infection and was treated with LAMISIL AT. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, chromaturia, epistaxis, gastroenteritis, haematemesis, nasopharyngitis, neoplasm malignant, . LAMISIL AT dosage: unknown. Patient recovered.

Reyataz Side Effects Report #5662354-8
Physician from FRANCE reported REYATAZ problem on Mar 10, 2008. Male patient, 50 years of age, was diagnosed with hiv infection and was treated with REYATAZ. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, . REYATAZ dosage: unknown. During the same period patient was treated with NORVIR. Patient died.


Lamictal Side Effects Report #5664465-X
LAMICTAL problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 06, 2008. Male patient, 59 years of age, weighting 135.4 lb, was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, chromaturia, hepatic enzyme increased, hepatitis, jaundice, nausea, . LAMICTAL dosage: 25MG IN THE MORNING. During the same period patient was treated with FLUOXETINE. Patient recovered.

Vfend Side Effects Report #5665007-5
Physician from JAPAN reported VFEND problem on Mar 03, 2008. Female patient, 27 years of age, was treated with VFEND. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, gamma-glutamyltransferase increased, prothrombin level decreased, pyrexia, . VFEND dosage: DAILY DOSE:400MG. Patient recovered.

Gleevec Side Effects Report #5669304-9
GLEEVEC problem was reported by a Physician from JAPAN on Mar 05, 2008. Female patient, 66 years of age, weighting 130.1 lb, was diagnosed with acute lymphocytic leukaemia, osteoporosis prophylaxis and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, disseminated intravascular coagulation, fibrin d dimer increased, fibrin decreased, fibrin degradation products increased, gastric haemorrhage, haemoglobin decreased, haemolytic anaemia, melaena, . GLEEVEC dosage: 600 MG/DAY. During the same period patient was treated with PREDNISOLONE, BONALON. Patient recovered.

Ambisome Side Effects Report #5671509-8
Health Professional from JAPAN reported AMBISOME problem on Feb 28, 2008. Female patient was diagnosed with aspergillosis and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, infection, . AMBISOME dosage: 3 MG/KG, UID/QD, IV NOS. Patient died.

Methadone Side Effects Report #5671627-4
METHADONE problem was reported by a Health Professional from IRELAND on Feb 29, 2008. Male patient, 34 years of age, was treated with METHADONE. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, blood pressure diastolic decreased, circulatory collapse, hyperhidrosis, incorrect dose administered, loss of consciousness, miosis, rales, . METHADONE dosage: unknown. During the same period patient was treated with FLURAZEPAM, ATAZANAVIR SULPHATE, RITONAVIR, TRUVADA. Patient was hospitalized. Patient recovered.


Ambisome Side Effects Report #5673964-6
Health Professional from JAPAN reported AMBISOME problem on Feb 28, 2008. Male patient, 55 years of age, weighting 114.6 lb, was diagnosed with bronchopulmonary aspergillosis and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, haemodialysis, metabolic acidosis, pneumonia, renal failure, respiratory failure, . AMBISOME dosage: 250 MG, UID/QD, IV NOS. During the same period patient was treated with FUNGUARD, PROGRAF, AZACTAM, BACTRIM, ACICLOVIR, FOSCAVIR, VANCOMYCIN HYDROCHLORIDE. Patient died on 11/21/2007.

Ambisome Side Effects Report #5673965-8
AMBISOME problem was reported by a Health Professional from ITALY on Feb 28, 2008. Male patient, 58 years of age, was diagnosed with myelofibrosis, graft versus host disease and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, blood creatinine increased, blood fibrinogen increased, diarrhoea, fatigue, pancreatitis, peritoneal effusion, thrombocytopenic purpura, . AMBISOME dosage: 3 MG/KG, 3XWEEKLY, IV NOS; 7 MG/KG, WEEKLY, IV NOS. During the same period patient was treated with CYCLOSPORINE, ATENOLOL, ACYCLOVIR, BACTRIM DS, OMEPRAZOLE, ASPIRIN, FOLIC ACID. Patient was hospitalized. Patient recovered.

Reyataz Side Effects Report #5675784-5
Physician from FRANCE reported REYATAZ problem on Mar 18, 2008. Male patient, 50 years of age, was diagnosed with hiv infection and was treated with REYATAZ. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, hepatic neoplasm malignant, metastases to bone, . REYATAZ dosage: unknown. During the same period patient was treated with NORVIR. Patient died on 01/01/2006.

Temozolomide Side Effects Report #5677627-2
TEMOZOLOMIDE problem was reported by a Physician from UNITED KINGDOM on Mar 06, 2008. Male patient, 40 years of age, weighting 181.7 lb, was diagnosed with metastatic malignant melanoma and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, blood lactate dehydrogenase increased, bone marrow toxicity, dehydration, dizziness, haemolytic anaemia, nausea, overdose, treatment noncompliance, . TEMOZOLOMIDE dosage: 320 MG. During the same period patient was treated with DOMPERIDONE, PREDNISOLONE. Patient was hospitalized. Patient recovered.

Erlotinib Side Effects Report #5679712-8
Health Professional from JAPAN reported ERLOTINIB problem on Mar 06, 2008. Male patient, 80 years of age, was diagnosed with non-small cell lung cancer and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, red blood cell morphology abnormal, thrombotic thrombocytopenic purpura, . ERLOTINIB dosage: (150 MG, QD), ORAL. Patient recovered.


Augmentin Side Effects Report #5680463-4
AUGMENTIN problem was reported by a Consumer or non-health professional from FRANCE on Mar 14, 2008. Male patient, 82 years of age, was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, cardiac disorder, cholelithiasis, hypoventilation, jaundice cholestatic, labile blood pressure, lung disorder, mixed liver injury, sinus arrest, . AUGMENTIN dosage: unknown. During the same period patient was treated with GENTAMICIN, PIPERACILLIN AND TAZOBACTAM, TAVANIC, VANCOMYCIN, SOLUPSAN, TENORMIN, ELISOR. Patient was hospitalized. Patient died on 02/23/2008.

Diclofenac Side Effects Report #5681107-8
Health Professional from FINLAND reported DICLOFENAC problem on Mar 12, 2008. Female patient, 80 years of age, was diagnosed with arthropathy and was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, jaundice, liver disorder, loss of consciousness, transaminases increased, . DICLOFENAC dosage: unknown. During the same period patient was treated with ALENDRONIC ACID, CLONAZEPAM, ZOPICLONE. Patient recovered.

Panaldine Side Effects Report #5685064-X
PANALDINE problem was reported by a Physician from FRANCE on Apr 05, 2000. Male patient, 70 years of age, was diagnosed with transient ischaemic attack, hypertension, insomnia and was treated with PANALDINE. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, cerebral arteriosclerosis, cholestasis, coma hepatic, dementia, depressed level of consciousness, headache, hepatic enzyme increased, hepatic failure, . PANALDINE dosage: unknown. During the same period patient was treated with PERSANTINE, GLYCYRON, NORVASC, MYSOLINE, INDOMETHACIN, RHYTHMY. Patient was hospitalized. Patient died on 01/19/2000.

Fludarabine Side Effects Report #5688357-5
Consumer or non-health professional from UNITED STATES reported FLUDARABINE PHOSPHATE problem on Mar 28, 2008. Male patient, weighting 138.9 lb, was diagnosed with non-hodgkin's lymphoma and was treated with FLUDARABINE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, blood creatinine increased, cardio-respiratory arrest, oxygen saturation decreased, . FLUDARABINE PHOSPHATE dosage: 55MG 5 DAYS IV. During the same period patient was treated with CYCLOPHOSPHAMIDE. Patient died on 03/27/2008.

Sporanox Side Effects Report #5689906-3
SPORANOX problem was reported by a Physician from UNITED STATES on Mar 31, 2008. Female patient, 52 years of age, weighting 145.0 lb, was diagnosed with onychomycosis and was treated with SPORANOX. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, haemoglobin decreased, haemolysis, jaundice, liver function test abnormal, . SPORANOX dosage: 100MG 1X/DAY PO. Patient was hospitalized. Patient recovered.

Gamunex Side Effects Report #5694074-8
Physician from CANADA reported GAMUNEX problem on Mar 11, 2008. Female patient, 76 years of age, weighting 154.3 lb, was diagnosed with thrombocytopenia and was treated with GAMUNEX. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, blood lactate dehydrogenase increased, chromaturia, haemolysis, myelodysplastic syndrome, pyrexia, . GAMUNEX dosage: unknown. During the same period patient was treated with PREDNISONE, SYNTHROID, SEROQUEL, STATEX, TRINIPATCH, ASPIRIN, METOPROLOL. Patient recovered.

Cymbalta Side Effects Report #5613893-7
CYMBALTA problem was reported by a Physician from UNITED STATES on Jan 23, 2008. Male patient, weighting 146.0 lb, was diagnosed with anxiety, gastrooesophageal reflux disease, blood pressure and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, urine bilirubin increased, . CYMBALTA dosage: 30 MG, DAILY (1/D). During the same period patient was treated with OMEPRAZOLE, NORVASC, COZAAR, SIMVASTATIN. Patient recovered.

Tavanic Side Effects Report #5616428-8
Physician from TURKEY reported TAVANIC problem on Jan 28, 2008. Male patient, 72 years of age, was diagnosed with pneumonia, chronic obstructive pulmonary disease and was treated with TAVANIC. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, blood urea increased, hepatic enzyme increased, leukocytosis, renal failure acute, sepsis, . TAVANIC dosage: unknown. During the same period patient was treated with TEOKAP, PREDNOL, SPIRIVA, SERETIDE, LANSOR. Patient recovered.

Gemcitabine Side Effects Report #5620741-8
GEMCITABINE problem was reported by a Physician from JAPAN on Jan 24, 2008. Female patient, weighting 97.00 lb, was diagnosed with gallbladder cancer recurrent and was treated with GEMCITABINE. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, intestinal ischaemia, . GEMCITABINE dosage: 1000 MG/M2, OTHER. Patient was hospitalized. Patient recovered.

Aredia Side Effects Report #5621602-0
Physician from UNITED STATES reported AREDIA problem on Feb 05, 2008. Female patient, 78 years of age, was diagnosed with multiple myeloma and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, blood creatinine increased, blood lactate dehydrogenase increased, haemoglobin decreased, plasmapheresis, platelet count decreased, renal disorder, thrombotic thrombocytopenic purpura, . AREDIA dosage: unknown. During the same period patient was treated with REVLIMID. Patient was hospitalized. Patient recovered.

Zyvox Side Effects Report #5623429-2
ZYVOX problem was reported by a Physician from CHINA on Jan 31, 2008. Male patient, 34 years of age, was diagnosed with enterococcal infection and was treated with ZYVOX. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, hepatic steatosis, liver transplant rejection, . ZYVOX dosage: unknown. During the same period patient was treated with SULPERAZON, DIFLUCAN, TEICOPLANIN. Patient recovered.

Lamictal Side Effects Report #5629644-6
Consumer or non-health professional from UNITED STATES reported LAMICTAL problem on Feb 11, 2008. Male patient, 59 years of age, weighting 135.4 lb, was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, chromaturia, hepatic enzyme increased, hepatitis, jaundice, . LAMICTAL dosage: 25MG IN THE MORNING. During the same period patient was treated with FLUOXETINE. Patient recovered.

Mirena Side Effects Report #5630137-0
MIRENA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 11, 2008. Female patient, 30 years of age, weighting 125.7 lb, was diagnosed with contraception, hypothyroidism and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, fatigue, jaundice, ocular icterus, . MIRENA dosage: unknown. During the same period patient was treated with SYNTHROID. Patient recovered.

Rilutek Side Effects Report #5632345-1
Physician from JAPAN reported RILUTEK problem on Feb 13, 2008. Female patient, 65 years of age, weighting 99.21 lb, was diagnosed with amyotrophic lateral sclerosis and was treated with RILUTEK. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, interstitial lung disease, . RILUTEK dosage: unknown. Patient recovered.

Cancidas Side Effects Report #5632933-2
CANCIDAS problem was reported by a Consumer or non-health professional from GERMANY on Jan 31, 2008. Male patient, 35 years of age, was diagnosed with stem cell transplant and was treated with CANCIDAS. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, graft versus host disease, . CANCIDAS dosage: unknown. During the same period patient was treated with CYCLOSPORINE. Patient was hospitalized. Patient recovered.

Lapatiniblet Side Effects Report #5644088-9
Physician from SPAIN reported LAPATINIBLET problem on Feb 13, 2008. Female patient, 53 years of age, weighting 358.9 lb, was diagnosed with breast cancer metastatic and was treated with LAPATINIBLET. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, blood potassium decreased, blood urea increased, diarrhoea, lymphocyte count decreased, mucosal inflammation, neutrophil count increased, . LAPATINIBLET dosage: 1250 MG/PER DAY/ORAL. During the same period patient was treated with CAPECITABINELET. Patient was hospitalized. Patient recovered.

Humalog Side Effects Report #5645007-1
HUMALOG problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 20, 2008. Female patient was diagnosed with tachycardia and was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, blood glucose increased, cardiac disorder, cognitive disorder, flatulence, magnesium deficiency, palpitations, pancreatic carcinoma, portal vein occlusion, . HUMALOG dosage: unknown. During the same period patient was treated with ATENOLOL, ACTIGALL, PANCREASE, NEXIUM, DEXAMETHASONE. Patient was hospitalized. Patient recovered.

Lamisil Side Effects Report #5646179-5
Pharmacist from JAPAN reported LAMISIL AT problem on Feb 08, 2008. Male patient was diagnosed with tinea infection and was treated with LAMISIL AT. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, diarrhoea, epistaxis, haematemesis, nasopharyngitis, protein urine present, . LAMISIL AT dosage: unknown. Patient recovered.

Tysabri Side Effects Report #5646315-0
TYSABRI problem was reported by a Health Professional from FRANCE on Feb 14, 2008. Male patient, 37 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, diarrhoea, nausea, pancreatic disorder, renal colic, ulcer, vomiting, . TYSABRI dosage: 300 MG; QM;. Patient was hospitalized. Patient recovered.

Januvia Side Effects Report #5654585-8
Physician from UNITED STATES reported JANUVIA problem on Jan 03, 2008. Female patient was diagnosed with type 2 diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, ejection fraction decreased, . JANUVIA dosage: unknown. Patient recovered.

Copegus Side Effects Report #5662004-0
COPEGUS problem was reported by a Physician from UNITED STATES on Oct 10, 2007. Female patient, 45 years of age, weighting 179.9 lb, was diagnosed with hepatitis c, hiv infection and was treated with COPEGUS. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, . COPEGUS dosage: unknown. During the same period patient was treated with REYATAZ, PEGASYS, COMBIVIR. Patient recovered.

Isotretinoin Side Effects Report #5581820-7
Physician from UNITED STATES reported ISOTRETINOIN problem on Dec 04, 2007. Female patient was treated with ISOTRETINOIN. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, treatment noncompliance, . ISOTRETINOIN dosage: 40 MG, UNK. Patient recovered.

Aredia Side Effects Report #5583832-6
AREDIA problem was reported by a Physician from UNITED STATES on Jan 02, 2008. Female patient, 78 years of age, was diagnosed with multiple myeloma and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, blood creatinine increased, blood lactate dehydrogenase increased, haemoglobin decreased, plasmapheresis, platelet count decreased, renal disorder, thrombotic thrombocytopenic purpura, . AREDIA dosage: unknown. During the same period patient was treated with REVLIMID. Patient was hospitalized. Patient recovered.

Simvastatin Side Effects Report #5583917-4
Pharmacist from UNITED STATES reported SIMVASTATIN problem on Jan 02, 2008. Male patient, 67 years of age, was diagnosed with myocardial infarction and was treated with SIMVASTATIN. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, jaundice, . SIMVASTATIN dosage: 10MG EVERY DAY PO. Patient recovered.

Aredia Side Effects Report #5587994-6
AREDIA problem was reported by a Physician from UNITED STATES on Jan 07, 2008. Female patient, 78 years of age, was diagnosed with multiple myeloma and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, blood creatinine increased, blood lactate dehydrogenase increased, haemoglobin decreased, plasmapheresis, platelet count decreased, renal disorder, thrombotic thrombocytopenic purpura, . AREDIA dosage: unknown. During the same period patient was treated with REVLIMID. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5590714-2
Health Professional from UNITED STATES reported SUTENT problem on Jan 07, 2008. Male patient, 58 years of age, weighting 142.0 lb, was diagnosed with metastatic renal cell carcinoma, pain and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, blood creatinine increased, cholelithiasis, hepatic enzyme increased, hepatitis, nausea, . SUTENT dosage: unknown. During the same period patient was treated with LORTAB, TENORMIN, ALTACE, NORVASC, DIABETA, GLUCOPHAGE, LIPITOR, CELEXA. Patient recovered.

Gleevec Side Effects Report #5591080-9
GLEEVEC problem was reported by a Physician from JAPAN on Jan 08, 2008. Female patient, 66 years of age, weighting 130.1 lb, was diagnosed with acute lymphocytic leukaemia, osteoporosis prophylaxis and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, disseminated intravascular coagulation, fibrin d dimer increased, fibrin decreased, fibrin degradation products increased, gastric haemorrhage, haemoglobin decreased, haemolytic anaemia, melaena, . GLEEVEC dosage: 600 MG/DAY. During the same period patient was treated with PREDNISOLONE, BONALON. Patient recovered.

Aptivus Side Effects Report #5592276-2
Physician from UNITED STATES reported APTIVUS problem on Jan 14, 2008. Male patient, 50 years of age, was treated with APTIVUS. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, hepatic steatosis, jaundice, . APTIVUS dosage: unknown. During the same period patient was treated with TRUVADA, RALTEGRAVIR, RITONAVIR. Patient was hospitalized. Patient recovered.

Taxotere Side Effects Report #5598364-9
TAXOTERE problem was reported by a Consumer or non-health professional from on Jan 14, 2008. Female patient, 69 years of age, weighting 154.3 lb, was treated with TAXOTERE. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, haemolytic anaemia, haptoglobin decreased, oedema, rash, . TAXOTERE dosage: unknown. During the same period patient was treated with DIFFU K, NEORECORMON. Patient was hospitalized. Patient recovered.

Campto Side Effects Report #5599367-0
Consumer or non-health professional from JAPAN reported CAMPTO problem on Jan 09, 2008. Male patient, weighting 125.7 lb, was diagnosed with large intestine carcinoma, fluid replacement, vomiting, antipyresis, dry mouth and was treated with CAMPTO. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, disseminated intravascular coagulation, febrile neutropenia, leukopenia, pneumonia bacterial, septic shock, thrombocytopenia, . CAMPTO dosage: DAILY DOSE:150MG/M2. During the same period patient was treated with VITAMIN B CAP, PRIMPERAN, POTACOL, AMINO ACIDS, LACTEC, ROPION, AMINO ACIDS, POTASSIUM PHOSPHATE DIBASIC. Patient died on 01/06/2008.

Norvir Side Effects Report #5602707-7
NORVIR problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 17, 2008. Female patient, 16 years of age, was diagnosed with hiv infection and was treated with NORVIR. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, blood bilirubin unconjugated increased, . NORVIR dosage: unknown. During the same period patient was treated with DIDANOSINE, EMTRICITABINE, ATAZANAVIR SULPHATE, MEDROXYPROGESTERONE ACETATE. Patient recovered.

Aspirin Side Effects Report #5603707-3
Health Professional from INDIA reported ASPIRIN problem on Nov 27, 2007. Male patient, child 8 years of age, weighting 41.89 lb, was diagnosed with pyrexia, inflammation and was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, haemoglobin decreased, haemolytic anaemia, hemiparesis, reticulocytosis, . ASPIRIN dosage: unknown. During the same period patient was treated with PENICILLIN. Patient recovered.

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