BLOOD LACTATE DEHYDROGENASE INCREASED side effect
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Drugs associated with BLOOD LACTATE DEHYDROGENASE INCREASED
ABILIFY ACETAMINOPHEN ACLASTA ACYCLOVIR ADAGEN ADRIBLASTINE ALDURAZYME ALLOPURINOL AMOXICILLIN ANAGRELIDE APROVEL AREDIA ARIMIDEX ARIXTRA ARTIST ASPIRIN ATACAND ATARAX ATOMOXETINE ATOVAQUONE AUGMENTIN AVANDIA AVASTIN AVELOX AVONEX AZATHIOPRINE BETAFERON BETAMETHASONE BETASERON BEVACIZUMAB BONIVA BRIPLATIN BUFFERIN BUSULFAN BUSULFEX BYETTA CAMPATH CANCIDAS CARBAMAZEPINE CARBOPLATIN CARVEDILOL CEFAZOLIN CEFEPIME CEFTRIAXONE CELANCE CELLCEPT CERTICAN CHAMPIX CHLORPROMAZINE CICLOSPORIN CIPROFLOXACIN CITALOPRAM CLARAVIS CLAVENTIN CLOFARABINE CLOZAPINE COMBIVIR COMTAN CONCERTA CONTROLOC COUMADIN CRESTOR CYCLOPHOSPHAMIDE CYCLOSPORINE CYMBALTA CYTARABINE DAONIL DECITABINE DEPAKINE DEROXAT DESLORATADINE DEXAMETHASONE DICLOFENAC DIGITOXIN DILTIAZEM DIOVAN EFAVIRENZ EFFEXOR ENALAPRIL ENBREL EPIRUBICIN ERLOTINIB ETHYOL ETODOLAC ETONOGESTREL EVEROLIMUS EXELON EXJADE FASTIC FEMARA FUNGUARD GABAPEN GAMUNEX GEMZAR GLEEVEC GLIVEC GLYBURIDE GONAL HEPARIN HEPSERA HUMIRA HYSRON HYZAAR IBUPROFEN IMATINIB IMMUNE IMMUNOSPORIN IMURAN INTERFERON IRESSA IRINOTECAN ITRIZOLE KALETRA KEPPRA KINERET KIVEXA KLARICIDLET LAMICTAL LAMISIL LANTUS LANVIS LAPATINIB LEFLUNOMIDE LEPONEX LESCOL LEUPROLIDE LOCHOL LOVENOX LUDIOMIL MABTHERA MALARONE MEFLOQUINE MELPHALAN MEMANTINE MENEST METFORMIN METHOTREXATE METRONIDAZOLE MIGLITOLLET MINOCYCLINE MIRTAZAPINE MYLOTARG NATALIZUMAB NAVELBINE NEORAL NEULASTA NEUPOGEN NEVIRAPINE NEXAVAR NICARDIPINE NORVASC NORVIR NOVANTRONE NOVOSEVEN OLMETEC OMNIPAQUE ONTAK ORTHO OXALIPLATIN OXCARBAZEPINE PANTOPRAZOLE PANTOZOL PAROXETINE PAXIL PEMETREXED PENICILLIN PENTASA PERDIPINE PERGOLIDE PLAVIX PLETAL PRAVASTATIN PREDNISOLONE PROGRAF PROPOFOL PROTOPIC RANEXA RANITIDINE RAPAMUNE REBIF REMICADE REQUIP REVATIO REVLIMID RHOPHYLAC RILUZOLE RIMSO RINLAXER RISEDRONATE RITALIN RITUXAN SANDIMMUNE SANDOSTATIN SEASONIQUE SIMVASTATIN SIROLIMUS SOLANAX SORIATANE STRATTERA SULFASALAZINE SUTENT TACROLIMUS TARCEVA TARGRETIN TASMAR TAVANIC TAVOR TAXOL TAXOTERE TAZOCILLINE TAZOCIN TEGRETOL TELBIVUDINE TELZIR TEMODAL TEMOZOLOMIDE TEMSIROLIMUS TERNELIN THALIDOMIDE TICLID TOFRANIL TRELSTAR TRILEPTAL TRISENOX TYZEKA VALTREX VANCOMIN VELCADE VESANOID VESICARE VIDEX VIRACEPT VIREAD VISKEN VOLTAREN VORICONAZOLE WINRHO ZEFIX ZELITREX ZETIA ZEVALIN ZIAGEN ZIDOVUDINE ZOCOR ZOFRAN ZOLOFT ZOMETA ZONISAMIDE ZOVIRAX ZYPREXADexamethasone Side Effects Report #5652214-0
Physician from GERMANY reported DEXAMETHASONE problem on Feb 22, 2008. Male patient, child 8 years of age, was diagnosed with prophylaxis of nausea and vomiting and was treated with DEXAMETHASONE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, blood phosphorus increased, hepatosplenomegaly, nausea, tumour lysis syndrome, vomiting, white blood cell count decreased, . DEXAMETHASONE dosage: 4 MG, ONCE/SINGLE, INTRAVENOUS. During the same period patient was treated with PROPOFOL, ALFENTANIL, DESFLURANE, REMIFENTANIL, ACETAMINOPHEN. Patient was hospitalized. Patient recovered.
Pravastatin Side Effects Report #5660423-X
PRAVASTATIN problem was reported by a Consumer or non-health professional from GREECE on Feb 25, 2008. Male patient, 60 years of age, was diagnosed with hypercholesterolaemia and was treated with PRAVASTATIN. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, lymphocyte percentage increased, neutrophil percentage decreased, pleural effusion, . PRAVASTATIN dosage: 40 MG; QD, 40 MG; QD. Patient recovered.
Zometa Side Effects Report #5661557-6
Physician from GERMANY reported ZOMETA problem on Mar 04, 2008. Male patient, 61 years of age, weighting 176.4 lb, was diagnosed with multiple myeloma, hypertension and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, haemoglobin decreased, haemolytic anaemia, red blood cell count decreased, reticulocyte count increased, . ZOMETA dosage: 4 MG, QMO. During the same period patient was treated with ENALAPRIL MALEATE, HYDROCHLOROTHIAZIDE, OMEPRAZOLE, METOPROLOL TARTRATE, ACETAMINOPHEN, SIRDALUD, FORTECORTIN, BALDRIPARAN. Patient recovered.
Soriatane Side Effects Report #5663735-9
SORIATANE problem was reported by a Physician from FRANCE on Feb 14, 2008. Male patient, 45 years of age, was treated with SORIATANE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, condition aggravated, dermatitis exfoliative, eosinophilia, gamma-glutamyltransferase increased, lymphadenopathy, no therapeutic response, oedema peripheral, psoriasis, . SORIATANE dosage: unknown. During the same period patient was treated with RHINUREFLEX, MUCICLAR, BRONCHODUAL. Patient was hospitalized. Patient recovered.
Tegretol Side Effects Report #5669334-7
Consumer or non-health professional from JAPAN reported TEGRETOL problem on Mar 06, 2008. Male patient, 69 years of age, was diagnosed with depression and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, c-reactive protein increased, eosinophil count increased, eosinophil percentage increased, gamma-glutamyltransferase increased, lymphocyte stimulation test positive, . TEGRETOL dosage: unknown. Patient was hospitalized. Patient recovered.
Azathioprine Side Effects Report #5670108-1
AZATHIOPRINE problem was reported by a Physician from BRAZIL on Feb 29, 2008. Female patient, 67 years of age, was diagnosed with immunosuppression and was treated with AZATHIOPRINE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, dyspnoea, epstein-barr virus infection, herpes virus infection, infectious mononucleosis, laboratory test abnormal, pleural effusion, primary effusion lymphoma, . AZATHIOPRINE dosage: 150 MG/DAY. During the same period patient was treated with CYCLOSPORINE, PREDNISONE, RAPAMYCIN. Patient died.
Leuprolide Side Effects Report #5679829-8
Consumer or non-health professional from JAPAN reported LEUPROLIDE ACETATE problem on Mar 18, 2008. Female patient, 51 years of age, weighting 126.8 lb, was diagnosed with breast cancer and was treated with LEUPROLIDE ACETATE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, cryptogenic organising pneumonia, hot flush, injection site induration, insomnia, nasopharyngitis, . LEUPROLIDE ACETATE dosage: 11.25 M (11.25 MG,1 IN 12 WK). During the same period patient was treated with NOLVADEX, TAKEPRON, BENET, ONEALFA, PURSENNID. Patient was hospitalized. Patient recovered.
Ticlid Side Effects Report #5685030-4
TICLID problem was reported by a Physician from UNITED STATES on Apr 27, 1998. Female patient, 81 years of age, was diagnosed with vertebrobasilar insufficiency and was treated with TICLID. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, myocardial infarction, thrombocytopenia, thrombotic thrombocytopenic purpura, . TICLID dosage: unknown. During the same period patient was treated with GLUCOTROL, PERSANTINE, ISORDIL, ZAROXOLYN, INDERAL LA, NORVASC, EQUANIL. Patient died on 04/21/1998.
Erlotinib Side Effects Report #5688183-7
Physician from ROMANIA reported ERLOTINIB problem on Mar 14, 2008. Male patient, 58 years of age, was diagnosed with non-small cell lung cancer metastatic and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, cardio-respiratory arrest, gamma-glutamyltransferase increased, rash, white blood cell count increased, . ERLOTINIB dosage: (150 MG, QD), ORAL. During the same period patient was treated with CARBOPLATIN, ETOPOSIDE, DOCETAXEL. Patient died on 11/10/2007.
Gleevec Side Effects Report #5615278-6
GLEEVEC problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 31, 2008. Male patient, 76 years of age, weighting 189.0 lb, was diagnosed with chronic myeloid leukaemia and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, catheter placement, cough, fluid retention, haemoptysis, hepatic cirrhosis, hiccups, thrombocytopenia, . GLEEVEC dosage: unknown. Patient was hospitalized. Patient died on 06/28/2006.
Methotrexate Side Effects Report #5616321-0
Physician from UNITED STATES reported METHOTREXATE problem on Jan 30, 2008. Male patient, 63 years of age, weighting 159.0 lb, was diagnosed with central nervous system lymphoma and was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, disease progression, hyperglycaemia, iiird nerve paralysis, muscular weakness, neck pain, neurological symptom, vith nerve paralysis, . METHOTREXATE dosage: 7000 MG. During the same period patient was treated with TEMODAR, DEXAMETHASONE, ENOXAPARIN. Patient was hospitalized. Patient recovered.
Depakine Side Effects Report #5618627-8
DEPAKINE CHRONOSPHERE GRANULE problem was reported by a Consumer or non-health professional from FRANCE on Jan 28, 2008. Female patient, 73 years of age, was treated with DEPAKINE CHRONOSPHERE GRANULE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, cholelithiasis, hepatocellular injury, hepatotoxicity, . DEPAKINE CHRONOSPHERE GRANULE dosage: unknown. During the same period patient was treated with DEPAKINE CHRONOSPHERE GRANULE, DEPAKINE CHRONOSPHERE GRANULE, OMEPRAZOLE. Patient was hospitalized. Patient recovered.
Mefloquine Side Effects Report #5618980-5
Consumer or non-health professional from reported MEFLOQUINE problem on Feb 04, 2008. Female patient, 67 years of age, was diagnosed with malaria prophylaxis, tinea versicolour and was treated with MEFLOQUINE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, c-reactive protein increased, eosinophilia, eosinophilic pneumonia, hypoxia, normochromic normocytic anaemia, pyrexia, red blood cell sedimentation rate increased, tachycardia, . MEFLOQUINE dosage: unknown. During the same period patient was treated with KETOCONAZOLE. Patient was hospitalized. Patient recovered.
Dexamethasone Side Effects Report #5619136-2
DEXAMETHASONE problem was reported by a Physician from UNITED STATES on Jan 24, 2008. Male patient, 71 years of age, was diagnosed with multiple myeloma and was treated with DEXAMETHASONE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, haemodialysis, renal failure acute, . DEXAMETHASONE dosage: 40 MG DAILY, DAYS 1-4 OF DISCHARGE. During the same period patient was treated with THALIDOMIDE, DARBEPOETIN ALPHA, ZOLEDRONIC ACID, WARFARIN. Patient was hospitalized. Patient recovered.
Prednisolone Side Effects Report #5622015-8
Consumer or non-health professional from JAPAN reported PREDNISOLONE problem on Jan 21, 2008. Female patient, 73 years of age, was diagnosed with systemic lupus erythematosus and was treated with PREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, disseminated intravascular coagulation, epistaxis, fibrin degradation products increased, haemoglobin decreased, metastases to bone marrow, neuroendocrine carcinoma of the skin, prothrombin time ratio increased, purpura, . PREDNISOLONE dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient was hospitalized. Patient died.
Nexavar Side Effects Report #5625714-7
NEXAVAR problem was reported by a Physician from NETHERLANDS on Feb 11, 2008. Female patient was diagnosed with follicular thyroid cancer, routine health maintenance and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, blood parathyroid hormone increased, hypocalcaemia, mucosal inflammation, palmar-plantar erythrodysaesthesia syndrome, pneumothorax, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG. During the same period patient was treated with DIETARY SUPPLEMENTS. Patient recovered.
Ceftriaxone Side Effects Report #5630637-3
Physician from UNITED STATES reported CEFTRIAXONE problem on Jan 26, 2008. Male patient, child 10 years of age, was diagnosed with abscess and was treated with CEFTRIAXONE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, blood phosphorus increased, haemolysis, heart rate increased, mental impairment, peritoneal dialysis, rash maculo-papular, renal failure acute, . CEFTRIAXONE dosage: unknown. During the same period patient was treated with CLINDAMYCIN, CEPHALEXIN. Patient was hospitalized. Patient recovered.
Revlimid Side Effects Report #5637484-7
REVLIMID problem was reported by a Physician from UNITED STATES on Feb 07, 2008. Male patient, 56 years of age, weighting 478.0 lb, was diagnosed with chronic lymphocytic leukaemia and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, dysphagia, dyspnoea, lymph node pain, lymphadenopathy, tumour flare, . REVLIMID dosage: 2.5 MG, DAYS 1-7, ORAL. During the same period patient was treated with DILAUDID, ALLOPURINOL, BACTRIM DS, VALTREX, METOPROLOL TARTRATE, ASPIRIN, HYDROCODONE BITARTRATE, MORPHINE. Patient was hospitalized. Patient recovered.
Concerta Side Effects Report #5579383-5
Physician from KOREA, REPUBLIC OF reported CONCERTA problem on Dec 27, 2007. Female patient, 16 years of age, weighting 132.3 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with CONCERTA. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, heart rate increased, overdose, . CONCERTA dosage: unknown. Patient recovered.
Revlimid Side Effects Report #5583701-1
REVLIMID problem was reported by a Physician from UNITED STATES on Dec 26, 2007. Male patient, 53 years of age, weighting 218.0 lb, was diagnosed with chronic lymphocytic leukaemia and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, condition aggravated, lymphadenopathy, nephrotic syndrome, pain, renal disorder, tumour lysis syndrome, vomiting, . REVLIMID dosage: 15 MG, DAILY FOR 21 OUT OF 28 DAYS, ORAL; 5 MG, DAILY, ORAL. During the same period patient was treated with TOPROL, LIPITOR, LISINOPRIL, FOSAMAX, CALCIUM WITH VITAMIN D, ZINC, ALDARA CREAM. Patient recovered.
Zelitrex Side Effects Report #5584288-X
Consumer or non-health professional from FRANCE reported ZELITREX problem on Dec 31, 2007. Male patient, child 12 years of age, was treated with ZELITREX. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, haemolytic anaemia, haptoglobin decreased, . ZELITREX dosage: 500MG TWICE PER DAY. During the same period patient was treated with ORACILLIN, FUNGIZONE, GARDENAL. Patient was hospitalized. Patient recovered.
Pergolide Side Effects Report #5584488-9
PERGOLIDE MESYLATE problem was reported by a Health Professional from FRANCE on Mar 27, 2007. Male patient, 83 years of age, was diagnosed with parkinson's disease and was treated with PERGOLIDE MESYLATE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, hyponatraemia, interstitial lung disease, pulmonary fibrosis, pulmonary hypertension, right ventricular failure, subileus, . PERGOLIDE MESYLATE dosage: 2 MG;QD;PO. During the same period patient was treated with CARBIDOPA, ENTACAPONE, LEVODOPA, PLAVIX, IKOREL. Patient was hospitalized. Patient died on 01/20/2007.
Cyclophosphamide Side Effects Report #5590366-1
Consumer or non-health professional from reported CYCLOPHOSPHAMIDE problem on Jan 08, 2008. Male patient, 46 years of age, was diagnosed with immunosuppression and was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, cerebral haemorrhage, haemolytic anaemia, thrombocytopenia, thrombotic microangiopathy, . CYCLOPHOSPHAMIDE dosage: unknown. During the same period patient was treated with TACROLIMUS, PROSTAYCLIN ANALOG INFUSION. Patient died.
Itrizole Side Effects Report #5594428-4
ITRIZOLE problem was reported by a Physician from JAPAN on Jan 07, 2008. Male patient, weighting 154.3 lb, was diagnosed with prophylaxis, multiple myeloma, purpura and was treated with ITRIZOLE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, c-reactive protein increased, hepatic function abnormal, platelet count decreased, purpura, pyrexia, white blood cell count decreased, . ITRIZOLE dosage: unknown. During the same period patient was treated with VELCADE, SULFAMETHOXAZOLE WITH TRIMETHOPRIM, AZULENE, DEPRODONE PROPIONATE. Patient recovered.
Itrizole Side Effects Report #5605650-2
Physician from JAPAN reported ITRIZOLE problem on Jan 21, 2008. Male patient, weighting 154.3 lb, was diagnosed with prophylaxis, multiple myeloma, purpura and was treated with ITRIZOLE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, c-reactive protein increased, hepatic function abnormal, platelet count decreased, purpura, pyrexia, white blood cell count decreased, . ITRIZOLE dosage: unknown. During the same period patient was treated with VELCADE, SULFAMETHOXAZOLE WITH TRIMETHOPRIM, AZULENE, DEPRODONE PROPIONATE. Patient recovered.
Prednisolone Side Effects Report #5535290-5
PREDNISOLONE problem was reported by a Physician from UNITED STATES on Nov 16, 2007. Female patient was diagnosed with haemangioma and was treated with PREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, cd4 lymphocytes decreased, ependymoma, pneumocystis jiroveci pneumonia, white blood cell count abnormal, . PREDNISOLONE dosage: 3.5 MG/KG;QD;PO. During the same period patient was treated with METHYLPREDNISOLONE, ORAPRED. Patient was hospitalized. Patient recovered.
Tegretol Side Effects Report #5541684-4
Physician from JAPAN reported TEGRETOL problem on Dec 03, 2007. Male patient, 43 years of age, weighting 154.3 lb, was diagnosed with nerve injury and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, c-reactive protein increased, pyrexia, . TEGRETOL dosage: 200 MG/DAY. During the same period patient was treated with LIPITOR, LUDIOMIL, PL GRAN, PL GRAN, MEXITIL, DIOVAN, MELBIN. Patient was hospitalized. Patient recovered.
Tegretol Side Effects Report #5543147-9
TEGRETOL problem was reported by a Physician from JAPAN on Dec 03, 2007. Male patient, 43 years of age, weighting 154.3 lb, was diagnosed with nerve injury and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, c-reactive protein increased, pyrexia, . TEGRETOL dosage: 200 MG/DAY. During the same period patient was treated with LIPITOR, LUDIOMIL, PL GRAN, PL GRAN, MEXITIL, DIOVAN, MELBIN. Patient was hospitalized. Patient recovered.
Velcade Side Effects Report #5552382-5
Physician from JAPAN reported VELCADE problem on Nov 28, 2007. Female patient, 76 years of age, weighting 119.0 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, c-reactive protein increased, deep vein thrombosis, disease progression, neuropathy peripheral, neutrophil count decreased, platelet count decreased, pulmonary embolism, pyrexia, . VELCADE dosage: 1.90 MG, INTRAVENOUS. During the same period patient was treated with DEXAMETHASONE, DEXAMETHASONE PHOSPHATE, LASIX, PIPERACILLIN AND TAZOBACTAM, NORVASC, MUCOSTA, LANSOPRAZOLE, RIZE. Patient died on 10/29/2007.
Lescol Side Effects Report #5553664-3
LESCOL problem was reported by a Physician from CHINA on Dec 05, 2007. Male patient, 53 years of age, was diagnosed with hyperlipidaemia and was treated with LESCOL. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, myalgia, . LESCOL dosage: 40 MG, QD. Patient recovered.
Mefloquine Side Effects Report #5564269-2
Physician from GREECE reported MEFLOQUINE problem on Dec 03, 2007. Female patient, 67 years of age, was diagnosed with malaria prophylaxis, tinea versicolour and was treated with MEFLOQUINE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, eosinophilic pneumonia, hypoxia, malaise, normochromic normocytic anaemia, pulmonary toxicity, tachycardia, . MEFLOQUINE dosage: 250 MG, QW, ORAL. During the same period patient was treated with KETOCONAZOLE. Patient was hospitalized. Patient recovered.
Prograf Side Effects Report #5564529-5
PROGRAF problem was reported by a Physician from BRAZIL on Nov 27, 2007. Female patient was diagnosed with renal and pancreas transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, cytomegalovirus infection, gastrointestinal haemorrhage, haematocrit decreased, haematuria, haemodialysis, kidney transplant rejection, pneumonia bacterial, proteinuria, . PROGRAF dosage: 0.15 MG/KG. During the same period patient was treated with PREDNISOLONE ACETATE. Patient recovered.
Prograf Side Effects Report #5564532-5
Physician from BRAZIL reported PROGRAF problem on Nov 27, 2007. Female patient was diagnosed with renal and pancreas transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, complications of transplanted kidney, cytomegalovirus oesophagitis, gastrointestinal haemorrhage, haematocrit decreased, haematuria, haemodialysis, haemolytic uraemic syndrome, kidney transplant rejection, . PROGRAF dosage: 0.15 MG/KG. During the same period patient was treated with PREDNISOLONE ACETATE. Patient recovered.
Prograf Side Effects Report #5564534-9
PROGRAF problem was reported by a Physician from BRAZIL on Nov 27, 2007. Female patient was diagnosed with renal and pancreas transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, complications of transplanted kidney, cytomegalovirus oesophagitis, gastrointestinal haemorrhage, haematocrit decreased, haematuria, haemodialysis, haemolytic uraemic syndrome, kidney transplant rejection, . PROGRAF dosage: 0.15 MG/KG. During the same period patient was treated with PREDNISOLONE ACETATE. Patient recovered.
Prograf Side Effects Report #5564536-2
Physician from BRAZIL reported PROGRAF problem on Nov 27, 2007. Female patient was diagnosed with renal and pancreas transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, complications of transplanted kidney, cytomegalovirus oesophagitis, gastrointestinal haemorrhage, haematocrit decreased, haematuria, haemodialysis, haemolytic uraemic syndrome, kidney transplant rejection, . PROGRAF dosage: 0.15 MG/KG. During the same period patient was treated with PREDNISOLONE ACETATE. Patient recovered.
Prograf Side Effects Report #5564543-X
PROGRAF problem was reported by a Physician from BRAZIL on Nov 27, 2007. Female patient was diagnosed with renal and pancreas transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, complications of transplanted kidney, cytomegalovirus oesophagitis, gastrointestinal haemorrhage, haematocrit decreased, haematuria, haemodialysis, haemolytic uraemic syndrome, kidney transplant rejection, . PROGRAF dosage: 0.15 MG/KG. During the same period patient was treated with PREDNISOLONE ACETATE. Patient recovered.
Prograf Side Effects Report #5564559-3
Physician from BRAZIL reported PROGRAF problem on Nov 27, 2007. Female patient was diagnosed with renal and pancreas transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, complications of transplanted kidney, cytomegalovirus oesophagitis, gastrointestinal haemorrhage, haematocrit decreased, haematuria, haemodialysis, haemolytic uraemic syndrome, kidney transplant rejection, . PROGRAF dosage: 0.15 MG/KG. During the same period patient was treated with PREDNISOLONE ACETATE. Patient recovered.
Velcade Side Effects Report #5570193-1
VELCADE problem was reported by a Physician from JAPAN on Dec 05, 2007. Female patient, 48 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, hepatic function abnormal, . VELCADE dosage: 2.00 MG/M2,. During the same period patient was treated with CALCIUM POLYSTYRENE SULFONATE, SIGMART. Patient was hospitalized. Patient recovered.
Zometa Side Effects Report #5570411-X
Physician from GERMANY reported ZOMETA problem on Dec 10, 2007. Male patient, 61 years of age, weighting 176.4 lb, was diagnosed with multiple myeloma, hypertension and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, haemoglobin decreased, haemolytic anaemia, red blood cell count decreased, reticulocyte count increased, . ZOMETA dosage: 4 MG, QMO. During the same period patient was treated with ENALAPRIL, HYDROCHLOROTHIAZIDE, OMEPRAZOLE, METOPROLOL, ACETAMINOPHEN, SIRDALUD, FORTECORTIN, BALDRIPARAN. Patient recovered.
Menest Side Effects Report #5505232-7
MENEST problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 28, 2007. Female patient was treated with MENEST. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, liver function test abnormal, . MENEST dosage: .3 MG, UNK. Patient recovered.
Protopic Side Effects Report #5506409-7
Physician from JAPAN reported PROTOPIC problem on Oct 17, 2007. Female patient, 28 years of age, weighting 101.4 lb, was diagnosed with dermatitis atopic and was treated with PROTOPIC. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, diffuse large b-cell lymphoma stage iii, . PROTOPIC dosage: unknown. During the same period patient was treated with ALLEGRA, METHADERM, TOPSYM, ACUATIM, STEROID EXTERNAL. Patient was hospitalized. Patient recovered.
Mylotarg Side Effects Report #5507775-9
MYLOTARG problem was reported by a Physician from JAPAN on Oct 30, 2007. Female patient, weighting 108.0 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 lactate dehydrogenase increased, blood potassium decreased, fibrin degradation products increased, neutrophil count decreased, pneumonia, sepsis, white blood cell count decreased, . MYLOTARG dosage: unknown. During the same period patient was treated with LIPOVAS, ENOCITABINE, FLUCONAZOLE, DAUNORUBICIN, FAMOTIDINE, MICARDIS. Patient died on 10/03/2006.
Prograf Side Effects Report #5509573-9
Physician from JAPAN reported PROGRAF problem on Oct 24, 2007. Female patient, 70 years of age, weighting 97.00 lb, was diagnosed with rheumatoid arthritis and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, condition aggravated, diffuse alveolar damage, interstitial lung disease, no therapeutic response, rheumatoid lung, . PROGRAF dosage: 1.5 MG, UID/QD, ORAL. During the same period patient was treated with PREDNISOLONE, VOLTAREN, BACACIL, RABEPRAZOLE, ONEALFA, CYTOTEC, FOSAMAC, DIOVAN. Patient died on 08/31/2007.
Prograf Side Effects Report #5509926-9
PROGRAF problem was reported by a Physician from JAPAN on Oct 24, 2007. Male patient, 31 years of age, was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, histiocytosis haematophagic, pyrexia, serum ferritin increased, weight increased, . PROGRAF dosage: unknown. Patient recovered.
Prograf Side Effects Report #5509949-X
Physician from JAPAN reported PROGRAF problem on Oct 24, 2007. Male patient, 59 years of age, was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, histiocytosis haematophagic, pyrexia, rash, serum ferritin increased, weight increased, . PROGRAF dosage: unknown. Patient recovered.
Tegretol Side Effects Report #5523127-X
TEGRETOL problem was reported by a Physician from JAPAN on Nov 13, 2007. Male patient, 43 years of age, weighting 154.3 lb, was diagnosed with nerve injury and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, c-reactive protein increased, pyrexia, . TEGRETOL dosage: 200 MG/DAY. During the same period patient was treated with LIPITOR, LUDIOMIL, PL GRAN, PL GRAN, MEXITIL, DIOVAN, MELBIN. Patient was hospitalized. Patient recovered.
Velcade Side Effects Report #5523796-4
Physician from JAPAN reported VELCADE problem on Nov 06, 2007. Female patient, 76 years of age, weighting 119.0 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, c-reactive protein increased, deep vein thrombosis, neuropathy peripheral, neutrophil count decreased, pulmonary embolism, pyrexia, tumour lysis syndrome, . VELCADE dosage: 1.90 MG, INTRAVENOUS ; 1.00 MG, INTRAVENOUS. During the same period patient was treated with DEXAMETHASONE, LASIX, PIPERACILLIN AND TAZOBACTAM. Patient died.
Revlimid Side Effects Report #5524922-3
REVLIMID problem was reported by a Physician from SWITZERLAND on Nov 06, 2007. Female patient was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, bone pain, c-reactive protein increased, renal failure, . REVLIMID dosage: 15 MG, EVERY SECOND DAY, ORAL; 15 MG, ORAL. Patient recovered.
Velcade Side Effects Report #5531246-7
Physician from NETHERLANDS reported VELCADE problem on Nov 13, 2007. Female patient, 69 years of age, weighting 213.8 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, chest pain, chills, dyspnoea, pyrexia, . VELCADE dosage: 1.30 MG/M2, INTRAVENOUS. Patient recovered.
Arimidex Side Effects Report #5472827-9
ARIMIDEX problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 21, 2006. Female patient, 67 years of age, weighting 142.0 lb, was diagnosed with breast cancer female and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, osteoporosis, . ARIMIDEX dosage: unknown. Patient recovered.
Velcade Side Effects Report #5480956-9
Physician from JAPAN reported VELCADE problem on Sept 26, 2007. Female patient, 75 years of age, weighting 97.00 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, hypoaesthesia, nausea, neutrophil count decreased, platelet count decreased, pyrexia, vomiting, . VELCADE dosage: 1.66 MG, INTRAVENOS, 1.28 MG, INTRAVENOUS. During the same period patient was treated with ACTONEL, METHYCOBAL, URALYT, KYTRIL. Patient recovered.