HAEMOGLOBIN DECREASED side effect
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ABACAVIR ABRAXANE ACETAMINOPHEN ACETYLSALICYLIC ACTIQ ACTONEL ACTOS ACYCLOVIR ADALAT ADVIL AGGRASTAT ALDACTONE ALEVE ALIMTA ALISKIREN ALTACE AMBISOME AMEVIVE AMIODARONE AMITIZA AMLODIN ANGIOMAX AOTAL ARANESP ARAVA AREDIA ARGATROBAN ARIMIDEX ARIXTRA ARSENIC ASAPHEN ASPIRIN ATIVAN ATORVASTATIN AUGMENTIN AVANDAMET AVANDIA AVASTIN AVONEX AZATHIOPRINE BECLOMETHASONE BETAFERON BETASERON BEVACIZUMAB BISOPROLOL BLOPRESS BONIVA BUFFERIN BUSULFAN BYETTA CALCIUM CAMPATH CAMPRAL CAMPTO CAMPTOSAR CAP CAPECITABINE CARBAMAZEPINE CARBOPLATIN CASODEX CEFAZOLIN CEFTRIAXONE CELEBREX CELECOXIB CELLCEPT CEREZYME CERTICAN CETUXIMAB CHAMPIX CHANTIX CHORIONIC CIFLOX CILOSTAZOL CIPROFLOXACIN CISPLATIN CITALOPRAM CLAMOXYL CLARITHROMYCIN CLEXANE CLOFARABINE CLOLAR CLOMIPRAMINE CLOZAPINE CLOZARIL COPAXONE COPEGUS CORDARONE COREG COSMEGEN COUMADIN COZAAR CPD CRESTOR CRIXIVAN CYCLOPHOSPHAMIDE CYCLOSPORINE CYMBALTA CYSTAGON CYTARABINE CYTOTEC CYTOXAN DACARBAZINE DACOGEN DACTINOMYCIN DASATINIB DECADRON DECITABINE DESFERRIOXAMINE DEXTROSE DICLOFENAC DIGOXIN DIOVAN DIPYRIDAMOLE DOCETAXEL DONEPEZIL DOXIL DOXORUBICIN DULOXETINE EFFEXOR EMEND ENBREL ENOXAPARIN EPIVIR EPOGEN EPTIFIBATIDE ERBITUX ERLOTINIB EROTINIB ESCITALOPRAM ETHYOL ETODOLAC EXELON EXJADE FABRAZYME FACTOR FASLODEX FEMARA FENOFIBRATE FENTANYL FLUDARA FLUDARABINE FLUOROURACIL FORADIL FORTAZ FORTEO FORTUM FOSAMAX FOSCAVIR FOSPHENYTOIN FRAGMIN FRESH FUNGUARD GAMUNEX GASTER GEMCITABINE GEMZAR GLEEVEC GLYCEOL GONAL GRTPA HALDOL HEPARIN HERCEPTIN HUMALOG HUMIRA HUMULIN HYDRODIURIL HYDROXYZINE IBUPROFEN IFOMIDE IFOSFAMIDE IMMUCYST IMPLANON INDOCIN INEXIUM INFLIXIMAB INOMAX INTERFERON INTRON IRESSA IRINOTECAN ISENTRESS ISOVORIN IXEMPRA JANUVIA KALETRA KARDEGIC KENALOG KEPPRA KINERET LAMICTAL LAMISIL LAMIVUDINE LANOXIN LANSOPRAZOLE LAPATINIB LASIX LASTET LEPONEX LETAIRIS LETROZOLE LEUCOVORIN LEUKINE LEVAQUIN LEVOFLOXACIN LEVOTHYROXINE LEXAPRO LIALDA LIORESAL LIPITOR LISINOPRIL LORAZEPAM LOTREL LOVAZA LOVENOX LYBREL LYRICA MABTHERA MACUGEN MAXIPIME MEGESTROL MELOXICAM MEMANTINE MERCAPTAMINE MERCAPTOPURINE MESALAMINE MESALAZINE METHOTREXATE METHYLPREDNISOLO METOPROLOL METRONIDAZOLE MICONAZOLE MINOFIT MIRALAX MIRENA MIRTAZAPINE MORPHINE MYCOPHENOLATE MYFORTIC MYLOTARG NAFCILLIN NANDROLONE NAPROSYN NATALIZUMAB NEOPHYLLINECTION NEORAL NEULASTA NEUPOGEN NEXAVAR NEXIUM NIASPAN NORDITROPIN NOVANTRONE NOVID NOVORAPID NOVOSEVEN NOXAFIL OFLOCET OLMETEC OMALIZUMAB OMEPRAZOLE OMNIPAQUE ONCASPAR ORFADIN ORSU OXALIPLATIN PACLITAXEL PARAPLATIN PAZOPANIB PEGASYS PEMETREXED PENTASA PEPCID PHENOBARBITAL PHENYTOIN PIROXICAM PLAVIX PRAVACHOL PREDNISOLONE PREDNISONE PRIMPERAN PROCARDIA PROCRIT PROGRAF PROPRANOLOL PROVIGIL QUETIAPINE RABEPRAZOLE RANEXA RAPAMUNE REBIF REMERON REMICADE RENAGEL REQUIP RETEPLASE RETROVIR REVATIO REVLIMID RIBAPAK RIBASPHERE RIBAVIRIN RISPERDAL RISPERIDONE RITUXAN RITUXIMAB ROCEPHIN ROSIGLITAZONE ROTIGOTINE ROZEREM RYTHMOL SALAZOPYRINE SALICYLATES SANDIMMUNE SEBIVO SENSIPAR SEPTRA SEROQUEL SERTRALINE SIBUTRAMINE SIMULECT SIMVASTATIN SIROLIMUS SOLAGE SORAFENIB SPORANOX SPRYCEL STALEVO STRATTERA SUNITINIB SUTENT SYMBICORT SYNAGIS SYNAREL SYNTOCINON TACROLIMUS TARCEVA TAREG TASIGNA TAVANIC TAXOL TAXOTERE TAZOCILLINE TEGRETOL TEMODAL TEMODAR TEMOZOLOIDE TEMOZOLOMIDE TEMSIROLIMUS TENOFOVIR THALIDOMIDE THALOMID THYMOGLOBULIN TICLODIPINE TIOTROPIUM TOPOTECAN TRACLEER TRAMADOL TRASTUZUMAB TREVILOR TRICOR TRILEPTAL TRIQUILAR TRISENOX TRUVADA TYSABRI URBANYL UROXATRAL VALACYCLOVIR VALSARTAN VALTREX VANCOMYCIN VASOTEC VELCADE VENOFER VFEND VIDAZA VINCRISTINE VIREAD VOLTAREN VYTORIN WARFARIN WINRHO XELODA XENICAL XIGRIS XOLAIR XOPENEX ZEFIX ZEVALIN ZIDOVUDINE ZOCOR ZOLOFT ZOMETA ZONEGRAN ZOVIRAX ZYPREXA ZYVOXSibutramine Side Effects Report #5647332-7
Physician from UNITED KINGDOM reported SIBUTRAMINE HYDROCHLORIDE MONOHYDRATE problem on Feb 25, 2008. Female patient, 29 years of age, weighting 176.4 lb, was diagnosed with weight control and was treated with SIBUTRAMINE HYDROCHLORIDE MONOHYDRATE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, pancytopenia, . SIBUTRAMINE HYDROCHLORIDE MONOHYDRATE dosage: unknown. Patient recovered.
Exjade Side Effects Report #5648473-0
EXJADE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 25, 2008. Female patient, 58 years of age, was diagnosed with iron overload and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, . EXJADE dosage: 10 MG/KG, QD. Patient recovered.
Rocephin Side Effects Report #5650782-6
Consumer or non-health professional from GERMANY reported ROCEPHIN problem on Feb 22, 2008. Female patient, 67 years of age, weighting 134.7 lb, was diagnosed with borrelia infection and was treated with ROCEPHIN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, hypertension, jarisch-herxheimer reaction, pleural effusion, pulmonary embolism, . ROCEPHIN dosage: unknown. During the same period patient was treated with CEFTRIAXONE, BISOPROLOL FUMARATE, KALINOR. Patient was hospitalized. Patient recovered.
Cetuximab Side Effects Report #5651423-4
CETUXIMAB problem was reported by a Consumer or non-health professional from FRANCE on Feb 26, 2008. Female patient, 70 years of age, was diagnosed with colon cancer stage iii and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, neutropenia, protein total increased, pyelonephritis, renal abscess, urinary tract infection, white blood cell count decreased, . CETUXIMAB dosage: unknown. During the same period patient was treated with OXALIPLATIN, FLUOROURACIL, FOLINIC ACID. Patient was hospitalized. Patient recovered.
Requip Side Effects Report #5654908-X
Consumer or non-health professional from UNITED STATES reported REQUIP problem on Sept 10, 2007. Male patient, 77 years of age, was diagnosed with parkinson's disease and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, . REQUIP dosage: 8MG THREE TIMES PER DAY. During the same period patient was treated with PROTONIX, COZAAR, FLOMAX. Patient recovered.
Arixtra Side Effects Report #5661256-0
ARIXTRA problem was reported by a Physician from JAPAN on Mar 07, 2008. Male patient, 59 years of age, weighting 130.1 lb, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemorrhage subcutaneous, pain, platelet count increased, red blood cell count decreased, white blood cell count increased, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with RHEUMATREX, AZULFIDINE EN, PROGRAF, PREDONINE, HEPARIN. Patient was hospitalized and became disabled. Patient recovered.
Pegasys Side Effects Report #5661513-8
Health Professional from CANADA reported PEGASYS problem on Mar 05, 2008. Male patient, 67 years of age, was diagnosed with hepatitis c, haemoglobin decreased and was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, insomnia, lung neoplasm malignant, weight decreased, . PEGASYS dosage: unknown. During the same period patient was treated with COPEGUS, EPREX, IMOVANE. Patient recovered.
Cisplatin Side Effects Report #5662471-2
CISPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 10, 2008. Female patient, weighting 123.0 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, heart rate increased, platelet count decreased, urinary tract infection, . CISPLATIN dosage: 47 MG. During the same period patient was treated with ERBITUX, COUMADIN, KLONOPIN, OXYCODONE. Patient was hospitalized. Patient recovered.
Erbitux Side Effects Report #5662617-6
Health Professional from UNITED STATES reported ERBITUX problem on Mar 08, 2008. Female patient, 50 years of age, weighting 123.5 lb, was diagnosed with cervix carcinoma and was treated with ERBITUX. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemolysis, hypocalcaemia, infection, platelet count decreased, pyrexia, white blood cell count decreased, . ERBITUX dosage: unknown. During the same period patient was treated with CISPLATIN, COUMADIN, KLONOPIN, OXYCODONE. Patient was hospitalized. Patient recovered.
Heparin Side Effects Report #5663637-8
HEPARIN problem was reported by a Health Professional from UNITED STATES on Mar 05, 2008. Female patient, weighting 108.0 lb, was diagnosed with prophylaxis and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemorrhage, hypotension, pain, rash, renal haemorrhage, syncope, . HEPARIN dosage: unknown. Patient was hospitalized. Patient recovered.
Mesalamine Side Effects Report #5664309-6
Physician from MEXICO reported MESALAMINE problem on Mar 07, 2008. Female patient, 32 years of age, weighting 121.3 lb, was diagnosed with cervix carcinoma and was treated with MESALAMINE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, platelet count decreased, rectal haemorrhage, . MESALAMINE dosage: unknown. During the same period patient was treated with STEROIDS NOS, GLEEVEC. Patient was hospitalized. Patient died on 05/27/2006.
Epogen Side Effects Report #5664332-1
EPOGEN problem was reported by a Physician from UNITED STATES on Feb 29, 2008. Female patient, 31 years of age, was diagnosed with renal failure chronic and was treated with EPOGEN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, platelet count increased, pneumonia klebsiella, pneumonia staphylococcal, therapeutic response decreased, white blood cell count increased, . EPOGEN dosage: unknown. During the same period patient was treated with ARANESP, LINEZOLID, IMIPENEM, TOBRAMYCIN, LISINOPRIL, METOPROLOL TARTRATE, CLONIDINE, SYNTHROID. Patient was hospitalized. Patient recovered.
Carboplatin Side Effects Report #5668823-9
Consumer or non-health professional from UNITED STATES reported CARBOPLATIN problem on Mar 12, 2008. Female patient, weighting 160.3 lb, was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, platelet count decreased, upper respiratory tract infection, . CARBOPLATIN dosage: 420 MG. During the same period patient was treated with TAXOL. Patient was hospitalized. Patient recovered.
Quetiapine Side Effects Report #5671037-X
QUETIAPINE FUMARATE problem was reported by a Health Professional from UNITED KINGDOM on Mar 12, 2008. Female patient, 86 years of age, was diagnosed with agitation, cerebrovascular accident, dementia, serum ferritin decreased, stomach discomfort and was treated with QUETIAPINE FUMARATE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, neutropenia, . QUETIAPINE FUMARATE dosage: unknown. During the same period patient was treated with ASPIRIN, BETAMETHASONE, CANDESARTAN CILEXETIL, CLEXANE, DONEPEZIL, FERROUS FUMARATE, HALOPERIDOL, LANSOPRAZOLE. Patient recovered.
Dipyridamole Side Effects Report #5671471-8
Physician from reported DIPYRIDAMOLE problem on Mar 12, 2008. Female patient, 74 years of age, weighting 112.4 lb, was diagnosed with transient ischaemic attack and was treated with DIPYRIDAMOLE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemorrhage, platelet count decreased, white blood cell count decreased, . DIPYRIDAMOLE dosage: 200MG TWICE DAILY. During the same period patient was treated with ARAVA, ASCORBIC ACID, CEPHALEXIN, COMBIVENT, METHYLPREDNISOLONE ACETATE, DURAGESIC, EFFEXOR, FLUVASTATIN. Patient recovered.
Tracleer Side Effects Report #5674055-0
TRACLEER problem was reported by a Consumer or non-health professional from GERMANY on Mar 05, 2008. Female patient, 51 years of age, weighting 147.7 lb, was diagnosed with pulmonary hypertension and was treated with TRACLEER. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, white blood cell count decreased, . TRACLEER dosage: unknown. During the same period patient was treated with MIRACUMAR, SILDENAFIL CITRATE, OXYGEN. Patient recovered.
Pazopanib Side Effects Report #5674662-5
Physician from PERU reported PAZOPANIB problem on Mar 12, 2008. Female patient, 34 years of age, weighting 109.3 lb, was treated with PAZOPANIB. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemorrhagic anaemia, vaginal haemorrhage, . PAZOPANIB dosage: 800MG PER DAY. During the same period patient was treated with LAPATINIB. Patient recovered.
Exjade Side Effects Report #5675699-2
EXJADE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 13, 2008. Female patient, 59 years of age, weighting 165.3 lb, was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, loss of consciousness, palpitations, transfusion, . EXJADE dosage: 1500 MG, QD. Patient was hospitalized. Patient recovered.
Fludara Side Effects Report #5676184-4
Physician from JAPAN reported FLUDARA problem on Mar 13, 2008. Male patient, 47 years of age, was diagnosed with follicle centre lymphoma, follicular grade i, ii, iii and was treated with FLUDARA. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, platelet count decreased, white blood cell count decreased, . FLUDARA dosage: TOTAL DAILY DOSE: 70 MG UNIT DOSE: 10 MG. Patient was hospitalized. Patient recovered.
Amevive Side Effects Report #5677816-7
AMEVIVE problem was reported by a Physician from UNITED STATES on Mar 04, 2008. Female patient, 41 years of age, weighting 175.0 lb, was diagnosed with psoriasis and was treated with AMEVIVE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, menometrorrhagia, . AMEVIVE dosage: 15 MG, WEEKLY, INTRAMUSCULAR. During the same period patient was treated with ENBREL, PREMARIN, FERROUS SULPHATE, FISH OIL, VITAMIN, LEVOTHYROXINE. Patient was hospitalized. Patient recovered.
Revlimid Side Effects Report #5678244-0
Health Professional from GERMANY reported REVLIMID problem on Mar 13, 2008. Female patient, 70 years of age, was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, platelet count decreased, sepsis, . REVLIMID dosage: 15 MG, ORAL; 8 MG, 1-4, 9-12. During the same period patient was treated with DEXAMETHASONE. Patient was hospitalized. Patient died on 03/11/2008.
Heparin Side Effects Report #5679346-5
HEPARIN problem was reported by a Physician from UNITED STATES on Mar 18, 2008. Female patient, 37 years of age, was diagnosed with prophylaxis and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemorrhage, . HEPARIN dosage: unknown. Patient recovered.
Dipyridamole Side Effects Report #5679641-X
Health Professional from UNITED KINGDOM reported DIPYRIDAMOLE problem on Mar 11, 2008. Female patient, 74 years of age, was diagnosed with transient ischaemic attack and was treated with DIPYRIDAMOLE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemorrhage, platelet count decreased, white blood cell count decreased, . DIPYRIDAMOLE dosage: 200 MG; BID; PO. During the same period patient was treated with ASCORBIC ACID, CEPHALEXIN, ARAVA, PLAVIX, FOLIC ACID, SALBUTAMOL, METHOTREXATE, FLUVASTATIN. Patient recovered.
Sprycel Side Effects Report #5682530-8
SPRYCEL problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 20, 2007. Female patient was diagnosed with chronic myeloid leukaemia and was treated with SPRYCEL. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, platelet count decreased, urticaria vesiculosa, white blood cell count increased, . SPRYCEL dosage: 70 MG TWICE A DAY THEN WENT DOWN TO 1 FORM = 70MG + 20MG (ALTERNATING EVERY OTHER DAY). Patient was hospitalized. Patient recovered.
Arixtra Side Effects Report #5682850-7
Physician from JAPAN reported ARIXTRA problem on Mar 25, 2008. Male patient, 59 years of age, weighting 130.1 lb, was diagnosed with thrombosis prophylaxis, rheumatoid arthritis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemorrhage subcutaneous, pain, platelet count increased, red blood cell count decreased, white blood cell count increased, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with RHEUMATREX, AZULFIDINE EN, PROGRAF, PREDONINE, HEPARIN. Patient was hospitalized and became disabled. Patient recovered.
Tenofovir Side Effects Report #5683229-4
TENOFOVIR DISOPROXIL FUMARATE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 19, 2008. Male patient, weighting 13.67 lb, was diagnosed with hiv infection and was treated with TENOFOVIR DISOPROXIL FUMARATE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, . TENOFOVIR DISOPROXIL FUMARATE dosage: unknown. Patient recovered.
Procrit Side Effects Report #5615861-8
Consumer or non-health professional from UNITED STATES reported PROCRIT problem on Jan 22, 2008. Male patient, weighting 155.2 lb, was diagnosed with renal failure chronic and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, t-cell lymphoma, . PROCRIT dosage: unknown. During the same period patient was treated with NEPHRO, FERROUS SULPHATE, FLOMAX, TRAMADOL, AVANDIA, ATENOLOL, ACETAMINOPHEN, LIPITOR. Patient recovered.
Erbitux Side Effects Report #5616503-8
ERBITUX problem was reported by a Health Professional from UNITED STATES on Feb 04, 2008. Female patient, 68 years of age, weighting 163.1 lb, was diagnosed with squamous cell carcinoma and was treated with ERBITUX. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, international normalised ratio increased, mucosal inflammation, neutrophil count decreased, platelet count decreased, rash, . ERBITUX dosage: 400 MG/M*2 DAY 1, THEN 250 MG/M*2 EVERY 8 DAYS.. During the same period patient was treated with ALIMTA, METOPROLOL TARTRATE, ACYCLOVIR, FENTANYL TRANSDERMAL SYSTEM, FOLIC ACID, LIPITOR, DECADRON. Patient was hospitalized. Patient recovered.
Primperan Side Effects Report #5621765-7
Physician from FRANCE reported PRIMPERAN problem on Jan 31, 2008. Male patient, 16 years of age, weighting 88.18 lb, was diagnosed with congenital aplastic anaemia, iron overload and was treated with PRIMPERAN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, . PRIMPERAN dosage: unknown. During the same period patient was treated with EXJADE. Patient recovered.
Remicade Side Effects Report #5624298-7
REMICADE problem was reported by a Health Professional from CANADA on Feb 05, 2008. Female patient, weighting 149.9 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, mouth ulceration, . REMICADE dosage: unknown. Patient was hospitalized. Patient recovered.
Epogen Side Effects Report #5624522-0
Health Professional from UNITED STATES reported EPOGEN problem on Jan 30, 2008. Male patient, 71 years of age, was diagnosed with dialysis and was treated with EPOGEN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, hospitalisation, . EPOGEN dosage: unknown. Patient was hospitalized. Patient recovered.
Cyclophosphamide Side Effects Report #5625554-9
CYCLOPHOSPHAMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 11, 2008. Female patient, weighting 132.3 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, headache, oedema peripheral, pharyngolaryngeal pain, platelet count decreased, pyrexia, white blood cell count decreased, . CYCLOPHOSPHAMIDE dosage: 1262 MG. During the same period patient was treated with DOXIL, PREDNISONE, RITUXIMAB, VINCRISTINE SULPHATE. Patient was hospitalized. Patient recovered.
Amevive Side Effects Report #5626623-X
Physician from UNITED STATES reported AMEVIVE problem on Jan 29, 2008. Female patient, 41 years of age, weighting 190.0 lb, was diagnosed with psoriasis and was treated with AMEVIVE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, menorrhagia, . AMEVIVE dosage: 15 MG, WEEKLY, INTRAMUSCULAR. During the same period patient was treated with ENBREL, PREMARIN, FERROUS SULPHATE, FISH OIL, VITAMIN, LEVOTHYROXINE. Patient was hospitalized. Patient recovered.
Procrit Side Effects Report #5627960-5
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 05, 2008. Female patient, 40 years of age, was diagnosed with renal failure chronic and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, . PROCRIT dosage: unknown. Patient recovered.
Procrit Side Effects Report #5627963-0
Consumer or non-health professional from UNITED STATES reported PROCRIT problem on Feb 05, 2008. Female patient, 65 years of age, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, . PROCRIT dosage: unknown. Patient recovered.
Viread Side Effects Report #5628230-1
VIREAD problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 12, 2008. Male patient, weighting 8.38 lb, was diagnosed with prophylaxis against hiv infection and was treated with VIREAD. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, . VIREAD dosage: 4 MG/KG ON DAY O, 3 AND 5. During the same period patient was treated with ZIDOVUDINE, LAMIVUDINE, SAQUINAVI. Patient recovered.
Cyclophosphamide Side Effects Report #5629393-4
Consumer or non-health professional from UNITED STATES reported CYCLOPHOSPHAMIDE problem on Feb 15, 2008. Female patient, weighting 114.6 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, neutrophil count decreased, tooth abscess, white blood cell count decreased, . CYCLOPHOSPHAMIDE dosage: 978 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE. Patient was hospitalized. Patient recovered.
Cyclophosphamide Side Effects Report #5629551-9
CYCLOPHOSPHAMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 14, 2008. Female patient, weighting 114.6 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, neutrophil count decreased, tooth abscess, white blood cell count decreased, . CYCLOPHOSPHAMIDE dosage: 978 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE. Patient was hospitalized. Patient recovered.
Clozaril Side Effects Report #5630076-5
Health Professional from NEW ZEALAND reported CLOZARIL problem on Feb 07, 2008. Male patient, 50 years of age, was diagnosed with schizophrenia and was treated with CLOZARIL. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, infection, plasma cells decreased, platelet count decreased, platelet count increased, white blood cell count increased, . CLOZARIL dosage: unknown. Patient was hospitalized. Patient recovered.
Syntocinon Side Effects Report #5630086-8
SYNTOCINON problem was reported by a Health Professional from AUSTRALIA on Feb 13, 2008. Female patient, 39 years of age, was diagnosed with caesarean section and was treated with SYNTOCINON. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, postpartum haemorrhage, . SYNTOCINON dosage: unknown. During the same period patient was treated with CEPHALEXIN, PARACETAMOL, VOLTAREN. Patient was hospitalized. Patient recovered.
Syntocinon Side Effects Report #5631787-8
Health Professional from AUSTRALIA reported SYNTOCINON problem on Feb 13, 2008. Female patient, 30 years of age, was diagnosed with third stage postpartum haemorrhage and was treated with SYNTOCINON. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, postpartum haemorrhage, . SYNTOCINON dosage: unknown. Patient was hospitalized. Patient recovered.
Seroquel Side Effects Report #5632199-3
SEROQUEL problem was reported by a Physician from JAPAN on Feb 06, 2008. Male patient, 37 years of age, was diagnosed with schizophrenia and was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, . SEROQUEL dosage: unknown. Patient recovered.
Decitabine Side Effects Report #5633774-2
Physician from VENEZUELA reported DECITABINE problem on Feb 07, 2008. Female patient, 74 years of age, weighting 103.6 lb, was diagnosed with myelodysplastic syndrome and was treated with DECITABINE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, necrotising fasciitis, platelet count decreased, red blood cell count decreased, skin infection, white blood cell count decreased, . DECITABINE dosage: 15 MG/M2, 2 IN 1 DAY, INTRAVENOUS; 20 MG/M2, INTRAVENOUS. Patient was hospitalized and became disabled. Patient recovered.
Bevacizumab Side Effects Report #5633937-6
BEVACIZUMAB problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Feb 07, 2008. Female patient, weighting 119.0 lb, was diagnosed with breast cancer metastatic and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, . BEVACIZUMAB dosage: 900 MG, 3/WEEK. During the same period patient was treated with TAXOTERE, CAPECITABINE, BENADON, CHLORPROMAZINE, DEROXAT, PANTOZOL, PASPERTIN. Patient recovered.
Aliskiren Side Effects Report #5634535-0
Consumer or non-health professional from UNITED KINGDOM reported ALISKIREN problem on Feb 18, 2008. Female patient, 55 years of age, was diagnosed with hypertension, pain, depression, dyspepsia, insomnia and was treated with ALISKIREN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, iron deficiency anaemia, . ALISKIREN dosage: 150MG / DAY. During the same period patient was treated with DICLOFENAC, SERTRALINE, ATENOLOL, LISINOPRIL, OMEPRAZOLE, ZOLPIDEM, ZOPICLONE. Patient recovered.
Pegasys Side Effects Report #5637129-6
PEGASYS problem was reported by a Health Professional from CANADA on Feb 12, 2008. Male patient, 67 years of age, was diagnosed with hepatitis c, haemoglobin decreased and was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, insomnia, lung neoplasm malignant, . PEGASYS dosage: unknown. During the same period patient was treated with COPEGUS, EPREX, IMOVANE. Patient recovered.
Gemzar Side Effects Report #5638149-8
Physician from JAPAN reported GEMZAR problem on Feb 14, 2008. Male patient, weighting 132.3 lb, was diagnosed with pancreatic carcinoma stage iv, prophylaxis and was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, malnutrition, renal disorder, white blood cell count decreased, . GEMZAR dosage: 1600 MG, OTHER. During the same period patient was treated with DECADRON, KYTRIL, NEUTROGIN. Patient was hospitalized. Patient recovered.
Heparin Side Effects Report #5641052-0
HEPARIN problem was reported by a Health Professional from UNITED STATES on Feb 22, 2008. Female patient, weighting 108.0 lb, was diagnosed with prophylaxis and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemorrhage, hypotension, renal haemorrhage, syncope, . HEPARIN dosage: unknown. Patient was hospitalized. Patient recovered.
Thalomid Side Effects Report #5644158-5
Physician from UNITED STATES reported THALOMID problem on Feb 19, 2008. Male patient, 61 years of age, was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemorrhage, . THALOMID dosage: 200 MG, 4 IN 1 D, ORAL; 100 MG, DAILY, ORAL; 150 MG, DAILY, ORAL. Patient recovered.
Urbanyl Side Effects Report #5644283-9
URBANYL problem was reported by a Physician from FRANCE on Feb 21, 2008. Male patient, 16 years of age, weighting 90.39 lb, was diagnosed with epilepsy, congenital aplastic anaemia, iron overload and was treated with URBANYL. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, . URBANYL dosage: unknown. During the same period patient was treated with PRIMPERAN, EXJADE. Patient recovered.
Decitabine Side Effects Report #5646197-7
Physician from VENEZUELA reported DECITABINE problem on Feb 18, 2008. Female patient, 74 years of age, weighting 103.6 lb, was diagnosed with myelodysplastic syndrome and was treated with DECITABINE. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, necrotising fasciitis, platelet count decreased, septic shock, skin infection, white blood cell count decreased, . DECITABINE dosage: 15 MG/M2, 2 IN 1 DAY, INTRAVENOUS. Patient was hospitalized and became disabled. Patient died on 02/15/2008.