BLOOD UREA INCREASED side effect
What is BLOOD UREA INCREASED ?
Help Community - Describe Your Side Effect
Search FDA Side Effects
Ask Health Expert
BLOOD UREA INCREASED and Recently Reported Side Effects
BLOOD UREA INCREASED and 15 most Active Side Effect polls
BLOOD UREA INCREASED and featured health surveys
Substances toxic to Health
Recent Hospital reviews
Comments about Side Effects
Hospital Quality reviews
Homecare Quality reviews
Drugs associated with BLOOD UREA INCREASED
ACLASTA ACTONEL ADALAT ALDACTONE ALENDRONIC ALEVE ALLOPURINOL ALTACE AMBISOME AMIODARONE AMLODIN AMLODIPINE AMPHOTERICIN APROTININ AREDIA ARICEPT ARIMIDEX ARIXTRA ASASANTIN ASPIRIN ATACAND ATENOLOL ATIVAN ATORVASTATIN AUGMENTIN AVANDIA AVAPRO AVASTIN AVELOX AVONEX AZATHIOPRINE AZITHROMYCIN BACLOFEN BACTRIM BENICAR BEVACIZUMAB BEXTRA BEXXAR BUFFERIN BUSULFEX BYETTA CALCITONIN CAMPATH CAMPTO CAP CAPECITABINE CARBAMAZEPINE CARBATROL CARBOPLATIN CARIMUNE CARVEDILOL CATAFLAM CEFEPIME CEFTAZIDIME CEFTRIAXONE CELLCEPT CEREZYME CERTICAN CETUXIMAB CGP CHANTIX CIPROFLOXACIN CISPLATIN CLARITHROMYCIN CLINDAMYCIN CLOFARABINE CLOZAPINE CLOZARIL COAPROVEL COLCHICINE COMTAN COTAREG COZAAR CRESTOR CYCLOPHOSPHAMIDE CYCLOSPORINE CYMBALTA CYTARABINE DACOGEN DEFERASIROX DEROXAT DESFERAL DIANEAL DICLOFENAC DIGOXIN DIOVAN DOCETAXEL DORIBAX DOXORUBICIN EFFEXOR ELSPAR EMTRIVA ENALAPRIL EPIVIR ERLOTINIB ESCITALOPRAM EXENATIDE EXJADE FABRAZYME FAMVIR FELDENE FEMARA FENOFIBRATE FENTANYL FINIBAX FLOMAX FLUDARABINE FLUOROURACIL FOLIC FORASEQ FORTEO FORTUM FOSINOPRIL FRONTAL FUROSEMIDE GADOLINIUM GASTER GEMFIBROZIL GEMZAR GENTAMICIN GLEEVEC GLUCOPHAGE GLYBURIDE HEPSERA HUMALOG HUMIRA HUMULIN HYDROCORTISONE HYDRODIURIL HYZAAR IBUPROFEN IDURSULFASE IMITREX IMMUCYST IMMUNE INDOCIN INTERFERON IRESSA ISENTRESS ISOTRETINOIN ISTIN ITRIZOLE JANUVIA KETEK KETOPROFEN KLARICID LAMICTAL LAMISIL LANOXIN LANTUS LAPATINIB LAPATINIBLET LASILIX LASIX LETAIRIS LEVAQUIN LEVEMIR LIPITOR LISINOPRIL LITHIUM LOCHOL LOTREL LOVASTATIN LUNESTA LYRICA MEMANTINE METFORMIN METHOTREXATE METHYLPREDNISOLO METOPROLOL METRONIDAZOLE MICARDIS MICONAZOLE MIRALAX MIRENA MODOPAR MODURETIC MORPHINE MOXIFLOXACIN MYLOTARG NADOLOL NAPROSYN NAPROXEN NATALIZUMAB NATEGLINIDE NATRECOR NEORAL NEUPRO NEXAVAR NEXIUM NITROFURANTOIN NORVASC NUTRITION NUTROPIN OLMESARTAN OPTIRAY OSMOPREP OXYBUTYNIN PAMIDRONATE PANCURONIUM PANITUMUMAB PAROXETINE PEGASYS PEMETREXED PEPCID PHOSPHOSODA PLETAL POLYMYXIN PRAVASTATIN PREDNISOLONE PREDNISONE PREGABALIN PREZOLON PROGRAF PROLEUKIN PROVIGIL PROZAC QUETIAPINE RAMIPRIL RAPAMUNE RASILEZ REBIF REMICADE RENAGEL REQUIP REVLIMID RIFAMPICIN RITONAVIR ROCALTROL ROSUVASTATIN SANDIMMUNE SANDOSTATIN SCOPE SEBIVO SECALIP SEGURIL SEROPLEX SEROQUEL SEVREDOL SIMULECT SIMVASTATIN SORAFENIB SORIATANE SOTALOL SPIRONOLACTONE STALEVO STARSIS STEROIDS SUTENT SYMLIN TAB TACROLIMUS TAMSULOSIN TARCEVA TAREG TARGOCID TASIGNA TASMAR TAVANIC TAXOL TAXOTERE TEKTURNA TEMERIT TEMODAL TEMODAR TEMOZOLOMIDE TENORETIC TERAZOSIN TERBINAFINE THALOMID THALOMIDE THYMOGLOBULIN TOPROL TRAMADOL TRASTUZUMAB TRICOR TRUVADA TYGACIL TYSABRI ULCEX VALACICLOVIR VALSARTAN VALTREX VELCADE VERAPAMIL VESICARE VIAGRA VISICOL VITAMIN VOLTAREN VYTORIN WINRHO XELODA XOLAIR XOPENEX ZESTRIL ZETIA ZOCOR ZOLADEX ZOLEDRONIC ZOMETA ZOPHREN ZOVIRAX ZYPREXASevredol Side Effects Report #5648716-3
Health Professional from FRANCE reported SEVREDOL problem on Feb 26, 2008. Female patient, 72 years of age, was diagnosed with pain and was treated with SEVREDOL. After drug was administered, patient experienced the following problems/side effects: blood urea increased, dehydration, hypochloraemia, renal failure, vomiting, . SEVREDOL dosage: 10 MG, DAILY. During the same period patient was treated with METFORMIN, RILMENIDINE, LESCOL, ACTRAPID MC, AMLOR, ZESTORETIC, VALIUM, KARDEGIC. Patient was hospitalized. Patient recovered.
Pletal Side Effects Report #5652208-5
PLETAL problem was reported by a Consumer or non-health professional from JAPAN on Feb 19, 2008. Male patient, 59 years of age, was diagnosed with cerebral infarction and was treated with PLETAL. After drug was administered, patient experienced the following problems/side effects: blood urea increased, cerebral infarction, gastric ulcer haemorrhage, helicobacter infection, iron deficiency anaemia, . PLETAL dosage: 100 MG, BID, ORAL, 100 MG, BID, ORAL. During the same period patient was treated with AMLODIPINE BESYLATE, FERROMIA. Patient was hospitalized. Patient recovered.
Idursulfase Side Effects Report #5657946-6
Physician from JAPAN reported IDURSULFASE problem on Feb 22, 2008. Male patient, 21 years of age, weighting 48.50 lb, was diagnosed with mucopolysaccharidosis i and was treated with IDURSULFASE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, cardiopulmonary failure, hepatic enzyme increased, oedema, pulmonary congestion, respiratory failure, urine output decreased, white blood cell count increased, . IDURSULFASE dosage: 12 MG, 1X/WEEK, IV DRIP. During the same period patient was treated with CARBOCISTEINE, CLARITHROMYCIN. Patient died on 02/15/2008.
Aleve Side Effects Report #5658659-7
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on May 15, 2007. Female patient, 71 years of age, weighting 180.8 lb, was diagnosed with arthritis and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, . ALEVE dosage: TOTAL DAILY DOSE: 220 MG UNIT DOSE: 220 MG. During the same period patient was treated with ZOCOR. Patient recovered.
Terbinafine Side Effects Report #5662642-5
Consumer or non-health professional from UNITED KINGDOM reported TERBINAFINE problem on Mar 06, 2008. Female patient, 65 years of age, weighting 134.5 lb, was diagnosed with tinea pedis, myocardial infarction, hypercholesterolaemia and was treated with TERBINAFINE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, glomerular filtration rate decreased, renal impairment, . TERBINAFINE dosage: 250 MG, QD. During the same period patient was treated with ASPIRIN, ATENOLOL, ATORVASTATIN CALCIUM, LOSARTAN POTASSIUM. Patient recovered.
Terbinafine Side Effects Report #5663793-1
TERBINAFINE problem was reported by a Health Professional from UNITED KINGDOM on Mar 03, 2008. Female patient was diagnosed with tinea pedis, myocardial infarction, hypercholesterolaemia and was treated with TERBINAFINE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, glomerular filtration rate decreased, renal impairment, . TERBINAFINE dosage: 250 MG, QD. During the same period patient was treated with DISPERSIBLE ASPIRIN, ATENOLOL BP, ATORVASTATIN CALCIUM, LOSARTAN POTASSIUM. Patient recovered.
Vesicare Side Effects Report #5663859-6
Physician from JAPAN reported VESICARE problem on Feb 25, 2008. Female patient, 74 years of age, weighting 136.7 lb, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, cerebral infarction, disease progression, renal impairment, . VESICARE dosage: 5 MG, UID/QD, ORAL. During the same period patient was treated with ACECOL, GLIMICRON, PRAVASTATIN, GASTER D ORODISPERSIBLE CRLET, ISOSORBIDE MONONITRATE, PANALDINE, CONIEL, SIGMART. Patient recovered.
Terbinafine Side Effects Report #5663961-9
TERBINAFINE problem was reported by a Health Professional from UNITED KINGDOM on Mar 03, 2008. Female patient, 65 years of age, weighting 134.5 lb, was diagnosed with tinea pedis and was treated with TERBINAFINE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, glomerular filtration rate decreased, renal impairment, . TERBINAFINE dosage: unknown. Patient recovered.
Lyrica Side Effects Report #5664994-9
Consumer or non-health professional from UNITED STATES reported LYRICA problem on Mar 03, 2008. Male patient, weighting 215.5 lb, was diagnosed with neuralgia and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: blood urea increased, dehydration, diarrhoea, dry mouth, feeling abnormal, increased appetite, monoplegia, oedema peripheral, . LYRICA dosage: unknown. During the same period patient was treated with INSULIN, LIPITOR, AVODART. Patient was hospitalized. Patient recovered.
Rocaltrol Side Effects Report #5669718-7
ROCALTROL problem was reported by a Consumer or non-health professional from BRAZIL on Mar 07, 2008. Female patient, 92 years of age, weighting 132.3 lb, was diagnosed with osteoporosis, mineral supplementation, depression, cardiomegaly, chronic obstructive pulmonary disease and was treated with ROCALTROL. After drug was administered, patient experienced the following problems/side effects: blood urea increased, cardiovascular insufficiency, dementia alzheimer's type, dry mouth, eating disorder, pneumonia, sinusitis, tongue disorder, . ROCALTROL dosage: unknown. During the same period patient was treated with CALTRATE, DAFLON, ASCORBIC ACID, CLORANA, SERTRALINE HYDROCHLORIDE, DIGOXIN, FORASEQ. Patient was hospitalized. Patient recovered.
Velcade Side Effects Report #5677804-0
Physician from JAPAN reported VELCADE problem on Mar 04, 2008. Male patient, 57 years of age, weighting 114.6 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, bone marrow failure, condition aggravated, diarrhoea, disease complication, faeces discoloured, gastritis erosive, gastritis haemorrhagic, haemoglobin decreased, . VELCADE dosage: 2.00 MG, INTRAVENOUS; 1.50 MG, INTRAVENOUS; 2.00 MG. During the same period patient was treated with ACYCLOVIR, ALLOPURINOL, PETROLATUM OINTEMENT, VIDARABINE, ALPROSTADIL, ZOMETA. Patient was hospitalized. Patient recovered.
Idursulfase Side Effects Report #5678103-3
IDURSULFASE problem was reported by a Physician from JAPAN on Mar 05, 2008. Male patient, 21 years of age, weighting 48.50 lb, was diagnosed with mucopolysaccharidosis ii and was treated with IDURSULFASE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, cardiac failure, hepatic enzyme increased, pulmonary congestion, respiratory failure, urine output decreased, white blood cell count increased, . IDURSULFASE dosage: 12 MG, 1X/WEEK, IV DRIP. During the same period patient was treated with CARBOCISTEINE, CLARITHROMYCIN. Patient died on 02/15/2008.
Alendronic Side Effects Report #5678793-5
Consumer or non-health professional from BELGIUM reported ALENDRONIC ACID problem on Mar 13, 2008. Female patient, 82 years of age, was diagnosed with bone density decreased, atrial fibrillation, temporal arteritis and was treated with ALENDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: blood urea increased, bone density decreased, calciphylaxis, cyanosis, decreased appetite, ecchymosis, fatigue, protein s decreased, skin necrosis, . ALENDRONIC ACID dosage: 70 MG/WEEK. During the same period patient was treated with PHENPROCOUMON, METHYLPREDNISOLONE, VIGTAMIN D SUPPLEMENTS, CALCIUM SUPPLEMENTS, FUROSEMIDE, LISINOPRIL. Patient died.
Renagel Side Effects Report #5625170-9
RENAGEL problem was reported by a Consumer or non-health professional from TAIWAN, PROVINCE OF CHINA on Feb 01, 2008. Male patient, 73 years of age, was diagnosed with hyperphosphataemia and was treated with RENAGEL. After drug was administered, patient experienced the following problems/side effects: blood urea increased, hepatic cirrhosis, hepatic neoplasm malignant recurrent, . RENAGEL dosage: unknown. During the same period patient was treated with DIOVAN, BETALOC SA, CEREMIN. Patient was hospitalized. Patient recovered.
Atenolol Side Effects Report #5643766-5
Consumer or non-health professional from UNITED STATES reported ATENOLOL problem on Feb 06, 2008. Male patient, 44 years of age, weighting 180.0 lb, was diagnosed with mitral valve prolapse and was treated with ATENOLOL. After drug was administered, patient experienced the following problems/side effects: blood urea increased, homicidal ideation, suicidal ideation, . ATENOLOL dosage: 25 MG; DAILY; ORAL. During the same period patient was treated with XANAX. Patient recovered.
Diovan Side Effects Report #5662193-8
DIOVAN problem was reported by a Physician from UNITED STATES on Dec 03, 2007. Female patient, 74 years of age, was diagnosed with hypertension and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: blood urea increased, creatinine renal clearance increased, renal failure, . DIOVAN dosage: 160 MG, QD, ORAL. During the same period patient was treated with TRIAMTERENE AND HYDROCHLOROTHIAZID, ASPIRIN. Patient was hospitalized. Patient recovered.
Rocaltrol Side Effects Report #5581316-2
Consumer or non-health professional from BRAZIL reported ROCALTROL problem on Dec 27, 2007. Female patient, 92 years of age, weighting 132.3 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with ROCALTROL. After drug was administered, patient experienced the following problems/side effects: blood urea increased, cardiovascular insufficiency, dementia alzheimer's type, dry mouth, eating disorder, pneumonia, sinusitis, tongue disorder, . ROCALTROL dosage: unknown. During the same period patient was treated with CALTRATE, DAFLON, ASCORBIC ACID, CLORANA, SERTRALINE HYDROCHLORIDE, DIGOXIN, FORASEQ. Patient was hospitalized. Patient recovered.
Diovan Side Effects Report #5594302-3
DIOVAN HCT problem was reported by a Physician from UNITED STATES on Jan 09, 2008. Male patient, 80 years of age, was treated with DIOVAN HCT. After drug was administered, patient experienced the following problems/side effects: blood urea increased, diabetes mellitus, hyperkalaemia, . DIOVAN HCT dosage: unknown. Patient recovered.
Scope Side Effects Report #5603856-X
Consumer or non-health professional from UNITED STATES reported SCOPE problem on Jan 09, 2008. Male patient, 67 years of age, was treated with SCOPE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, malignant melanoma, oral disorder, . SCOPE dosage: unknown. Patient recovered.
Miralax Side Effects Report #5614658-2
MIRALAX problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 16, 2008. Female patient was treated with MIRALAX. After drug was administered, patient experienced the following problems/side effects: blood urea increased, . MIRALAX dosage: unknown. Patient recovered.
Immucyst Side Effects Report #5562983-6
Health Professional from JAPAN reported IMMUCYST problem on Dec 05, 2007. Male patient, 76 years of age, was diagnosed with bladder cancer and was treated with IMMUCYST. After drug was administered, patient experienced the following problems/side effects: blood urea increased, prostatitis, pyelonephritis, white blood cell count increased, . IMMUCYST dosage: unknown. During the same period patient was treated with SILODOSIN, DISTIGMINE BROMIDE, MITOMYCIN. Patient was hospitalized. Patient recovered.
Immucyst Side Effects Report #5564796-8
IMMUCYST problem was reported by a Health Professional from JAPAN on Dec 05, 2007. Male patient, 76 years of age, was diagnosed with bladder cancer and was treated with IMMUCYST. After drug was administered, patient experienced the following problems/side effects: blood urea increased, prostatitis, pyelonephritis, white blood cell count increased, . IMMUCYST dosage: unknown. During the same period patient was treated with SILODOSIN, DISTIGMINE BROMIDE, MITOMYCIN. Patient was hospitalized. Patient recovered.
Exjade Side Effects Report #5504847-X
Physician from UNITED KINGDOM reported EXJADE problem on Oct 25, 2007. Male patient, child 10 years of age, weighting 66.14 lb, was diagnosed with iron overload and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, serum ferritin increased, . EXJADE dosage: 750MG/DAY. Patient recovered.
Tamsulosin Side Effects Report #5505805-1
TAMSULOSIN problem was reported by a Physician from JAPAN on Oct 26, 2007. Male patient, 85 years of age, was diagnosed with benign prostatic hyperplasia, hypertonic bladder and was treated with TAMSULOSIN. After drug was administered, patient experienced the following problems/side effects: blood urea increased, . TAMSULOSIN dosage: unknown. During the same period patient was treated with VESICARE, ARTIST, LASIX, ALDACTONE, ENALAPRIL MALEATE, AMIODARONE, LOCOL. Patient recovered.
Forteo Side Effects Report #5510205-4
Physician from UNITED STATES reported FORTEO problem on Oct 29, 2007. Female patient, weighting 208.0 lb, was diagnosed with osteoporosis, hypersensitivity and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: blood urea increased, renal impairment, . FORTEO dosage: unknown. During the same period patient was treated with COUMADIN, RYTHMOL, LISINOPRIL, LIPITOR, CLARITIN, GLUCOSAMINE, FISH OIL, CENTRUM SILVER. Patient recovered.
Vesicare Side Effects Report #5511271-2
VESICARE problem was reported by a Physician from JAPAN on Oct 26, 2007. Male patient, 85 years of age, was diagnosed with hypertonic bladder, benign prostatic hyperplasia and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, . VESICARE dosage: 5 MG, /D, ORAL. During the same period patient was treated with TAMSULOSIN, ARTIST, LASIX, ALDACTONE PER ORAL NOS, RENIVACE, ANCARON, LOCOL PER ORAL NOS. Patient recovered.
Escitalopram Side Effects Report #5512334-8
Health Professional from FRANCE reported ESCITALOPRAM problem on Oct 23, 2007. Female patient, 93 years of age, was diagnosed with transient ischaemic attack and was treated with ESCITALOPRAM. After drug was administered, patient experienced the following problems/side effects: blood urea increased, haematoma, haemorrhagic stroke, hyperkalaemia, hyperthermia, hyponatraemia, increased bronchial secretion, intraventricular haemorrhage, meningorrhagia, . ESCITALOPRAM dosage: 10 MG QD PO. During the same period patient was treated with KARDEGIC, ZALDIAR, ACETAMINOPHEN, MOVICOL, DENSICAL D. Patient died on 06/22/2007.
Humalog Side Effects Report #5521740-7
HUMALOG problem was reported by a Consumer or non-health professional from TURKEY on Nov 05, 2007. Male patient, 52 years of age, weighting 187.4 lb, was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: blood urea increased, kidney infection, . HUMALOG dosage: unknown. Patient recovered.
Xopenex Side Effects Report #5528003-4
Physician from UNITED STATES reported XOPENEX HFA problem on Nov 13, 2007. Male patient, 57 years of age, weighting 309.7 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with XOPENEX HFA. After drug was administered, patient experienced the following problems/side effects: blood urea increased, hypokalaemia, hypomagnesaemia, leukocytosis, neutrophil percentage decreased, . XOPENEX HFA dosage: unknown. During the same period patient was treated with VALIUM, ASPIRIN, NEXIUM, ATORVASTATIN CALCIUM, ZANAFLEX, ALLOPURINOL, LORTAB. Patient was hospitalized. Patient recovered.
Januvia Side Effects Report #5533101-5
JANUVIA problem was reported by a Physician from UNITED STATES on July 31, 2007. Male patient, 68 years of age, weighting 205.0 lb, was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: blood urea increased, . JANUVIA dosage: PO ; 50 MG/DAILY/PO. During the same period patient was treated with LASIX. Patient recovered.
Xopenex Side Effects Report #5475336-6
Physician from UNITED STATES reported XOPENEX HFA problem on Sept 18, 2007. Male patient, 57 years of age, weighting 309.7 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with XOPENEX HFA. After drug was administered, patient experienced the following problems/side effects: blood urea increased, condition aggravated, hypokalaemia, hypomagnesaemia, leukocytosis, neutrophil percentage decreased, oedema peripheral, . XOPENEX HFA dosage: unknown. During the same period patient was treated with VALIUM, ASPIRIN, NEXIUM, ATORVASTATIN CALCIUM, ZANAFLEX, ALLOPURINOL, LORTAB. Patient was hospitalized. Patient recovered.
Olmesartan Side Effects Report #5477562-9
OLMESARTAN MEDOXOMIL problem was reported by a Consumer or non-health professional from FRANCE on Sept 18, 2007. Female patient, 93 years of age, was diagnosed with hypertension, dementia alzheimer's type and was treated with OLMESARTAN MEDOXOMIL. After drug was administered, patient experienced the following problems/side effects: blood urea increased, dehydration, hypernatraemia, oral intake reduced, somnolence, . OLMESARTAN MEDOXOMIL dosage: 20 MG (20 MG,1 IN 1 D), ORAL. During the same period patient was treated with RISPERDAL, KARDEGIC. Patient was hospitalized. Patient died on 08/02/2007.
Klaricid Side Effects Report #5482306-0
Physician from JAPAN reported KLARICID problem on Oct 03, 2007. Male patient was diagnosed with pneumonia, gastritis, constipation and was treated with KLARICID. After drug was administered, patient experienced the following problems/side effects: blood urea increased, urine output decreased, . KLARICID dosage: unknown. During the same period patient was treated with AZULENE SULFONATE, FAMOTIDINE, MAGNESIUM OXIDE, DAIKEN, SULPERAZON. Patient was hospitalized. Patient recovered.
Temodal Side Effects Report #5483215-3
TEMODAL problem was reported by a Physician from JAPAN on Oct 03, 2007. Male patient, child 6 years of age, weighting 35.27 lb, was diagnosed with brain neoplasm and was treated with TEMODAL. After drug was administered, patient experienced the following problems/side effects: blood urea increased, bone marrow failure, hypernatraemia, infection, lymphocyte count decreased, neoplasm progression, neutrophil count decreased, platelet count decreased, pneumonia bacterial, . TEMODAL dosage: 75 MG/M2; QD; PO. During the same period patient was treated with VEPESID, BAKTAR, LASTET S, NASEA, PRIMPERAN, DECADRON, MANNITOL, BUPRENORPHINE. Patient died on 10/26/2006.
Temodal Side Effects Report #5483255-4
Physician from JAPAN reported TEMODAL problem on Oct 01, 2007. Male patient, 77 years of age, weighting 165.3 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAL. After drug was administered, patient experienced the following problems/side effects: blood urea increased, c-reactive protein increased, platelet count decreased, red blood cell count decreased, sepsis, white blood cell count decreased, . TEMODAL dosage: 75 MG/M2; QD; PO. During the same period patient was treated with FERON, MUCOSTA, FAMOTIDINE, PRAVASTATIN, AMLODIPINE, EXCEGRAN, GLYCYRON. Patient died on 01/30/2007.
Exjade Side Effects Report #5483289-X
EXJADE problem was reported by a Physician from UNITED KINGDOM on Oct 04, 2007. Male patient was diagnosed with thalassaemia and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, serum ferritin increased, . EXJADE dosage: 30MG/KG. Patient recovered.
Feldene Side Effects Report #5485194-1
Health Professional from UNITED STATES reported FELDENE problem on Oct 10, 2007. Male patient, 97 years of age, weighting 180.0 lb, was diagnosed with osteoarthritis and was treated with FELDENE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, cardiac failure congestive, peptic ulcer haemorrhage, . FELDENE dosage: unknown. Patient was hospitalized. Patient recovered.
Tekturna Side Effects Report #5489103-0
TEKTURNA problem was reported by a Health Professional from UNITED STATES on Aug 28, 2007. Male patient was diagnosed with hypertension and was treated with TEKTURNA. After drug was administered, patient experienced the following problems/side effects: blood urea increased, creatinine renal clearance increased, . TEKTURNA dosage: unknown. Patient recovered.
Klaricid Side Effects Report #5491173-0
Physician from JAPAN reported KLARICID problem on Oct 12, 2007. Male patient was diagnosed with pneumonia, gastritis, constipation and was treated with KLARICID. After drug was administered, patient experienced the following problems/side effects: blood urea increased, urine output decreased, . KLARICID dosage: unknown. During the same period patient was treated with AZULENE SULFONATE, FAMOTIDINE, MAGNESIUM OXIDE, DAIKEN, SULPERAZON. Patient was hospitalized. Patient recovered.
Stalevo Side Effects Report #5500173-3
STALEVO problem was reported by a Consumer or non-health professional from GERMANY on Sept 27, 2007. Male patient, 74 years of age, was diagnosed with parkinson's disease and was treated with STALEVO. After drug was administered, patient experienced the following problems/side effects: blood urea increased, condition aggravated, parkinson's disease, psychotic disorder, red blood cell count decreased, rhabdomyolysis, . STALEVO dosage: 600 MG (150 MG,4 IN 1 D) ORAL. During the same period patient was treated with SEROQUEL. Patient was hospitalized. Patient recovered.
Immucyst Side Effects Report #5502568-0
Health Professional from JAPAN reported IMMUCYST problem on Oct 29, 2007. Male patient, 76 years of age, was diagnosed with bladder cancer and was treated with IMMUCYST. After drug was administered, patient experienced the following problems/side effects: blood urea increased, prostatitis, pyelonephritis, white blood cell count increased, . IMMUCYST dosage: unknown. During the same period patient was treated with MITOMYCIN. Patient was hospitalized. Patient recovered.
Requip Side Effects Report #5444727-1
REQUIP problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 19, 2007. Male patient was diagnosed with restless legs syndrome and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: blood urea increased, . REQUIP dosage: 2MG PER DAY. Patient recovered.
Mylotarg Side Effects Report #5451515-9
Physician from JAPAN reported MYLOTARG problem on Sept 04, 2007. Male patient, weighting 132.3 lb, was diagnosed with acute myeloid leukaemia, prophylaxis and was treated with MYLOTARG. After drug was administered, patient experienced the following problems/side effects: blood urea increased, cerebral haemorrhage, condition aggravated, disseminated intravascular coagulation, febrile neutropenia, hypernatraemia, pneumonia, renal impairment, . MYLOTARG dosage: unknown. During the same period patient was treated with MAGNESIUM OXIDE, ROXATIDINE ACETATE, GLUCOSEECTION, DIFLUCAN, VITAMEDIN, SOLDEM, STRONG NEO MINOPHAGEN C. Patient was hospitalized. Patient died on 02/23/2007.
Memantine Side Effects Report #5466864-8
MEMANTINE problem was reported by a Health Professional from FRANCE on Aug 13, 2007. Male patient, 85 years of age, was treated with MEMANTINE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, cerebral atrophy, dehydration, rhabdomyolysis, . MEMANTINE dosage: 10 MG BID PO. During the same period patient was treated with GALANTAMINE HYDROBROMIDE, RISPERDAL. Patient was hospitalized. Patient recovered.
Amlodipine Side Effects Report #5406975-6
Consumer or non-health professional from TURKEY reported AMLODIPINE problem on July 04, 2007. Female patient, 77 years of age, was diagnosed with essential hypertension and was treated with AMLODIPINE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, respiratory rate increased, . AMLODIPINE dosage: 10 MG (10 MG, 1 IN 1 D). Patient was hospitalized. Patient recovered.
Avonex Side Effects Report #5410325-9
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on July 30, 2007. Female patient, 57 years of age, weighting 140.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood urea increased, cardiac disorder, diabetes mellitus, fatigue, hypertension, hypoacusis, injection site bruising, lung neoplasm, trigeminal neuralgia, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Lithium Side Effects Report #5411530-8
Consumer or non-health professional from reported LITHIUM CARBONATE problem on Aug 06, 2007. Female patient, 16 years of age, was diagnosed with mania, major depression and was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, catatonia, dehydration, mania, therapeutic agent toxicity, white blood cell count increased, . LITHIUM CARBONATE dosage: unknown. During the same period patient was treated with OLANZAPINE, ESCITALOPRAM. Patient was hospitalized. Patient recovered.
Gleevec Side Effects Report #5416340-3
GLEEVEC problem was reported by a Physician from UNITED STATES on Aug 09, 2007. Male patient, 71 years of age, was diagnosed with gastrointestinal stromal tumour and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: blood urea increased, creatinine renal clearance decreased, tumour lysis syndrome, . GLEEVEC dosage: 400 MG, QD. Patient was hospitalized. Patient recovered.
Lithium Side Effects Report #5423141-9
Consumer or non-health professional from INDIA reported LITHIUM CARBONATE problem on Aug 08, 2007. Female patient, 16 years of age, was diagnosed with major depression and was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: blood urea increased, catatonia, decreased appetite, dehydration, diet refusal, hyperreflexia, immobile, mutism, negativism, . LITHIUM CARBONATE dosage: unknown. During the same period patient was treated with OLANZAPINE. Patient was hospitalized. Patient recovered.
Olmesartan Side Effects Report #5424326-8
OLMESARTAN MEDOXOMIL problem was reported by a Consumer or non-health professional from FRANCE on Aug 10, 2007. Female patient, 93 years of age, was diagnosed with hypertension, dementia alzheimer's type and was treated with OLMESARTAN MEDOXOMIL. After drug was administered, patient experienced the following problems/side effects: blood urea increased, creatine urine increased, dehydration, hypernatraemia, oral intake reduced, somnolence, . OLMESARTAN MEDOXOMIL dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with RISPERDAL, KARDEGIC. Patient was hospitalized. Patient recovered.
Natalizumab Side Effects Report #5424464-X
Physician from GERMANY reported NATALIZUMAB problem on Aug 10, 2007. Female patient, 53 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: blood urea increased, haemoglobin decreased, herpes zoster, hypertension, monocyte percentage increased, neutrophil percentage decreased, red blood cell count decreased, . NATALIZUMAB dosage: 300 MG; QM; IV. During the same period patient was treated with CORTISONE ACETATE, BETAFERON, MITOXANTRONE, ENDOXAN. Patient was hospitalized. Patient recovered.