BLOOD URIC ACID INCREASED side effect
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Drugs associated with BLOOD URIC ACID INCREASED
ADDERALL ALTACE ARAVA ARCALION AVANDIA AVASTIN AVONEX BASOFORTINA BYETTA CADUET CEREZYME CITRUCEL CLOLAR COREG COZAAR CRESTOR CYCLOPHOSPHAMIDE CYCLOSPORINE DIOVAN DIPRIVAN EFAVIRENZ ELITEK ENALAPRIL EXEMESTANE FLUOROURACIL FORASEQ FORTEO HYZAAR INTRON INVEGA IRESSA KALETRA LIPITOR METHOTREXATE MIACALCIN MYLOTARG NEUPOGEN NEXAVAR NIACIN PEGETRON PHENTERMINE PROPECIA QUINAPRIL RASILEZ REBETOL REMICADE REVLIMID STOCRIN SUTENT TEKTURNA TRUVADA VELCADE VESICARE XELODA ZOLADEX ZOLEDRONICPropecia Side Effects Report #5689578-8
Physician from JAPAN reported PROPECIA problem on Mar 21, 2008. Male patient, 33 years of age, was diagnosed with androgenetic alopecia and was treated with PROPECIA. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, carcinoembryonic antigen increased, . PROPECIA dosage: unknown. Patient recovered.
Invega Side Effects Report #5583821-1
INVEGA problem was reported by a Physician from GERMANY on Jan 02, 2008. Female patient, 40 years of age, was treated with INVEGA. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, . INVEGA dosage: unknown. Patient recovered.
Cerezyme Side Effects Report #5591420-0
Physician from UNITED STATES reported CEREZYME problem on Jan 07, 2008. Female patient, 70 years of age, weighting 194.0 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, carotid artery occlusion, . CEREZYME dosage: unknown. Patient recovered.
Cyclosporine Side Effects Report #5595588-1
CYCLOSPORINE problem was reported by a Health Professional from CROATIA (local name: Hrvatska) on Jan 09, 2008. Male patient, 68 years of age, was diagnosed with liver transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, c-reactive protein increased, calculus urinary, crystal urine present, hydronephrosis, nephrostomy, renal colic, stent placement, . CYCLOSPORINE dosage: 100 MG, BID. Patient was hospitalized. Patient recovered.
Invega Side Effects Report #5602385-7
Physician from GERMANY reported INVEGA problem on Jan 18, 2008. Female patient, weighting 207.2 lb, was diagnosed with schizophrenia and was treated with INVEGA. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, . INVEGA dosage: unknown. Patient recovered.
Kaletra Side Effects Report #5558589-5
KALETRA problem was reported by a Consumer or non-health professional from SERBIA on Dec 10, 2007. Male patient, 41 years of age, weighting 165.3 lb, was diagnosed with hiv infection, non-hodgkin's lymphoma and was treated with KALETRA. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, myalgia, non-hodgkin's lymphoma, pain, . KALETRA dosage: 133.3/33.3 MG. During the same period patient was treated with RITUXIMAB. Patient died on 06/28/2007.
Citrucel Side Effects Report #5562990-3
Consumer or non-health professional from UNITED STATES reported CITRUCEL CAPLETS problem on Dec 14, 2007. Male patient, 57 years of age, was treated with CITRUCEL CAPLETS. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, nephrolithiasis, ph urine decreased, . CITRUCEL CAPLETS dosage: unknown. Patient recovered.
Citrucel Side Effects Report #5563089-2
CITRUCEL CAPLETS problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 14, 2007. Male patient, 57 years of age, was treated with CITRUCEL CAPLETS. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, nephrolithiasis, ph urine decreased, . CITRUCEL CAPLETS dosage: unknown. Patient recovered.
Stocrin Side Effects Report #5566237-3
Health Professional from UNITED STATES reported STOCRIN CAPS problem on Dec 12, 2007. Male patient, 48 years of age, was diagnosed with acquired immunodeficiency syndrome and was treated with STOCRIN CAPS. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, cholelithiasis, dizziness, haemoglobin decreased, hepatic function abnormal, hyperlactacidaemia, . STOCRIN CAPS dosage: unknown. During the same period patient was treated with ZERIT, EPIVIR, COMBIVIR, DEPAKENE, LASIX, ZIDOVUDINE, ABACAVIR. Patient was hospitalized. Patient recovered.
Stocrin Side Effects Report #5576937-7
STOCRIN CAPS problem was reported by a Health Professional from UNITED STATES on Dec 12, 2007. Male patient, 48 years of age, was diagnosed with acquired immunodeficiency syndrome and was treated with STOCRIN CAPS. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, cholelithiasis, dizziness, haemoglobin decreased, hepatic function abnormal, hyperlactacidaemia, . STOCRIN CAPS dosage: unknown. During the same period patient was treated with ZERIT, EPIVIR, COMBIVIR, DEPAKENE, LASIX, ZIDOVUDINE, ABACAVIR. Patient was hospitalized. Patient recovered.
Coreg Side Effects Report #5515561-9
Health Professional from UNITED STATES reported COREG problem on June 05, 2007. Female patient, 66 years of age, was diagnosed with hypertension, tuberculosis and was treated with COREG. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, haematocrit decreased, haemoglobin decreased, hepatic enzyme increased, . COREG dosage: 25MG TWICE PER DAY. During the same period patient was treated with RIFAMPIN, MIDODRINE, ASPIRIN, LASIX, ALLEGRA. Patient recovered.
Intron Side Effects Report #5522138-8
INTRON A problem was reported by a Physician from GERMANY on Nov 07, 2007. Male patient, 51 years of age, weighting 257.9 lb, was diagnosed with metastatic malignant melanoma and was treated with INTRON A. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, nephrolithiasis, . INTRON A dosage: unknown. During the same period patient was treated with INTRON A, METOPROLOL. Patient was hospitalized. Patient recovered.
Fluorouracil Side Effects Report #5523049-4
Consumer or non-health professional from UNITED STATES reported FLUOROURACIL problem on Nov 19, 2007. Male patient, weighting 240.5 lb, was treated with FLUOROURACIL. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, diarrhoea, . FLUOROURACIL dosage: 20880 MG. During the same period patient was treated with BEVACIZUMAB, CAMPTOSAR, LEUCOVORIN CALCIUM. Patient was hospitalized. Patient recovered.
Byetta Side Effects Report #5582153-5
BYETTA problem was reported by a Physician from UNITED STATES on Aug 09, 2007. Female patient was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, pain, pain in extremity, . BYETTA dosage: unknown. Patient recovered.
Forteo Side Effects Report #5475199-9
Consumer or non-health professional from UNITED STATES reported FORTEO problem on Sept 21, 2007. Female patient, 72 years of age, was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, fall, hypoaesthesia, pain in extremity, pelvic fracture, . FORTEO dosage: unknown. During the same period patient was treated with AMBIEN, DIURETICS. Patient recovered.
Avastin Side Effects Report #5476190-9
AVASTIN problem was reported by a Physician from UNITED KINGDOM on Sept 18, 2007. Male patient, weighting 218.3 lb, was diagnosed with colon cancer and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, disease progression, insomnia, tachycardia, . AVASTIN dosage: unknown. During the same period patient was treated with FLUOROURACIL, FOLINIC ACID, TRAMADOL, ESTAZOLAM, MILURIT, KETONAL. Patient died on 09/12/2007.
Avastin Side Effects Report #5489439-3
Physician from UNITED KINGDOM reported AVASTIN problem on Oct 04, 2007. Male patient, weighting 218.3 lb, was diagnosed with colon cancer and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, disease progression, insomnia, tachycardia, . AVASTIN dosage: unknown. During the same period patient was treated with FLUOROURACIL, FOLINIC ACID, TRAMADOL, ESTAZOLAM, MILURIT, KETONAL. Patient died on 09/12/2007.
Zoladex Side Effects Report #5494624-0
ZOLADEX problem was reported by a Consumer or non-health professional from BRAZIL on Oct 18, 2007. Male patient, 88 years of age, weighting 180.8 lb, was diagnosed with prostate cancer, gout, dyspepsia, hypertension and was treated with ZOLADEX. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, dysuria, obstruction, oedema peripheral, urine colour abnormal, . ZOLADEX dosage: unknown. During the same period patient was treated with DICLOFENAC, ZYLORIC, OMEPRAZOLE, MODURETIC. Patient was hospitalized. Patient recovered.
Intron Side Effects Report #5500190-3
Physician from GERMANY reported INTRON A problem on Sept 25, 2007. Male patient, 51 years of age, weighting 257.9 lb, was diagnosed with metastatic malignant melanoma and was treated with INTRON A. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, nephrolithiasis, . INTRON A dosage: unknown. During the same period patient was treated with METOPROLOL. Patient was hospitalized. Patient recovered.
Propecia Side Effects Report #5446417-8
PROPECIA problem was reported by a Physician from JAPAN on Sept 03, 2007. Male patient, 24 years of age, was diagnosed with male pattern baldness and was treated with PROPECIA. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, hepatic function abnormal, . PROPECIA dosage: unknown. Patient recovered.
Efavirenz Side Effects Report #5408234-4
Health Professional from UNITED STATES reported EFAVIRENZ problem on July 27, 2007. Male patient, 36 years of age, was diagnosed with hiv infection and was treated with EFAVIRENZ. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, cholecystitis acute, cholelithiasis, convulsion, gait disturbance, neurogenic bladder, nightmare, pyelonephritis, pyrexia, . EFAVIRENZ dosage: unknown. During the same period patient was treated with VIDEX EC, VIDEX EC, ZIAGEN, EPIVIR, ZERIT, VIRACEPT, EXCEGRAN, PHENOBARBITAL. Patient was hospitalized. Patient recovered.
Cerezyme Side Effects Report #5425844-9
CEREZYME problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 15, 2007. Female patient, 70 years of age, weighting 194.0 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, carotid artery occlusion, . CEREZYME dosage: unknown. Patient recovered.
Propecia Side Effects Report #5377316-8
Physician from JAPAN reported PROPECIA problem on June 18, 2007. Male patient, 24 years of age, was diagnosed with male pattern baldness and was treated with PROPECIA. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, hepatic function abnormal, . PROPECIA dosage: unknown. Patient recovered.
Efavirenz Side Effects Report #5384154-9
EFAVIRENZ problem was reported by a Health Professional from UNITED STATES on June 20, 2007. Male patient, 36 years of age, was diagnosed with hiv infection and was treated with EFAVIRENZ. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, cholecystitis acute, cholelithiasis, convulsion, gait disturbance, neurogenic bladder, nightmare, pyelonephritis, pyrexia, . EFAVIRENZ dosage: unknown. During the same period patient was treated with VIDEX EC, VIDEX EC, ZIAGEN, EPIVIR, ZERIT, VIRACEPT, EXCEGRAN, PHENOBARBITAL. Patient was hospitalized. Patient recovered.
Diovan Side Effects Report #5397410-5
Consumer or non-health professional from UNITED STATES reported DIOVAN problem on July 21, 2007. Female patient was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, gout, . DIOVAN dosage: unknown. Patient recovered.
Propecia Side Effects Report #5377316-8
PROPECIA problem was reported by a Physician from JAPAN on June 18, 2007. Male patient, 24 years of age, was diagnosed with male pattern baldness and was treated with PROPECIA. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, hepatic function abnormal, . PROPECIA dosage: unknown. Patient recovered.
Efavirenz Side Effects Report #5384154-9
Health Professional from UNITED STATES reported EFAVIRENZ problem on June 20, 2007. Male patient, 36 years of age, was diagnosed with hiv infection and was treated with EFAVIRENZ. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, cholecystitis acute, cholelithiasis, convulsion, gait disturbance, neurogenic bladder, nightmare, pyelonephritis, pyrexia, . EFAVIRENZ dosage: unknown. During the same period patient was treated with VIDEX EC, VIDEX EC, ZIAGEN, EPIVIR, ZERIT, VIRACEPT, EXCEGRAN, PHENOBARBITAL. Patient was hospitalized. Patient recovered.
Diovan Side Effects Report #5397410-5
DIOVAN problem was reported by a Consumer or non-health professional from UNITED STATES on July 21, 2007. Female patient was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, gout, . DIOVAN dosage: unknown. Patient recovered.
Propecia Side Effects Report #5759932-4
Physician from JAPAN reported PROPECIA problem on May 29, 2008. Male patient, 33 years of age, was diagnosed with androgenetic alopecia and was treated with PROPECIA. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, carcinoembryonic antigen increased, . PROPECIA dosage: unknown. Patient recovered.
Quinapril Side Effects Report #5763172-2
QUINAPRIL AND HYDROCHLOROTHIAZIDE problem was reported by a Physician from ALGERIA on June 02, 2008. Female patient, 55 years of age, was diagnosed with hypertension and was treated with QUINAPRIL AND HYDROCHLOROTHIAZIDE. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, swelling, . QUINAPRIL AND HYDROCHLOROTHIAZIDE dosage: TEXT:20MG/12.5MG DAILY. Patient recovered.
Tekturna Side Effects Report #5763192-8
Consumer or non-health professional from UNITED STATES reported TEKTURNA problem on Jan 25, 2008. Female patient was diagnosed with hypertension and was treated with TEKTURNA. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, gout, . TEKTURNA dosage: 150 MG. Patient recovered.
Quinapril Side Effects Report #5774442-6
QUINAPRIL AND HYDROCHLOROTHIAZIDE problem was reported by a Physician from ALGERIA on June 07, 2008. Female patient, 55 years of age, was diagnosed with hypertension and was treated with QUINAPRIL AND HYDROCHLOROTHIAZIDE. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, swelling, . QUINAPRIL AND HYDROCHLOROTHIAZIDE dosage: TEXT:20MG/12.5MG-FREQ:FREQUENCY: DAILY. Patient recovered.
Clolar Side Effects Report #5733313-1
Physician from UNITED STATES reported CLOLAR problem on Apr 28, 2008. Male patient, 60 years of age, weighting 197.3 lb, was diagnosed with myelodysplastic syndrome and was treated with CLOLAR. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, diarrhoea, liver function test abnormal, oedema, pericardial effusion, rash, . CLOLAR dosage: 40 MG/M2, QDX5, INTRAVENOUS. During the same period patient was treated with CYTARABINE, THYMOGLOBULIN, NORVASC, CEFEPIME, NEXIUM, FLUCONAZOLE, FLONASE. Patient recovered.
Clolar Side Effects Report #5734935-4
CLOLAR problem was reported by a Physician from UNITED STATES on May 02, 2008. Male patient, 60 years of age, weighting 197.3 lb, was diagnosed with myelodysplastic syndrome and was treated with CLOLAR. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, bone marrow transplant, chest pain, diarrhoea, dilatation ventricular, dyspnoea, ebstein's anomaly, liver function test abnormal, oedema, . CLOLAR dosage: 40 MG/M2, QDX5, INTRAVENOUS. During the same period patient was treated with CYTARABINE, THYMOGLOBULINE, NORVASC, CEFEPIME, NEXIUM, FLUCONAZOLE, FLONASE, COMPAZINE. Patient was hospitalized. Patient recovered.
Elitek Side Effects Report #5695736-9
Pharmacist from UNITED STATES reported ELITEK problem on Mar 27, 2008. Female patient was treated with ELITEK. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, tumour lysis syndrome, . ELITEK dosage: unknown. Patient was hospitalized. Patient recovered.
Clolar Side Effects Report #5720932-1
CLOLAR problem was reported by a Physician from UNITED STATES on Apr 18, 2008. Male patient, 60 years of age, weighting 197.3 lb, was diagnosed with myelodysplastic syndrome and was treated with CLOLAR. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, diarrhoea, liver function test abnormal, oedema, pericardial effusion, rash, . CLOLAR dosage: 40 MG/M2, QDX5, INTRAVENOUS. During the same period patient was treated with CYTARABINE, THYMOGLOBULINE, FLUCONAZOLE. Patient recovered.
Propecia Side Effects Report #5374019-0
Physician from JAPAN reported PROPECIA problem on June 18, 2007. Male patient, 24 years of age, was diagnosed with male pattern baldness and was treated with PROPECIA. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, hepatic function abnormal, . PROPECIA dosage: unknown. Patient recovered.
Revlimid Side Effects Report #5324974-X
REVLIMID problem was reported by a Physician from UNITED STATES on Apr 27, 2007. Male patient, 78 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, dehydration, haemodialysis, multiple myeloma, renal disorder, renal failure acute, renal failure chronic, urate nephropathy, . REVLIMID dosage: 20 MG, 2 IN 1 D, ORAL. During the same period patient was treated with PAMIDRONATE DI, ALLOPURINOL, DECADRON, PRILOSEC, VITAMIN, ASPIRIN, PERCOCET, FENTANYL. Patient was hospitalized. Patient recovered.
Velcade Side Effects Report #5331814-1
Physician from JAPAN reported VELCADE problem on May 07, 2007. Female patient, 58 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 uric acid increased, bronchitis, diarrhoea, discomfort, haemoglobin decreased, injury asphyxiation, obstructive airways disorder, productive cough, respiratory arrest, . VELCADE dosage: 1.30 MG/M2. During the same period patient was treated with BAKTAR, MAGNESIUM OXIDE, FENTANYL, EBRANTIL, BESACOLIN, RED BLOOD CELLS, MUCOSOLVAN, ASTOMIN. Patient was hospitalized. Patient died on 02/03/2007.
Adderall Side Effects Report #5334248-9
ADDERALL problem was reported by a Consumer or non-health professional from UNITED STATES on May 07, 2007. Male patient, 31 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with ADDERALL. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, gout, hepatic steatosis, hepatomegaly, liver disorder, pain in extremity, . ADDERALL dosage: unknown. Patient recovered.
Altace Side Effects Report #5283686-1
Consumer or non-health professional from UNITED KINGDOM reported ALTACE problem on Mar 23, 2007. Female patient was diagnosed with hypertension, gout, angina pectoris and was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, gout, . ALTACE dosage: 5 MG, QD. During the same period patient was treated with ASPIRIN, DICLOFENAC, NITROLINGUAL. Patient recovered.
Neupogen Side Effects Report #5283803-3
NEUPOGEN problem was reported by a Health Professional from UNITED STATES on Mar 19, 2007. Female patient, weighting 110.0 lb, was diagnosed with neutropenia and was treated with NEUPOGEN. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, chills, cyanosis, dyspnoea, fluid overload, hyponatraemia, pyrexia, . NEUPOGEN dosage: unknown. During the same period patient was treated with ARANESP, NABUMETONE, NEXIUM, PROPOXYPHENE NAPSYLATE, PHAZYME, SINGULAIR, MINOCYCLINE, FOLIC ACID. Patient was hospitalized. Patient recovered.
Crestor Side Effects Report #5284931-9
Pharmacist from BELGIUM reported CRESTOR problem on Mar 28, 2007. Male patient, weighting 165.3 lb, was diagnosed with prophylaxis, hypertension and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, gamma-glutamyltransferase increased, . CRESTOR dosage: unknown. During the same period patient was treated with CHOLESTIN, EMCONCOR. Patient recovered.
Mylotarg Side Effects Report #5270234-5
MYLOTARG problem was reported by a Physician from JAPAN on Mar 12, 2007. Female patient, weighting 81.57 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 uric acid increased, disseminated intravascular coagulation, hypoalbuminaemia, pneumonia, renal failure, . MYLOTARG dosage: unknown. During the same period patient was treated with ISCOTIN, ISEPAMICIN SULPHATE, AMLODIN, STREPTOCOCCUS FAECALIS, FAMOTIDINE, CIPROFLOXACIN, BAKTAR. Patient was hospitalized. Patient recovered.
Efavirenz Side Effects Report #5274144-9
Health Professional from UNITED STATES reported EFAVIRENZ problem on Mar 13, 2007. Male patient, 36 years of age, was diagnosed with hiv infection and was treated with EFAVIRENZ. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, cholecystitis acute, cholelithiasis, convulsion, gait disturbance, neurogenic bladder, nightmare, pyelonephritis, pyrexia, . EFAVIRENZ dosage: unknown. During the same period patient was treated with VIDEX EC, VIDEX EC, ZIAGEN, EPIVIR, ZERIT, VIRACEPT, EXCEGRAN, PHENOBARBITAL. Patient was hospitalized. Patient recovered.
Crestor Side Effects Report #5278499-0
CRESTOR problem was reported by a Pharmacist from BELGIUM on Mar 19, 2007. Male patient, weighting 165.3 lb, was diagnosed with prophylaxis, hypertension and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: blood uric acid increased, gamma-glutamyltransferase increased, . CRESTOR dosage: unknown. During the same period patient was treated with CHOLESTIN, EMCONCOR. Patient recovered.
Remicade Side Effects Report #5670432-2
Consumer or non-health professional from UNITED STATES reported REMICADE problem on Mar 07, 2008. Male patient, weighting 175.0 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: ankle fracture, blood uric acid increased, rash, skin striae, weight increased, . REMICADE dosage: unknown. During the same period patient was treated with OXYCODONE, CLONIPINE, AMITRIPTALINE, BECLOMETHASONE DIPROPIONATE, HYDROCORTISONE, ALLEGRA, NEOSPORIN. Patient recovered.
Enalapril Side Effects Report #5679780-3
ENALAPRIL MALEATE problem was reported by a Consumer or non-health professional from TAIWAN, PROVINCE OF CHINA on Mar 06, 2008. Male patient, 66 years of age, was treated with ENALAPRIL MALEATE. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase increased, blood uric acid increased, collagen disorder, dermatitis exfoliative, granuloma, lymph node palpable, . ENALAPRIL MALEATE dosage: unknown. During the same period patient was treated with TAMSULOSIN HYDROCHLORIDE, TERAZOSIN HYDROCHLORIDE. Patient recovered.
Miacalcin Side Effects Report #5626020-7
Physician from BULGARIA reported MIACALCIN problem on Feb 04, 2008. Female patient, 63 years of age, weighting 176.4 lb, was diagnosed with osteoporosis, hypertension and was treated with MIACALCIN. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, blood uric acid increased, condition aggravated, hip fracture, renal impairment, x-ray abnormal, . MIACALCIN dosage: unknown. During the same period patient was treated with ACLASTA, ENALAPRIL MALEATE, VITAMIN D, CALCIUM. Patient recovered.
Lipitor Side Effects Report #5633349-5
LIPITOR problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 13, 2008. Female patient, weighting 130.1 lb, was diagnosed with blood cholesterol and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: blood cholesterol increased, blood uric acid increased, limb operation, . LIPITOR dosage: unknown. During the same period patient was treated with COLCHICINE, ALLOPURINOL, ACCUPRIL, PLAVIX, ASPIRIN, VITAMIN E, ESTER. Patient recovered.
Phentermine Side Effects Report #5583783-7
Consumer or non-health professional from UNITED STATES reported PHENTERMINE problem on Jan 03, 2008. Female patient, weighting 150.0 lb, was diagnosed with appetite disorder and was treated with PHENTERMINE. After drug was administered, patient experienced the following problems/side effects: alopecia, blood uric acid increased, gout, localised infection, pain in extremity, skin discolouration, toe operation, . PHENTERMINE dosage: 1/2 OF 37.5 MG ONCE A DAY PO. Patient recovered.