Menu

• Ask a Health Expert about BLOOD CREATININE ABNORMAL
• Post Your Side Effect related to BLOOD CREATININE ABNORMAL
• BLOOD CREATININE ABNORMAL and FDA Warnings
• BLOOD CREATININE ABNORMAL in Patients Wiki
• Report BLOOD CREATININE ABNORMAL in Drug Side Effect Survey

BLOOD CREATININE ABNORMAL side effect

What is BLOOD CREATININE ABNORMAL ?

A Health Expert wants to answer your question. Please provide details below.

Type your question here

 letters left

Naproxen Side Effects Report #5646887-6
Health Professional from UNITED KINGDOM reported NAPROXEN problem on Feb 14, 2008. Male patient, 81 years of age, was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, glomerular filtration rate decreased, renal impairment, . NAPROXEN dosage: 500 MG;TWICE A DAY;ORAL. During the same period patient was treated with ASPIRIN, CITALOPRAM, METFORMIN, RAMIPRIL, SIMVASTATIN. Patient was hospitalized. Patient recovered.

Teriparatide Side Effects Report #5591930-6
TERIPARATIDE problem was reported by a Physician from HONDURAS on Jan 07, 2008. Female patient, 69 years of age, was diagnosed with osteoporosis and was treated with TERIPARATIDE. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, dysgeusia, hypercalcaemia, joint injury, multiple myeloma, nausea, . TERIPARATIDE dosage: unknown. Patient recovered.

Theophylline Side Effects Report #5593689-5
Health Professional from CZECH REPUBLIC reported THEOPHYLLINE problem on Jan 15, 2008. Female patient, 17 years of age, was treated with THEOPHYLLINE. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, blood glucose abnormal, hypokalaemia, intentional overdose, myoglobin blood increased, ventricular extrasystoles, . THEOPHYLLINE dosage: unknown. Patient was hospitalized. Patient recovered.

Tekturna Side Effects Report #5641668-1
TEKTURNA problem was reported by a Physician from UNITED STATES on Nov 19, 2007. Male patient, 57 years of age, weighting 201.9 lb, was diagnosed with hypertension and was treated with TEKTURNA. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, blood urea abnormal, joint swelling, pain, . TEKTURNA dosage: 300 MG, QD, ORAL. During the same period patient was treated with ATACAND, LIPITOR, COVERA, LANOXIN. Patient recovered.


Byetta Side Effects Report #5567171-5
Physician from UNITED STATES reported BYETTA problem on Dec 12, 2007. Male patient, 56 years of age, was diagnosed with renal disorder and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, hepatic enzyme abnormal, hepatic steatosis, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN. Patient recovered.

Amlodipine Side Effects Report #5576105-9
AMLODIPINE problem was reported by a Physician from NETHERLANDS on Dec 11, 2007. Female patient, 47 years of age, was treated with AMLODIPINE. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, blood ph increased, bradycardia, hyperglycaemia, hypotension, respiratory rate increased, . AMLODIPINE dosage: 5 MG X 40 TABLETS, ORAL. During the same period patient was treated with LORAZEPAM. Patient was hospitalized. Patient recovered.

Byetta Side Effects Report #5519496-7
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Nov 06, 2007. Male patient, 56 years of age, was diagnosed with renal disorder and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, blood glucose abnormal, hepatic enzyme abnormal, hepatic steatosis, urinary tract infection, urosepsis, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN. Patient was hospitalized. Patient recovered.

Dasatinib Side Effects Report #5521674-8
DASATINIB problem was reported by a Health Professional from UNITED STATES on Nov 13, 2007. Female patient, 70 years of age, was diagnosed with sarcoma and was treated with DASATINIB. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, dehydration, diarrhoea, renal failure acute, urinary tract infection, . DASATINIB dosage: unknown. During the same period patient was treated with ALLOPURINOL, THYROID, COMPAZINE, FOLIC ACID, GABAPENTIN, LOMOTIL, SERTRALINE, TOPROL. Patient was hospitalized. Patient recovered.

Sandostatin Side Effects Report #5479315-4
Consumer or non-health professional from UNITED STATES reported SANDOSTATIN LAR problem on Oct 02, 2007. Male patient was treated with SANDOSTATIN LAR. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, . SANDOSTATIN LAR dosage: unknown. Patient was hospitalized. Patient recovered.


Sandostatin Side Effects Report #5481205-8
SANDOSTATIN LAR problem was reported by a Physician from UNITED STATES on Oct 03, 2007. Male patient, weighting 162.0 lb, was diagnosed with carcinoid syndrome and was treated with SANDOSTATIN LAR. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, renal impairment, . SANDOSTATIN LAR dosage: 20 MG, QMO. During the same period patient was treated with SANDOSTATIN LAR, EPOGEN, CALCIUM CARBONATE, LASIX, BICITRA, NIFEDIPINE, INSULIN, CREON. Patient was hospitalized. Patient recovered.

Topotecan Side Effects Report #5481556-7
Health Professional from UNITED STATES reported TOPOTECAN problem on Oct 05, 2007. Female patient, weighting 268.5 lb, was treated with TOPOTECAN. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, female genital tract fistula, obstructive uropathy, prothrombin time prolonged, . TOPOTECAN dosage: 18 MG. During the same period patient was treated with COUMADIN, MIRALAX, SENOKOT, VICODIN. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5490409-X
GLEEVEC problem was reported by a Physician from JAPAN on Oct 11, 2007. Female patient, child 10 years of age, weighting 74.96 lb, was diagnosed with chronic myeloid leukaemia and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, bone pain, creatinine renal clearance, haematocrit decreased, haemoglobin decreased, hypercalcaemia, hyponatraemia, marasmus, normochromic normocytic anaemia, . GLEEVEC dosage: 100 MG/D. During the same period patient was treated with HYDREA. Patient died on 09/15/2007.

Letrozole Side Effects Report #5491492-8
Health Professional from UNITED STATES reported LETROZOLE problem on Oct 11, 2007. Female patient, 66 years of age, weighting 238.0 lb, was diagnosed with breast cancer metastatic and was treated with LETROZOLE. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, blood disorder, blood urea abnormal, dehydration, diarrhoea, dysphagia, epistaxis, exercise tolerance decreased, myalgia, . LETROZOLE dosage: 2.5 MG, QD. During the same period patient was treated with LUNESTA, ADVIL LIQUI, TARCEVA, LEVOTHYROXINE, SYNTHROID, CARDURA, IMODIUM, ACCUPRIL. Patient was hospitalized. Patient recovered.

Vesicare Side Effects Report #5487782-5
VESICARE problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 07, 2007. Female patient, 67 years of age, was diagnosed with incontinence and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, dry mouth, . VESICARE dosage: 5 MG, UID/QD, ORAL. During the same period patient was treated with COUMADIN, VERAPAMIL, VITAMIN. Patient recovered.


Altace Side Effects Report #5415566-2
Consumer or non-health professional from SWEDEN reported ALTACE problem on Aug 06, 2007. Female patient was diagnosed with hypertension and was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, c-reactive protein increased, diarrhoea, fluid intake reduced, gastroenteritis viral, nephropathy toxic, pyrexia, vomiting, . ALTACE dosage: 10 MG, QD. During the same period patient was treated with METOPROLOL SUCCINATE. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5427185-2
GLEEVEC problem was reported by a Physician from AUSTRALIA on Aug 16, 2007. Male patient, 58 years of age, was diagnosed with chordoma and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, dehydration, escherichia urinary tract infection, nausea, oral intake reduced, renal impairment, vomiting, . GLEEVEC dosage: 600 MG, QD. Patient was hospitalized. Patient recovered.

Azathioprine Side Effects Report #5397010-7
Consumer or non-health professional from reported AZATHIOPRINE problem on July 17, 2007. Male patient, 32 years of age, was treated with AZATHIOPRINE. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, oliguria, pyrexia, thrombotic microangiopathy, . AZATHIOPRINE dosage: unknown. During the same period patient was treated with STEROID, CYCLOSPORINE, BASILIXIMAB. Patient recovered.

Azathioprine Side Effects Report #5397010-7
AZATHIOPRINE problem was reported by a Consumer or non-health professional from on July 17, 2007. Male patient, 32 years of age, was treated with AZATHIOPRINE. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, oliguria, pyrexia, thrombotic microangiopathy, . AZATHIOPRINE dosage: unknown. During the same period patient was treated with STEROID, CYCLOSPORINE, BASILIXIMAB. Patient recovered.

Lipitor Side Effects Report #5781138-3
Consumer or non-health professional from UNITED STATES reported LIPITOR problem on June 11, 2008. Male patient, weighting 200.0 lb, was diagnosed with blood cholesterol increased and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, . LIPITOR dosage: unknown. During the same period patient was treated with HYZAAR, CARDIZEM, PROSCAR, NEXIUM, ASTHALIN, ZYRTEC. Patient recovered.


Exjade Side Effects Report #5803532-4
EXJADE problem was reported by a Physician from UNITED STATES on Mar 26, 2008. Female patient was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, renal failure, . EXJADE dosage: unknown. Patient recovered.

Neoral Side Effects Report #5699731-5
Consumer or non-health professional from JAPAN reported NEORAL problem on Apr 02, 2008. Female patient, 78 years of age, weighting 108.0 lb, was diagnosed with myasthenia gravis, diabetes mellitus, hypertension and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, blood potassium increased, blood urea increased, dysarthria, hypoglycaemia, hyponatraemia, renal impairment, vomiting, . NEORAL dosage: 150 MG/D. During the same period patient was treated with EUGLUCON, MELBIN, BASEN, MESTINON, KINEDAK, CONIEL, CARDENALIN. Patient recovered.

Neoral Side Effects Report #5707972-3
NEORAL problem was reported by a Consumer or non-health professional from JAPAN on Apr 10, 2008. Female patient, 78 years of age, weighting 108.0 lb, was diagnosed with myasthenia gravis, diabetes mellitus, hypertension and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, blood potassium increased, blood urea increased, dysarthria, hypoglycaemia, hyponatraemia, renal disorder, renal impairment, vomiting, . NEORAL dosage: 150 MG/D. During the same period patient was treated with EUGLUCON, MELBIN, BASEN, MESTINON, KINEDAK, CONIEL, CARDENALIN. Patient recovered.

Mavik Side Effects Report #5351910-2
Physician from CANADA reported MAVIK problem on May 31, 2007. Female patient, weighting 136.7 lb, was diagnosed with hypertension and was treated with MAVIK. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, glomerular filtration rate decreased, renal artery stenosis, . MAVIK dosage: unknown. Patient recovered.

Xyrem Side Effects Report #5352236-3
XYREM problem was reported by a Health Professional from UNITED STATES on May 30, 2007. Female patient, 72 years of age, weighting 178.0 lb, was diagnosed with cataplexy and was treated with XYREM. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, dry mouth, hypertension, sinusitis, stomach discomfort, . XYREM dosage: unknown. During the same period patient was treated with CHOLESTEROL MEDICINE. Patient was hospitalized. Patient recovered.

Zoloft Side Effects Report #5381495-6
Health Professional from UNITED STATES reported ZOLOFT problem on Feb 06, 2007. Female patient, 47 years of age, weighting 115.1 lb, was diagnosed with myelodysplastic syndrome and was treated with ZOLOFT. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, blood urea abnormal, pancreatitis, . ZOLOFT dosage: 100 MG (100 MG, 1 IN 1 D);. During the same period patient was treated with AZACITIDINE, QUINAPRIL AND HYDROCHLOROTHIAZIDE, PRAVASTATIN, NISOLDIPINE, LORATADINE, ACCURETIC. Patient was hospitalized. Patient recovered.

Atomoxetine Side Effects Report #5291157-1
ATOMOXETINE HYDROCHLORIDE problem was reported by a Physician from UNITED STATES on Mar 26, 2007. Female patient, 53 years of age, weighting 123.0 lb, was diagnosed with attention deficit/hyperactivity disorder, pain, prophylaxis, depression, chorea, sleep disorder and was treated with ATOMOXETINE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, . ATOMOXETINE HYDROCHLORIDE dosage: 40 MG, 2/D. During the same period patient was treated with NAPROXEN, LEXAPRO, CREATINE, COENZYME Q, FISH OIL, LUNESTA. Patient recovered.

Fentanyl Side Effects Report #5294653-6
Pharmacist from UNITED STATES reported FENTANYL problem on Apr 09, 2007. Male patient, weighting 244.1 lb, was diagnosed with sedation and was treated with FENTANYL. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, blood glucose increased, blood urea increased, body temperature decreased, haemoglobin decreased, respiratory arrest, . FENTANYL dosage: unknown. During the same period patient was treated with MIDAZOLAM IV. Patient was hospitalized. Patient recovered.

Revlimid Side Effects Report #5300955-7
REVLIMID problem was reported by a Physician from UNITED STATES on Apr 03, 2007. Male patient, 71 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 creatinine abnormal, platelet count decreased, . REVLIMID dosage: unknown. Patient was hospitalized. Patient recovered.

Neoral Side Effects Report #5268472-0
Pharmacist from JAPAN reported NEORAL problem on Mar 13, 2007. Female patient, 78 years of age, weighting 108.0 lb, was diagnosed with myasthenia gravis, diabetes mellitus, hypertension and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, blood potassium increased, blood urea increased, dysarthria, hypoglycaemia, hyponatraemia, renal impairment, vomiting, . NEORAL dosage: 150 MG/D. During the same period patient was treated with EUGLUCON, MELBIN, BASEN, MESTINON, KINEDAK, CONIEL, CARDENALIN. Patient recovered.

Lyrica Side Effects Report #5272163-X
LYRICA problem was reported by a Physician from PORTUGAL on Mar 09, 2007. Male patient, 55 years of age, was diagnosed with paraesthesia and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, . LYRICA dosage: unknown. Patient was hospitalized. Patient recovered.

Diltiazem Side Effects Report #5663635-4
Health Professional from FRANCE reported DILTIAZEM HYDROCHLORIDE problem on Feb 22, 2008. Male patient, 86 years of age, was treated with DILTIAZEM HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: atrioventricular block, blood creatinine abnormal, cardiomegaly, pulmonary embolism, troponin increased, . DILTIAZEM HYDROCHLORIDE dosage: (200 MG QD ORAL). During the same period patient was treated with FONZYLANE, PLAVIX, FUROSEMIDE, DISCOTRINE. Patient was hospitalized. Patient recovered.

Altace Side Effects Report #5672751-2
ALTACE problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 11, 2007. Female patient was diagnosed with hypertension and was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, blood creatinine abnormal, cheilitis, lip exfoliation, lip swelling, pancreatitis, renal failure chronic, . ALTACE dosage: 2.5 MG, QD. During the same period patient was treated with ATENOLOL, PROCARDIA. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5614087-1
Consumer or non-health professional from BRAZIL reported HUMIRA problem on Jan 31, 2008. Female patient, weighting 85.98 lb, was diagnosed with rheumatoid arthritis, pain and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: anaemia, blood creatinine abnormal, blood urea abnormal, c-reactive protein increased, rheumatoid factor increased, scar, sepsis, streptococcal identification test positive, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISONE, TRAMADOL. Patient was hospitalized. Patient died on 01/07/2008.

Boniva Side Effects Report #5570872-6
BONIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 14, 2007. Female patient, 91 years of age, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: anaemia, blood creatinine abnormal, blood urea abnormal, diarrhoea, fall, nausea, urinary tract infection, vomiting, . BONIVA dosage: unknown. During the same period patient was treated with VITAMIN D, CALCIUM, GABAPENTIN, DICLOFENAC, VITAMINS NOS, ARICEPT. Patient was hospitalized. Patient recovered.

Zoledronic Side Effects Report #5519298-1
Physician from POLAND reported ZOLEDRONIC ACID problem on Nov 14, 2007. Female patient, 80 years of age, weighting 160.7 lb, was diagnosed with osteoporosis postmenopausal and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: asthenia, blood creatinine abnormal, blood potassium abnormal, blood urea, c-reactive protein increased, cardiac failure chronic, cardiac failure congestive, concomitant disease progression, cough, . ZOLEDRONIC ACID dosage: unknown. During the same period patient was treated with CALCIUM, VITAMIN D, DICLOFENAC. Patient was hospitalized. Patient died on 10/08/2007.

Zoledronic Side Effects Report #5520244-5
ZOLEDRONIC ACID problem was reported by a Physician from POLAND on Nov 14, 2007. Female patient, 80 years of age, weighting 160.7 lb, was diagnosed with osteoporosis postmenopausal and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: asthenia, blood creatinine abnormal, blood potassium abnormal, blood urea, c-reactive protein increased, cardiac failure chronic, cardiac failure congestive, concomitant disease progression, cough, . ZOLEDRONIC ACID dosage: unknown. During the same period patient was treated with CALCIUM, VITAMIN D, DICLOFENAC. Patient was hospitalized. Patient died on 10/08/2007.

Gemcitabine Side Effects Report #5476788-8
Health Professional from UNITED STATES reported GEMCITABINE problem on Oct 03, 2007. Male patient, weighting 200.0 lb, was diagnosed with pancreatic carcinoma and was treated with GEMCITABINE. After drug was administered, patient experienced the following problems/side effects: ascites, blood creatinine abnormal, disease progression, dyspnoea, fatigue, left ventricular dysfunction, pain, . GEMCITABINE dosage: 1GM/M2 - 2100 MG WKLY X 3 IV. During the same period patient was treated with LAPATINIB. Patient was hospitalized. Patient recovered.

Cyclophosphamide Side Effects Report #5479442-1
CYCLOPHOSPHAMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 03, 2007. Female patient, weighting 129.0 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: atrial flutter, blood creatinine abnormal, diastolic dysfunction, dyspnoea, febrile neutropenia, haemodialysis, haemoglobin abnormal, herpes simplex serology positive, hypotension, . CYCLOPHOSPHAMIDE dosage: 1155 MG. During the same period patient was treated with DOXIL, HEPARIN LOCK, LORAZEPAM, LUCENTIS, NORVASC, PRILOSEC, PROCRIT, PROPOXYPHENE. Patient was hospitalized. Patient recovered.

Lipitor Side Effects Report #5491133-X
Physician from AUSTRALIA reported LIPITOR problem on Oct 11, 2007. Female patient, 70 years of age, weighting 286.6 lb, was diagnosed with metabolic syndrome, cardiac failure congestive, oedema peripheral and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: ankle fracture, blood creatinine abnormal, blood creatinine increased, blood uric acid abnormal, fractured sacrum, myalgia, . LIPITOR dosage: unknown. During the same period patient was treated with SPIRONOLACTONE, FUROSEMIDE, DIURETICS, INSULINS AND ANALOGUES, INSULINS AND ANALOGUES, METFORMIN. Patient recovered.

Lipitor Side Effects Report #5442340-3
LIPITOR problem was reported by a Physician from UNITED STATES on Aug 27, 2007. Female patient, 70 years of age, was diagnosed with lipids increased and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, blood creatinine abnormal, myalgia, . LIPITOR dosage: unknown. During the same period patient was treated with METOPROLOL SUCCINATE, SYNTHROID. Patient recovered.

Atorvastatin Side Effects Report #5468861-5
Physician from AUSTRALIA reported ATORVASTATIN CALCIUM problem on Sept 16, 2007. Female patient, 70 years of age, weighting 213.8 lb, was treated with ATORVASTATIN CALCIUM. After drug was administered, patient experienced the following problems/side effects: ankle fracture, blood creatinine abnormal, blood uric acid abnormal, fractured sacrum, . ATORVASTATIN CALCIUM dosage: unknown. During the same period patient was treated with SPIRONOLACTONE, FRUSEMIDE, INSULINS AND ANALOGUES, INSULINS AND ANALOGUES, METFORMIN, ACARBOSE. Patient recovered.

Certican Side Effects Report #5404836-X
CERTICAN problem was reported by a Physician from AUSTRIA on July 23, 2007. Female patient, 61 years of age, weighting 158.7 lb, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: blood cholesterol abnormal, blood creatinine abnormal, blood creatinine increased, blood triglycerides abnormal, diabetes mellitus inadequate control, glomerulonephritis membranous, haemoglobin abnormal, nephropathy toxic, oedema peripheral, . CERTICAN dosage: unknown. During the same period patient was treated with MYFORTIC. Patient recovered.

Certican Side Effects Report #5423859-8
Physician from AUSTRIA reported CERTICAN problem on Aug 13, 2007. Female patient, 61 years of age, weighting 158.7 lb, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: blood cholesterol abnormal, blood creatinine abnormal, blood creatinine increased, blood triglycerides abnormal, chronic allograft nephropathy, diabetes mellitus inadequate control, haemoglobin abnormal, nephropathy toxic, oedema peripheral, . CERTICAN dosage: unknown. During the same period patient was treated with MYFORTIC. Patient was hospitalized. Patient recovered.

Fosrenol Side Effects Report #5460945-0
FOSRENOL problem was reported by a Consumer or non-health professional from UNITED STATES on May 04, 2007. Male patient, 69 years of age, weighting 164.9 lb, was diagnosed with hyperphosphataemia and was treated with FOSRENOL. After drug was administered, patient experienced the following problems/side effects: blood calcium abnormal, blood creatinine abnormal, blood phosphorus abnormal, blood sodium abnormal, dialysis device complication, . FOSRENOL dosage: unknown. During the same period patient was treated with OMEPRAZOLE, COREG, PLAVIX, AMBIEN, ZOLOFT, ALLOPURINOL. Patient recovered.

Sertraline Side Effects Report #5392935-0
Consumer or non-health professional from UNITED STATES reported SERTRALINE problem on July 06, 2007. Female patient was diagnosed with obsessive-compulsive disorder and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, blood creatinine abnormal, cholelithiasis, hepatic steatosis, musculoskeletal pain, . SERTRALINE dosage: 125 MG, QD, ORAL. During the same period patient was treated with DIAZEPAM, DIHYDROCODEINE, LOPERAMIDE, OMEPRAZOLE. Patient recovered.

Sertraline Side Effects Report #5392935-0
SERTRALINE problem was reported by a Consumer or non-health professional from UNITED STATES on July 06, 2007. Female patient was diagnosed with obsessive-compulsive disorder and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, blood creatinine abnormal, cholelithiasis, hepatic steatosis, musculoskeletal pain, . SERTRALINE dosage: 125 MG, QD, ORAL. During the same period patient was treated with DIAZEPAM, DIHYDROCODEINE, LOPERAMIDE, OMEPRAZOLE. Patient recovered.

Boniva Side Effects Report #5690219-4
Physician from UNITED STATES reported BONIVA problem on Mar 24, 2008. Female patient, 91 years of age, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: anaemia, blood creatinine abnormal, blood urea abnormal, diarrhoea, fall, nausea, urinary tract infection, vomiting, . BONIVA dosage: unknown. During the same period patient was treated with VITAMIN D, CALCIUM, GABAPENTIN, DICLOFENAC, VITAMINS NOS, ARICEPT. Patient was hospitalized. Patient recovered.

Coreg Side Effects Report #5716259-4
COREG problem was reported by a Physician from UNITED STATES on Apr 15, 2008. Female patient, 44 years of age, weighting 84.22 lb, was treated with COREG. After drug was administered, patient experienced the following problems/side effects: anaemia, blood creatinine abnormal, bone marrow failure, haematocrit abnormal, haemoglobin decreased, hyperparathyroidism, pneumonia, . COREG dosage: unknown. During the same period patient was treated with PROCRIT, PHENYTOIN. Patient was hospitalized. Patient recovered.

Sertraline Side Effects Report #5369644-7
Physician from UNITED KINGDOM reported SERTRALINE problem on June 13, 2007. Female patient, weighting 103.6 lb, was diagnosed with obsessive-compulsive disorder, abdominal pain, anxiety and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, blood creatinine abnormal, cholelithiasis, hepatic steatosis, herpes zoster, liver function test abnormal, musculoskeletal pain, . SERTRALINE dosage: unknown. During the same period patient was treated with LOPERAMIDE, OMEPRAZOLE, DIAZEPAM, DIHYDROCODEINE BITARTRATE. Patient recovered.

Viramune Side Effects Report #5327924-5
VIRAMUNE problem was reported by a Consumer or non-health professional from UNITED STATES on May 10, 2007. Female patient, weighting 6.61 lb, was diagnosed with vertical infection transmission and was treated with VIRAMUNE. After drug was administered, patient experienced the following problems/side effects: blood bicarbonate decreased, blood creatinine abnormal, . VIRAMUNE dosage: unknown. During the same period patient was treated with ZIDOVUDINE, DIDANOSINE, VITAMIN K1. Patient recovered.

Lipitor Side Effects Report #5335360-0
Physician from UNITED STATES reported LIPITOR problem on May 16, 2007. Female patient, 70 years of age, was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, blood creatinine abnormal, myalgia, . LIPITOR dosage: unknown. Patient recovered.