Menu

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

BLOOD CREATININE DECREASED side effect

What is BLOOD CREATININE DECREASED ?

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

Type your question here

 letters left

Mucodyne Side Effects Report #5657370-6
Physician from JAPAN reported MUCODYNE problem on Feb 28, 2008. Female patient, 78 years of age, was diagnosed with urticaria and was treated with MUCODYNE. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, blood glucose increased, blood lactate dehydrogenase decreased, cheilitis, dermatitis exfoliative, feeling hot, lymphocyte count decreased, neutrophil count increased, . MUCODYNE dosage: unknown. During the same period patient was treated with ONEALFA, BONALON, ZADITEN, MUCOSTA, ALESION. Patient recovered.

Cyclophosphamide Side Effects Report #5638991-3
CYCLOPHOSPHAMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 25, 2008. Female patient, weighting 209.0 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, blood sodium decreased, hyperglycaemia, incontinence, nausea, oral intake reduced, vision blurred, vomiting, . CYCLOPHOSPHAMIDE dosage: 1200 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE. Patient recovered.

Aggrenox Side Effects Report #5587467-0
Physician from reported AGGRENOX problem on Jan 08, 2008. Male patient, weighting 198.4 lb, was diagnosed with embolic stroke, hypertension, thrombocythaemia, myelofibrosis and was treated with AGGRENOX. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, diarrhoea, headache, renal failure, . AGGRENOX dosage: unknown. During the same period patient was treated with XAGRID, CANDESARTAN CILEXETIL, ATACAND HCT, ATACAND HCT, TRIAMTEREN HCT. Patient was hospitalized. Patient recovered.

Paroxetine Side Effects Report #5574960-X
PAROXETINE HYDROCHLORIDE problem was reported by a Consumer or non-health professional from NETHERLANDS on Dec 18, 2007. Female patient, 78 years of age, was diagnosed with depression, hypertension and was treated with PAROXETINE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, blood osmolarity decreased, blood potassium decreased, creatinine urine decreased, decreased appetite, headache, hyponatraemia, ill-defined disorder, malaise, . PAROXETINE HYDROCHLORIDE dosage: 20MG PER DAY. During the same period patient was treated with AMILORIDE AND HYDROCHLOROTHIAZIDE, OXAZEPAM, CORTICOSTEROID, NORVASC. Patient was hospitalized. Patient recovered.


Finibax Side Effects Report #5511432-2
Health Professional from JAPAN reported FINIBAX problem on Oct 31, 2007. Male patient, 81 years of age, was diagnosed with pneumonia and was treated with FINIBAX. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, . FINIBAX dosage: unknown. During the same period patient was treated with URSO, UNIPHYL LA, DASEN, MUCOSTA, TERSIGAN, CERCINE. Patient was hospitalized. Patient recovered.

Prozac Side Effects Report #5513239-9
PROZAC problem was reported by a Physician from FRANCE on Nov 08, 2007. Male patient was diagnosed with depression, hypertension and was treated with PROZAC. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, hallucination, visual, hypochloraemia, hyponatraemia, . PROZAC dosage: 20 MG, EACH MORNING. During the same period patient was treated with LOPRESSOR. Patient was hospitalized. Patient recovered.

Doribax Side Effects Report #5518538-2
Physician from JAPAN reported DORIBAX problem on Nov 05, 2007. Male patient, 81 years of age, was diagnosed with pneumonia and was treated with DORIBAX. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, . DORIBAX dosage: unknown. During the same period patient was treated with URSO, UNIPHYL LA, DASEN, MUCOSTA, TERSIGAN, CERCINE. Patient was hospitalized. Patient recovered.

Tarceva Side Effects Report #5483232-3
TARCEVA problem was reported by a Physician from GERMANY on Sept 21, 2007. Male patient, 53 years of age, was diagnosed with non-small cell lung cancer and was treated with TARCEVA. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, blood glucose increased, blood lactate dehydrogenase increased, blood uric acid increased, bronchial neoplasm, bronchostenosis, c-reactive protein increased, cerebral infarction, cerebral ischaemia, . TARCEVA dosage: 150 MG (QD), ORAL. During the same period patient was treated with METOPROLOL TARTRATE, RAMIPRIL COMP, HYDROCHLOROTHIAZIDE, ESOMEPRAZOLE, ACETYLCYSTEINE, DEXAMETHASONE, PROMETHAZINE, PARACODINE. Patient was hospitalized. Patient recovered.

Seroquel Side Effects Report #5490747-0
Physician from PORTUGAL reported SEROQUEL problem on Oct 09, 2007. Female patient, 57 years of age, was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, leukocytosis, lymphocyte percentage decreased, muscle rigidity, neuroleptic malignant syndrome, neutrophil percentage increased, rhabdomyolysis, . SEROQUEL dosage: unknown. During the same period patient was treated with LORAZEPAM, VENLAFAXINE, MIRTAZAPINE. Patient was hospitalized. Patient recovered.


Prozac Side Effects Report #5447837-8
PROZAC problem was reported by a Physician from FRANCE on Aug 30, 2007. Male patient, 60 years of age, was diagnosed with depression, hypertension and was treated with PROZAC. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, hallucination, visual, hypochloraemia, hyponatraemia, . PROZAC dosage: 20 MG, EACH MORNING. During the same period patient was treated with LOPRESSOR. Patient was hospitalized. Patient recovered.

Cyclophosphamide Side Effects Report #5451358-6
Consumer or non-health professional from UNITED STATES reported CYCLOPHOSPHAMIDE problem on Sept 11, 2007. Female patient, weighting 150.4 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, culture urine positive, haematocrit decreased, haemoglobin decreased, nausea, neutrophil count increased, vomiting, white blood cell count increased, . CYCLOPHOSPHAMIDE dosage: 1080 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Norvasc Side Effects Report #5461126-7
NORVASC problem was reported by a Physician from JAPAN on Sept 13, 2007. Female patient, 69 years of age, weighting 108.0 lb, was diagnosed with hypertension and was treated with NORVASC. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, chest x-ray abnormal, interstitial lung disease, . NORVASC dosage: 5 MG, UNK. During the same period patient was treated with DIOVAN. Patient recovered.

Infergen Side Effects Report #5431645-8
Consumer or non-health professional from UNITED STATES reported INFERGEN problem on Aug 14, 2007. Male patient, 49 years of age, weighting 170.0 lb, was diagnosed with hepatitis c and was treated with INFERGEN. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, blood magnesium decreased, blood potassium decreased, condition aggravated, depression, haemoglobin decreased, hepatic enzyme increased, hypotension, influenza like illness, . INFERGEN dosage: unknown. During the same period patient was treated with RIBAVIRIN, AMBIEN CR, REQUIP. Patient was hospitalized. Patient recovered.

Modacin Side Effects Report #5384195-1
MODACIN problem was reported by a Pharmacist from JAPAN on July 06, 2007. Male patient, 67 years of age, weighting 152.1 lb, was diagnosed with spondylitis, arteriosclerosis obliterans, gastric mucosal lesion, pain, neuropathy peripheral and was treated with MODACIN. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, c-reactive protein increased, haematocrit decreased, haemoglobin decreased, leukopenia, lymphopenia, monocyte count increased, red blood cell count decreased, . MODACIN dosage: unknown. During the same period patient was treated with MINOCYCLINE, ALPROSTADIL, MUCOSTA, ANPLAG, LORCAM, CEFMETAZON, TIENAM, NEOLAMIN. Patient was hospitalized. Patient recovered.


Exenatide Side Effects Report #5414179-6
Consumer or non-health professional from UNITED STATES reported EXENATIDE problem on Apr 02, 2007. Male patient, 67 years of age, weighting 192.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, blood glucose increased, blood urea decreased, decreased appetite, nasopharyngitis, sinus congestion, tooth infection, weight decreased, . EXENATIDE dosage: unknown. During the same period patient was treated with METFORMIN, HUMALOG, LANTUS, GLIPIZIDE. Patient recovered.

Modacin Side Effects Report #5384195-1
MODACIN problem was reported by a Pharmacist from JAPAN on July 06, 2007. Male patient, 67 years of age, weighting 152.1 lb, was diagnosed with spondylitis, arteriosclerosis obliterans, gastric mucosal lesion, pain, neuropathy peripheral and was treated with MODACIN. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, c-reactive protein increased, haematocrit decreased, haemoglobin decreased, leukopenia, lymphopenia, monocyte count increased, red blood cell count decreased, . MODACIN dosage: unknown. During the same period patient was treated with MINOCYCLINE, ALPROSTADIL, MUCOSTA, ANPLAG, LORCAM, CEFMETAZON, TIENAM, NEOLAMIN. Patient was hospitalized. Patient recovered.

Exenatide Side Effects Report #5414179-6
Consumer or non-health professional from UNITED STATES reported EXENATIDE problem on Apr 02, 2007. Male patient, 67 years of age, weighting 192.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, blood glucose increased, blood urea decreased, decreased appetite, nasopharyngitis, sinus congestion, tooth infection, weight decreased, . EXENATIDE dosage: unknown. During the same period patient was treated with METFORMIN, HUMALOG, LANTUS, GLIPIZIDE. Patient recovered.

Casodex Side Effects Report #5762934-5
CASODEX problem was reported by a Consumer or non-health professional from CANADA on June 03, 2008. Male patient, 76 years of age, was diagnosed with glaucoma and was treated with CASODEX. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, constipation, fatigue, feeling abnormal, intestinal obstruction, lethargy, paraesthesia, peripheral coldness, sensation of pressure, . CASODEX dosage: unknown. During the same period patient was treated with ZOLADEX, FOSAMAX, COSOPT, XALATAN. Patient recovered.

Mycophenolate Side Effects Report #5776902-0
Pharmacist from UNITED STATES reported MYCOPHENOLATE MOFETIL problem on June 17, 2008. Male patient, weighting 202.6 lb, was diagnosed with immunosuppression and was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, platelet count decreased, transplant rejection, white blood cell count decreased, . MYCOPHENOLATE MOFETIL dosage: 500MG PO Q12H. During the same period patient was treated with PREDNISONE, TACROLIMUS, NYSTATIN, ACYCLOVIR, BACTRIM, RANITIDINE, PRAVASTATIN, INSULIN. Patient was hospitalized. Patient recovered.


Mucodyne Side Effects Report #5742264-8
MUCODYNE problem was reported by a Physician from JAPAN on May 12, 2008. Female patient, 78 years of age, was diagnosed with urticaria and was treated with MUCODYNE. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, blood glucose increased, blood lactate dehydrogenase decreased, cheilitis, dermatitis exfoliative, feeling hot, lymphocyte count decreased, neutrophil count increased, . MUCODYNE dosage: unknown. During the same period patient was treated with ONEALFA, BONALON, ZADITEN, MUCOSTA, ALESION. Patient recovered.

Mucodyne Side Effects Report #5703694-3
Physician from JAPAN reported MUCODYNE problem on Apr 07, 2008. Female patient, 78 years of age, was diagnosed with urticaria and was treated with MUCODYNE. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, blood glucose increased, blood lactate dehydrogenase decreased, cheilitis, dermatitis exfoliative, feeling hot, lymphocyte count decreased, neutrophil count increased, . MUCODYNE dosage: unknown. During the same period patient was treated with ONEALFA, BONALON, ZADITEN, MUCOSTA, ALESION. Patient recovered.

Synagis Side Effects Report #5712698-6
SYNAGIS problem was reported by a Health Professional from IRELAND on Apr 03, 2008. Female patient was diagnosed with antiviral prophylaxis and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, gastritis, . SYNAGIS dosage: 120 MG, INTRAMUSCULAR. During the same period patient was treated with FUROSEMIDE, SPIRONOLACTONE. Patient was hospitalized. Patient recovered.

Zoladex Side Effects Report #5723598-X
Consumer or non-health professional from BRAZIL reported ZOLADEX problem on Apr 23, 2008. Male patient, 80 years of age, weighting 138.9 lb, was diagnosed with prostate cancer recurrent, pollakiuria, anaemia and was treated with ZOLADEX. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, blood urea decreased, decreased appetite, dizziness, labyrinthitis, nausea, pollakiuria, prostatic specific antigen increased, renal disorder, . ZOLADEX dosage: unknown. During the same period patient was treated with DOXAZOSIN MESYLATE, PROPATYLNITRATE, CILOSTAZOLE, SOMALGIN CARDIO, NORIPURUM, PAPAVERINE, TORLOS H. Patient was hospitalized. Patient recovered.

Aggrenox Side Effects Report #5326710-X
AGGRENOX problem was reported by a Physician from on May 14, 2007. Male patient, weighting 198.4 lb, was diagnosed with thromboembolic stroke, hypertension, thrombocythaemia, myelofibrosis and was treated with AGGRENOX. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, diarrhoea, headache, renal failure, . AGGRENOX dosage: unknown. During the same period patient was treated with XAGRID, CANDESARTAN, ATACAND HCT, ATACAND HCT, TRIAMTEREN HCT. Patient was hospitalized. Patient recovered.

Lithium Side Effects Report #5343892-4
Pharmacist from UNITED STATES reported LITHIUM CARBONATE problem on May 31, 2007. Male patient, 48 years of age, was diagnosed with bipolar i disorder and was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, confusional state, convulsion, tremor, . LITHIUM CARBONATE dosage: 450MG HS PO. Patient was hospitalized. Patient recovered.

Keflex Side Effects Report #5347845-1
KEFLEX problem was reported by a Health Professional from UNITED STATES on June 12, 2006. Female patient, 89 years of age, weighting 150.4 lb, was treated with KEFLEX. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, hip fracture, hyponatraemia, infection, . KEFLEX dosage: unknown. During the same period patient was treated with DARVOCET, REMERON, EFFEXOR, ADVAIR DISKUS, ULTRAM, ACETAMINOPHEN, DOCUSATE, ASPIRIN. Patient was hospitalized. Patient recovered.

Byetta Side Effects Report #5364111-9
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Jan 03, 2007. Male patient, 67 years of age, weighting 192.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, blood glucose increased, blood urea decreased, decreased appetite, sinus congestion, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN, HUMALOG, LANTUS, GLIPIZIDE, OVER THE COUNTER NASAL SPRAY. Patient recovered.

Citalopram Side Effects Report #5277995-X
CITALOPRAM HYDROBROMIDE problem was reported by a Consumer or non-health professional from FRANCE on Mar 09, 2007. Male patient, 82 years of age, was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, brain natriuretic peptide increased, cardiac failure, fall, hypoalbuminaemia, hyponatraemia, muscular weakness, oedema, pleural disorder, . CITALOPRAM HYDROBROMIDE dosage: 10 MG BID PO. During the same period patient was treated with TENORMIN, PREVISCAN, RAMIPRIL, VASTAREL, DIOVENOR. Patient was hospitalized. Patient recovered.

Escitalopram Side Effects Report #5278427-8
Health Professional from DENMARK reported ESCITALOPRAM problem on Mar 15, 2007. Female patient, 84 years of age, was treated with ESCITALOPRAM. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, blood magnesium decreased, haemoglobin decreased, hyponatraemia, . ESCITALOPRAM dosage: unknown. During the same period patient was treated with LEKOVIT CA, METOPROLOL SUCCINATE, COZAAR, VITAMIN B12 DEPOT. Patient was hospitalized. Patient recovered.

Temozolomide Side Effects Report #5663906-1
TEMOZOLOMIDE problem was reported by a Physician from UNITED KINGDOM on Mar 06, 2008. Female patient, 78 years of age, weighting 145.3 lb, was diagnosed with glioblastoma, swelling and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood creatinine decreased, hyperglycaemia, lymphocyte count decreased, monocyte count decreased, platelet count decreased, pneumonia aspiration, urinary tract infection, . TEMOZOLOMIDE dosage: unknown. During the same period patient was treated with DEXAMETHASONE, PHENYTOIN, PARACETAMOL, DOMPERIDONE. Patient was hospitalized. Patient died on 01/29/2008.

Temozolomide Side Effects Report #5625275-2
Physician from UNITED KINGDOM reported TEMOZOLOMIDE problem on Feb 01, 2008. Female patient, 78 years of age, weighting 145.3 lb, was diagnosed with glioblastoma, swelling and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood creatinine decreased, c-reactive protein increased, hyperglycaemia, lymphocyte count decreased, monocyte count decreased, platelet count decreased, protein total decreased, urinary tract infection, . TEMOZOLOMIDE dosage: unknown. During the same period patient was treated with DEXAMETHASONE, PHENYTOIN, ACETAMINOPHEN, DOMPERIDONE. Patient was hospitalized. Patient died on 01/29/2008.

Natalizumab Side Effects Report #5510863-4
NATALIZUMAB problem was reported by a Health Professional from UNITED STATES on Oct 29, 2007. Female patient, 43 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: basophil percentage increased, blood creatinine decreased, blood lactate dehydrogenase increased, blood urea decreased, cardiac failure congestive, cholesterol granuloma, condition aggravated, depression, low density lipoprotein increased, . NATALIZUMAB dosage: 300 MG; QM; IV. During the same period patient was treated with BIRTH CONTROL S, EFFEXOR, AMBIEN, HYDROCODONE W, ZANAFLEX, PROVIGIL, LASIX, VITAMIN E. Patient died on 10/11/2007.

Sandostatin Side Effects Report #5524513-4
Physician from CANADA reported SANDOSTATIN LAR problem on Nov 19, 2007. Male patient, 49 years of age, was diagnosed with acromegaly and was treated with SANDOSTATIN LAR. After drug was administered, patient experienced the following problems/side effects: asthenia, blood creatinine decreased, blood pressure increased, dizziness, fatigue, headache, heart rate increased, lymphocyte count, mean platelet volume decreased, . SANDOSTATIN LAR dosage: 20 MG, QMO. During the same period patient was treated with ADVAIR DISKUS, BACLOFEN, ACETYLSALICYLIC ACID SRT, CODEINE SUL, FLONASE, OTRIVIN, VENTOLIN. Patient recovered.

Voltaren Side Effects Report #5526866-X
VOLTAREN problem was reported by a Physician from JAPAN on Nov 21, 2007. Male patient, 52 years of age, was diagnosed with spinal cord injury cervical and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood creatinine decreased, nephrotic syndrome, oedema peripheral, protein total decreased, protein urine present, renal impairment, . VOLTAREN dosage: 50 MG, UNK. During the same period patient was treated with LORCAM, TERNELIN, CYANOCOBALAMIN, SOLON. Patient was hospitalized. Patient recovered.

Sandostatin Side Effects Report #5527605-9
Physician from CANADA reported SANDOSTATIN LAR problem on Nov 19, 2007. Male patient, 49 years of age, was diagnosed with acromegaly and was treated with SANDOSTATIN LAR. After drug was administered, patient experienced the following problems/side effects: asthenia, blood creatinine decreased, blood pressure increased, dizziness, fatigue, headache, heart rate increased, lymphocyte count, mean platelet volume decreased, . SANDOSTATIN LAR dosage: 20 MG, QMO. During the same period patient was treated with ADVAIR DISKUS, BACLOFEN, ACETYLSALICYLIC ACID SRT, CODEINE SUL, FLONASE, OTRIVIN, VENTOLIN. Patient recovered.

Prilosec Side Effects Report #5474670-3
PRILOSEC problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 26, 2007. Male patient, 82 years of age, weighting 149.9 lb, was diagnosed with gastric disorder and was treated with PRILOSEC. After drug was administered, patient experienced the following problems/side effects: anorexia, blood creatinine decreased, lethargy, malaise, nephropathy toxic, . PRILOSEC dosage: unknown. During the same period patient was treated with PREDNISONE, PREVACID. Patient recovered.

Zometa Side Effects Report #5494196-0
Consumer or non-health professional from JAPAN reported ZOMETA problem on Oct 19, 2007. Male patient, 69 years of age, weighting 213.8 lb, was diagnosed with bone pain, prophylaxis and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, blood creatinine decreased, blood pressure decreased, cardiac failure congestive, cardioversion, disseminated intravascular coagulation, heart rate increased, oliguria, renal failure acute, . ZOMETA dosage: 4 MG, UNK. During the same period patient was treated with DECADRON, SEROTONE, TAXOTERE. Patient died on 04/09/2007.

Cisplatin Side Effects Report #5452234-5
CISPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 12, 2007. Male patient, weighting 187.4 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: anxiety, blood creatinine decreased, blood phosphorus decreased, cough, dehydration, haemoglobin decreased, infection, influenza, . CISPLATIN dosage: 200 MG. During the same period patient was treated with LEXAPRO, TYLENOL. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5465851-3
Consumer or non-health professional from JAPAN reported ZOMETA problem on Sept 20, 2007. Male patient, 69 years of age, weighting 213.8 lb, was diagnosed with bone pain, prophylaxis and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, blood creatinine decreased, blood pressure decreased, cardiac failure congestive, cardioversion, disseminated intravascular coagulation, heart rate increased, oliguria, renal failure acute, . ZOMETA dosage: 4 MG, UNK. During the same period patient was treated with DECADRON, SEROTONE. Patient died on 04/08/2007.

Cisplatin Side Effects Report #5415203-7
CISPLATIN problem was reported by a Consumer or non-health professional from IRELAND on Aug 14, 2007. Male patient, 60 years of age, was diagnosed with gastric cancer, cancer pain, diabetes mellitus, constipation, prophylaxis of nausea and vomiting, stomatitis and was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: biliary sepsis, blood creatinine decreased, blood sodium decreased, blood urea increased, cholangitis, electrocardiogram t wave abnormal, lung infection, malignant neoplasm progression, metastases to liver, . CISPLATIN dosage: unknown. During the same period patient was treated with FLUOROURACIL, INFUMORPH, GLICLAZIDE, METFORMIN, DOMPERIDONE, ORAMORPH, DIFFLAM. Patient was hospitalized. Patient died on 02/27/2006.

Prednisone Side Effects Report #5395662-9
Consumer or non-health professional from reported PREDNISONE problem on July 17, 2007. Male patient, 34 years of age, was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood creatinine decreased, blood creatinine increased, focal glomerulosclerosis, haemodialysis, hypertension, oedema peripheral, proteinuria, renal impairment, . PREDNISONE dosage: 0.25 MG/DAY. During the same period patient was treated with BASILIXIMAB, SIROLIMUS, MYCOPHENOLATE MOFETIL. Patient recovered.

Myozyme Side Effects Report #5402043-8
MYOZYME problem was reported by a Physician from JAPAN on July 13, 2007. Male patient, 25 years of age, weighting 66.14 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: back pain, blood creatinine decreased, calculus ureteric, eosinophil percentage decreased, hydronephrosis, lymphocyte percentage decreased, neutrophil percentage increased, pyelonephritis, white blood cell count increased, . MYOZYME dosage: 20 MG/ KG Q2WKS IV. Patient was hospitalized. Patient recovered.

Prednisone Side Effects Report #5395662-9
Consumer or non-health professional from reported PREDNISONE problem on July 17, 2007. Male patient, 34 years of age, was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood creatinine decreased, blood creatinine increased, focal glomerulosclerosis, haemodialysis, hypertension, oedema peripheral, proteinuria, renal impairment, . PREDNISONE dosage: 0.25 MG/DAY. During the same period patient was treated with BASILIXIMAB, SIROLIMUS, MYCOPHENOLATE MOFETIL. Patient recovered.

Myozyme Side Effects Report #5402043-8
MYOZYME problem was reported by a Physician from JAPAN on July 13, 2007. Male patient, 25 years of age, weighting 66.14 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: back pain, blood creatinine decreased, calculus ureteric, eosinophil percentage decreased, hydronephrosis, lymphocyte percentage decreased, neutrophil percentage increased, pyelonephritis, white blood cell count increased, . MYOZYME dosage: 20 MG/ KG Q2WKS IV. Patient was hospitalized. Patient recovered.

Viramune Side Effects Report #5344422-3
Consumer or non-health professional from UNITED STATES reported VIRAMUNE problem 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 decreased, . VIRAMUNE dosage: unknown. During the same period patient was treated with ZIDOVUDINE, DIDANOSINE, VITAMIN K1. Patient recovered.

Nifluril Side Effects Report #5372432-9
NIFLURIL problem was reported by a Health Professional from FRANCE on June 20, 2007. Female patient, child 10 years of age, weighting 68.34 lb, was treated with NIFLURIL. After drug was administered, patient experienced the following problems/side effects: asthenia, blood creatinine decreased, blood culture positive, blood pressure diastolic decreased, condition aggravated, gait disturbance, haemoglobin decreased, heart rate increased, . NIFLURIL dosage: unknown. During the same period patient was treated with AMOXICILLIN, DOLIPRANE, ADVIL. Patient was hospitalized. Patient recovered.

Lopid Side Effects Report #5318177-2
Physician from UNITED STATES reported LOPID problem on Apr 25, 2007. Male patient, weighting 200.0 lb, was diagnosed with blood triglycerides increased and was treated with LOPID. After drug was administered, patient experienced the following problems/side effects: asthenia, blood creatinine decreased, muscle atrophy, muscular weakness, pain, pyrexia, . LOPID dosage: unknown. During the same period patient was treated with LEVOTHYROXINE. Patient recovered.

Advil Side Effects Report #5284199-3
ADVIL problem was reported by a Health Professional from FRANCE on Mar 29, 2007. Female patient, weighting 22.05 lb, was treated with ADVIL. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood creatinine decreased, blood glucose increased, blood sodium decreased, carbon dioxide decreased, condition aggravated, dysphagia, enanthema, haemoglobin decreased, . ADVIL dosage: unknown. During the same period patient was treated with DOLIPRANE, PRIMALAN. Patient was hospitalized. Patient recovered.

Zelnorm Side Effects Report #5306895-1
Consumer or non-health professional from UNITED STATES reported ZELNORM problem on Apr 17, 2007. Female patient was diagnosed with irritable bowel syndrome and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: abdominal pain, blood creatinine decreased, blood urea, dizziness, dysstasia, hypokalaemia, muscle spasms, . ZELNORM dosage: 6 MG 2-3 TIMES A DAY. Patient was hospitalized. Patient recovered.

Lopid Side Effects Report #5254624-2
LOPID problem was reported by a Health Professional from UNITED STATES on Feb 20, 2007. Male patient, weighting 200.0 lb, was diagnosed with blood triglycerides increased and was treated with LOPID. After drug was administered, patient experienced the following problems/side effects: asthenia, blood creatinine decreased, muscle atrophy, muscular weakness, pain, pyrexia, . LOPID dosage: unknown. During the same period patient was treated with LEVOTHYROXINE. Patient recovered.

Nutropin Side Effects Report #5274516-2
Physician from UNITED STATES reported NUTROPIN problem on Mar 14, 2007. Male patient, child 3 years of age, was diagnosed with growth hormone deficiency and was treated with NUTROPIN. After drug was administered, patient experienced the following problems/side effects: adrenal insufficiency, blood creatinine decreased, blood ph decreased, blood pressure immeasurable, coma, diarrhoea, electrocardiogram abnormal, hypoglycaemia, . NUTROPIN dosage: unknown. During the same period patient was treated with HYDROCORTISONE, SYNTHROID. Patient died.