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BIOPSY KIDNEY ABNORMAL side effect

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Desferal Side Effects Report #5653070-7
Consumer or non-health professional from GERMANY reported DESFERAL problem on Feb 27, 2008. Male patient, 58 years of age, weighting 155.4 lb, was diagnosed with haemosiderosis and was treated with DESFERAL. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood creatinine increased, blood urea increased, cardiac murmur, chronic allograft nephropathy, condition aggravated, creatinine renal clearance decreased, heart rate irregular, kidney fibrosis, . DESFERAL dosage: unknown. During the same period patient was treated with SANDIMMUNE, IMUREK, BENZBROMARONE, ASPIRIN, PANTOZOL, PRAVASTATIN, EZETROL, FUROSEMIDE. Patient was hospitalized. Patient recovered.

Myfortic Side Effects Report #5654677-3
MYFORTIC problem was reported by a Physician from GERMANY on Feb 27, 2008. Male patient, 53 years of age, was diagnosed with renal transplant and was treated with MYFORTIC. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood creatinine increased, catheter removal, epididymal infection, femoral nerve palsy, hydronephrosis, nephrostomy, post procedural infection, transplant rejection, . MYFORTIC dosage: 400 MG, BID. Patient was hospitalized. Patient recovered.

Mycophenolate Side Effects Report #5669298-6
Consumer or non-health professional from JAPAN reported MYCOPHENOLATE MOFETIL problem on Mar 06, 2008. Male patient, 16 years of age, was diagnosed with renal transplant and was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, cyst drainage, disease recurrence, focal segmental glomerulosclerosis, lymphocele, nephropathy toxic, proteinuria, renal impairment, ureteric obstruction, . MYCOPHENOLATE MOFETIL dosage: unknown. During the same period patient was treated with PREDNISOLONE, SIMULECT, NEORAL. Patient was hospitalized. Patient recovered.

Mycophenolate Side Effects Report #5669299-8
MYCOPHENOLATE MOFETIL problem was reported by a Consumer or non-health professional from JAPAN on Mar 06, 2008. Male patient, 16 years of age, was diagnosed with renal transplant and was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, cyst drainage, disease recurrence, focal segmental glomerulosclerosis, lymphocele, nephropathy toxic, proteinuria, renal impairment, ureteric obstruction, . MYCOPHENOLATE MOFETIL dosage: unknown. During the same period patient was treated with PREDNISOLONE, SIMULECT, NEORAL. Patient was hospitalized. Patient recovered.


Neoral Side Effects Report #5619814-5
Consumer or non-health professional from JAPAN reported NEORAL problem on Jan 31, 2008. Male patient, 60 years of age, weighting 125.7 lb, was diagnosed with aplastic anaemia and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood albumin decreased, blood cholesterol increased, blood creatinine increased, blood lactate dehydrogenase increased, blood urea increased, blood urine present, face oedema, focal glomerulosclerosis, . NEORAL dosage: 150 MG/DAY. During the same period patient was treated with PREDONINE. Patient was hospitalized and became disabled. Patient recovered.

Neoral Side Effects Report #5607538-X
NEORAL problem was reported by a Consumer or non-health professional from JAPAN on Jan 22, 2008. Male patient, 59 years of age, was diagnosed with aplastic anaemia and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood albumin decreased, blood urine present, face oedema, focal glomerulosclerosis, haemoglobin decreased, low density lipoprotein apheresis, oedema peripheral, platelet count decreased, . NEORAL dosage: 150 MG/DAY. During the same period patient was treated with PREDNISOLONE. Patient was hospitalized. Patient recovered.

Desferal Side Effects Report #5533221-5
Consumer or non-health professional from GERMANY reported DESFERAL problem on Nov 27, 2007. Male patient, 58 years of age, weighting 155.4 lb, was diagnosed with haemosiderosis and was treated with DESFERAL. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood creatinine increased, blood urea increased, cardiac murmur, chronic allograft nephropathy, condition aggravated, creatinine renal clearance decreased, heart rate irregular, kidney fibrosis, . DESFERAL dosage: unknown. During the same period patient was treated with SANDIMMUNE, IMUREK, BENZBROMARONE, ACETYLSALICYLIC ACID SRT, PANTOPRAZOLE, PRAVASTATIN, EZETROL, FUROSEMIDE. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5541685-6
ZOMETA problem was reported by a Physician from UNITED STATES on Dec 03, 2007. Female patient, 59 years of age, was diagnosed with multiple myeloma and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood creatinine increased, dialysis, diarrhoea, nephritis interstitial, renal failure acute, . ZOMETA dosage: unknown. During the same period patient was treated with REVLIMID, DEXAMETHASONE. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5542842-5
Physician from UNITED STATES reported PROGRAF problem on Nov 27, 2007. Male patient, 17 years of age, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood fibrinogen decreased, blood lactate dehydrogenase increased, complement factor c3 decreased, fibrin d dimer increased, haemoglobin decreased, hydronephrosis, hypertension, . PROGRAF dosage: 4 MG,BID. During the same period patient was treated with MYCOPHENOLATE MOFETIL, CYTOMEGALOVIRUS IMMUNE GLOBIN, VALGANCICLOVIR, FLUCONAZOLE, TRIMETHOPRIM COMP. Patient recovered.


Neoral Side Effects Report #5573093-6
NEORAL problem was reported by a Consumer or non-health professional from JAPAN on Dec 21, 2007. Male patient, 21 years of age, was diagnosed with bone marrow transplant and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood creatinine increased, blood lactate dehydrogenase increased, infection, occult blood positive, proteinuria, renal failure acute, septic shock, . NEORAL dosage: unknown. During the same period patient was treated with PREDNISOLONE, ANTITHYMOCYTE IMMUNOGLOBULIN. Patient died.

Myfortic Side Effects Report #5575376-2
Physician from GERMANY reported MYFORTIC problem on Dec 20, 2007. Male patient, 53 years of age, was diagnosed with renal transplant and was treated with MYFORTIC. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood creatinine increased, catheter removal, epididymal infection, femoral nerve palsy, hydronephrosis, nephrostomy, post procedural infection, transplant rejection, . MYFORTIC dosage: 400 MG, BID. Patient was hospitalized. Patient recovered.

Carboplatin Side Effects Report #5506021-X
CARBOPLATIN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Oct 17, 2007. Male patient, 43 years of age, was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood potassium increased, haemodialysis, renal failure acute, renal tubular disorder, tumour lysis syndrome, . CARBOPLATIN dosage: unknown. During the same period patient was treated with ALLOPURINOL, DAUNORUBICIN, HYDROXYCARBAMIDE, ELITEK. Patient was hospitalized. Patient recovered.

Thalidomide Side Effects Report #5509994-4
Pharmacist from UNITED STATES reported THALIDOMIDE problem on Nov 07, 2007. Female patient, weighting 174.2 lb, was diagnosed with multiple myeloma and was treated with THALIDOMIDE. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, glomerulonephritis proliferative, nephritis interstitial, tubulointerstitial nephritis, . THALIDOMIDE dosage: 100MG DAILY PO. Patient recovered.

Ciprofloxacin Side Effects Report #5513575-6
CIPROFLOXACIN problem was reported by a Consumer or non-health professional from ITALY on Oct 29, 2007. Female patient, 78 years of age, weighting 123.5 lb, was diagnosed with bronchitis and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood creatinine increased, cough, crystal urine present, red blood cells urine positive, specific gravity urine decreased, urine output decreased, . CIPROFLOXACIN dosage: 750MG TWICE DAILY PO. Patient was hospitalized. Patient recovered.


Rebif Side Effects Report #5477597-6
Consumer or non-health professional from GERMANY reported REBIF problem on Sept 14, 2007. Female patient, 39 years of age, weighting 198.4 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, cerebral infarction, condition aggravated, coombs test negative, disorientation, gastritis erosive, gastrointestinal haemorrhage, leukocytosis, . REBIF dosage: unknown. During the same period patient was treated with MITOXANTRONE HYDROCHLORIDE. Patient was hospitalized and became disabled. Patient recovered.

Neoral Side Effects Report #5482089-4
NEORAL problem was reported by a Consumer or non-health professional from JAPAN on Oct 05, 2007. Male patient, 21 years of age, was diagnosed with bone marrow transplant and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood creatinine increased, blood lactate dehydrogenase increased, infection, occult blood positive, proteinuria, renal failure acute, thrombotic microangiopathy, . NEORAL dosage: 200 MG/DAY. During the same period patient was treated with PREDNISOLONE, ANTITHYMOCYTE IMMUNOGLOBULIN. Patient died.

Neoral Side Effects Report #5483357-2
Consumer or non-health professional from JAPAN reported NEORAL problem on Oct 05, 2007. Male patient, 21 years of age, was diagnosed with bone marrow transplant and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood creatinine increased, blood lactate dehydrogenase increased, infection, occult blood positive, proteinuria, renal failure acute, thrombotic microangiopathy, . NEORAL dosage: 200 MG/DAY. During the same period patient was treated with PREDNISOLONE, ANTITHYMOCYTE IMMUNOGLOBULIN. Patient died.

Fabrazyme Side Effects Report #5485654-3
FABRAZYME problem was reported by a Physician from DENMARK on Sept 28, 2007. Male patient, 40 years of age, weighting 202.8 lb, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, complications of transplanted kidney, renal impairment, tubulointerstitial nephritis, . FABRAZYME dosage: 90 MG Q2WKS IV. During the same period patient was treated with PANTOPRAZOLE, BUMETANIZDE, PREDNISOLONE, CIPROFLOXACIN, CYCLOSPORINE, MYCOPHENOLATE MOFETIL, OXYCARBAMAZEPINE. Patient was hospitalized. Patient recovered.

Asacol Side Effects Report #5452345-4
Consumer or non-health professional from UNITED STATES reported ASACOL problem on Sept 12, 2007. Male patient, 46 years of age, weighting 150.0 lb, was diagnosed with colitis ulcerative and was treated with ASACOL. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, kidney fibrosis, renal impairment, . ASACOL dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.


Fabrazyme Side Effects Report #5474886-6
FABRAZYME problem was reported by a Physician from DENMARK on Sept 14, 2007. Male patient, 40 years of age, weighting 202.8 lb, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, renal impairment, . FABRAZYME dosage: 90MG Q2WKS IV. During the same period patient was treated with PANTOPRAZOL, BUMETANID, PREDNISOLONE, CIPROFLOXACIN, CYCLOSPORINE, MYCOPHENOLATMOFETIL, ACETYLSALICYLACID, OXCARBAZEPIN. Patient was hospitalized. Patient recovered.

Diovan Side Effects Report #5376800-0
Physician from JAPAN reported DIOVAN problem on June 25, 2007. Female patient, 52 years of age, weighting 105.8 lb, was diagnosed with hypertension, gastritis, hypersensitivity and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, eyelid oedema, hypoalbuminaemia, hypoproteinaemia, malaise, nephritis interstitial, nephrotic syndrome, oedema peripheral, protein urine present, . DIOVAN dosage: 80 MG/DAY. During the same period patient was treated with NORVASC, GASTER, ZYRTEC, CELESTAMINE, CYANOCOBALAMIN. Patient was hospitalized. Patient recovered.

Cyclosporine Side Effects Report #5387327-4
CYCLOSPORINE problem was reported by a Physician from AUSTRIA on July 05, 2007. Male patient, 43 years of age, was diagnosed with renal transplant, hepatitis b, hypertension and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood creatinine increased, blood urea increased, disease recurrence, glomerulonephritis membranoproliferative, oedema peripheral, proteinuria, renal failure, . CYCLOSPORINE dosage: unknown. During the same period patient was treated with CERTICAN, CELLCEPT, PREDNISOLONE, ZEFFIX, LIDOPRINTE, NIFEDIPINE, REPRIL. Patient was hospitalized and became disabled. Patient recovered.

Diovan Side Effects Report #5376800-0
Physician from JAPAN reported DIOVAN problem on June 25, 2007. Female patient, 52 years of age, weighting 105.8 lb, was diagnosed with hypertension, gastritis, hypersensitivity and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, eyelid oedema, hypoalbuminaemia, hypoproteinaemia, malaise, nephritis interstitial, nephrotic syndrome, oedema peripheral, protein urine present, . DIOVAN dosage: 80 MG/DAY. During the same period patient was treated with NORVASC, GASTER, ZYRTEC, CELESTAMINE, CYANOCOBALAMIN. Patient was hospitalized. Patient recovered.

Cyclosporine Side Effects Report #5387327-4
CYCLOSPORINE problem was reported by a Physician from AUSTRIA on July 05, 2007. Male patient, 43 years of age, was diagnosed with renal transplant, hepatitis b, hypertension and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood creatinine increased, blood urea increased, disease recurrence, glomerulonephritis membranoproliferative, oedema peripheral, proteinuria, renal failure, . CYCLOSPORINE dosage: unknown. During the same period patient was treated with CERTICAN, CELLCEPT, PREDNISOLONE, ZEFFIX, LIDOPRINTE, NIFEDIPINE, REPRIL. Patient was hospitalized and became disabled. Patient recovered.

Tacrolimus Side Effects Report #5792333-1
Physician from JAPAN reported TACROLIMUS problem on June 12, 2008. Female patient, child 12 years of age, weighting 58.86 lb, was diagnosed with renal transplant and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood phosphorus decreased, cytomegalovirus infection, disease recurrence, escherichia sepsis, focal segmental glomerulosclerosis, haemodialysis, hyperlipidaemia, . TACROLIMUS dosage: 4.00 MG, BID, ORAL, 4 MG, UID/QD, ORAL, 2 MG, D, ORAL, 1.5 MG, BID, ORAL, 2 MG, BID, ORAL,. During the same period patient was treated with PROGRAF. Patient recovered.

Rasilez Side Effects Report #5699716-9
RASILEZ problem was reported by a Physician from on Apr 03, 2008. Male patient was diagnosed with hypertension and was treated with RASILEZ. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, glomerulonephritis membranous, glucose tolerance test abnormal, glycosylated haemoglobin increased, haematuria, hyperkalaemia, metabolic syndrome, proteinuria, . RASILEZ dosage: unknown. During the same period patient was treated with ACETYLSALICYLIC ACID SRT, ALLOPURINOL, ATENOLOL, TROMCARDINTE, ENALAPRIL MALEATE, TOREM, CARMEN, NOVALGIN. Patient recovered.

Rasilez Side Effects Report #5716428-3
Physician from reported RASILEZ problem on Apr 21, 2008. Male patient, 75 years of age, weighting 187.4 lb, was diagnosed with hypertension, hyperuricaemia and was treated with RASILEZ. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, glomerulonephritis membranous, glucose tolerance test abnormal, glycosylated haemoglobin increased, haematuria, hyperkalaemia, metabolic syndrome, protein total decreased, proteinuria, . RASILEZ dosage: unknown. During the same period patient was treated with ACETYLSALICYLIC ACID SRT, ALLOPURINOL, ATENOLOL, TROMCARDINTE, TOREM, CARMEN, NOVALGIN, DOXAZOSIN MESYLATE. Patient recovered.

Enalapril Side Effects Report #5339500-9
ENALAPRIL MALEATE problem was reported by a Physician from INDIA on Nov 05, 2003. Male patient was diagnosed with hypertension and was treated with ENALAPRIL MALEATE. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, congenital anomaly, neonatal anuria, oligohydramnios, peritoneal dialysis, premature baby, renal tubular disorder, skull malformation, . ENALAPRIL MALEATE dosage: MATERNAL DOSE (5 MG, MATERNAL DOSE). Patient was hospitalized. Patient recovered.

Nisisco Side Effects Report #5282882-7
Consumer or non-health professional from FRANCE reported NISISCO problem on Mar 19, 2007. Male patient, 67 years of age, was diagnosed with hypertension, diabetes mellitus non-insulin-dependent and was treated with NISISCO. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood albumin decreased, glomerulonephritis membranous, nephrotic syndrome, protein urine present, weight increased, . NISISCO dosage: unknown. During the same period patient was treated with LOGIMAX, AVANDAMET. Patient was hospitalized. Patient recovered.

Claventin Side Effects Report #5278615-0
CLAVENTIN problem was reported by a Consumer or non-health professional from FRANCE on Mar 22, 2007. Male patient, 60 years of age, was diagnosed with hyperthermia, hypertension, acute myeloid leukaemia and was treated with CLAVENTIN. After drug was administered, patient experienced the following problems/side effects: biopsy kidney abnormal, blood creatinine increased, renal failure acute, urinary retention, . CLAVENTIN dosage: unknown. During the same period patient was treated with CIPROFLOXACIN, TARGOCID, NISIS, VFEND, ZOPHREN, ARACYTINE, CERUBIDINE, CEFTRIAXONE. Patient was hospitalized. Patient recovered.

Cyclosporine Side Effects Report #5616671-8
Health Professional from NETHERLANDS reported CYCLOSPORINE problem on Jan 28, 2008. Male patient, 51 years of age, weighting 275.6 lb, was diagnosed with liver transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, biopsy kidney abnormal, blood albumin decreased, blood creatinine increased, blood immunoglobulin g decreased, blood immunoglobulin m increased, blood pressure increased, complement factor c3 decreased, complement factor c4 decreased, . CYCLOSPORINE dosage: unknown. During the same period patient was treated with PREDNISONE, LAMIVUDINE, INSULIN. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5403618-2
ZOMETA problem was reported by a Physician from BELGIUM on July 25, 2007. Female patient, 83 years of age, was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: anuria, biopsy kidney abnormal, blood creatinine increased, blood immunoglobulin g increased, dialysis, inflammation, light chain analysis increased, multiple myeloma, renal failure acute, . ZOMETA dosage: unknown. During the same period patient was treated with LIPANTHYL, AMLODIPINE, CONTRAMAL, LEVOTHYROXINE, ASPIRIN, LOORTAN, MOXON, LANITOP. Patient recovered.

Zometa Side Effects Report #5411737-X
Physician from BELGIUM reported ZOMETA problem on Aug 06, 2007. Female patient, 83 years of age, was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: anuria, biopsy kidney abnormal, blood creatinine increased, blood immunoglobulin g increased, dialysis, inflammation, light chain analysis increased, multiple myeloma, nephrosclerosis, . ZOMETA dosage: unknown. During the same period patient was treated with LIPANTHYL, AMLODIPINE, CONTRAMAL, LEVOTHYROXINE, ASPIRIN, LOORTAN, MOXON, LANITOP. Patient recovered.

Zometa Side Effects Report #5399841-6
ZOMETA problem was reported by a Physician from BELGIUM on July 24, 2007. Female patient was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: anuria, biopsy kidney abnormal, blood creatinine increased, dialysis, inflammation, multiple myeloma, renal failure, . ZOMETA dosage: unknown. During the same period patient was treated with LIPANTHYL, AMLODIPINE, CONTRAMAL, LEVOTHYROXINE, ASPIRIN, LOORTAN, MOXON, LANITOP. Patient recovered.

Zometa Side Effects Report #5399841-6
Physician from BELGIUM reported ZOMETA problem on July 24, 2007. Female patient was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: anuria, biopsy kidney abnormal, blood creatinine increased, dialysis, inflammation, multiple myeloma, renal failure, . ZOMETA dosage: unknown. During the same period patient was treated with LIPANTHYL, AMLODIPINE, CONTRAMAL, LEVOTHYROXINE, ASPIRIN, LOORTAN, MOXON, LANITOP. Patient recovered.

Ibuprofen Side Effects Report #5341638-7
IBUPROFEN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on May 18, 2007. Female patient, 36 years of age, was diagnosed with headache and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, biopsy kidney abnormal, blood alkaline phosphatase increased, blood creatinine increased, dermatitis exfoliative, granuloma, hepatic function abnormal, lymphadenopathy, . IBUPROFEN dosage: unknown. Patient was hospitalized. Patient recovered.

Tegretol Side Effects Report #5504841-9
Consumer or non-health professional from JAPAN reported TEGRETOL problem on Oct 24, 2007. Female patient, 41 years of age, was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: anorexia, arthralgia, biopsy kidney abnormal, blood creatinine increased, c-reactive protein increased, diarrhoea, eosinophilia, haemodialysis, nephritis interstitial, . TEGRETOL dosage: unknown. During the same period patient was treated with PEROSPIRONE HYDROCHLORIDE, CLOMIPRAMINE HYDROCHLORIDE, VALPROATE, TEPRENONE. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5479158-1
ZOMETA problem was reported by a Health Professional from SWITZERLAND on Sept 28, 2007. Female patient, 67 years of age, was diagnosed with breast cancer metastatic and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: anorexia, asthenia, biopsy kidney abnormal, blood creatinine increased, fatigue, haemodialysis, nephritis interstitial, . ZOMETA dosage: unknown. During the same period patient was treated with HERCEPTIN. Patient recovered.

Zometa Side Effects Report #5448277-8
Health Professional from SWITZERLAND reported ZOMETA problem on Sept 03, 2007. Female patient, 67 years of age, was diagnosed with breast cancer metastatic and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: anorexia, asthenia, biopsy kidney abnormal, blood creatinine increased, fatigue, haemodialysis, nephritis interstitial, . ZOMETA dosage: unknown. During the same period patient was treated with HERCEPTIN. Patient recovered.

Ciprofloxacin Side Effects Report #5473386-7
CIPROFLOXACIN problem was reported by a Physician from UNITED STATES on Aug 29, 2007. Female patient, 20 years of age, was diagnosed with bronchopneumonia and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: anion gap increased, azotaemia, biopsy kidney abnormal, blood bicarbonate decreased, cough, decreased appetite, fatigue, flank pain, . CIPROFLOXACIN dosage: 1500 MG (750 MG). During the same period patient was treated with TOBRAMYCIN, PULMOZYME, PANCREATIC, CONTRACEPTIVE ORAL. Patient was hospitalized. Patient recovered.

Furosemide Side Effects Report #5387420-6
Consumer or non-health professional from CANADA reported FUROSEMIDE problem on June 30, 2007. Female patient, 18 years of age, was diagnosed with oedema and was treated with FUROSEMIDE. After drug was administered, patient experienced the following problems/side effects: alkalosis hypochloraemic, alkalosis hypokalaemic, biopsy kidney abnormal, blood pressure decreased, face oedema, glomerulonephritis minimal lesion, heart rate increased, hypercapnia, hyponatraemia, . FUROSEMIDE dosage: 120MG DAILY. Patient was hospitalized. Patient recovered.

Furosemide Side Effects Report #5387420-6
FUROSEMIDE problem was reported by a Consumer or non-health professional from CANADA on June 30, 2007. Female patient, 18 years of age, was diagnosed with oedema and was treated with FUROSEMIDE. After drug was administered, patient experienced the following problems/side effects: alkalosis hypochloraemic, alkalosis hypokalaemic, biopsy kidney abnormal, blood pressure decreased, face oedema, glomerulonephritis minimal lesion, heart rate increased, hypercapnia, hyponatraemia, . FUROSEMIDE dosage: 120MG DAILY. Patient was hospitalized. Patient recovered.

Aredia Side Effects Report #5287706-X
Consumer or non-health professional from UNITED STATES reported AREDIA problem on Mar 26, 2007. Female patient, 70 years of age, was diagnosed with osteoporosis and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, albumin globulin ratio decreased, biopsy kidney abnormal, blood albumin decreased, blood calcium decreased, blood creatinine increased, blood glucose increased, blood urea increased, cachexia, . AREDIA dosage: 45MG QMOS. During the same period patient was treated with PREDNISONE, ATENOLOL, LISINOPRIL, NORVASC, ASPIRIN, MAGNESIUM OXIDE, LASIX. Patient was hospitalized. Patient recovered.

Phosphosoda Side Effects Report #5311700-3
PHOSPHOSODA FLAVER NOT SPECIFIED problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 26, 2007. Female patient, 75 years of age, was diagnosed with colonoscopy and was treated with PHOSPHOSODA FLAVER NOT SPECIFIED. After drug was administered, patient experienced the following problems/side effects: anaemia, arterial disorder, biopsy kidney abnormal, discomfort, ischaemia, nephritis interstitial, renal failure acute, renal failure chronic, . PHOSPHOSODA FLAVER NOT SPECIFIED dosage: 45 ML X1 PO. During the same period patient was treated with FLEET PREP, NORVASC, FOSAMAX, LIPITOR, DIOVAN, CEFPROZIL, COREG, PROCRIT. Patient was hospitalized. Patient recovered.

Zoledronic Side Effects Report #5254092-0
Consumer or non-health professional from UNITED STATES reported ZOLEDRONIC ACID problem on Feb 13, 2007. Female patient, 50 years of age, was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: asthenia, back pain, biopsy kidney abnormal, blood creatinine increased, blood urea increased, cardiac tamponade, cholelithiasis, cough, creatinine renal clearance decreased, . ZOLEDRONIC ACID dosage: unknown. During the same period patient was treated with GEMZAR, ANTIHYPERTENSIVES, DARBEPOETIN ALFA, ANASTROZOLE, PALONOSETRON, DEXAMETHASONE PHOSPHATE, GOSERELIN. Patient was hospitalized. Patient recovered.

Cyclophosphamide Side Effects Report #5261503-3
CYCLOPHOSPHAMIDE problem was reported by a Physician from UNITED STATES on Feb 26, 2007. Female patient, 49 years of age, weighting 162.0 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: arthralgia, benign familial haematuria, biopsy kidney abnormal, condition aggravated, protein urine present, rash, red blood cell abnormality, . CYCLOPHOSPHAMIDE dosage: unknown. During the same period patient was treated with PREDNISOLONE, PLAQUENIL, LISINOPRIL, NIFEDIPINE. Patient died.