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Fioricet Side Effects Report #5578982-4
Health Professional from UNITED STATES reported FIORICET problem on Dec 21, 2007. Male patient, 76 years of age, was diagnosed with headache, gout and was treated with FIORICET. After drug was administered, patient experienced the following problems/side effects: kidney fibrosis, nephropathy toxic, renal atrophy, . FIORICET dosage: unknown. During the same period patient was treated with SULINDAC, ACETYLSALICYLIC ACID SRT, ALLOPURINOL, COLCHICINE. Patient recovered.

Ciprofloxacin Side Effects Report #5513576-8
CIPROFLOXACIN problem was reported by a Consumer or non-health professional from ITALY on Oct 29, 2007. Male patient, 74 years of age, weighting 132.3 lb, was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: kidney fibrosis, renal ischaemia, renal tubular disorder, . CIPROFLOXACIN dosage: 750MG TWICE DAILY PO. Patient was hospitalized. Patient recovered.

Ciprofloxacin Side Effects Report #5455074-6
Consumer or non-health professional from ITALY reported CIPROFLOXACIN problem on Aug 27, 2007. Male patient, 74 years of age, was diagnosed with diarrhoea, malaise and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: kidney fibrosis, nephrolithiasis, renal impairment, . CIPROFLOXACIN dosage: 1500 MG (750 MG, 2 IN 1 D). Patient recovered.

Ciprofloxacin Side Effects Report #5455139-9
CIPROFLOXACIN problem was reported by a Physician from ITALY on Aug 31, 2007. Male patient, 74 years of age, weighting 132.3 lb, was diagnosed with diarrhoea and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: kidney fibrosis, nephropathy, renal failure acute, . CIPROFLOXACIN dosage: 750 MG, BID. During the same period patient was treated with ANGIOTENSIN CONVERTING ENZYME BLOCKERS. Patient was hospitalized. Patient recovered.


Ortho Side Effects Report #5413730-X
Physician from UNITED STATES reported ORTHO EVRA problem on May 04, 2007. Female patient, 19 years of age, weighting 135.1 lb, was diagnosed with contraception, ovarian disorder and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: kidney fibrosis, renal vein thrombosis, . ORTHO EVRA dosage: unknown. During the same period patient was treated with ORTHO EVRA. Patient was hospitalized. Patient recovered.

Ortho Side Effects Report #5413730-X
ORTHO EVRA problem was reported by a Physician from UNITED STATES on May 04, 2007. Female patient, 19 years of age, weighting 135.1 lb, was diagnosed with contraception, ovarian disorder and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: kidney fibrosis, renal vein thrombosis, . ORTHO EVRA dosage: unknown. During the same period patient was treated with ORTHO EVRA. Patient was hospitalized. Patient recovered.

Truvada Side Effects Report #5315060-3
Health Professional from SPAIN reported TRUVADA problem on Apr 23, 2007. Male patient, 74 years of age, was treated with TRUVADA. After drug was administered, patient experienced the following problems/side effects: kidney fibrosis, renal failure acute, . TRUVADA dosage: unknown. During the same period patient was treated with KALETRA, SEPTRA. Patient was hospitalized. Patient recovered.

Osmoprep Side Effects Report #5481633-0
OSMOPREP problem was reported by a Physician from UNITED STATES on Sept 27, 2007. Female patient, 58 years of age, weighting 160.0 lb, was diagnosed with colonoscopy and was treated with OSMOPREP. After drug was administered, patient experienced the following problems/side effects: arteriosclerosis, kidney fibrosis, nephrocalcinosis, nephrosclerosis, procedural pain, renal failure acute, renal tubular atrophy, . OSMOPREP dosage: unknown. During the same period patient was treated with LISINOPRIL, ASACOL, IBUPROFEN. Patient was hospitalized. Patient recovered.

Ciprofloxacin Side Effects Report #5495507-2
Consumer or non-health professional from ITALY reported CIPROFLOXACIN problem on Oct 10, 2007. Male patient, 74 years of age, was diagnosed with diarrhoea and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, kidney fibrosis, nephropathy, . CIPROFLOXACIN dosage: 750MG,BID,ORAL. Patient was hospitalized. Patient recovered.


Lithium Side Effects Report #5504477-X
LITHIUM CARBONATE problem was reported by a Consumer or non-health professional from GERMANY on Oct 16, 2007. Female patient, 51 years of age, was diagnosed with affective disorder and was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: hypothyroidism, kidney fibrosis, nephrogenic diabetes insipidus, nephropathy, overweight, renal cyst, renal failure, renal tubular atrophy, . LITHIUM CARBONATE dosage: unknown. Patient was hospitalized. Patient recovered.

Urso Side Effects Report #5449609-7
Consumer or non-health professional from CANADA reported URSO problem on Aug 24, 2007. Male patient, 67 years of age, was diagnosed with cholangitis sclerosing and was treated with URSO. After drug was administered, patient experienced the following problems/side effects: autoimmune disorder, kidney fibrosis, pancreatitis, tubulointerstitial nephritis, . URSO dosage: 1000 MG ORAL. During the same period patient was treated with NEXIUM, METFORMIN. Patient recovered.

Asacol Side Effects Report #5452345-4
ASACOL problem was reported by a Consumer or non-health professional from UNITED STATES 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.

Aspirin Side Effects Report #5413403-3
Health Professional from JAPAN reported ASPIRIN problem on Aug 10, 2007. Male patient, 74 years of age, was diagnosed with hypertension and was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: fat embolism, kidney fibrosis, renal impairment, renal tubular atrophy, . ASPIRIN dosage: unknown. During the same period patient was treated with WARFARIN, STATIN, CALCIUM CHANNEL BLOCKERS, ANGIOTENSIN II RECEPTOR BLOCKERS. Patient was hospitalized. Patient recovered.

Phosphosoda Side Effects Report #5422137-0
PHOSPHOSODA FLAVOR NOT SPECIFIED problem was reported by a Physician from UNITED STATES on Aug 21, 2007. Female patient, 60 years of age, was diagnosed with colonoscopy and was treated with PHOSPHOSODA FLAVOR NOT SPECIFIED. After drug was administered, patient experienced the following problems/side effects: glomerulosclerosis, kidney fibrosis, nephritis interstitial, nephrocalcinosis, nephrosclerosis, post procedural complication, renal failure acute, renal ischaemia, renal tubular disorder, . PHOSPHOSODA FLAVOR NOT SPECIFIED dosage: unknown. Patient recovered.


Neoral Side Effects Report #5386204-2
Consumer or non-health professional from JAPAN reported NEORAL problem on July 05, 2007. Male patient, 15 years of age, weighting 136.7 lb, was diagnosed with nephrotic syndrome and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: glomerulosclerosis, kidney fibrosis, nephropathy toxic, nephrotic syndrome, therapeutic response decreased, . NEORAL dosage: 125 MG/DAY. Patient recovered.

Neoral Side Effects Report #5386204-2
NEORAL problem was reported by a Consumer or non-health professional from JAPAN on July 05, 2007. Male patient, 15 years of age, weighting 136.7 lb, was diagnosed with nephrotic syndrome and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: glomerulosclerosis, kidney fibrosis, nephropathy toxic, nephrotic syndrome, therapeutic response decreased, . NEORAL dosage: 125 MG/DAY. Patient recovered.

Phosphosoda Side Effects Report #5352529-X
Consumer or non-health professional from UNITED STATES reported PHOSPHOSODA GINGER LEMON problem on June 07, 2007. Male patient, weighting 240.0 lb, was diagnosed with colonoscopy and was treated with PHOSPHOSODA GINGER LEMON. After drug was administered, patient experienced the following problems/side effects: focal glomerulosclerosis, kidney fibrosis, nephrocalcinosis, postoperative renal failure, renal arteriosclerosis, renal failure chronic, tubulointerstitial nephritis, . PHOSPHOSODA GINGER LEMON dosage: 45 ML;X1;PO. During the same period patient was treated with FLEET ENEMA, VERSED, FENTANYL, XANAX, FLOMAX, ZESTORETIC, TOPROL. Patient recovered.

Carbamazepine Side Effects Report #5367668-7
CARBAMAZEPINE problem was reported by a Consumer or non-health professional from GERMANY on June 11, 2007. Female patient, 39 years of age, was diagnosed with epilepsy and was treated with CARBAMAZEPINE. After drug was administered, patient experienced the following problems/side effects: haemodialysis, kidney fibrosis, renal failure chronic, . CARBAMAZEPINE dosage: unknown. Patient recovered.

Phosphosoda Side Effects Report #5377212-6
Consumer or non-health professional from UNITED STATES reported PHOSPHOSODA UNFLAVORED problem on June 29, 2007. Male patient, 58 years of age, weighting 198.0 lb, was diagnosed with sigmoidoscopy and was treated with PHOSPHOSODA UNFLAVORED. After drug was administered, patient experienced the following problems/side effects: glomerulosclerosis, kidney fibrosis, nephritis interstitial, nephrogenic anaemia, renal failure acute, . PHOSPHOSODA UNFLAVORED dosage: 45 ML;X1;PO. During the same period patient was treated with HYDROCHLOROTHIAZIDE, LOVASTATIN, VIAGRA. Patient was hospitalized. Patient recovered.


Cyclosporine Side Effects Report #5661606-5
CYCLOSPORINE problem was reported by a Health Professional from JAPAN on Mar 07, 2008. Male patient, 56 years of age, was diagnosed with psoriasis and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, focal glomerulosclerosis, kidney fibrosis, nephritis interstitial, oedema peripheral, proteinuria, renal failure, urine protein/creatinine ratio increased, . CYCLOSPORINE dosage: unknown. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5637179-X
Consumer or non-health professional from UNITED KINGDOM reported HUMIRA problem on Feb 15, 2008. Female patient, weighting 103.6 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: cardiac failure congestive, chronic obstructive pulmonary disease, kidney fibrosis, myocardial ischaemia, renal ischaemia, . HUMIRA dosage: unknown. During the same period patient was treated with LEFLUNOMIDE, ATENOLOL, CELECOXIB, PARAMOL, DIHYDROCODEINE BITARTRATE, NITROGLYCERIN, LANSOPRAZOLE, RAMIPRIL. Patient died on 10/03/2007.

Ifosfamide Side Effects Report #5510154-1
IFOSFAMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 31, 2007. Male patient, 31 years of age, was diagnosed with neuroectodermal neoplasm and was treated with IFOSFAMIDE. After drug was administered, patient experienced the following problems/side effects: fanconi syndrome, febrile neutropenia, kidney fibrosis, nausea, osteomalacia, vomiting, . IFOSFAMIDE dosage: unknown. During the same period patient was treated with DOXORUBICIN, ETOPOSIDE, VINCRISTINE SULPHATE. Patient was hospitalized. Patient recovered.

Azasan Side Effects Report #5510687-8
Consumer or non-health professional from UNITED STATES reported AZASAN problem on Oct 29, 2007. Male patient, 33 years of age, was diagnosed with colitis ulcerative and was treated with AZASAN. After drug was administered, patient experienced the following problems/side effects: dehydration, glomerulosclerosis, kidney fibrosis, meniere's disease, nephritis interstitial, pyrexia, renal arteriosclerosis, renal failure acute, renal tubular atrophy, . AZASAN dosage: 50 MG;QD;. During the same period patient was treated with COLAZAL, PRIMAL DEFENSE, PREDNISONE, MECLIZINE. Patient was hospitalized. Patient recovered.

Ifosfamide Side Effects Report #5500298-2
IFOSFAMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 24, 2007. Male patient, 31 years of age, was diagnosed with neuroectodermal neoplasm and was treated with IFOSFAMIDE. After drug was administered, patient experienced the following problems/side effects: fanconi syndrome, febrile neutropenia, kidney fibrosis, nausea, osteomalacia, vomiting, . IFOSFAMIDE dosage: unknown. During the same period patient was treated with DOXORUBICIN, ETOPOSIDE, VINCRISTINE SULPHATE. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5500643-8
Physician from UNITED STATES reported PROGRAF problem on Oct 10, 2007. Male patient, 48 years of age, was diagnosed with liver transplant, osteopenia and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: focal glomerulosclerosis, hyperplasia, kidney fibrosis, liver transplant rejection, osteopenia, renal tubular atrophy, renal vessel disorder, . PROGRAF dosage: ORAL; 9 MG, UID/QD, ORAL. During the same period patient was treated with CORTICOSTEROIDS, MYCOPHENOLATE MOFETIL, PREDNISONE, ALENDRONATE. Patient recovered.

Ifosfamide Side Effects Report #5463275-6
IFOSFAMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 12, 2007. Male patient, 31 years of age, was diagnosed with neuroectodermal neoplasm and was treated with IFOSFAMIDE. After drug was administered, patient experienced the following problems/side effects: fanconi syndrome, febrile neutropenia, kidney fibrosis, nausea, osteomalacia, vomiting, . IFOSFAMIDE dosage: unknown. During the same period patient was treated with VINCRISTINE, DOXORUBICIN, ETOPOSIDE. Patient was hospitalized. Patient recovered.

Neoral Side Effects Report #5388992-8
Consumer or non-health professional from JAPAN reported NEORAL problem on July 06, 2007. Male patient, 15 years of age, weighting 136.7 lb, was diagnosed with nephrotic syndrome and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: chronic sinusitis, glomerulosclerosis, kidney fibrosis, nephritis, nephropathy toxic, nephrotic syndrome, protein urine present, therapeutic response decreased, . NEORAL dosage: 125 MG/DAY. Patient recovered.

Certican Side Effects Report #5389842-6
CERTICAN problem was reported by a Physician from BRAZIL on July 12, 2007. Female patient, 30 years of age, weighting 116.8 lb, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemolytic anaemia, kidney fibrosis, oedema, post procedural haemorrhage, red blood cell abnormality, renal impairment, renal tubular necrosis, renal vessel disorder, . CERTICAN dosage: 1.5 MG, BID. During the same period patient was treated with NEORAL, PREDNISONE. Patient was hospitalized. Patient recovered.

Certican Side Effects Report #5399861-1
Physician from BRAZIL reported CERTICAN problem on July 19, 2007. Female patient, 30 years of age, weighting 116.8 lb, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemolytic anaemia, kidney fibrosis, oedema, post procedural haemorrhage, red blood cell abnormality, renal impairment, renal tubular necrosis, renal vessel disorder, . CERTICAN dosage: 1.5 MG, BID. During the same period patient was treated with NEORAL, PREDNISONE. Patient was hospitalized. Patient recovered.

Neoral Side Effects Report #5388992-8
NEORAL problem was reported by a Consumer or non-health professional from JAPAN on July 06, 2007. Male patient, 15 years of age, weighting 136.7 lb, was diagnosed with nephrotic syndrome and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: chronic sinusitis, glomerulosclerosis, kidney fibrosis, nephritis, nephropathy toxic, nephrotic syndrome, protein urine present, therapeutic response decreased, . NEORAL dosage: 125 MG/DAY. Patient recovered.

Certican Side Effects Report #5389842-6
Physician from BRAZIL reported CERTICAN problem on July 12, 2007. Female patient, 30 years of age, weighting 116.8 lb, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemolytic anaemia, kidney fibrosis, oedema, post procedural haemorrhage, red blood cell abnormality, renal impairment, renal tubular necrosis, renal vessel disorder, . CERTICAN dosage: 1.5 MG, BID. During the same period patient was treated with NEORAL, PREDNISONE. Patient was hospitalized. Patient recovered.

Certican Side Effects Report #5399861-1
CERTICAN problem was reported by a Physician from BRAZIL on July 19, 2007. Female patient, 30 years of age, weighting 116.8 lb, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemolytic anaemia, kidney fibrosis, oedema, post procedural haemorrhage, red blood cell abnormality, renal impairment, renal tubular necrosis, renal vessel disorder, . CERTICAN dosage: 1.5 MG, BID. During the same period patient was treated with NEORAL, PREDNISONE. Patient was hospitalized. Patient recovered.

Furosemide Side Effects Report #5758086-8
Consumer or non-health professional from UNITED STATES reported FUROSEMIDE problem on June 02, 2008. Male patient, 73 years of age, weighting 149.9 lb, was treated with FUROSEMIDE. After drug was administered, patient experienced the following problems/side effects: haemodialysis, hyperoxaluria, kidney fibrosis, nephropathy, renal failure, . FUROSEMIDE dosage: unknown. During the same period patient was treated with VITAMIN D, ASCORBIC ACID, LISINOPRIL, VITAMIN A, CACO, LEVOTHYROXINE, MAGNESIUM OXIDE, NIACIN. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5753055-6
PROGRAF problem was reported by a Health Professional from SWITZERLAND on May 09, 2008. Male patient, 26 years of age, was diagnosed with stem cell transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, haemoglobin decreased, kidney fibrosis, platelet count decreased, renal tubular atrophy, thrombotic microangiopathy, . PROGRAF dosage: unknown. During the same period patient was treated with RAPAMUNE, CYCLOSPORINE, CELLCEPT, PREDNISOLONE ACETATE, DIFLUCAN, BACTRIM, FAMVIR. Patient was hospitalized. Patient recovered.

Certican Side Effects Report #5363777-7
Physician from BRAZIL reported CERTICAN problem on June 08, 2007. Female patient, 30 years of age, weighting 116.8 lb, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemolytic anaemia, kidney fibrosis, oedema, post procedural haemorrhage, red blood cell abnormality, renal impairment, renal tubular necrosis, renal vessel disorder, . CERTICAN dosage: 1.5 MG, BID. During the same period patient was treated with NEORAL, PREDNISONE. Patient was hospitalized. Patient recovered.

Phosphosoda Side Effects Report #5333199-3
PHOSPHOSODA FLAVOR NOT SPECIFIED problem was reported by a Physician from UNITED STATES on May 21, 2007. Female patient, 66 years of age, was diagnosed with colonoscopy and was treated with PHOSPHOSODA FLAVOR NOT SPECIFIED. After drug was administered, patient experienced the following problems/side effects: feeling cold, gait disturbance, kidney fibrosis, nephrocalcinosis, renal impairment, renal tubular disorder, sensation of heaviness, . PHOSPHOSODA FLAVOR NOT SPECIFIED dosage: 45 ML;X1;PO. During the same period patient was treated with PREMARIN, CLONIDINE. Patient was hospitalized and became disabled. Patient recovered.

Pentasa Side Effects Report #5334161-7
Health Professional from DENMARK reported PENTASA problem on May 11, 2007. Male patient, 51 years of age, was diagnosed with colitis ulcerative and was treated with PENTASA. After drug was administered, patient experienced the following problems/side effects: haematuria, kidney fibrosis, malaise, nephritis interstitial, renal tubular atrophy, . PENTASA dosage: unknown. During the same period patient was treated with BUDESONIDE, DOLEX, BISOPROLOL FUMARATE. Patient recovered.

Certican Side Effects Report #5334373-2
CERTICAN problem was reported by a Physician from BRAZIL on May 14, 2007. Female patient, 30 years of age, weighting 116.8 lb, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, haemolytic anaemia, kidney fibrosis, oedema, post procedural haemorrhage, red blood cell abnormality, renal impairment, renal tubular necrosis, renal vessel disorder, . CERTICAN dosage: 1.5 MG, BID. During the same period patient was treated with NEORAL, PREDNISONE. Patient was hospitalized. Patient recovered.

Omniscan Side Effects Report #5258614-5
Consumer or non-health professional from DENMARK reported OMNISCAN problem on Feb 20, 2007. Female patient, 50 years of age, was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: depression, insomnia, kidney fibrosis, myalgia, weight decreased, . OMNISCAN dosage: 50 ML, SINGLE DOSE, IV. Patient recovered.