Menu

• Ask a Health Expert about CHRONIC ALLOGRAFT NEPHROPATHY
• Post Your Side Effect related to CHRONIC ALLOGRAFT NEPHROPATHY
• CHRONIC ALLOGRAFT NEPHROPATHY and FDA Warnings
• CHRONIC ALLOGRAFT NEPHROPATHY in Patients Wiki
• Report CHRONIC ALLOGRAFT NEPHROPATHY in Drug Side Effect Survey

CHRONIC ALLOGRAFT NEPHROPATHY side effect

What is CHRONIC ALLOGRAFT NEPHROPATHY ?

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

Type your question here

 letters left

Ultra Side Effects Report #5619808-X
Physician from BELGIUM reported ULTRA problem on Feb 01, 2008. Female patient, 53 years of age, weighting 145.5 lb, was diagnosed with renal transplant and was treated with ULTRA. After drug was administered, patient experienced the following problems/side effects: chronic allograft nephropathy, transplant rejection, . ULTRA dosage: unknown. During the same period patient was treated with PYRIDOXINE, CALCIUM CARBONATE, ALPHA, XANAX, MEDROL, NEORAL, BACTRIM. Patient was hospitalized. Patient recovered.

Cyclosporine Side Effects Report #5624220-3
CYCLOSPORINE problem was reported by a Consumer or non-health professional from JAPAN on Feb 06, 2008. Male patient, 52 years of age, was diagnosed with renal transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: chronic allograft nephropathy, liver disorder, ureteric perforation, . CYCLOSPORINE dosage: unknown. During the same period patient was treated with SIMULECT, MYCOPHENOLATE MOFETIL, METHYLPREDNISOLONE. Patient recovered.

Basiliximab Side Effects Report #5625984-5
Consumer or non-health professional from reported BASILIXIMAB problem on Feb 06, 2008. Male patient, 38 years of age, was diagnosed with renal transplant and was treated with BASILIXIMAB. After drug was administered, patient experienced the following problems/side effects: chronic allograft nephropathy, kidney transplant rejection, polyomavirus-associated nephropathy, . BASILIXIMAB dosage: 20 MG, UNK. During the same period patient was treated with PROGRAF, CELLCEPT, METHYLPREDNISOLONE. Patient recovered.

Prograf Side Effects Report #5521068-5
PROGRAF problem was reported by a Health Professional from UNITED STATES on Nov 06, 2007. Female patient, 63 years of age, weighting 133.8 lb, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: chronic allograft nephropathy, . PROGRAF dosage: 2.5 MG, BID, ORAL. During the same period patient was treated with CELLCEPT. Patient was hospitalized. Patient recovered.


Azathioprine Side Effects Report #5479872-8
Consumer or non-health professional from reported AZATHIOPRINE problem on Oct 01, 2007. Female patient, 59 years of age, was diagnosed with immunosuppression, renal impairment and was treated with AZATHIOPRINE. After drug was administered, patient experienced the following problems/side effects: chronic allograft nephropathy, complications of transplanted kidney, graft dysfunction, proteinuria, scedosporium infection, transplant rejection, . AZATHIOPRINE dosage: unknown. During the same period patient was treated with CYCLOSPORINE, METHYLPREDNISOLONE, MYCOPHENOLATE MOFETIL. Patient recovered.

Tacrolimus Side Effects Report #5500150-2
TACROLIMUS problem was reported by a Physician from TAIWAN, PROVINCE OF CHINA on Oct 11, 2007. Male patient, child 12 years of age, was diagnosed with renal transplant and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: chronic allograft nephropathy, complications of transplanted kidney, kidney transplant rejection, peritoneal dialysis, transitional cell carcinoma, . TACROLIMUS dosage: unknown. During the same period patient was treated with MYCOPHENOLIC ACID, METHYLPREDNISOLONE, CYCLOSPORINE. Patient recovered.

Prograf Side Effects Report #5452036-X
Health Professional from UNITED STATES reported PROGRAF problem on Sept 04, 2007. Male patient was diagnosed with prophylaxis against transplant rejection and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: chronic allograft nephropathy, . PROGRAF dosage: 2 MG, BID, ORAL. Patient died.

Prograf Side Effects Report #5429224-1
PROGRAF problem was reported by a Physician from JAPAN on Aug 08, 2007. Female patient, 55 years of age, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: chronic allograft nephropathy, cytomegalovirus infection, glomerulonephritis, transplant rejection, . PROGRAF dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL, METHYLPREDNISOLONE, SIMULECT, GANCICLOVIR, STEROID, GUSPERIMUS HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Mycophenolate Side Effects Report #5400274-4
Physician from KUWAIT reported MYCOPHENOLATE MOFETIL problem on July 17, 2007. Male patient, 40 years of age, was diagnosed with diabetes mellitus and was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: chronic allograft nephropathy, crohn's disease, diabetes mellitus, lower respiratory tract infection, lymphopenia, sepsis, skin infection, transplant rejection, upper respiratory tract infection, . MYCOPHENOLATE MOFETIL dosage: unknown. During the same period patient was treated with TACROLIMUS, PREDNISOLONE, BASILIXIMAB, CYCLOSPORINE, METHYLPREDNISOLONE, ORTHOCLONE OKT, INSULIN. Patient was hospitalized. Patient recovered.


Mycophenolate Side Effects Report #5400274-4
MYCOPHENOLATE MOFETIL problem was reported by a Physician from KUWAIT on July 17, 2007. Male patient, 40 years of age, was diagnosed with diabetes mellitus and was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: chronic allograft nephropathy, crohn's disease, diabetes mellitus, lower respiratory tract infection, lymphopenia, sepsis, skin infection, transplant rejection, upper respiratory tract infection, . MYCOPHENOLATE MOFETIL dosage: unknown. During the same period patient was treated with TACROLIMUS, PREDNISOLONE, BASILIXIMAB, CYCLOSPORINE, METHYLPREDNISOLONE, ORTHOCLONE OKT, INSULIN. Patient was hospitalized. Patient recovered.

Sirolimus Side Effects Report #5316503-1
Health Professional from FRANCE reported SIROLIMUS problem on Apr 24, 2007. Male patient, 54 years of age, was diagnosed with prophylaxis against transplant rejection, lung neoplasm malignant and was treated with SIROLIMUS. After drug was administered, patient experienced the following problems/side effects: chronic allograft nephropathy, non-small cell lung cancer, thrombotic microangiopathy, . SIROLIMUS dosage: unknown. During the same period patient was treated with CARBOPLATIN, GEMCITABINE, MYCOPHENOLATE MOFETIL, MYCOPHENOLATE MOFETIL, PREDNISONE. Patient was hospitalized. Patient recovered.

Sirolimus Side Effects Report #5253365-5
SIROLIMUS problem was reported by a Physician from UNITED KINGDOM on Feb 23, 2007. Female patient, weighting 110.2 lb, was diagnosed with renal transplant, immunosuppression and was treated with SIROLIMUS. After drug was administered, patient experienced the following problems/side effects: chronic allograft nephropathy, . SIROLIMUS dosage: unknown. During the same period patient was treated with RANITIDINE, FERROUS SULPHATE, ADALAT PA, LISINOPRIL, FUROSEMIDE, CEPHALEXIN, PREDNISOLONE. Patient was hospitalized. Patient recovered.

Cyclosporine Side Effects Report #5254213-X
Consumer or non-health professional from UNITED STATES reported CYCLOSPORINE problem on Feb 19, 2007. Male patient, 46 years of age, was diagnosed with renal transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: chronic allograft nephropathy, complications of transplant surgery, complications of transplanted kidney, kidney anastomosis, thrombotic microangiopathy, . CYCLOSPORINE dosage: 800 MG, QD. During the same period patient was treated with PREDNISONE, MYCOPHENOLATE MOFETIL. Patient recovered.

Azathioprine Side Effects Report #5689583-1
AZATHIOPRINE problem was reported by a Physician from FRANCE on Mar 17, 2008. Female patient, 62 years of age, was treated with AZATHIOPRINE. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, chronic allograft nephropathy, haemodialysis, hydrocephalus, meningitis cryptococcal, nephropathy toxic, . AZATHIOPRINE dosage: unknown. During the same period patient was treated with PREDNISONE. Patient was hospitalized. Patient recovered.


Cyclosporine Side Effects Report #5597114-X
Health Professional from AUSTRALIA reported CYCLOSPORINE problem on Jan 09, 2008. Female patient, 36 years of age, was diagnosed with renal transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, chronic allograft nephropathy, deep vein thrombosis, focal glomerulosclerosis, haemodialysis, nephritis interstitial, nephrogenic systemic fibrosis, nephropathy toxic, rash papular, . CYCLOSPORINE dosage: 75 MG, BID. During the same period patient was treated with AZATHIOPRINE, MYCOPHENOLATE MOFETIL, PREDNISOLONE. Patient recovered.

Certican Side Effects Report #5607616-5
CERTICAN problem was reported by a Physician from GERMANY on Jan 21, 2008. Female patient, 48 years of age, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, chronic allograft nephropathy, proteinuria, . CERTICAN dosage: 1.25 MG, BID. During the same period patient was treated with URBASON, MYFORTIC. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5573978-0
Physician from UNITED STATES reported PROGRAF problem on Dec 04, 2007. Female patient, 23 years of age, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, chronic allograft nephropathy, pre-eclampsia, pregnancy, . PROGRAF dosage: 6 MG, BID, ORAL. Patient died.

Prograf Side Effects Report #5413451-3
PROGRAF problem was reported by a Physician from JAPAN on July 26, 2007. Female patient, 29 years of age, weighting 103.6 lb, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: antibody test positive, chronic allograft nephropathy, meningitis cryptococcal, nephritis interstitial, nephropathy toxic, polyomavirus-associated nephropathy, renal arteriosclerosis, renal tubular disorder, transplant rejection, . PROGRAF dosage: 4 MG, D, IV NOS. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISOLONE, PREDNISONE, DEOXYSPERGUALIN, AZATHIOPRINE, NEROL. Patient was hospitalized. Patient recovered.

Mycophenolate Side Effects Report #5736061-7
Health Professional from AUSTRALIA reported MYCOPHENOLATE MOFETIL problem on May 02, 2008. Female patient, 36 years of age, was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, chronic allograft nephropathy, deep vein thrombosis, focal glomerulosclerosis, nephritis interstitial, nephrogenic systemic fibrosis, nephropathy toxic, rash papular, . MYCOPHENOLATE MOFETIL dosage: unknown. During the same period patient was treated with AZATHIOPRINE, CYCLOSPORINE, PREDNISOLONE. Patient recovered.


Neoral Side Effects Report #5336469-8
NEORAL problem was reported by a Physician from UNITED KINGDOM on May 22, 2007. Female patient, weighting 154.3 lb, was diagnosed with immunosuppression, glaucoma, restless legs syndrome, hypertension, hypercholesterolaemia, prophylaxis against gastrointestinal ulcer, angina pectoris, left ventricular failure and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, chronic allograft nephropathy, dehydration, diarrhoea, hypokalaemia, lower respiratory tract infection, syncope, white blood cell count decreased, . NEORAL dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL, TRAVOPROST, GABAPENTIN, ATENOLOL, PRAVASTATIN, OMEPRAZOLE, ISOSORBIDE MONONITRATE, ISOSORBIDE MONONITRATE. Patient was hospitalized. Patient recovered.

Basiliximab Side Effects Report #5626009-8
Health Professional from FRANCE reported BASILIXIMAB problem on Feb 06, 2008. Male patient, 63 years of age, was diagnosed with renal transplant and was treated with BASILIXIMAB. After drug was administered, patient experienced the following problems/side effects: ascites, cardiac tamponade, chronic allograft nephropathy, complications of transplanted kidney, kidney transplant rejection, pericarditis, pleural effusion, primary effusion lymphoma, renal impairment, . BASILIXIMAB dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISONE, RAPAMYCIN, CYCLOSPORINE. Patient was hospitalized. Patient died.

Basiliximab Side Effects Report #5629885-8
BASILIXIMAB problem was reported by a Consumer or non-health professional from on Feb 13, 2008. Male patient, 38 years of age, was diagnosed with renal transplant and was treated with BASILIXIMAB. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, cells in urine, chronic allograft nephropathy, kidney transplant rejection, polyomavirus-associated nephropathy, renal impairment, . BASILIXIMAB dosage: 20 MG, UNK. During the same period patient was treated with PROGRAF, CELLCEPT, METHYLPREDNISOLONE. Patient recovered.

Predonine Side Effects Report #5633563-9
Consumer or non-health professional from reported PREDONINE problem on Feb 15, 2008. Male patient, 38 years of age, was diagnosed with renal transplant and was treated with PREDONINE. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, cells in urine, chronic allograft nephropathy, kidney transplant rejection, polyomavirus-associated nephropathy, renal impairment, . PREDONINE dosage: unknown. During the same period patient was treated with SIMULECT, DEOXYSPERGUALIN, PROGRAF, CELLCEPT, METHYLPREDNISOLONE. Patient recovered.

Mycophenolate Side Effects Report #5582923-3
MYCOPHENOLATE MOFETIL problem was reported by a Health Professional from AUSTRALIA on Jan 02, 2008. Female patient, 39 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: anal ulcer, blood creatinine increased, chronic allograft nephropathy, cytomegalovirus infection, herpes simplex, . MYCOPHENOLATE MOFETIL dosage: unknown. During the same period patient was treated with CYCLOSPORINE, PREDNISOLONE. Patient was hospitalized. Patient recovered.

Rapamune Side Effects Report #5594656-8
Health Professional from FRANCE reported RAPAMUNE problem on Jan 14, 2008. Female patient, weighting 119.0 lb, was diagnosed with prophylaxis against transplant rejection, actinic keratosis and was treated with RAPAMUNE. After drug was administered, patient experienced the following problems/side effects: asthenia, blood lactate dehydrogenase increased, chronic allograft nephropathy, cryptogenic organising pneumonia, interstitial lung disease, left ventricular failure, systemic inflammatory response syndrome, tremor, . RAPAMUNE dosage: unknown. During the same period patient was treated with LASIX, COZAAR, TAVANIC, MOPRAL, ARANESP, LEXOMIL. Patient was hospitalized. Patient recovered.

Rapamune Side Effects Report #5479444-5
RAPAMUNE problem was reported by a Health Professional from FRANCE on Sept 28, 2007. Female patient, weighting 119.0 lb, was diagnosed with prophylaxis against transplant rejection, actinic keratosis and was treated with RAPAMUNE. After drug was administered, patient experienced the following problems/side effects: asthenia, blood lactate dehydrogenase increased, chronic allograft nephropathy, cryptogenic organising pneumonia, left ventricular failure, lung disorder, systemic inflammatory response syndrome, tremor, . RAPAMUNE dosage: unknown. During the same period patient was treated with LASIX, ARANESP, TAHOR, OMEPRAZOLE, MYFORTIC, COZAAR. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5448187-6
Physician from FRANCE reported TACROLIMUS problem on Aug 22, 2007. Female patient, 62 years of age, was diagnosed with renal transplant and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: acute vestibular syndrome, blood pressure increased, chronic allograft nephropathy, diabetes mellitus, enterocolitis haemorrhagic, escherichia infection, haemodialysis, headache, herpes zoster, . TACROLIMUS dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL, CORTICOSTEROIDS, ANTITHYMOCYTE IMMUNOGLOBULIN, ORTHOCLONE OKT, AZATHIOPRINE. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5401451-9
PROGRAF problem was reported by a Physician from JAPAN on July 09, 2007. Male patient, 58 years of age, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: aortic aneurysm, aortic calcification, chronic allograft nephropathy, continuous haemodiafiltration, diabetes mellitus, post procedural complication, renal failure chronic, renal impairment, . PROGRAF dosage: 4 MG, D, ORAL. During the same period patient was treated with PREDNISOLONE, MIZORIBINE. Patient died.

Prograf Side Effects Report #5401451-9
Physician from JAPAN reported PROGRAF problem on July 09, 2007. Male patient, 58 years of age, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: aortic aneurysm, aortic calcification, chronic allograft nephropathy, continuous haemodiafiltration, diabetes mellitus, post procedural complication, renal failure chronic, renal impairment, . PROGRAF dosage: 4 MG, D, ORAL. During the same period patient was treated with PREDNISOLONE, MIZORIBINE. Patient died.

Cyclosporine Side Effects Report #5355943-1
CYCLOSPORINE problem was reported by a Health Professional from FRANCE on June 01, 2007. Female patient, 55 years of age, was diagnosed with renal transplant, chronic myeloid leukaemia and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, breast cancer, chronic allograft nephropathy, diabetes mellitus inadequate control, diarrhoea, kidney transplant rejection, mastectomy, neutropenia, renal impairment, . CYCLOSPORINE dosage: 4.1-1.32 MG/KG/D. During the same period patient was treated with IMATINIB MESYLATE, IMATINIB MESYLATE, MYCOPHENOLATE MOFETIL, ANTIDIABETICS, INSULIN, AZATHIOPRINE. Patient recovered.

Cyclosporine Side Effects Report #5267091-X
Health Professional from FRANCE reported CYCLOSPORINE problem on Mar 02, 2007. Female patient, 55 years of age, was diagnosed with renal transplant, chronic myeloid leukaemia and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, breast cancer, chronic allograft nephropathy, diabetes mellitus inadequate control, diarrhoea, kidney transplant rejection, mastectomy, neutropenia, renal impairment, . CYCLOSPORINE dosage: 4.1-1.32 MG/KG/D. During the same period patient was treated with IMATINIB MESYLATE, IMATINIB MESYLATE, MYCOPHENOLATE MOFETIL, ANTIDIABETICS, INSULIN, AZATHIOPRINE. Patient recovered.