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COMPLICATIONS OF TRANSPLANT SURGERY side effect

What is COMPLICATIONS OF TRANSPLANT SURGERY ?
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Drugs associated with COMPLICATIONS OF TRANSPLANT SURGERY

ACYCLOVIR  ALDURAZYME  ALKERAN  BETAMETHASONE  BONVIVA  CERTICAN  CHANTIX  CORTANCYL  CYCLOSPORINE  CYTARABINE  ETOPOSIDE  EYE  FLUDARABINE  FORTEO  HEMATOPOETIC  LUCENTIS  LYODURA  MUSCULOSKELETAL  MYCOPHENOLATE  PREDNISOLONE  PREDNISONE  PROGRAF  REVLIMID  SANDIMMUNE  SIMULECT  SIROLIMUS  THALOMID  THYMOGLOBULIN  TRACE  TRACLEER  TRETINOIN  VFEND  


Sirolimus Side Effects Report #5655336-3
Physician from BELGIUM reported SIROLIMUS problem on Feb 26, 2008. Female patient was diagnosed with immunosuppression, type 1 diabetes mellitus and was treated with SIROLIMUS. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, . SIROLIMUS dosage: LOADING DOSE OF 0.2 MG/KG/DAY AND 0.1 MG/KG/DAY THEREAFTER. During the same period patient was treated with METHYLPREDNISOLONE, INSULIN, ANTITHYMOCYTE IMMUNOGLOBULIN. Patient recovered.

Sirolimus Side Effects Report #5655402-2
SIROLIMUS problem was reported by a Physician from BELGIUM on Feb 26, 2008. Female patient was diagnosed with immunosuppression, type 1 diabetes mellitus and was treated with SIROLIMUS. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, lymphocyte count decreased, white blood cell count decreased, . SIROLIMUS dosage: LOADING DOSE OF 0.2 MG/KG/DAY AND 0.1 MG/KG/DAY THEREAFTER. During the same period patient was treated with INSULIN, TACROLIMUS, ANTITHYMOCYTE IMMUNOGLOBULIN, METHYLPREDNISOLONE. Patient recovered.

Sirolimus Side Effects Report #5655404-6
Physician from BELGIUM reported SIROLIMUS problem on Feb 26, 2008. Female patient was diagnosed with immunosuppression, type 1 diabetes mellitus and was treated with SIROLIMUS. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, insulin c-peptide decreased, lymphocyte count decreased, white blood cell count decreased, . SIROLIMUS dosage: LOADING DOSE OF 0.2 MG/KG/DAY AND 0.1 MG/KG/DAY THEREAFTER. During the same period patient was treated with INSULIN, TACROLIMUS, ANTITHYMOCYTE IMMUNOGLOBULIN, METHYLPREDNISOLONE. Patient recovered.

Sirolimus Side Effects Report #5655405-8
SIROLIMUS problem was reported by a Physician from BELGIUM on Feb 26, 2008. Female patient was diagnosed with immunosuppression, type 1 diabetes mellitus and was treated with SIROLIMUS. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, lymphocyte count decreased, white blood cell count decreased, . SIROLIMUS dosage: LOADING DOSE OF 0.2 MG/KG/DAY AND 0.1 MG/KG/DAY THEREAFTER. During the same period patient was treated with METHYLPREDNISOLONE, INSULIN, ANTITHYMOCYTE IMMUNOGLOBULIN. Patient recovered.


Sirolimus Side Effects Report #5655416-2
Physician from BELGIUM reported SIROLIMUS problem on Feb 26, 2008. Female patient was diagnosed with immunosuppression, type 1 diabetes mellitus and was treated with SIROLIMUS. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, . SIROLIMUS dosage: LOADING DOSE OF 0.2 MG/KG/DAY AND 0.1 MG/KG/DAY THEREAFTER. During the same period patient was treated with METHYLPREDNISOLONE, INSULIN, ANTITHYMOCYTE IMMUNOGLOBULIN. Patient recovered.

Prograf Side Effects Report #5664316-3
PROGRAF problem was reported by a Health Professional from UNITED STATES on Mar 04, 2008. Female patient, 27 years of age, weighting 110.0 lb, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, feeling abnormal, kidney transplant rejection, . PROGRAF dosage: ORAL; 5 MG, OTHER, ORAL. During the same period patient was treated with PREDNISOLONE ACETATE, CELLCEPT, ALLESE, COZAAR. Patient was hospitalized. Patient recovered.

Lucentis Side Effects Report #5665277-3
Consumer or non-health professional from UNITED STATES reported LUCENTIS problem on Mar 07, 2008. Female patient was treated with LUCENTIS. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, corneal graft rejection, visual disturbance, . LUCENTIS dosage: unknown. During the same period patient was treated with ECONOPRED PLUS, RESTASIS. Patient recovered.

Lucentis Side Effects Report #5622234-0
LUCENTIS problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 05, 2008. Female patient was treated with LUCENTIS. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, corneal transplant, visual disturbance, . LUCENTIS dosage: unknown. During the same period patient was treated with ECONOPRED PLUS, RESTASIS. Patient recovered.

Alkeran Side Effects Report #5623110-X
Health Professional from UNITED STATES reported ALKERAN problem on Feb 06, 2008. Female patient, 61 years of age, weighting 167.3 lb, was diagnosed with multiple myeloma and was treated with ALKERAN. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, disease progression, interstitial lung disease, respiratory failure, . ALKERAN dosage: unknown. During the same period patient was treated with REVLIMID. Patient died on 01/16/2007.


Prograf Side Effects Report #5634096-6
PROGRAF problem was reported by a Physician from JAPAN on Jan 31, 2008. Male patient, 26 years of age, was diagnosed with bone marrow transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, microangiopathy, . PROGRAF dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient died.

Revlimid Side Effects Report #5637182-X
Physician from UNITED STATES reported REVLIMID problem on Feb 15, 2008. Female patient, 35 years of age, was diagnosed with myelodysplastic syndrome and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, stem cell transplant, . REVLIMID dosage: 5 MG, 1 IN 1 D, ORAL. Patient died.

Betamethasone Side Effects Report #5638995-0
BETAMETHASONE PHOSPHATE problem was reported by a Physician from JAPAN on Feb 08, 2008. Female patient, 85 years of age, was diagnosed with procedural site reaction and was treated with BETAMETHASONE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, corneal deposits, corneal disorder, . BETAMETHASONE PHOSPHATE dosage: unknown. During the same period patient was treated with CRAVIT. Patient recovered.

Chantix Side Effects Report #5645775-9
Consumer or non-health professional from UNITED STATES reported CHANTIX problem on Feb 19, 2008. Female patient, weighting 149.9 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, condition aggravated, failure of implant, gingival bleeding, gingivitis, periodontal disease, resorption bone increased, tooth loss, . CHANTIX dosage: unknown. During the same period patient was treated with LIPITOR, PREMARIN, BUPROPION, FOSAMAX, CELEBREX. Patient recovered.

Alkeran Side Effects Report #5535812-4
ALKERAN problem was reported by a Health Professional from UNITED STATES on Nov 27, 2007. Female patient, 61 years of age, was diagnosed with multiple myeloma and was treated with ALKERAN. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, interstitial lung disease, respiratory failure, . ALKERAN dosage: unknown. During the same period patient was treated with REVLIMID. Patient died on 01/01/2006.


Prograf Side Effects Report #5564530-1
Physician from BRAZIL reported PROGRAF problem on Nov 27, 2007. Female patient was diagnosed with renal and pancreas transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, complications of transplanted kidney, haematocrit decreased, haemodialysis, kidney transplant rejection, shock haemorrhagic, thrombotic microangiopathy, . PROGRAF dosage: 0.15 MG/KG. During the same period patient was treated with PREDNISOLONE ACETATE. Patient recovered.

Tretinoin Side Effects Report #5565296-1
TRETINOIN problem was reported by a Physician from AUSTRALIA on Sept 26, 2002. Male patient, 58 years of age, was diagnosed with acute promyelocytic leukaemia and was treated with TRETINOIN. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, cytogenetic abnormality, . TRETINOIN dosage: unknown. During the same period patient was treated with CYTOSINE ARABINOSIDE, CYTOSINE ARABINOSIDE, CYTOSINE ARABINOSIDE, IDARUBICIN. Patient died.

Cortancyl Side Effects Report #5577660-5
Physician from FRANCE reported CORTANCYL problem on Dec 26, 2007. Female patient, 66 years of age, weighting 151.5 lb, was diagnosed with renal transplant and was treated with CORTANCYL. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, disease progression, disseminated intravascular coagulation, oesophageal haemorrhage, . CORTANCYL dosage: unknown. During the same period patient was treated with CERTICAN, NEORAL. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5580225-2
PROGRAF problem was reported by a Physician from JAPAN on Dec 17, 2007. Female patient, child 12 years of age, was diagnosed with bone marrow transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, dermatitis atopic, eczema, eosinophilic pustular folliculitis, . PROGRAF dosage: unknown. During the same period patient was treated with METHOTREXATEMULATION. Patient recovered.

Prograf Side Effects Report #5524905-3
Physician from UNITED STATES reported PROGRAF problem on Nov 02, 2007. Female patient, 58 years of age, was diagnosed with lung transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, gingival hyperplasia, . PROGRAF dosage: 6MG, UID/QD, ORAL. During the same period patient was treated with PREDNISOLONE ACETATE, MYCOPHENOLATE MOFETIL, CITALOPRAM, NYSTATIN, OMEPRAZOLE, VALGANCICLOVIR, TRIMETOPRIM, DOCUSATE. Patient died.


Prograf Side Effects Report #5524906-5
PROGRAF problem was reported by a Health Professional from UNITED STATES on Nov 02, 2007. Male patient, 63 years of age, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, fluid retention, retroperitoneal effusion, . PROGRAF dosage: 2 MG, BID, ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISONE, FUROSEMIDE, CLONIDINE, OMEPRAZOLE, ROSIGLITAZONE, VALGANCICLOVIR, BACTRIM DS. Patient was hospitalized. Patient recovered.

Thalomid Side Effects Report #5494110-8
Physician from UNITED STATES reported THALOMID problem on Oct 16, 2007. Male patient was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, organ failure, sepsis, stem cell transplant, stomach discomfort, . THALOMID dosage: 200 MG, 1 IN 1 D, ORAL. Patient died.

Eye Side Effects Report #5467652-9
EYE problem was reported by a Physician from UNITED STATES on Aug 20, 2007. Female patient, 75 years of age, was diagnosed with ulcerative keratitis and was treated with EYE. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, corneal infection, eye infection staphylococcal, graft infection, . EYE dosage: unknown. Patient recovered.

Musculoskeletal Side Effects Report #5468089-9
Consumer or non-health professional from UNITED STATES reported MUSCULOSKELETAL SOFT problem on Sept 12, 2007. Female patient, 28 years of age, was treated with MUSCULOSKELETAL SOFT. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, failure of implant, graft complication, . MUSCULOSKELETAL SOFT dosage: unknown. Patient recovered.

Lyodura Side Effects Report #5294247-2
LYODURA DURA MATER TRI problem was reported by a Physician from UNITED STATES on Apr 09, 2007. Male patient, 26 years of age, was diagnosed with spina bifida and was treated with LYODURA DURA MATER TRI. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, creutzfeldt-jakob disease, . LYODURA DURA MATER TRI dosage: unknown. Patient died.

Certican Side Effects Report #5387235-9
Physician from CHILE reported CERTICAN problem on July 03, 2007. Female patient, 45 years of age, weighting 151.0 lb, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, kidney transplant rejection, maculopathy, nephropathy toxic, oliguria, removal of renal transplant, renal tubular necrosis, vision blurred, . CERTICAN dosage: 0.75 MG, QD. During the same period patient was treated with NEORAL. Patient was hospitalized and became disabled. Patient recovered.

Thymoglobulin Side Effects Report #5423747-7
THYMOGLOBULIN problem was reported by a Health Professional from UNITED STATES on June 29, 2004. Male patient, 54 years of age, weighting 213.8 lb, was diagnosed with renal transplant and was treated with THYMOGLOBULIN. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, nephrectomy, . THYMOGLOBULIN dosage: 75 MG. During the same period patient was treated with TACROLIMUS, CELLCEPT, FAMOTIDINE, SULFAMETHOXAZOLE AND TRIMETHOPRIM. Patient recovered.

Lyodura Side Effects Report #5294247-2
Physician from UNITED STATES reported LYODURA DURA MATER TRI problem on Apr 09, 2007. Male patient, 26 years of age, was diagnosed with spina bifida and was treated with LYODURA DURA MATER TRI. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, creutzfeldt-jakob disease, . LYODURA DURA MATER TRI dosage: unknown. Patient died.

Certican Side Effects Report #5387235-9
CERTICAN problem was reported by a Physician from CHILE on July 03, 2007. Female patient, 45 years of age, weighting 151.0 lb, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, kidney transplant rejection, maculopathy, nephropathy toxic, oliguria, removal of renal transplant, renal tubular necrosis, vision blurred, . CERTICAN dosage: 0.75 MG, QD. During the same period patient was treated with NEORAL. Patient was hospitalized and became disabled. Patient recovered.

Thymoglobulin Side Effects Report #5423747-7
Health Professional from UNITED STATES reported THYMOGLOBULIN problem on June 29, 2004. Male patient, 54 years of age, weighting 213.8 lb, was diagnosed with renal transplant and was treated with THYMOGLOBULIN. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, nephrectomy, . THYMOGLOBULIN dosage: 75 MG. During the same period patient was treated with TACROLIMUS, CELLCEPT, FAMOTIDINE, SULFAMETHOXAZOLE AND TRIMETHOPRIM. Patient recovered.

Cytarabine Side Effects Report #5776182-6
CYTARABINE problem was reported by a Consumer or non-health professional from UNITED STATES on June 05, 2008. Male patient was diagnosed with acute myeloid leukaemia and was treated with CYTARABINE. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, myelodysplastic syndrome, stem cell transplant, . CYTARABINE dosage: 100 MG/M2 DAILY. During the same period patient was treated with NEUPOGEN, BUSULFAN, ETOPOSIDE, DAUNORUBICIN. Patient recovered.

Cortancyl Side Effects Report #5727191-4
Physician from FRANCE reported CORTANCYL problem on Apr 30, 2008. Female patient, 66 years of age, weighting 151.5 lb, was diagnosed with renal transplant and was treated with CORTANCYL. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, disease progression, disseminated intravascular coagulation, lung infection, oesophageal haemorrhage, osteitis, urinary tract infection, . CORTANCYL dosage: unknown. During the same period patient was treated with CERTICAN, NEORAL. Patient was hospitalized. Patient recovered.

Fludarabine Side Effects Report #5316829-1
FLUDARABINE problem was reported by a Health Professional from UNITED STATES on May 01, 2007. Male patient, 28 years of age, weighting 190.3 lb, was diagnosed with acute lymphocytic leukaemia and was treated with FLUDARABINE. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, dialysis, multi-organ failure, . FLUDARABINE dosage: 70 MG QD IV. During the same period patient was treated with CYTOXAN, UMBILICAL CORD BLOOD, UMBILICAL CORD BLOOD. Patient was hospitalized. Patient died on 04/28/2007.

Thymoglobulin Side Effects Report #5321792-3
Pharmacist from UNITED STATES reported THYMOGLOBULIN problem on Apr 27, 2007. Male patient, 53 years of age, was diagnosed with pancreas transplant and was treated with THYMOGLOBULIN. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, graft thrombosis, . THYMOGLOBULIN dosage: 100 MG QD IV. Patient recovered.

Eye Side Effects Report #5341421-2
EYE problem was reported by a Physician from UNITED STATES on May 31, 2007. Female patient, 79 years of age, was treated with EYE. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, eye excision, keratitis, keratitis fungal, . EYE dosage: unknown. Patient recovered.

Cyclosporine Side Effects Report #5284260-3
Health Professional from UNITED STATES reported CYCLOSPORINE problem on Mar 28, 2007. Female patient, 55 years of age, was diagnosed with angioimmunoblastic t-cell lymphoma and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, . CYCLOSPORINE dosage: unknown. Patient died.

Prograf Side Effects Report #5291926-8
PROGRAF problem was reported by a Physician from JAPAN on Mar 19, 2007. Male patient, 38 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: complications of transplant surgery, hypomagnesaemia, reversible posterior leukoencephalopathy syndrome, . PROGRAF dosage: unknown. Patient recovered.

Lyodura Side Effects Report #5294247-2
Physician from UNITED STATES reported LYODURA DURA MATER TRI problem on Apr 09, 2007. Male patient, 26 years of age, was diagnosed with spina bifida and was treated with LYODURA DURA MATER TRI. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, creutzfeldt-jakob disease, . LYODURA DURA MATER TRI dosage: unknown. Patient died.

Cyclosporine Side Effects Report #5280203-7
CYCLOSPORINE problem was reported by a Pharmacist from UNITED STATES on Mar 26, 2007. Female patient, 35 years of age, weighting 203.0 lb, was diagnosed with heart transplant, immunosuppression and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, convulsion, reversible posterior leukoencephalopathy syndrome, . CYCLOSPORINE dosage: unknown. Patient was hospitalized. Patient recovered.

Sirolimus Side Effects Report #5286903-7
Physician from NETHERLANDS reported SIROLIMUS problem on Mar 13, 2007. Female patient was diagnosed with immunosuppression and was treated with SIROLIMUS. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, haemodialysis, haemorrhage, proteinuria, pulmonary embolism, transplant failure, . SIROLIMUS dosage: 6 MG; QD; PO. During the same period patient was treated with METHYLPREDNISOLONE, ORAPRED, MYCOPHENOLATE MOFETIL. Patient recovered.

Prednisolone Side Effects Report #5290077-6
PREDNISOLONE PHOSPHATE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 22, 2007. Male patient, 35 years of age, was diagnosed with renal transplant and was treated with PREDNISOLONE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, epstein-barr virus infection, histology abnormal, lymphoproliferative disorder, skin lesion, . PREDNISOLONE PHOSPHATE dosage: 10 MILLIGRAMS;CYCLICAL. During the same period patient was treated with AZATHIOPRINE, CYCLOSPORINE. Patient recovered.

Prograf Side Effects Report #5674468-7
Physician from JAPAN reported PROGRAF problem on Feb 29, 2008. Female patient, 53 years of age, was diagnosed with bone marrow transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, complications of transplant surgery, dysuria, pain, pain in extremity, thrombotic microangiopathy, . PROGRAF dosage: unknown. During the same period patient was treated with PREDNISOLONE, MYCOPHENOLATE MOFETIL. Patient died.

Prograf Side Effects Report #5509503-X
PROGRAF problem was reported by a Physician from UNITED STATES on Oct 23, 2007. Female patient, 58 years of age, was diagnosed with lung transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: buccal polyp, complications of transplant surgery, gingival hyperplasia, . PROGRAF dosage: 6 MG, UID/QD, ORAL ; 1.5 MG, UID/QD, ORAL. During the same period patient was treated with PREDNISONE, MYCOPHENOLATE MOFETIL, CITALOPRAM, NYSTATIN, OMEPRAZOLE, VALGANCICLOVIR, TRIMETOPRIM, DOCUSATE. Patient died.

Mycophenolate Side Effects Report #5511241-4
Physician from NETHERLANDS reported MYCOPHENOLATE MOFETIL problem on Oct 30, 2007. Male patient, 58 years of age, was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: bile duct stenosis, complications of transplant surgery, liver transplant rejection, . MYCOPHENOLATE MOFETIL dosage: unknown. During the same period patient was treated with LAMIVUDINE, BACTRIM, PIPERACILLIN AND TAZOBACTAM, GENTAMICIN, FLUCONAZOLE. Patient was hospitalized. Patient recovered.

Prednisone Side Effects Report #5512345-2
PREDNISONE problem was reported by a Physician from INDIA on Oct 22, 2007. Female patient, 40 years of age, was diagnosed with glomerulonephritis rapidly progressive and was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: catheter related infection, complications of transplant surgery, klebsiella infection, malnutrition, no therapeutic response, pneumonia, renal transplant, strongyloidiasis, . PREDNISONE dosage: 50 MG QD. During the same period patient was treated with ORAPRED, METHYLPREDNISOLONE, CYCLOPHOSPHAMIDE. Patient was hospitalized. Patient recovered.

Certican Side Effects Report #5475478-5
Physician from ARGENTINA reported CERTICAN problem on Sept 26, 2007. Male patient, 27 years of age, weighting 138.2 lb, was diagnosed with renal transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: abdominal pain, complications of transplant surgery, complications of transplanted kidney, diarrhoea, haematoma evacuation, haemodynamic instability, hyperplasia, hypotension, intra-abdominal haematoma, . CERTICAN dosage: unknown. During the same period patient was treated with NEORAL. Patient was hospitalized. Patient recovered.

Fludarabine Side Effects Report #5483742-9
FLUDARABINE PHOSPHATE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 09, 2007. Male patient, weighting 150.1 lb, was diagnosed with myeloproliferative disorder and was treated with FLUDARABINE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: acute graft versus host disease in intestine, complications of transplant surgery, myeloproliferative disorder, neoplasm recurrence, stem cell transplant, . FLUDARABINE PHOSPHATE dosage: 70 MG DAILY FOR 5 DAYS IV. During the same period patient was treated with CYCLOPHOSPHAMIDE, MYCOFUNGIN, ZOSYN, VANCOMYCIN, URSODIAL, DESONIDE CREAM, BUDESONIDE, METHOXALON. Patient died on 10/06/2007.

Sirolimus Side Effects Report #5410919-0
Physician from MEXICO reported SIROLIMUS problem on Aug 07, 2007. Female patient, weighting 132.7 lb, was diagnosed with prophylaxis against transplant rejection, hypertension, hyperuricaemia, hypercholesterolaemia, hyperlipidaemia, gastritis and was treated with SIROLIMUS. After drug was administered, patient experienced the following problems/side effects: azotaemia, complications of transplant surgery, . SIROLIMUS dosage: unknown. During the same period patient was treated with DILTIAZEM, ENALAPRIL MALEATE, CANDESARTAN CILEXETIL, ALLOPURINOL, MACRODANTIN, PRAVASTATINE, BEZAFIBRATE, OMEPRAZOLE. Patient was hospitalized. Patient recovered.

Mycophenolate Side Effects Report #5412643-7
MYCOPHENOLATE MOFETIL problem was reported by a Physician from NETHERLANDS on Aug 01, 2007. Male patient, 58 years of age, was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: bile duct stenosis, complications of transplant surgery, liver transplant rejection, therapeutic agent toxicity, . MYCOPHENOLATE MOFETIL dosage: unknown. During the same period patient was treated with LAMIVUDINE, BACTRIM, PIPERACILLIN AND TAZOBACTAM, GENTAMICIN, FLUCONAZOLE. Patient was hospitalized. Patient recovered.

Aldurazyme Side Effects Report #5417132-1
Health Professional from UNITED STATES reported ALDURAZYME problem on Aug 01, 2007. Female patient, child 1 years of age, weighting 53.35 lb, was diagnosed with mucopolysaccharidosis i and was treated with ALDURAZYME. After drug was administered, patient experienced the following problems/side effects: blood stem cell transplant failure, complications of transplant surgery, hyperbilirubinaemia, mucosal inflammation, . ALDURAZYME dosage: 0.58 MG/KG QWK IV. During the same period patient was treated with CYCLOSPORINE, MYCOPHENOLATE MOFETIL, NORVASC, ATIVAN, BACTRIM, NEUPOGEN, DIGOXIN, FLUCONAZOLE. Patient recovered.

Forteo Side Effects Report #5376882-6
FORTEO problem was reported by a Physician from IRELAND on June 22, 2007. Female patient, 53 years of age, was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: bronchiectasis, complications of transplant surgery, respiratory failure, . FORTEO dosage: unknown. Patient died on 07/16/2006.

Prograf Side Effects Report #5383236-5
Physician from JAPAN reported PROGRAF problem on June 22, 2007. Male patient, 58 years of age, weighting 147.7 lb, was diagnosed with bone marrow transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: coma hepatic, complications of transplant surgery, dialysis, graft versus host disease, hepatitis fulminant, pyrexia, renal impairment, tremor, . PROGRAF dosage: unknown. During the same period patient was treated with PREDNISOLONE, MUCOSTA, LAC B, DEPAS, DIFLUCAN. Patient died on 10/24/2004.

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