Tacrolimus and blood urea increased 
Tacrolimus and blood urea increased Patient Reports February 12, 2012
Tacrolimus Side Effects Report #5280638-2
Tacrolimus side effect was reported by a Physician from JAPAN on Mar 06, 2007. Male patient, 78 years of age, weighting 145.5 lb, was diagnosed with rheumatoid arthritis
and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: blood cholesterol increased, blood triglycerides increased, blood urea increased, spinal compression fracture, white blood cell count increased. Tacrolimus dosage: 1.5 MG, D, ORAL, 2 MG, D, ORAL. During the same period patient was treated with TACROLIMUS CAPSULES, TACROLIMUS CAPSULES, PREDNISOLONE, ETODOLAC, SELBEX, RISEDRONATE. Patient was hospitalized. Patient recovered.Tacrolimus Side Effects Report #5297617-1
Tacrolimus side effect was reported by a Physician from JAPAN on Mar 26, 2007. Male patient, 78 years of age, weighting 145.5 lb, was diagnosed with rheumatoid arthritis
and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: blood cholesterol increased, blood triglycerides increased, blood urea increased, spinal compression fracture, white blood cell count increased. Tacrolimus dosage: unknown. During the same period patient was treated with PREDNISOLONE, ETODOLAC, SELBEX, BENET. Patient was hospitalized. Patient recovered.Tacrolimus Side Effects Report #5341398-X
Tacrolimus side effect was reported by a Physician from JAPAN on May 14, 2007. Male patient, 78 years of age, weighting 145.5 lb, was diagnosed with rheumatoid arthritis
and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: blood cholesterol increased, blood triglycerides increased, blood urea increased, spinal compression fracture, white blood cell count increased. Tacrolimus dosage: unknown. During the same period patient was treated with PREDNISOLONE, ETODOLAC, SELBEX, RISEDRONATE. Patient was hospitalized. Patient recovered.Tacrolimus Side Effects Report #5117963-1
Tacrolimus side effect was reported by a Physician from JAPAN on Sept 13, 2006. Female patient, 76 years of age, weighting 77.16 lb, was diagnosed with rheumatoid arthritis
and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: acute respiratory failure, blood creatinine increased, blood urea increased, decubitus ulcer, dislocation of vertebra, infected skin ulcer, joint sprain, septic shock. Tacrolimus dosage: unknown. During the same period patient was treated with PREDNISOLONE, VOLTAREN CAPSULE, LANSOPRAZOLE, AMLODIPINE BESYLATE, NEUQUINON, ONEALFA, FOSAMAC. Patient died on 09/07/2006.Tacrolimus Side Effects Report #5122639-0
Tacrolimus side effect was reported by a Physician from JAPAN on Sept 13, 2006. Female patient, 76 years of age, weighting 77.16 lb, was diagnosed with rheumatoid arthritis
and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: acute respiratory failure, blood creatinine increased, blood urea increased, decreased appetite, dislocation of vertebra, infected skin ulcer, joint sprain, septic shock. Tacrolimus dosage: 1.5 MG, D, ORAL. During the same period patient was treated with PREDNISOLONE, VOLTAREN CAPSULE, LANSOPRAZOLE, AMLODIN, NEUQUINON, ONEALFA, FOSAMAC. Patient died on 09/07/2006.Tacrolimus Side Effects Report #5122642-0
Tacrolimus side effect was reported by a Physician from JAPAN on Sept 13, 2006. Female patient, 76 years of age, weighting 77.16 lb, was diagnosed with rheumatoid arthritis
and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: acute respiratory failure, blood creatinine increased, blood urea increased, decreased appetite, dislocation of vertebra, infected skin ulcer, joint sprain, septic shock. Tacrolimus dosage: 1.5 MG, D, ORAL. During the same period patient was treated with PREDNISOLONE, VOLTAREN CAPSULE, LANSOPRAZOLE, AMLODIN, NEUQUINON, ONEALFA, FOSAMAC. Patient died on 09/07/2006.Tacrolimus Side Effects Report #5139697-X
Tacrolimus side effect was reported by a Physician from JAPAN on Oct 11, 2006. Female patient, 76 years of age, weighting 77.16 lb, was diagnosed with rheumatoid arthritis
and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: acute respiratory failure, blood creatinine increased, blood ph decreased, blood urea increased, decreased appetite, infected skin ulcer, joint sprain, ligament injury, restlessness. Tacrolimus dosage: 1.5 MG/D, ORAL. During the same period patient was treated with PREDNISOLONE, VOLTAREN CAPSULE, LANSOPRAZOLE, AMLODIPINE BESYLATE, NEUQUINON, ONEALFA, FOSAMAC. Patient died on 09/07/2006.Tacrolimus Side Effects Report #5292084-6
Tacrolimus side effect was reported by a Physician from JAPAN on Mar 19, 2007. Male patient, 69 years of age, weighting 104.7 lb, was diagnosed with rheumatoid arthritis
and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: arteriosclerosis obliterans, beta 2 microglobulin increased, blood urea increased, diabetes mellitus, extremity necrosis, feeling cold, pulmonary fibrosis , skin ulcer. Tacrolimus dosage: unknown. During the same period patient was treated with PREDNISOLONE, TAMSULOSIN, LIPITOR, MOBIC, ASPIRIN, DIOVAN. Patient was hospitalized and became disabled. Patient recovered.Tacrolimus Side Effects Report #5314201-1
Tacrolimus side effect was reported by a Physician from JAPAN on Apr 09, 2007. Male patient, 69 years of age, weighting 104.7 lb, was diagnosed with rheumatoid arthritis
and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: beta 2 microglobulin increased, blood urea increased, condition aggravated, diabetes mellitus, extremity necrosis, skin ulcer. Tacrolimus dosage: unknown. During the same period patient was treated with PREDNISOLONE, TAMSULOSIN, LIPITOR, MOBIC, ASPIRIN, DIOVAN. Patient was hospitalized and became disabled. Patient recovered.Tacrolimus Side Effects Report #5705530-8
Tacrolimus side effect was reported by a Health Professional from FRANCE on Mar 26, 2008. Male patient, 75 years of age, was diagnosed with renal transplant and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: anorexia, bk virus infection, blood creatinine increased, blood urea increased, dehydration, dialysis
, hypernatraemia, leukocytosis, lung disorder. Tacrolimus dosage: unknown. During the same period patient was treated with NEORAL, CELLCEPT, PREDNISONE, CATAPRES, AMLODIPINE BESYLATE, IMUREL. Patient was hospitalized. Patient recovered.Tacrolimus Side Effects Report #4564065-9
Tacrolimus side effect was reported by a Physician from on Jan 13, 2005. Male patient, 38 years of age, was diagnosed with renal transplant and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: blood creatinine increased, blood urea increased, folate deficiency, pneumocystis jiroveci pneumonia, white blood cell count increased. Tacrolimus dosage: unknown. During the same period patient was treated with TACROLIMUS CAPSULES, TACROLIMUS CAPSULES, TACROLIMUS CAPSULES, TACROLIMUS CAPSULES, TACROLIMUS CAPSULES, TACROLIMUS CAPSULES, TACROLIMUS CAPSULES, TACROLIMUS CAPSULES. Patient was hospitalized. Patient recovered.
Tacrolimus Side Effects Report #4751378-0
Tacrolimus side effect was reported by a Health Professional from UNITED STATES on Aug 08, 2005. Male patient, 56 years of age, weighting 129.1 lb, was diagnosed with prophylaxis against transplant rejection and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: blood creatinine increased, blood urea increased, kidney transplant rejection. Tacrolimus dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISONE, ZENAPAX. Patient recovered.
Tacrolimus Side Effects Report #5158508-X
Tacrolimus side effect was reported by a Consumer or non-health professional from FRANCE on Nov 08, 2006. Female patient, 49 years of age, was diagnosed with prophylaxis against transplant rejection and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: blood creatinine increased, blood urea increased, complications of transplanted kidney. Tacrolimus dosage: 8 MG 1X PER 1 DAY. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISONE. Patient was hospitalized. Patient recovered.
Tacrolimus Side Effects Report #4656939-5
Tacrolimus side effect was reported by a Consumer or non-health professional from on Apr 26, 2005. Male patient, 33 years of age, was diagnosed with prophylaxis against transplant rejection and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: acute coronary syndrome, blood creatinine increased, blood urea increased, complications of transplanted kidney, gastric ulcer, haematocrit decreased, haemodialysis, haemoglobin decreased, pseudomonal sepsis. Tacrolimus dosage: unknown. During the same period patient was treated with CORTICOSTEROID NOS, MYCOPHENOLATE MOFETIL. Patient was hospitalized. Patient recovered.
Tacrolimus Side Effects Report #4999428-0
Tacrolimus side effect was reported by a Consumer or non-health professional from UNITED STATES on May 09, 2006. Male patient, 60 years of age, weighting 160.9 lb, was diagnosed with immunosuppression and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: abdominal pain
, blood creatinine increased, blood urea increased, haemodialysis, multi-organ failure, pancytopenia, pyrexia. Tacrolimus dosage: unknown. During the same period patient was treated with CLOTRIMAZOLE, INSULIN, DOCUSATE, FLUCONAZOLE, GENTAMICIN, LANSOPRAZOLE, LEVOFLOXACIN, METHYLPREDNISOLONE. Patient recovered.Tacrolimus Side Effects Report #6079781-X
Tacrolimus side effect was reported by a Physician from TAIWAN, PROVINCE OF CHINA on Feb 02, 2009. Male patient, 74 years of age, was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: abdominal tenderness, alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood creatine increased, blood lactate dehydrogenase increased, blood pressure decreased, blood urea increased, cardiac murmur. Tacrolimus dosage: 1 MG, BID,; 0.5 MG, BID,. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISOLONE. Patient was hospitalized. Patient recovered.
Tacrolimus Side Effects Report #4678618-0
Tacrolimus side effect was reported by a Pharmacist from on Jan 07, 2002. Male patient, 57 years of age, was diagnosed with urinary tract infection
, renal failure, depression , bone marrow conditioning regimen and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: agranulocytosis, blood albumin decreased, blood chloride increased, blood creatinine increased, blood urea increased, haemodialysis, haemoglobin decreased, liver function test abnormal, nephrotic syndrome. Tacrolimus dosage: 4 MG, BID. During the same period patient was treated with CEFRADINE, RAMIPRIL, PAROXETINE, CLOZARIL, MYCOPHENOLATE. Patient was hospitalized. Patient recovered.Tacrolimus Side Effects Report #4682851-1
Tacrolimus side effect was reported by a Pharmacist from on Jan 07, 2002. Male patient, 57 years of age, was diagnosed with urinary tract infection
, renal failure, depression , bone marrow conditioning regimen and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: agranulocytosis, blood albumin decreased, blood chloride increased, blood creatinine increased, blood potassium increased, blood urea increased, haemoglobin decreased, hepatic failure, liver function test abnormal. Tacrolimus dosage: 4 MG, BID. During the same period patient was treated with CEFRADINE, RAMIPRIL, PAROXETINE, CLOZARIL, MYCOPHENOLATE, OLANZAPINE. Patient was hospitalized. Patient recovered.Tacrolimus Side Effects Report #4687962-2
Tacrolimus side effect was reported by a Pharmacist from on Jan 07, 2002. Male patient, 57 years of age, was diagnosed with urinary tract infection
, renal failure, depression , bone marrow conditioning regimen and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: agranulocytosis, blood albumin decreased, blood chloride increased, blood creatinine increased, blood potassium increased, blood urea increased, haemoglobin decreased, hepatic failure, liver function test abnormal. Tacrolimus dosage: 4 MG, BID. During the same period patient was treated with CEFRADINE, RAMIPRIL, PAROXETINE, CLOZARIL, MYCOPHENOLATE, OLANZAPINE. Patient was hospitalized. Patient recovered.Tacrolimus Side Effects Report #4693490-0
Tacrolimus side effect was reported by a Pharmacist from on Jan 07, 2002. Male patient, 57 years of age, was diagnosed with urinary tract infection
, renal failure, depression , bone marrow conditioning regimen and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: agranulocytosis, blood albumin decreased, blood chloride increased, blood creatinine increased, blood potassium increased, blood urea increased, haemoglobin decreased, hepatic failure, liver function test abnormal. Tacrolimus dosage: 4 MG, BID. During the same period patient was treated with CEFRADINE, RAMIPRIL, PAROXETINE, CLOZARIL, MYCOPHENOLATE, OLANZAPINE. Patient was hospitalized. Patient recovered.Tacrolimus Side Effects Report #4565161-2
Tacrolimus side effect was reported by a Pharmacist from on Jan 27, 2005. Male patient, 46 years of age, weighting 246.0 lb, was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: blood creatinine increased, blood urea increased. Tacrolimus dosage: unknown. Patient was hospitalized. Patient died on 10/27/2004.