Tacrolimus and haemoglobin decreased Patient Reports February 12, 2012

Tacrolimus Side Effects Report #5207358-4
Tacrolimus side effect was reported by a Physician from JAPAN on Dec 26, 2006. Male patient was diagnosed with rheumatoid arthritis  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: blood amylase increased, condition aggravated, haematocrit decreased, haemoglobin decreased, interstitial lung disease, lymphocyte count decreased, neurogenic bladder, red blood cell count decreased, rheumatoid arthritis . Tacrolimus dosage: 1 MG, UID/QD, ORAL. During the same period patient was treated with TACROLIMUS CAPSULES, PREDNISOLONE, ENBREL, MINOCYCLINE HYDROCHLORIDE, PLETAL, LANSOPRAZOLE, RHEUMATREX, NEO MINOPHAGEN C. Patient died on 11/05/2006.

Tacrolimus Side Effects Report #5186571-9
Tacrolimus side effect was reported by a Physician from JAPAN on Nov 28, 2006. Female patient, weighting 105.8 lb, was diagnosed with rheumatoid arthritis  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: blood creatinine increased, haematocrit decreased, haemoglobin decreased, melaena. Tacrolimus dosage: 3 MG, ORAL. During the same period patient was treated with VOLTAREN, PREDNISOLONE, ADOFEED. Patient recovered.

Tacrolimus Side Effects Report #5839488-8
Tacrolimus side effect was reported by a Health Professional from TAIWAN, PROVINCE OF CHINA on July 31, 2008. Male patient, 39 years of age, weighting 143.3 lb, was diagnosed with renal transplant and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: abdominal distension, abdominal pain lower, compartment syndrome, haematoma infection, haemoglobin decreased, haemorrhage, hypotension, loss of consciousness, oliguria. Tacrolimus dosage: 5 MG, BID, ORAL; 4 MG, BID, ORAL; 3 MG, BID, ORAL. During the same period patient was treated with CELLCEPT, GASTER PER ORAL NOS, METISONE, LASIX, CIPROXIN, ZEFFIX. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5849028-5
Tacrolimus side effect was reported by a Physician from TAIWAN, PROVINCE OF CHINA on Aug 04, 2008. Male patient, 39 years of age, weighting 143.3 lb, was diagnosed with renal transplant and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: abdominal pain lower, altered state of consciousness, blood pressure systolic decreased, compartment syndrome, haematoma infection, haemodialysis, haemoglobin decreased, haemorrhage, oliguria. Tacrolimus dosage: 5 MG, BID, ORAL, 4 MG, BID, ORAL, 3 MG BID,ORAL. During the same period patient was treated with CELLCEPT, FAMOTIDINE, METISONE, LASIX, CIPROFLOXACIN, LAMIVUDINE. Patient was hospitalized. Patient recovered.


Tacrolimus Side Effects Report #5444333-9
Tacrolimus side effect was reported by a Physician from TUNISIA on Aug 16, 2007. Male patient, 14 years of age, was diagnosed with renal transplant and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: blood lactate dehydrogenase increased, haematocrit decreased, haemoglobin decreased, renal impairment, thrombotic microangiopathy, white blood cell count decreased. Tacrolimus dosage: unknown. During the same period patient was treated with PREDNISONE, MYCOPHENOLATE MOFETIL. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #4665450-7
Tacrolimus side effect was reported by a Consumer or non-health professional from on May 18, 2005. Female patient, 59 years of age, weighting 135.4 lb, was diagnosed with prophylaxis against transplant rejection and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: blood pressure abnormal, cardiomegaly, haemodialysis, haemoglobin decreased, infection , platelet count decreased, post procedural complication, pulmonary embolism . Tacrolimus dosage: 4 MG 2X PER 1 DAY, NASOGASTRIC. During the same period patient was treated with CORTICOSTEROIDS, MYCOPHENOLATE MOFETIL, METRONIDAZOLE, BACTRIM, MEROPENEM. Patient was hospitalized. Patient died on 05/05/2005.

Tacrolimus Side Effects Report #4682526-9
Tacrolimus side effect was reported by a Consumer or non-health professional from on May 27, 2005. Female patient, 59 years of age, weighting 135.4 lb, was diagnosed with prophylaxis against transplant rejection and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: blood pressure decreased, cardiomegaly, condition aggravated, deep vein thrombosis , haemodialysis, haemodynamic instability, haemoglobin decreased, infection . Tacrolimus dosage: 4 MG 2X PER 1 DAY; NASOGASTRIC. During the same period patient was treated with CORTICOSTEROIDS, MYCOPHENOLATE MOFETIL, METRONIDAZOLE, BACTRIM, MEROPENEM. Patient was hospitalized. Patient died on 05/05/2005.

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 #4692294-2
Tacrolimus side effect was reported by a Consumer or non-health professional from on June 01, 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, complications of transplanted kidney, gastric ulcer, gastric ulcer haemorrhage, haematocrit decreased, haemodialysis, haemoglobin decreased, pseudomonal sepsis. Tacrolimus dosage: unknown. During the same period patient was treated with CORTICOSTEROID NOS CORTICOSTEROID NOS, MYCOPHENOLATE MOFETIL, ZENAPAX. Patient was hospitalized. Patient recovered.


Tacrolimus Side Effects Report #4743673-6
Tacrolimus side effect was reported by a Consumer or non-health professional from AUSTRALIA on July 27, 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, complications of transplanted kidney, coronary artery stenosis, gastric ulcer, haematocrit decreased, haemodialysis, haemoglobin decreased, myocardial ischaemia, pseudomonal sepsis. Tacrolimus dosage: unknown. During the same period patient was treated with CORTICOSTEROID NOS, MYCOPHENOLATE MOFETIL, ZENAPAX. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5482475-2
Tacrolimus side effect was reported by a Physician from UNITED STATES on Oct 09, 2007. Female patient, weighting 135.4 lb, was diagnosed with prophylaxis against transplant rejection and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: cardiac hypertrophy, deep vein thrombosis , haemodialysis, haemoglobin decreased, hyperglycaemia, infection , platelet count decreased, pulmonary embolism . Tacrolimus dosage: unknown. During the same period patient was treated with PREDNISONE, MEROPENEM, MYCOPHENOLATE MOFETIL, METRONIDAZOLE, BACTRIM. Patient was hospitalized. Patient died on 05/05/2005.

Tacrolimus Side Effects Report #4738835-8
Tacrolimus side effect was reported by a Health Professional from UNITED KINGDOM on July 26, 2005. Male patient, 54 years of age, was diagnosed with liver transplant  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: abdominal sepsis, arrhythmia , collapse of lung, confusional state, haemoglobin decreased, hepatic enzyme increased, multi-organ failure, neutrophilia. Tacrolimus dosage: unknown. During the same period patient was treated with TACROLIMUS CAP, MYCOPHENOLATE MOFETIL, HYDROCORTISONE, PROPOFOL, AMITRIPTYLINE, LANSOPRAZOLE, PARACETAMOL, PREDNISONE. Patient was hospitalized. Patient died on 06/02/2005.

Tacrolimus Side Effects Report #5325851-0
Tacrolimus side effect was reported by a Health Professional from FRANCE on Apr 27, 2007. Female patient, 40 years of age, was diagnosed with liver transplant  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: haemoglobin decreased, peritoneal haemorrhage, sepsis . Tacrolimus dosage: 3 MG, UID/QD; ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, MYCOPHENOLATE MOFETIL, MYCOPHENOLATE MOFETIL, PREDNISOLONE, TAZOCILLINE, AMPHOTERICIN B, COLISTIN, GANCICLOVIR. Patient recovered.

Tacrolimus Side Effects Report #5282400-3
Tacrolimus side effect was reported by a Physician from UNITED KINGDOM on Mar 08, 2007. Male patient, 24 years of age, was diagnosed with liver transplant  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: arterial aneurysm repair, candidiasis, haemoglobin decreased, hepatic artery aneurysm, shock. Tacrolimus dosage: 1 MG, UID/QD, ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, MYCOPHENOLATE MOFETIL, METHYLPREDNISOLONE, TAZOCILLINE, TARGOCID, ABELCET, ZOVIRAX. Patient was hospitalized. Patient recovered.


Tacrolimus Side Effects Report #6137535-X
Tacrolimus side effect was reported by a Health Professional from UNITED KINGDOM on Mar 18, 2009. Female patient, 60 years of age, was diagnosed with liver transplant  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: aspartate aminotransferase increased, blood alkaline phosphatase increased, blood creatinine increased, cytomegalovirus infection , haemoglobin decreased, night sweats, pallor, pericardial effusion, pericarditis tuberculous. Tacrolimus dosage: 9 MG, UID/QD,. During the same period patient was treated with AZATHIOPRINE, GANCICLOVIR, PIPERACILLIN AND TAZOBACTAM. 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.