Tacrolimus and vomiting Patient Reports February 12, 2012

Tacrolimus Side Effects Report #5117972-2
Tacrolimus side effect was reported by a Physician from JAPAN on Sept 15, 2006. Female patient, 74 years of age, was diagnosed with rheumatoid arthritis  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: aspiration, injury asphyxiation, shock, vomiting. Tacrolimus dosage: unknown. During the same period patient was treated with AMLODIPINE BESYLATE, FOSAMAC, ALFAROL, LOXONIN, PREDNISOLONE, KENACORT, LIMETHASONE, VOLTAREN. Patient died on 01/10/2006.

Tacrolimus Side Effects Report #5515804-1
Tacrolimus side effect was reported by a Health Professional from JAPAN on Oct 25, 2007. Female patient, 60 years of age, weighting 127.9 lb, was diagnosed with rheumatoid arthritis  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: bone neoplasm, vomiting. Tacrolimus dosage: 3 MG, ORAL; 3 MG, ORAL. During the same period patient was treated with METHOTREXATELET, LOXONIN, SEVEN EP, MARZULENE S, MOHRUS. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5594019-5
Tacrolimus side effect was reported by a Health Professional from JAPAN on Dec 27, 2007. Female patient, 60 years of age, weighting 127.9 lb, was diagnosed with rheumatoid arthritis  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: bone giant cell tumour benign, vomiting. Tacrolimus dosage: 3 MG, ORAL; 3 MG, ORAL. During the same period patient was treated with METHOTREXATELET, LOXONIN, SEVEN EP, MARZULENE S, MOHRUS, FLOMOX, DASEN. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5633049-1
Tacrolimus side effect was reported by a Physician from JAPAN on Jan 29, 2008. Female patient, 60 years of age, weighting 127.9 lb, was diagnosed with rheumatoid arthritis  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: accident, bone giant cell tumour benign, vomiting. Tacrolimus dosage: 3 MG, D, ORAL. During the same period patient was treated with RHEUMATREX, LOXONIN, SEVEN EP, MARZULENE S, MOHRUS, FLOMOX, DASEN. Patient was hospitalized. Patient recovered.


Tacrolimus Side Effects Report #5877342-6
Tacrolimus side effect was reported by a Health Professional from JAPAN on July 24, 2008. Female patient, 60 years of age, weighting 127.9 lb, was diagnosed with rheumatoid arthritis  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: bone neoplasm, vomiting. Tacrolimus dosage: 3 MG, ORAL. During the same period patient was treated with RHEUMATREX, LOXONIN, SEVEN EP, MARZULENE S, MOHRUS, FLOMOX, DASEN. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #4830958-8
Tacrolimus side effect was reported by a Physician from JAPAN on Nov 02, 2005. Female patient, 59 years of age, weighting 99.21 lb, was diagnosed with rheumatoid arthritis  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: amyloidosis, condition aggravated, pulmonary embolism , vomiting. Tacrolimus dosage: unknown. During the same period patient was treated with TACROLIMUS CAPSULES, PREDNISONE, METHYLPREDNISOLONE, VOLTAREN, DOGMATYL, TOLEDOMIN, RABEPRAZOLE, LUPRAC. Patient died on 08/19/2005.

Tacrolimus Side Effects Report #4852960-2
Tacrolimus side effect was reported by a Physician from JAPAN on Nov 30, 2005. Female patient, 59 years of age, weighting 99.21 lb, was diagnosed with rheumatoid arthritis  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: amyloidosis, condition aggravated, pulmonary embolism , vomiting. Tacrolimus dosage: 1.50 MG, D, ORAL; 3 MG, D, ORAL. During the same period patient was treated with TACROLIMUS CAPSULES, PREDNISONE, METHYLPREDNISOLONE, VOLTAREN, DOGMATYL, TOLEDOMIN, RABEPRAZOLE, LUPRAC. Patient died on 08/19/2005.

Tacrolimus Side Effects Report #5589593-9
Tacrolimus side effect was reported by a Physician from JAPAN on Dec 24, 2007. Female patient, 57 years of age, weighting 109.8 lb, was diagnosed with rheumatoid arthritis  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: blood pressure increased, muscular weakness, subarachnoid haemorrhage, vomiting. Tacrolimus dosage: 3 MG, ORAL. During the same period patient was treated with RHEUMATREX, ETODOLAC, FOLIC ACID, OLMETEC, GASTER, MARZULENE S, SELBEX, NORVASC. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5054131-6
Tacrolimus side effect was reported by a Physician from JAPAN on June 29, 2006. Female patient, 25 years of age, weighting 72.75 lb, was diagnosed with rheumatoid arthritis  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: condition aggravated, depression , mental disorder, persecutory delusion, suicide attempt, vomiting. Tacrolimus dosage: 1 MG, UID/QD, ORAL; 2 MG UID/QD, ORAL; 54 DF D, ORAL. During the same period patient was treated with TACROLIMUS CAPSULES, TACROLIMUS CAPSULES, RHEUMATREX, VOLTAREN, LENDORMIN, PREDNISOLONE, RIMATIL. Patient was hospitalized. Patient recovered.


Tacrolimus Side Effects Report #5025511-X
Tacrolimus side effect was reported by a Physician from JAPAN on May 24, 2006. Female patient, 25 years of age, weighting 72.75 lb, was diagnosed with rheumatoid arthritis  and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: depressed level of consciousness, depression , mental disorder, persecutory delusion, suicide attempt, vomiting. Tacrolimus dosage: unknown. During the same period patient was treated with RHEUMATREX, VOLTAREN, LENDORM, PREDNISOLONE, RIMATIL. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5920040-0
Tacrolimus side effect was reported by a Pharmacist from UNITED STATES on Sept 29, 2008. Female patient, 71 years of age, was diagnosed with renal transplant and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: malaise, nausea . Tacrolimus dosage: 0.5 MG, BID, ORAL : 5 MG, BID, ORAL. Patient recovered.

Tacrolimus Side Effects Report #4983559-5
Tacrolimus side effect was reported by a Physician from AUSTRALIA on Apr 04, 2006. Male patient, 45 years of age, weighting 125.4 lb, was diagnosed with renal transplant and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: dehydration, enteritis, nausea , oesophagitis ulcerative. Tacrolimus dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISOLONE, NIFEDIPINE, PHOSPHATE NOVARTIS. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5883343-4
Tacrolimus side effect was reported by a Physician from KOREA, REPUBLIC OF on Sept 04, 2008. Male patient, 34 years of age, was diagnosed with renal transplant and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: burning sensation, loss of consciousness, renal transplant, respiratory arrest, shock, vomiting. Tacrolimus dosage: unknown. Patient recovered.

Tacrolimus Side Effects Report #4900729-2
Tacrolimus side effect was reported by a Physician from JAPAN on Jan 18, 2006. Female patient, 66 years of age, weighting 117.3 lb, was diagnosed with myasthenia gravis and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: atrioventricular block second degree, nausea , palpitations. Tacrolimus dosage: 1 MG, ORAL. During the same period patient was treated with PREDNISOLONE, MYTELASE, MARZULENE S, SELBEX, BIOFERMIN. Patient was hospitalized. Patient recovered.


Tacrolimus Side Effects Report #4678601-5
Tacrolimus side effect was reported by a Health Professional from on May 31, 2005. Male patient, 59 years of age, weighting 145.0 lb, was diagnosed with immunosuppression and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: decreased appetite, nausea , pyrexia. Tacrolimus dosage: 2 MG BID PO. During the same period patient was treated with CELLCEPT, PREDNIZINE. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5401906-7
Tacrolimus side effect was reported by a Consumer or non-health professional from BELGIUM on July 02, 2007. Female patient, 15 years of age, was diagnosed with immunosuppression, helicobacter gastritis and was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: convulsion, dehydration, diarrhoea, haemoconcentration, oliguria, renal disorder, vomiting. Tacrolimus dosage: unknown. During the same period patient was treated with CLARITHROMYCIN, AMOXICILLIN, OMEPRAZOLE. Patient recovered.

Tacrolimus Side Effects Report #5593184-3
Tacrolimus side effect was reported by a Consumer or non-health professional from UNITED STATES on Jan 15, 2008. Female patient, weighting 196.9 lb, was treated with Tacrolimus. After drug was administered, patient experienced the following side effects: diarrhoea, nausea , renal failure acute. Tacrolimus dosage: 78 MG 1.5 MG PO BID STARTING ON DAY -1 OF ALLOGENEIC TRANSPLANT. During the same period patient was treated with CYCLOPHOSPHAMIDE, FLUDARABINE PHOSPHATE, MELPHALAN. Patient was hospitalized. Patient recovered.