The bioavailability of mycophenolic acid (MPA) after oral administration of mycophenolate mofetil (MMF) has been reported to be more than 90% in healthy volunteers, and in kidney and thoracic organ transplant patients. Such information is limited in liver transplant (LTx) patients. The present study
Pharmacokinetics (PK) of intravenous mycophenolate mofetil (MMF) in liver transplant patients.
โ Scribed by Hebert, M.F.; Chang, T.; Linna, T.J.; Hale, M.D.; Roberts, J.P.
- Book ID
- 110019663
- Publisher
- Nature Publishing Group
- Year
- 1996
- Tongue
- English
- Weight
- 178 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0009-9236
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๐ SIMILAR VOLUMES
There are few pharmacokinetic data for mycophenolate mofetil (MMF) when used in combination with cyclosporine (CsA) in pediatric liver transplant recipients. The aim of this study was to assess the pharmacokinetics of MMF in stable pediatric liver transplant patients and estimate the dose of MMF req
Renal transplant recipients who are chronically immunosuppressed by drugs are at a higher risk of developing malignancies. Commonly observed malignancies are several forms of posttransplant lymphoproliferative disorders (PTLD), skin, lip and gynaecological cancers. The risk is associated with many r
The aim of the study was to evaluate the effect of t-tube clamping on the pharmacokinetics of mycophenolic acid (MPA) after oral administration of mycophenolate mofetil (MMF) in primary liver transplant recipients treated with tacrolimus as the primary immunosuppressive drug. We evaluated the pharma