| Literature DB >> 2757905 |
M Frisk-Holmberg1, P Kerth, P Meyer.
Abstract
1. This study, involving eight healthy volunteers, revealed that food intake does not have a clinically significant effect on vigabatrin kinetics. 2. Kinetics of vigabatrin in the fasting state showed low inter-individual variation. 3. The plasma concentration vs time profile followed a bi-exponential decline with a terminal half-life of 6.8 h and a relative bioavailability of 92% +/- 11%. 4. In the clinical setting, vigabatrin may be taken at times convenient for the patient.Entities:
Mesh:
Substances:
Year: 1989 PMID: 2757905 PMCID: PMC1379675 DOI: 10.1111/j.1365-2125.1989.tb03457.x
Source DB: PubMed Journal: Br J Clin Pharmacol ISSN: 0306-5251 Impact factor: 4.335