The pharmacokinetics of oral ranitidine were studied in 24 Mexican mal
e healthy volunteers. Subjects received a tablet containing 150 mg of
ranitidine (Azantac(TM), Glare de Mexico, Mexico City) after an overni
ght fast and blood samples were drawn at several times for a period of
24 h. Ranitidine concentration in plasma was measured by high perform
ance liquid chromatography and pharmacokinetic parameters were determi
ned by non-compartmental analysis. Ranitidine plasma concentration inc
reased with time, reaching a maximum of (mean +/- SEM) 484 +/- 34 ng/m
l in 2.7 +/- 0.2 h. plasma levels then decayed with a terminal half-li
fe of 4.8 +/- 0.3 h. The area under the plasma concentration against t
ime curve was 2440 +/- 126 ngh/ml. Oral ranitidine pharmacokinetic par
ameters in Mexicans appeared to be similar to those previously reporte
d for Caucasians.