## Abstract The bioavailability of the thiazide diuretic bemetizide from a tablet containing 25 mg of this drug and 50 mg of the chemically unrelated diuretic triamterene was lower than, and significantly different (__P__ < 0.01) from that from a tablet containing 25mg bemetizide alone. The mean pe
Absorption and disposition of a new low-dose combination formulation of hydrochlorothiazide and triamterene
β Scribed by Dr. R. L. Williams; E. T. Lin; W. Liang-Gee; C. D. Blume; L. Z. Benet
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 549 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0142-2782
No coin nor oath required. For personal study only.
β¦ Synopsis
Two studies are reported that assess the bioequivalence of a new half-strength drug combination containing 25 mg hydrochlorothiazide and 37.5 mg triamterene compared to a full-strength formulation containing 50 mg hydrochlorothiazide and 75 mg triamterene. The first study (I) compared the absorption and disposition of the two drugs after administration of two tablets of the half-strength product as a single dose compared to a single dose of the full-strength product. The second study (11) assessed the bioavailability of the new product given as a single tablet on two occasions separated by an interval of 12 h compared to the full-strength product given as a single dose. Urine parameters in the first study indicated bioequivalence of the half-strength to the full product for both rate and extent of absorption. When given in divided doses, the halfstrength product demonstrated bioequivalence to the full-strength product for extent of absorption. Additional data from the second study suggest that absorption of triamterene is greater when given in smaller divided doses and when given at night.
π SIMILAR VOLUMES
The dissolution profiles of two brands of triamterene-hydrochlorothiazide (TRM-HCT) combination tablets and two brands of TRM-HCT combination capsules were studied using the USP paddle method at 100revmin-' in acid medium (0.1N). The tablets represent two products marketed in Germany, whereas the ca
The pharmacokinetics of cyclosporin A (CyA) were investigated in the rat following intravenous doses of 1.7, 3 . 3 , and 6-4mg kg-' and oral doses of 3.1, 6.8, and 12.9 mg kg-I . The blood concentration-time profile after intravenous administration was adequately described by a twocompartment model
## Abstract Experiments have been carried out in dogs and man to determine the effect of hydrochlorothiazide (HCT) on the pharmacokinetics of propranlol and to evaluate the bioavailability of two dosage forms containing both propranolol and HCT (40/25 and 80/25 mg, respectively). In adult male beag
## Abstract Angiogenesis is critical to the growth and metastasis of solid tumors, and acquired drug resistance is one of the major hindrances to chemotherapy. Thus, we sought a rational strategy using the combination of antiangiogenic biotherapy and chemotherapy for cancer therapy. We explored the