9553683 15255087 11033571 19856796 12968816 7996375 - Search Results

Year	Number of Results
1994	1
1998	1
2000	1
2003	1
2004	1
2009	1
2023	0

1

Single dose study of the bioequivalence of two sustained-release theophylline formulations.

Contreras J, Pérez N, González R, Ontivero E, López M. Contreras J, et al. Arzneimittelforschung. 1998 Mar;48(3):259-62. Arzneimittelforschung. 1998. PMID: 9553683 Clinical Trial.

2

Potential savings from increased use of generic drugs in the elderly: what the experience of Medicaid and other insurance programs means for a Medicare drug benefit.

Fischer MA, Avorn J. Fischer MA, et al. Pharmacoepidemiol Drug Saf. 2004 Apr;13(4):207-14. doi: 10.1002/pds.872. Pharmacoepidemiol Drug Saf. 2004. PMID: 15255087

3

A practical approach for evaluating population and individual bioequivalence.

Gould AL. Gould AL. Stat Med. 2000 Oct 30;19(20):2721-40. doi: 10.1002/1097-0258(20001030)19:20<2721::aid-sim541>3.0.co;2-8. Stat Med. 2000. PMID: 11033571

4

Substitution of theophylline slow-release formulations according to the rebate contracts in the German statutory health insurance.

Weissenfeld J, Lüngen M, Stock S, Drabik A, Gerber A. Weissenfeld J, et al. Arzneimittelforschung. 2009;59(9):476-81. doi: 10.1055/s-0031-1296428. Arzneimittelforschung. 2009. PMID: 19856796

5

Economic consequences of underuse of generic drugs: evidence from Medicaid and implications for prescription drug benefit plans.

Fischer MA, Avorn J. Fischer MA, et al. Health Serv Res. 2003 Aug;38(4):1051-63. doi: 10.1111/1475-6773.00162. Health Serv Res. 2003. PMID: 12968816 Free PMC article.

6

Bioequivalence of a generic slow-release theophylline tablet in children.

Kanthawatana S, Ahrens RC, McCubbin M, Bronsky E, Blake K, Hendeles L. Kanthawatana S, et al. J Pediatr. 1994 Dec;125(6 Pt 1):987-91. doi: 10.1016/s0022-3476(05)82021-9. J Pediatr. 1994. PMID: 7996375 Clinical Trial.

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