MODELING THE MARKET UPTAKE OF NEW DRUGS FOLLOWING LISTING FOR SUBSIDYIN AUSTRALIA - A REPORT FROM THE DRUG-UTILIZATION-SUBCOMMITTEE OF THETRALIAN-PHARMACEUTICAL-BENEFITS-ADVISORY-COMMITTEE

Citation
Dj. Birkett et P. Mcmanus, MODELING THE MARKET UPTAKE OF NEW DRUGS FOLLOWING LISTING FOR SUBSIDYIN AUSTRALIA - A REPORT FROM THE DRUG-UTILIZATION-SUBCOMMITTEE OF THETRALIAN-PHARMACEUTICAL-BENEFITS-ADVISORY-COMMITTEE, British journal of clinical pharmacology, 40(4), 1995, pp. 407-410
Citations number
5
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
03065251
Volume
40
Issue
4
Year of publication
1995
Pages
407 - 410
Database
ISI
SICI code
0306-5251(1995)40:4<407:MTMUON>2.0.ZU;2-J
Abstract
The market uptake of five drugs following subsidy listing in Australia during the period 1990 to 1992 has been modelled using the sigmoid E( max) model for drug-receptor binding. Utilisation trends for simvastat in, omeprazole, budesonide, fluoxetine and moclobemide in defined dail y dose (DDD) per 1000 population per day were smoothed by expressing a s rolling annual averages. The results indicate good fits of the model to the data except for omeprazole, with good estimates of uptake rate and eventual maximum utilisation. Substantial differences between the drugs occurred in uptake rate which may be related to public educatio n campaigns on asthma and coronary heart disease occurring during the release period. The very slow uptake of omeprazole relative to other d rugs is likely to be due to restrictions on subsidised use. Modelling the market uptake rate and eventual utilisation of new drugs is useful as an aid to regulatory, quality use of medicines and financial decis ions and allows comparisons between drugs to investigate factors impor tant in market uptake.