首页> 美国卫生研究院文献>British Journal of Clinical Pharmacology >Modelling the market uptake of new drugs following listing for subsidy in Australia. A report from the Drug Utilisation Subcommittee of the Australian Pharmaceutical Benefits Advisory Committee.
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Modelling the market uptake of new drugs following listing for subsidy in Australia. A report from the Drug Utilisation Subcommittee of the Australian Pharmaceutical Benefits Advisory Committee.

机译:在澳大利亚上市后模拟新药的市场吸收情况。澳大利亚药品福利咨询委员会药品使用小组委员会的报告。

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摘要

The market uptake of five drugs following subsidy listing in Australia during the period 1990 to 1992 has been modelled using the sigmoid Emax model for drug-receptor binding. Utilisation trends for simvastatin, omeprazole, budesonide, fluoxetine and moclobemide in defined daily dose (DDD) per 1000 population per day were smoothed by expressing as 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 education campaigns on asthma and coronary heart disease occurring during the release period. The very slow uptake of omeprazole relative to other drugs 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 decisions and allows comparisons between drugs to investigate factors important in market uptake.
机译:1990年至1992年在澳大利亚补贴上市后,五种药物的市场吸收已使用S型Emax模型进行药物受体结合建模。通过以滚动年度平均值表示,可以消除每天每1000人口定义的日剂量(DDD)中辛伐他汀,奥美拉唑,布地奈德,氟西汀和莫洛贝米的使用趋势。结果表明除奥美拉唑外,该模型与数据的拟合良好,对摄取率和最终的最大利用率均具有良好的估计。药物之间的吸收率存在很大差异,这可能与在释放期间发生的关于哮喘和冠心病的公众教育运动有关。相对于其他药物,奥美拉唑的吸收非常缓慢,这可能是由于补贴使用受到限制。对市场吸收率和新药的最终利用进行建模,有助于提高药物的监管,质量使用和财务决策的效率,并使药物之间的比较可以调查对市场吸收重要的因素。

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