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本文引用的文献

1
An improved approach to measuring drug innovation finds steady rates of first-in-class pharmaceuticals, 1987-2011.一种改进的药物创新衡量方法发现，1987-2011 年，首创类药物的研发速度稳定。
Health Aff (Millwood). 2013 Aug;32(8):1433-9. doi: 10.1377/hlthaff.2012.0541.
2
Communicating uncertainties about prescription drugs to the public: a national randomized trial.向公众传达处方药的不确定性：一项全国性随机试验。
Arch Intern Med. 2011 Sep 12;171(16):1463-8. doi: 10.1001/archinternmed.2011.396.
3
Building comparative efficacy and tolerability into the FDA approval process.将比较疗效和耐受性纳入美国食品药品监督管理局的批准流程。
JAMA. 2010 Mar 10;303(10):979-80. doi: 10.1001/jama.2010.257.
4
Relative efficacy of drugs: an emerging issue between regulatory agencies and third-party payers.药物的相对疗效：监管机构与第三方支付者之间的一个新兴问题。
Nat Rev Drug Discov. 2010 Apr;9(4):277-91. doi: 10.1038/nrd3079. Epub 2010 Feb 26.
5
Medicines regulation and health technology assessment.药品监管与卫生技术评估。
Clin Pharmacol Ther. 2010 Feb;87(2):152-4. doi: 10.1038/clpt.2009.261.
6
Incremental advance or seismic shift? The need to raise the bar of efficacy for drug approval.渐进式进步还是重大变革？提高药物审批效力标准的必要性。
J Clin Oncol. 2009 Dec 10;27(35):5868-73. doi: 10.1200/JCO.2009.22.4162. Epub 2009 Oct 13.
7
How much is life worth: cetuximab, non-small cell lung cancer, and the $440 billion question.生命价值几何：西妥昔单抗、非小细胞肺癌与那4400亿美元的问题
J Natl Cancer Inst. 2009 Aug 5;101(15):1044-8. doi: 10.1093/jnci/djp177. Epub 2009 Jun 29.

Response to Michael Wonder's comments on the article 'Assessment of the therapeutic value of new medicines marketed in Australia'.

作者信息

Vitry Agnes I

机构信息

Quality Use of Medicines and Pharmacy Research Centre, Sansom Institute for Health Sciences, School of Pharmacy and Medical Sciences, University of South Australia, Adelaide Australia.

出版信息

J Pharm Policy Pract. 2013 Oct 10;6:8. doi: 10.1186/2052-3211-6-8. eCollection 2013.

DOI:10.1186/2052-3211-6-8
PMID:25848537
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4366930/
Abstract
摘要