估计COVID-19对全球化活跃制药成分市场的影响
Melissa Barber1, Reshma Ramachandran2, Suerie Moon3
1Melissa Barber (melissa.barber@yale.edu), Yale University, New Haven, Connecticut.
Health affairs (Project Hope)
|July 1, 2024
概括
由于COVID-19大流行,印度的活性药物成分 (API) 出口量大幅减少. 非COVID-19基本药物的价格保持稳定,而重定向药物的价格升,凸显了供应链的脆弱性.
科学领域:
- 制药经济学 制药经济学
- 全球卫生安全 全球卫生安全
- 供应链管理 供应链管理
背景情况:
- 全球活性药物成分 (API) 供应链高度集中,在公共卫生危机期间构成风险.
- 缺乏系统监测和全球协调,阻碍了有效的风险管理和公平的药物获取.
- COVID-19 流行病暴露了制药供应链中的关键漏洞.
研究的目的:
- 分析COVID-19大流行对印度API价格和出口量的影响.
- 评估对基本药物的差异性影响与针对COVID-19的猜测性重用药物的差异性影响.
主要方法:
- 在从印度的货物级别海关数据上使用了准实验方法.
- 在世界卫生组织宣布流行病之前和之后,比较API价格和出口量.
- 对必需药物的API和用于投机性COVID-19重新用途的API之间的差异化分析.
主要成果:
- 印度的API出口量在疫情宣布后下降了80%.
- 与COVID-19无关的基本药品的价格没有显著变化.
- 投机性地重新定制的药物价格,如氧化和甲胺,上了高达250%,甲胺也经历了体积下降.
结论:
- 该研究强调了全球API供应链的脆弱性,以及在卫生紧急情况期间价格投机的潜力.
- 建议包括系统的API市场监测,投资供应多样化,以及政策改革以防止价格操纵.
- 提高供应链的弹性对于确保全球持续获得必需药物的安全至关重要.
相关概念视频
Drug Control Governance: Regulatory Bodies and Their Impact
150
Drug control governance involves the oversight and regulation of pharmaceuticals to ensure their safety and efficacy while preventing illegal drug use and trafficking. Regulatory bodies, including the US Food and Drug Administration (FDA) and the European Union's European Medicines Agency (EMA), play a central role in this process. These agencies evaluate the safety and efficacy of drugs before they can be marketed. They fund clinical trials and assess the benefits and risks associated with...
150
Pharmacovigilance
817
Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
817
Factors Influencing Drug Absorption: Pharmaceutical Parameters
129
Solid dosage forms such as tablets and capsules undergo rigorous manufacturing processes to ensure stability and effectiveness. Their dissolution and absorption properties are influenced significantly by the choice of excipients (inactive ingredients that serve various roles in the formulation), and the methodology applied during production. The manufacturing parameters, such as compression force and granulation techniques, significantly affect dissolution rates. Elevated compression forces...
129
Bioequivalence: Overview
983
Pharmaceutical equivalents, by definition, are drug products with the same active ingredient in the same quantities, encapsulated in identical dosage forms, and intended for the same administration routes. These pharmaceutical equivalents are deemed bioequivalent if the bioavailability of the active entity in the drug preparations is similar. Moreover, pharmaceutical equivalents demonstrating bioequivalence are also regarded as therapeutically equivalent. This means that when used as directed,...
983
Biopharmaceutics and Pharmacokinetics: Overview
1.9K
Understanding drugs, drug products, and their performance in pharmaceutical science is pivotal. Drugs, whether simple molecules or complex compounds, are designed to interact with the body's biological systems to diagnose, treat, or prevent diseases. Drug products include various delivery systems such as tablets, capsules, injections, and inhalers. The performance of these drug products is gauged by their ability to deliver the active ingredient to the desired site of action at the...
1.9K
Time Course of Drug Effect
2.0K
The progression of a drug's impact can be analyzed by examining both the concentration-time course and the effect-time course. The concentration-time course is determined by the drug's half-life and is influenced by factors such as its pharmacokinetics, including absorption, distribution, metabolism, and elimination. The effect of the drug is often related to its concentration in the plasma and is calculated using the maximum drug effect and the plasma concentration that generates 50...
2.0K


