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Legal Status Reviews of Household Medicines

ปรุฬห์ รุจนธำรงค์; Parun Rutjanathamrong; ตวงรัตน์ โพธะ; Tuangrat Phodha; กิตติยา จันทรธานีวัฒน์; Kittiya Jantarathaneewat; ธนะวัฒน์ วงศ์ผัน; Thanawat Wongphan;
Date: 2568-07
Abstract
Background Drug classification should not consider only accessibility but also the risks associated with drug use as a classification criterion. This study aims to examine the pain points and concepts related to household medicine classification criteria in Thailand. Methods This research employs a multi-method qualitative approach comprising two phases. Phase 1 involves a literature review of Thailand's household medicine classification criteria over the past 20 years (2005-2024), analyzing the conceptual framework of the criteria. Phase 2 consists of in-depth interviews with stakeholders involved in establishing household medicine classification criteria. Content analysis was performed, followed by a synthesis of findings from both phases to develop policy recommendations addressing gaps in the current Thai household medicine classification system. Results Previous household medicine classification criteria in Thailand were established based on two types of data: (1) epidemiological disease data, which indicates the public health necessity for basic selfcare and drug accessibility, and (2) drug safety data, which is determined by various risk factors including drug abuse, antimicrobial resistance, and severe adverse reactions. Results from in-depth interviews identified gaps in the household medicine classification criteria, specifically the need for risk-benefit study data and therapeutic category information that aligns with current treatment guidelines. However, criteria improvements should involve public consultation with citizens, who are directly affected by drug classification in terms of self-care, drug accessibility, and drug information access. Additionally, consultation with pharmaceutical manufacturers is necessary, as changes may impact drug production processes, production costs, and manufacturing feasibility, ensuring alignment with public needs. Conclusion Future classification criteria should maintain a balance between improving drug accessibility and maintaining public safety, while considering the dynamic nature of medical advances and evolving healthcare needs. These findings provide valuable insights for policymakers and healthcare authorities in developing more robust and responsive drug classification systems in Thailand.
Copyright ผลงานวิชาการเหล่านี้เป็นลิขสิทธิ์ของสถาบันวิจัยระบบสาธารณสุข หากมีการนำไปใช้อ้างอิง โปรดอ้างถึงสถาบันวิจัยระบบสาธารณสุข ในฐานะเจ้าของลิขสิทธิ์ตามพระราชบัญญัติสงวนลิขสิทธิ์สำหรับการนำงานวิจัยไปใช้ประโยชน์ในเชิงพาณิชย์
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