校際選修

115-1 選課時程

進行中

  • 初選第一階段 6/15/2026
  • 初選第二階段 6/22/2026
  • 校際選修 8/24/2026
  • 初選第三階段 8/31/2026
  • 開學後加退選 9/7/2026
  • 逾期加退選 9/21/2026
選課資源

藥物流行病學

Pharmacoepidemiology

學期
113-1
學分
2 學分
當期課號
132017
永久課號
PSPM30029
開課單位
藥學系
授課教師
黃彥銘、謝斯婷、黃薇伊、周千瀅、許家禎、東雅惠、黃莉茵、簡伶蓁、張釗銘、王孟廷
校區
陽明
類別
必修
上課時間表
週二
5
13:20–14:10
藥物流行病學
YL405
2 節連堂
6
14:20–15:10

* 根據陽明交大上課時間表所列

週次計畫
週次主題
第 1 週Course overview and introduction to pharmacoepidemiology
第 2 週Studies of drug utilization and prescribing patterns
第 3 週中秋節放假
第 4 週Studies of medication adherence
第 5 週Cohort studies and corresponding methodological considerations
第 6 週Case studies
第 7 週Case-control studies and corresponding methodological considerations
第 8 週Case studies **調課至 10/23 3-4節 圖資404教室**
第 9 週Case-only studies and corresponding methodological considerations
第 10 週Case studies
第 11 週Comorbidity measures and control for confounding
第 12 週Randomized controlled trials
第 13 週Special topic: Application of primary data collection in healthcare services research
第 14 週Special topic: Spontaneous Pharmacovigilance Reporting System & Postmarketing Drug Safety Surveillance
第 15 週Special topic: Health Technology Assessment
第 16 週Student report
第 17 週Student report
教科書

1. Pharmacoepidemiology. Brian L. Strom, Stephen E. Kimmel, Sean Hennessy. New York: Wiley-Blackwell. 6th ed., 2019. 2. International Society for Pharmacoepidemiology. Guidelines for Good Pharmacoepidemiology Practices (GPP). https://www.pharmacoepi.org/resources/policies/guidelines-08027 3. European Network of Centers for Pharmacoepidemiology and Pharmacovigilance. Guide on Methodological Standards in Pharmacoepidemiology. http://encepp.eu/standards_and_guidances/methodologicalGuide.shtml 4. US Food and Drug Administration. Framework for FDA’s real-world evidence program. https://www.fda.gov/media/120060/download 5. Guidance for Industry and FDA Staff -- Best Practices for Conducting and Reporting Pharmacoepidemiologic Safety Studies Using Electronic Healthcare Data. https://www.fda.gov/media/79922/download 6. European Medicines Agency. Guideline on good pharmacovigilance practices (GVP) Module VIII – Post-authorisation safety studies (Rev 3) http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2012/06/WC500129137.pdf 7. 授課教師指定參考教材