Available in 2017

Course handbook

Description

Provides students with core training in appropriate methods for pharmacoepidemiology. The role of post-marketing drug surveillance and voluntary drug reporting systems are examined. Study methodologies explored in this course include cohort studies, case control studies, and meta-analysis of observational studies.


Availability2017 Course Timetables

WebLearn GradSchool

  • Semester 2 - 2017

Learning outcomes

On successful completion of the course students will be able to:

1. An appreciation of the importance of systematic evaluation of drug effects following licensing.

2. The strengths and limitations of controlled observational designs in quantifying drug effects.

3. The role of systematic review and meta-analysis in making an overview of pharmacoepidemiological studies.

4. The capacity to perform critical appraisals of published observational studies and systematic reviews.


Content

Module 1: The role of postmarketing drug evaluation

Module 2: Voluntary reporting systems

Module 3: Case control studies in pharmacoepidemiology

Module 4: Cohort studies in pharmacoepidemiology

Module 5: Automated data-bases in pharmacoepidemiology

Module 6: Systematic reviews and meta-analysis in pharmacoepidemiology


Assumed knowledge

Students are required to have a background in Epidemiology and Biostatistics.


Assessment items

Written Assignment: Written Assignment / Essay 1 - 25%

Written Assignment: Written Assignment / Essay 2 - 25%

Written Assignment: Written Assignment / Essay 3 - 25%

Written Assignment: Written Assignment / Essay 4 - 25%


Contact hours

WebLearn GradSchool

Online Activity

Online 2 hour(s) per Week for Full Term

Contact hours are an indication only. Blackboard Discussion and Email Discussion as Required