Honors Theses
Date of Award
Spring 5-9-2026
Document Type
Undergraduate Thesis
Department
Public Health
First Advisor
Neil A. Manson
Second Advisor
Nathan Oakes
Third Advisor
Vivian Ibrahim
Relational Format
Dissertation/Thesis
Abstract
The United States pharmaceutical system is highly advanced but faces growing ethical concerns related to drug development and marketing, overprescription, and high drug costs. This thesis examines how pharmaceutical marketing, regulatory practices, and prescribing behaviors may conflict with the ethical principle of “first, do no harm.”
Using a narrative review of interdisciplinary literature in public health, medical ethics, and applied ethics, this thesis analyzes patterns in drug development, marketing strategies, and regulatory oversight. The findings suggest that ethical issues are systemic, driven by commercial incentives, inconsistent regulatory standards, and an increasing reliance on pharmaceutical solutions. These factors contribute to overmedicalization, expanded disease definitions, and reduced emphasis on preventive care.
This thesis concludes that addressing these challenges requires a shift toward greater transparency, stronger regulatory oversight, and increased investment in preventive healthcare. Emphasizing prevention over treatment may better align pharmaceutical practices with long-term patient well-being and ethical medical standards.
Recommended Citation
Bailey, Rebekah R., ""First, Do No Harm": Ethical Failures and Preventive Solutions in the United States Pharmaceutical System - A Narrative Review" (2026). Honors Theses. 3431.
https://egrove.olemiss.edu/hon_thesis/3431
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Included in
Applied Ethics Commons, Bioethics and Medical Ethics Commons, Pharmacy Administration, Policy and Regulation Commons