What are the public health effects of direct-to-consumer drug advertising?
Elizabeth A Almasi1, Randall S Stafford, Richard L Kravitz
1Stanford University, Stanford, California, USA. ealmasi@stanford.edu
Background To The Debate:
Only two industrialized countries, the United States and New Zealand, allow direct-to-consumer advertising (DTCA) of prescription medicines, although New Zealand is planning a ban. The challenge for these governments is ensuring that DTCA is more beneficial than harmful. Proponents of DTCA argue that it helps to inform the public about available treatments and stimulates appropriate use of drugs for high-priority illnesses (such as statin use in people with ischemic heart disease). Critics argue that the information in the adverts is often biased and misleading, and that DTCA raises prescribing costs without net evidence of health benefits.
More Related Videos
Related Concept Videos
Drug Regulation
Pharmacovigilance
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...
Effects of Chemicals: Overview
Drug Control Governance: Regulatory Bodies and Their Impact
Drug Toxicity: Overview
Drug Toxicity: Dose-Dependent Reactions


