Professor O\u27Reilly\u27s study of recent drug review legislation applies a historical and holistic view of promotion practices for unapproved uses of prescription drugs. He faults Congress for moving public health protections away from a strictly protective mode and toward assistance to drug marketers. He argues that the adverse health consequences of off-label promotion of drugs are not well understood, and that the 1997 amendments disserved the public health interest while expanding pharmaceutical company profits
The U.S. Food and Drug Administration’s (FDA) policies have been a battleground for litigation about...
The Food and Drug Administration (FDA) engages in a premarketing approval process established by Con...
Off-label drug promotion is commonplace in the United States, but it is not without its dangers. Whi...
Professor O\u27Reilly\u27s study of recent drug review legislation applies a historical and holistic...
Off-label promotion occurs when pharmaceutical manufacturers engage in promo-tion of unapproved or &...
Last year alone, doctors filled out over four billion drug prescriptions in the United States. But a...
Physicians often prescribe prescription drugs and other medications for uses that are not approved b...
Off-label promotion occurs when pharmaceutical manufacturers engage in promotion of unapproved or o...
The Federal Food, Drug, and Cosmetic Act (FDCA) does not expressly prohibit companies from marketing...
Off-label promotion occurs when pharmaceutical manufacturers engage in promo-tion of unapproved or “...
In the United States, the term off-label use means usingapproved drugs for clinical indications that...
Off-label promotion has attracted intense scrutiny from regulators in recent decades resulting in ma...
After Caronia: First Amendment Concerns in Off-Label Promotion by Stephanie M. Greene* Abstract The ...
In this article, Professor Orentlicher explores free speech and federalism issues arising from FDA r...
This Essay posits that the FDA should protect the current regime put in place by the Kefauver-Harris...
The U.S. Food and Drug Administration’s (FDA) policies have been a battleground for litigation about...
The Food and Drug Administration (FDA) engages in a premarketing approval process established by Con...
Off-label drug promotion is commonplace in the United States, but it is not without its dangers. Whi...
Professor O\u27Reilly\u27s study of recent drug review legislation applies a historical and holistic...
Off-label promotion occurs when pharmaceutical manufacturers engage in promo-tion of unapproved or &...
Last year alone, doctors filled out over four billion drug prescriptions in the United States. But a...
Physicians often prescribe prescription drugs and other medications for uses that are not approved b...
Off-label promotion occurs when pharmaceutical manufacturers engage in promotion of unapproved or o...
The Federal Food, Drug, and Cosmetic Act (FDCA) does not expressly prohibit companies from marketing...
Off-label promotion occurs when pharmaceutical manufacturers engage in promo-tion of unapproved or “...
In the United States, the term off-label use means usingapproved drugs for clinical indications that...
Off-label promotion has attracted intense scrutiny from regulators in recent decades resulting in ma...
After Caronia: First Amendment Concerns in Off-Label Promotion by Stephanie M. Greene* Abstract The ...
In this article, Professor Orentlicher explores free speech and federalism issues arising from FDA r...
This Essay posits that the FDA should protect the current regime put in place by the Kefauver-Harris...
The U.S. Food and Drug Administration’s (FDA) policies have been a battleground for litigation about...
The Food and Drug Administration (FDA) engages in a premarketing approval process established by Con...
Off-label drug promotion is commonplace in the United States, but it is not without its dangers. Whi...