HealthDay News – Misconceptions of U.S. Food and Drug Administration drug terminology exist among prescribing physicians, according to a research letter published in  the Journal of the American Medical Association.

The U.S. Congress in 2012 gave FDA the power to designate a drug as a “breakthrough therapy” if preliminary clinical evidence suggests an advantage over existing medications. But a survey of 692 doctors revealed that many tended to misinterpret the term “breakthrough.” 

Doctors often believed the drugs were supported by stronger evidence than the law requires to achieve that designation, lead author Aaron Kesselheim, MD, JD, MPH, a faculty member at Brigham and Women’s Hospital in Boston, told HealthDay.

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In the survey, nine out of 10 doctors chose one hypothetical drug over another identical one solely based on the “breakthrough” designation, even though both were taken on the same schedule, had similar side effects, and were equally covered by the patient’s insurance. 

In addition, 52% incorrectly believed that strong evidence from randomized trials is needed to earn the breakthrough designation. The survey also revealed a widespread lack of understanding about the meaning of FDA approval for a new drug, the researchers reported.

The FDA released the following statement in response to the study: “In general, the FDA does not comment on specific studies, but evaluates them as part of the body of evidence to further our understanding about a particular issue and assist in our mission to protect public health.”

Summary and Clinical Applicability

Physician misconceptions regarding the FDA drug approval terminology may have an effect on prescribing habits. FDA drug approval terminology should be more widely taught to prescribers.


Kesselheim AS, Woloshin S, Eddings W, et al.Physicians’ Knowledge About FDA Approval Standards and Perceptions of the “Breakthrough Therapy” DesignationJAMA. 2016;315(14):1516-1518. doi:10.1001/jama.2015.16984.