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Why & How Our Biologic Drug Discussion with Patients Should Evolve

Paul H. Caldron, DO, PhD, MBA, & John R.P. Tesser, MD  |  Issue: February 2019  |  

Conclusion

Our patients and the community at large deserve a more measured and representative briefing on the risks of serious infection events with biologic agents, not only from us, but also from regulatory agencies and pharmaceutical firms. Even if the low rates are the result of our adherence to the cautionary practice guidance in the boxed warning, truly informed consent compels a shift from emphasis on dire risks toward responsible optimism. 

Paul H. Caldron, DO, PhD, MBAPaul H. Caldron, DO, PhD, MBA, is a clinical associate professor at Midwestern University, Arizona College of Osteopathic Medicine; a clinical assistant professor at the University of Arizona College of Medicine; and a practicing rheumatologist at Arizona Arthritis and Rheumatology Associates in Phoenix.

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John R.P. Tesser, MDJohn R.P. Tesser, MD, is a clinical assistant professor at Midwestern University, Arizona College of Osteopathic Medicine and a practicing rheumatologist at Arizona Arthritis and Rheumatology Associates in Phoenix.

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