Clinical risk management for allergist focuses primarily on concerns r
egarding adverse occurrences and the possibility of civil litigation a
s a result of negligence or professional liability. Risk is substantia
lly reduced with an understanding of such predictable drug reactions a
s overdosage, side effects, secondary effects, and drug interactions.
In addition, all clinicians who prescribe have a duty to disclose to t
heir patients the possibility of unpredictable reactions, including in
tolerance, idiosyncrasy, and allergy or hypersensitivity. This disclos
ure should be part of a comprehensive discussion of the risks and bene
fits of, and alternatives to, therapeutic agents and procedures they r
ecommend. The process of informed consent becomes even more critical w
ith the increasing influence of hospital and managed care formularies
on prescribing decisions. Although cost effectiveness is an important
factor in prescribing.