The rationale for the 1992 changes in the Food and Drug Administration regulations to permit accelerated approval of drugs for the treatment of life-threatening or severely debilitating disease was:

A. to allow for marketing before completion of Phase II of drug trials.
B. to ensure that the unknown risks associated with early approval are balanced by the need for effective drugs.
C. to change the rules because existing FDA regulations were too stringent for potentially effective drugs.
D. to accelerate approval of new drugs to give physicians the option of using them without research findings.


B

Nursing

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The nurse anticipates that drug therapy for an acute severe attack of multiple sclerosis (MS) will be:

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