Which of the following could be an implication if postmarketing (phase 4) were taken out of the drug approval process?
A) Additional safety information could be collected while on the market.
B) Safety and efficacy would be determined when the drug is used in real-world conditions.
C) Not all adverse reactions would be known,and the drug could be on the market longer than necessary.
D) Long-term side effects could be identified when used in the mass population.
Correct Answer:
Verified
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