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- W2001029816 abstract "When prescribing a generic drug, there should be confidence the patient would see the same results as a patient taking the brand-name drug. Current Federal Drug Administration (FDA) protocol allows generic drugs to be marketed after having met the criteria for bioequivalence to brand-name drugs, but should that classification be equated with therapeutic equivalence as done by the FDA? Such is the concern of physicians each time they note “generic substitution acceptable” rather than “brand necessary”." @default.
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- W2001029816 date "2012-08-07" @default.
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- W2001029816 title "Brand versus Generic Drugs: Should We Be Cautious?" @default.
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- W2001029816 doi "https://doi.org/10.7759/cureus.53" @default.
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