Prescription Medicine Introduction -
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All
medications sold in the US can be divided into 2 categories:
The first "Prescription medications" that require
a prescription to be sold and "Free prescription" -
without Rx - or over-the-counter medications that do not
require a directive from a doctor.Rx/Prescription meds are
generally more potent than those sold over-the-counter (OTC)
and may have more various side effects in case inappropriately
used. Therefore, Rx meds products are only sold under a doctor’s
direction. These directions are written on a prescription
by your local doctor, then double-checked, packaged, and
offer for sale by a pharmacist.
History of FDA :The
Food and Drug Administration (FDA), established in 1930 as
a part of the US Department of Health and Human Services
(HHS), regulates products accounting for roughly 25% of the United
States gross national product.You may not realize the number
of products you use in a given day that are regulated by
the
FDA. The label on the juice you drink for breakfast, the
cosmetics you apply before work, the array of dietary supplements
you
take before dashing out the door, the food you feed your
pets, the aspirin you take after a long day, and the contact
lenses
you place on your eyes are all regulated by this Rockville,
Maryland-based agency. Because of the FDA, Americans largely
can take for granted that these products are safe.By examining
the history of food and drug regulation, you can get a sense
of the breadth of the agency’s mission and the forces
that have led to the agency’s present size and role as
one of the world’s most respected public health agencies.
(An extensive bibliography included at the end of this article
provides detailed references.)Until the 20th century, drugs
were regulated primarily by state and local governments. Drugs "could
be bought and sold like any other consumer good" (US
Regulatory Affairs History, Chapter 1). Regulation became
more stringent
as medical technology improved and high-profile incidents
highlighted the need for at least some degree of government
monitoring
of these products.
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