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phenylpropanolamine

Phenylpropanolamine, commonly abbreviated as PPA, is a synthetic sympathomimetic amine that was used in pharmaceutical products as a decongestant and, in some formulations, as an appetite suppressant. It belongs to the class of phenethylamines and was found in various over-the-counter cold and flu remedies as well as weight-loss products.

Pharmacology and use: PPA exerts its effects by stimulating adrenergic receptors, producing vasoconstriction that reduces nasal

Safety and regulatory history: Concerns about safety led to significant regulatory action. In the late 1990s

Current status: In the United States, phenylpropanolamine is no longer approved for OTC use, and products containing

swelling
and
congestion.
It
also
has
central
nervous
system
activity
that
contributed
to
appetite
suppression
in
some
weight-control
regimens.
Its
actions
are
related
to
other
phenylephrine-
and
ephedrine-like
compounds,
but
its
potency
and
safety
profile
differed
among
formulations.
and
early
2000s,
studies
associated
phenylpropanolamine
with
an
increased
risk
of
hemorrhagic
stroke,
particularly
in
women.
In
2000,
the
U.S.
Food
and
Drug
Administration
advised
manufacturers
to
withdraw
PPA-containing
over-the-counter
products
from
the
market.
By
the
following
years,
PPA
had
been
largely
removed
from
U.S.
OTC
decongestants
and
diet
aids.
Some
other
countries
imposed
ongoing
restrictions
or
bans,
while
certain
formulations
and
restrictions
persisted
in
different
markets.
PPA
have
been
withdrawn
from
sale.
In
other
countries,
regulatory
decisions
vary,
but
safety
concerns
have
led
many
manufacturers
to
discontinue
PPA-containing
products.
Researchers
continue
to
review
its
risk–benefit
profile
relative
to
alternative
decongestants
and
appetite
suppressants.