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oxycodone HCl controlled-release
The cravings for Oxycontin are the result of the impact on
the person's memory with feelings of pleasure and euphoria
that the person associates with the taking of medication.
The subconscious memory then motivates the person to seek
for oxycontin because of its false imprint of Oxycontin.
Oxycontin contains oxycodone, a really strong narcotic pain
killer with similarity to morphine. Oxycontin is made in a
way that the oxycodone is slowly released over time.
Oxycontin Addiction is a physical dependency that you cannot
avoid when a person is exposed to high dosages of the oxycontin
for a extended lenght of time. The body then adapts and start
having a tolerance for Oxycontin. Oxycontin is so powerful
that it produces a great amount cravings.
Regulation
Regulation of oxycodone (and opioids in general) varies according
to nations, with different places focusing on different parts
of the "supply chain".
Regulation in Canada
In Canada, Oxycodone is a regulated drug under Schedule I
of the Controlled Drugs and Substances Act (CDSA). Every individual
who looks for or obtain the substance without disclosing authorization
to obtain such substances 30 days prior to obtaining another
prescription from a practitioner is guilty of an indictable
offence and liable to imprisonment for a term not exceeding
seven years. Possession for purpose of trafficking is guilty
of an indictable crime and liable to life imprisonment.
Regulation in the USA
Regulation of prescription substances comes from many different
regions. The Food and Drug Administration (FDA) authorizes
drugs for medical use, as well as sets regulations for the
marketing of drugs, including regulated substances. The Drug
Enforcement Administration (DEA) on the other hand, receives
its regulatory authority from the Controlled Substances Act
(CSA) [21 U.S.C. §§ 801-971], which "mandates
that DEA prevent, detect and investigate the diversion of
legitimately produced controlled substances while, at the
same time, ensuring that there are adequate supplies to meet
the legitimate medical needs in the United States".
Part of the regulation of prescription substances is connected
to their marketing and advertising. The FDA has authority
over this sector under the Food, Drug, and Cosmetic (FD&C)
Act and its implementing regulations. The Division of Drug
Marketing, Advertising, and Communications (DDMAC) is "responsible
for controlling prescription substance advertising and promotion,"
and has a "mission is to protect the public health by
ensuring that prescription drug information is truthful, balanced,
and accurately communicated".
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