RNSG 1301 EXAM ONE Questions And Answers Rated 100% Correct!!
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Course
RNSG 1301
Institution
RNSG 1301
Genetic drugs vs Brand name - ️️Once the patent on a brand name runs out
manufactures develop genetic drugs which are intended work on in the same way
(quality, dosage, strength, and route of administration).
The bioavailability of the generic drugs may differ from the brand name. This is wh...
RNSG 1301 EXAM ONE
Genetic drugs vs Brand name - ✔️✔️Once the patent on a brand name runs out
manufactures develop genetic drugs which are intended work on in the same way
(quality, dosage, strength, and route of administration).
The bioavailability of the generic drugs may differ from the brand name. This is why
providers might specify "dispense as written" so brand name product may use
especially in drugs that have narrow safety margins.
Pregnancy category C - ✔️✔️Animal studies have shown an adverse effect on the
fetus but there are no adequate studies in humans; the benefits from the use of the drug
in pregnant women may be acceptable despite its potential risks, or there are no animal
reproduction studies and no adequate studies in humans.
Generic drugs - ✔️✔️drugs sold by their generic name; not brand (or trade) name
products
Brand name - ✔️✔️name given to a drug by the pharmaceutical company that
developed it; also called a trade name
Control substance - (C-I) Schedule I - ✔️✔️High abuse potential and no accepted
medical use (heroin, marijuana, LSD)
Control substance - (C-II) Schedule II - ✔️✔️High abuse potential with severe
dependence liability (narcotics, amphetamines, and barbiturates)
Control substance - (C-III) Schedule III - ✔️✔️Less abuse potential than schedule II
drugs and moderate dependence liability (nonbarbiturate sedatives, nonamphetamine
stimulants, limited amounts of certain narcotics)
< 15 mg hydrocodone per dosage unit (Vicodin) ; < 90 mg of codeine p3er dosage unit
(Tylenol w/ codeine); ketamine; anabolic steroids; testosterone
Written/Oral Rx that expired w/n 6mos. No more than 5 refills.
, Control substance - (C-IV) Schedule IV - ✔️✔️Less abuse potential than schedule III
and limited dependence liability (some sedatives, antianxiety agents, and nonnarcotic
analgesics)
Written Rx or OTC; must be 18 yo, ID must be showed, and dispensing must be
recorded
The Controlled Substances Act of 1970 - ✔️✔️Control over the coding of drugs and the
enforcement of these codes to the FDA and the Drug Enforcement Agency (DEA), a
part of the U.S. Department of Justice.
Pregnancy category A - ✔️✔️Adequate studies in pregnant women have not
demonstrated a risk to the fetus in the first trimester of pregnancy, and there is no
evidence of risk in later trimesters.
Pregnancy category B - ✔️✔️Animal studies have not demonstrated a risk to the fetus
but there are no adequate studies in pregnant women.
Pregnancy category D - ✔️✔️There is evidence of human fetal risk, but the potential
benefits from the use of the drug in pregnant women may be acceptable despite its
potential risks.
Pregnancy category X - ✔️✔️Studies in animals or humans demonstrate fetal
abnormalities or adverse reaction; reports indicate evidence of fetal risk. The risk of use
in a pregnant woman clearly outweighs any possible benefit.
Pharmacotherapeutics - ✔️✔️clinical pharmacology—the branch of pharmacology that
deals with drugs; chemicals that are used in medicine for the treatment, prevention, and
diagnosis of disease in humans
Pharmacodynamics - ✔️✔️The process by which a medication works on the body.
The study of the interactions between the chemical components of living systems and
the foreign chemicals, including drugs, that enter living organisms; the way a drug
affects a body.
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