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PHARMACOLOGY_NEW_EXAM_UPDATE_QUESTIONS_AND_ANSWERS_SOLUTION
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  • Nursing
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  • University Of Wales Insitute, Cardiff

PHARMACOLOGY_NEW_EXAM_UPDATE_QUESTIONS_AND_ANSWERS_SOLUTION PHARMACOLOGY_NEW_EXAM_UPDATE_QUESTIONS_AND_ANSWERS_SOLUTION PHARMACOLOGY_NEW_EXAM_UPDATE_QUESTIONS_AND_ANSWERS_SOLUTION

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Document information

  • June 11, 2023
  • 6
  • 2022/2023
  • Exam (elaborations)
  • Questions & answers

Subjects

  • pharmacologynewexamupdatequestionsandanswers
  • pharmacologynewexamupdatequestionsandanswer2

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  • University of Wales Insitute, Cardiff
  • Unknown
  • Nursing
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2022-2023 PHARMACOLOGY NEW EXAM UPDATE QUESTIONS AND ANSWERS
SOLUTION

molecular pharmacology - ANS IS the study of the chemical structures of drugs and
their actions at the molecular level within a cell is called

Pharmacogenomics - ANS IS use of information about a person's genetic makeup, or
genome, to choose the drugs and drug doses that are likely to work best for that person

generic name - ANS IS The United Stated Adopted name is considered to be the drugs
____________

Trade Name - ANS IS The brand name that a manufacturer gives a medication; the
name is capitalized.

In Vivo - ANS IS This term means testing on animals or humans

In Vitro - ANS IS This term means testing in glass

Pharmacodynamics - ANS IS drug effects based on time and dose

half-life - ANS IS The time required for the drug level in the blood to decrease form
100% to 50%

Pharmacokinetics - ANS IS the study of drug movement throughout the body

Inert ingredients - ANS IS Filler / non-drug ingredients in medication which are inactive.

Desiccant - ANS IS a substance used to absorb moisture from the air and create a dry
atmosphere

National Drug Code (NDC) - ANS IS Unique 10 or 11 identification number given to
drugs that contains 3 sections Manufacturer, drug strength/dose and drug size/type

Federal Trade Commission (FTC) - ANS IS The agency that regulates the marketing
and advertising of over the counter drugs

Post-marketing surveillance - ANS IS Monitoring safety of medications/devices
AFTER they have been released on the market

drug recall - ANS IS Medications are taken off the market if there is a reasonable
probability that use will result in serious adverse health consequences or death

Bioavailability - ANS IS the rate at and the extent to which a nutrient is absorbed and
used




This study source was downloaded by 100000835004878 from CourseHero.com on 01-23-2023 12:30:38 GMT -06:00


https://www.coursehero.com/file/186262267/2022-2023-PHARMACOLOGY-NEW-EXAM-UPDATE-QUESTIONS-AND-ANSWERS-SOLUTIONpdf/

, Control Group - ANS IS the group that does not receive the experimental treatment.

Placebo - ANS IS A harmless pill, that is usually received by the control group is called

Pharmacogenetics - ANS IS the study of how genetic variation affects an individual's
response to drugs

Isomers - ANS IS Compounds with the same formula but different structures.

Recombinant DNA technology - ANS IS technology that combines genes from different
sources into a single DNA molecule

Recombinant DNA Advisory Committee - ANS IS group of physicians and pharmacists
that review clinical trials of genetically engineered drugs and then makes
recommendations to the FDA

therapeutic index - ANS IS the ratio between the toxic and therapeutic concentrations of
a drug

median effective dose - ANS IS Dose required to produce a specified intensity of effect
in 50% of the animals

active ingredient - ANS IS Generic drugs and trade name drugs that are in the same
drug form and drug strength--even if they are from different drug companies-must
contain exactly the same amount of

It can be marketed - ANS IS No matter how a drug was originally discovered or
designed, it must be thoroughly tested by the drug company
before_____________________.

FTC (Federal Trade Commission) - ANS IS ___________is over advertising of over the
counter drugs

MedWatch - ANS IS ________________________ is the FDA safety information and
adverse event reporting system on the Internet.

MEDMARX - ANS IS A national Internet-accessible database that hospitals and health
care systems use to track adverse drug reactions and medication errors.

Investigational new drug application - ANS IS When animal studies are completed, the
drug company submits a(n) ____________ application to the FDA.

Median effective dose (ED50) - ANS IS the dose of a drug that produces a therapeutic
response in 50% of the animals tested




This study source was downloaded by 100000835004878 from CourseHero.com on 01-23-2023 12:30:38 GMT -06:00


https://www.coursehero.com/file/186262267/2022-2023-PHARMACOLOGY-NEW-EXAM-UPDATE-QUESTIONS-AND-ANSWERS-SOLUTIONpdf/

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