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NURS 316 Exam Questions And Accurate Answers

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NURS 316 Exam Questions And Accurate Answers...

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  • October 2, 2024
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  • 2024/2025
  • Exam (elaborations)
  • Questions & answers
  • NURS 316
  • NURS 316
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NURS 316 Exam Questions And Accurate Answers


Pharmacology



The study of medicines (Pharmakon)that includes: indication, administration, transport
around the body, responses produced

Pharmacotherapeutics

Administration of drugs for the purpose of disease prevention or treatment and relief of
suffering.

Physiology

Normal function of the body

Pathophysiology

Abnormal changes caused by (or resulting in) disease

Pharmacodynamics

What a drug does to the body

Pharmacokinetics

What the body does to the drug

Drug

chemical agent capable of producing biologic responses within the body

Therapeutic effect

Desirable response

Adverse effect

Undesirable response

Biologics

Agents naturally produced in Aminal cells, used to treat and prevent various illnesses

Natural health products (NHP)

,Naturally occurring health substances use to maintain or restore health

Drug Regulation

Health Products and Food Branch (HPFB) of Health Canada has a mandate to "maximize
the safety provided by the regulatory system for health products and food"

Canadian federal law demands that the manufacturer of a drug demonstrate that it is
safe as well as effective for a particular purpose. Laws and regulations of drugs safe
and effective Step 1 in the approval process of drugs Preliminary research on drugs is
done Step 2 in the approval process of drugs Preclinical studies in cultured cells, living
tissues, and animal species Step 3 Phase I

safety phase: small group of healthy humans

Step 3 Phase II

The effective phase: small group of humans with the target disorder

Step 3 Phase III

The confirmation phase: larger groups of patients with the target disorder. Double blind
study. Only 10% make it to phase III

Step 3 Phase IV

Ongoing research

Step 4 for approval of drugs

The pharmaceutical company completes a New Drug Submission to Health Canada. This
report outlines significant safety and effectiveness information including testing data on
how the drug product will be manufactured and packaged, expected therapeutic
benefits, and adverse reactions.

Step 5 for approval of drugs

A committee of drug experts comprises medical and drugs scientists, reviews the NDS
to identify protection, drug benefits, and risks.

Step 6 for approval of drugs

Health Canada reviews the information relating to the drug product and releases crucial
information to health professionals and consumers.

Step 7 for approval of the drugs

Health Canada gives Notice of Compliance, NOC, and Drug Identification Number, DIN.
Both are required by the manufacturer for marketing the drug product.

Step 8 for the approval of the drugs

, Health Canada also monitors the effectiveness of the drug and any safety concerns
once it reaches the market. This is accomplished through routine inspection, notices,
newsletters, and consumer and health care provider feedback.

Pricing and Access to Prescription

The role of Patented Medicine Prices Review Board independent of Health Canada is to
make sure that prices by manufactures for patented medicines do not become
excessive.

drug that is medically therapeutic is commonly referred

Drug regulations requires that a drug be what for a specific purpose?

safe and effective

Drug indication

intended or indicated uses for any drug

Mechanism of Action

how a drug produces its physiological effect in the body

2 drugs having the same effect, but at different doses, which one is more effective?

ideal drug produces a rapid, predictable response at a relatively low doses

Therapeutic classification of a drug

Organises drugs according to therapeutic usefulness in the treatment of a disease.

Pharmacological classification of a drug

Describes how drug acts at molecular, tissue and body system level

Chemical drug names

Drugs named for chemical composition or by IUPAC naming

Generic drug name

Assigned International Non-proprietary name. ONE generic name per drug

Brand/Trade drug name

Name chosen by the company manufacturing it. Many trade names for each generic
drug.

Bio-avaialability

the quantity of drug absorbed into the systemic circulation and available to reach target

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