Intro to Pharmacology (Exam 1) Flashcards

1
Q

Definition of Pharmacology

A

The study of the biological effects of DRUGS that are introduced into the body to cause some sort of change

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2
Q

Definition of Pharmacokinetics

A

-What happens to drugs in the body

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3
Q

Pharmacodynamics

A

-Mechanism of action

-Effects on the body

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4
Q

Chemical Name

A

-Long and Complex

-Used in research

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5
Q

Generic name

A

-Official name of drug

-Only 1 generic name

-Usually more complicated than trade name

-Lower case

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6
Q

Trade Name

A

-Brand Name

-Easier to remember and pronounce

-Upper case

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7
Q

Prototype Drug

A

One drug-typically the first-that represents a group or class of medication

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8
Q

New drugs int eh class are compared to the prototype to examine what?

A

Effectiveness and Side Effects

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9
Q

Therapeutic Effects

A

-Intended effects of the drug

-What we want to happen

Blood pressure medication to decrease blood pressure

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10
Q

Side effects

A

-Unintended Effects of Medication

-Unavoidable

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11
Q

When taking a medication a person has to weigh what?

A

The therapeutic effects vs the adverse (side effects)

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12
Q

Toxicties

A

Harmful effects of medication

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13
Q

Allergic reactions

A

-Unexpected can be dangerous

-Involves immune system response

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14
Q

What do we needs to know with each medication?

A

-Name: Generic Names

-Classification (drug class): Given to a describe a group of medication that work similarly (SAME MOA)

-Mechanism of action: How the drug works in the body

-Indications: Why are we giving this med? What is it used to treat?

-Common/Serious Adverse Effects

-Contrindications

-Nursing indications: What the nurses need to worry about with the medication. What do we need to assess before giving the said medication. Serious interactions? is it a CYP drug?

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15
Q

How are new drugs approved

A

-approved by the FDA

-chemical identified and undergoes strict clinical test

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16
Q

Preclinical Trials

A

Tested on lab animals for therapeutic and adverse effects

17
Q

Phase I studies

A

Human Volunteers are used to test the drug

-Showing us big side effects

18
Q

Phase II Studies

A

-drug is tried on patients who have the disease that the drug is designed to treat

-showing use rare and new side effects

19
Q

Phase III studies

A

The drug is used in a VAST CLINICAL MARKET.

20
Q

Phase IV studies

A

-CONTINUED EVALUATION by the FDA

21
Q

Controlled Substances

A

-Schedule I-V

22
Q

Schedule I Medications

A

-Chemical substances or drugs that are not approved for medical use. No reason to prescribe

-Herion-LSD-Ecstasy

-VERY HIGH POTENTIAL FOR ABUSE

23
Q

Schedule II Medications

A

-Used medically, but HIGH potential for abuse

-Narcotics and amphetamines

-Hydromorphone - Oxycodone

-NO REFILLS ALLOWED

24
Q

Schedule III Medications

A

Less potential for abuse (moderate to low)

-None barbiturate sedatives, non-amphetamines, stimulants

-Ketamine, testosterone, anabolic steroids

25
Q

Schedule IV Medications

A

-Some potential for Abuse

-Primarily sedatives, anti-anxiety medications

-Xanax, Valium, Ambien

26
Q

Schedule 5

A

Low potential for abuse

-Mediations containing small amounts of certain narcotics or stimulants. Antitussives

-Cough suppressants with some codeine, ephedrine containing medications

27
Q

Over the Counter Medications

A

-80 different classes

-Antihistamines, sleep aids, analgesics, antacids, laxatives

-Low risk of side effects and Low abuse potential

28
Q

For a medication to be classified as OTC

A

Consumers must be able to diagnose own conditions and monitor effectiveness EASILY

Benedryll for poison Ivey rash

29
Q

Some OTC medications are available only behind the pharmacy counter due to abuse possibility

A

-Pseudoephedrine containing medications

30
Q

Dietary and Herbal Supplements can only

A

Claim affect on BODY STRUCTURE or FUNCTION (not medical condition)

EX. St John’s Wort- affects emotional balance (not treat depression)

Not evaluated by the FDA

31
Q

Adverse interactions between drugs and herbals

A

-Some herbals can INCREASE the toxicity of prescription medication or cause DECREASED therapeutic effects

32
Q

Teaching Points for Drug and Herbals

A

When getting a medication history always ask SPECIFICALLY about other medications, supplements, OTC, herbals, vitamins, etc.

33
Q

Example: of adverse interaction

A

GINKO biloba platelet aggregation

Therefore can increase the risk of bleeding in patients on antiplatelet and antiocoagulant drugs (blood thinners)

34
Q

Teratogens

A

Substances that can cause congenital malformations in developing fetus

35
Q

Common teratogens

A

Alcohol, marijuana, and nicotine all known teratogens

36
Q

FDA Pregnancy Risk Categories

A

Category A- Safe for fetus

Category B- Lack of studies to show benefit/risk

Category C- No studies, animal studies possible risk

Category D- drugs that have possible risk to the fetus

Category X- drugs that have KNOWN RISK, that CANNOT be outweighed by possible benefit

37
Q

Pregnancy and Lactation Labeling Rule (PLLR) categories

A

Pregnancy

Lactation

Females and Males of Reproductive Potential

38
Q

Pharmacogenomics

A

-The study of how genes affect a person’s response to drugs

-New field combines pharmacology and genomics to develop effective, safe medications and doses that will be tailored to a persons makeup