Definition of Pharmacology Flashcards

The study of the actions of drugs on humans and animals

1
Q

Elimination Half - Life (T1/2)

A

The time it takes for 50% of a particular drug to be cleared from the blood stream

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2
Q

Routes of Elimination

A

Kidney, Lung or Bowel

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3
Q

Anatomical Barriers to Distribution

A

Blood - Brain Barrier
Placental Barrier

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4
Q

Pharmacokinetic Phase (ADME)

A

Absorption
Distribution
Metabolism
Elimination

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5
Q

Duration of Action

A

The time between the onset of action and the discontinuation of drug action

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6
Q

Peak Effect

A

The maximum effect produced by a drug after it has reached its maximum concentration in the body.

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7
Q

Onset of Action

A

The time it takes for a drug to produce a therapeutic effect

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8
Q

Food and Drug Amendments Act (2007)

A

Set guidelines for post market clinical studies

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9
Q

Comprehensive Drug Abuse Prevention and Control Act (1970)

A

Places controlled substances into categories C-1 through C-V, regulating drugs with a history of abuse

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10
Q

Pharmaceutical Equivalent

A

Different inactive ingredients, dosage form, and exhibits different absorption rates than brand name product

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10
Q

Kefauver-Harris Amendment (1962)

A

Requires drugs to be safe and effective

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10
Q

Durham- Humphrey Amendment (1950)

A

Categorized drugs as either legend (prescription only) or over -the -counter (no prescription required

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11
Q

Whey are drugs used

A

Diagnosis
Treatment
Mitigation of Symptoms
Cure Disease
Prevent Disease

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11
Q

Routes of Administration

A

Oral
Topical
Inhalation
Parenteral

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11
Q

Pure Food and Drug Act (1906)

A

sets the standards for allowing new drugs onto the market

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11
Q

Therapeutic Alternative

A

Different active ingredients, yet produce the same desired therapeutic outcome

12
Q

First Pass Effect

A

A process in which the liver metabolizes nearly all of a drug to an inactive metabolite before the drug passes into the general circulation.

12
Q

Pharmaceutical Alternative

A

Same active ingredient as the brand name, strength and dosage form may be different

13
Q

Bioequivalence

A

No statistical differences are found in the rate and extent of absorption between the generic product and the brand name product.

14
Q

Bioavailability

A

The extent to which an administered amount of drug reaches the site of action and is available to produce the desired drug effects.

15
Q

Generic Drug Basics

A

contains the same active ingredients as the brand name drug

May be offered b the generic manufacturer after the patient period of the brand drug ends

Can receive an A rating from the FDA if not significantly different from the original drug

16
Q

Why is knowledge of pharmacology important for technicians

A

Help reduce dispensing errors

Improves recognition of possible problems with drug orders, such as drug interactions and therapeutic duplications