Basic Pharmacology Flashcards

1
Q

The science that deals with the study of drugs in all its aspects.

A

Pharmacology

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2
Q

The study of the drug in terms of its history, source of chemical and physical properties, mechanism of action, absorption, distribution, bio-transformations and other uses of the drug.

A

Pharmacology

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3
Q

The study of the way a drug is ABSORBED, then DISTRIBUTED to the tissues of the body, METABOLIZED and EXCRETED.
MOVEMENT of the drug in the body

A

Pharmacokinetics

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4
Q
  • The study of a DRUG’s ACTIVITY, describing the nature and magnitude of the response, once it reaches its SITE OF ACTION.
  • What the drug DOES to a body
A

Pharmacodynamics

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5
Q

Determines the DOSAGE of the drug recommended for patients, and HOW they should TAKE it.

A

Pharmacokinetic Profile

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6
Q

What are the 4 Pharmacokinetic Processes?

A

Absorption
Digestion
Metabolism
Excretion

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7
Q

The process by which a drug moves from the SITE OF ADMINISTRATION into the BLOODSTREAM.

A

Absorption

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8
Q

The process by which a drug, when taken, is PARTITIONED among THE VARIOUS ORGANS and TISSUES in the body where the drug EXERTS ITS ACTION.

A

Distribution

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9
Q

The process by which a drug in the body may be changed into other, usually smaller, molecules called METABOLITES.

A

Metabolism

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10
Q

The process by which drugs or their metabolites are eliminated from the body

A

Excretion

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11
Q

Rate of absorption affects _______ and ______.

A

Duration

Intensity of Action

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12
Q

Factors affecting absorption are:

A
Gastric Motility
Rate of Blood Flow
Area of Absorbing Surface
Molecular Size
Solubility

GRAMS

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13
Q

Body compartments in which drugs accumulate

A

Reservoir

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14
Q

Also known as biotransformation

A

Metabolism

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15
Q

True or False.

Metabolites may be active or inactive, usually lees active than the parent drug

A

True

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16
Q

Metabolism happens in the _____, if drug is taken orally.

A

Liver

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17
Q

True or False.

Lipid Soluble drugs are eliminated faster

A

False. They are eliminated slowly

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18
Q

True or False.

Drugs are eliminated in the body either unchanged or as metabolites

A

True

19
Q

What are the 7 excretory Routes.

A
Sweat
Tears
Respiratory Gases
Saliva
Mother's Milk
Urine
Stool
20
Q

What are the 6 Pharmacokinetic Parameters?

A
Bioavailability
Area under the curve
Peak serum concentration
Half life
First-pass effect
Blood protein binding
21
Q

The amount of the ADMINISTERED drug which arrives in its THERAPEUTIC form at the SITE OF ACTION

A

Bioavailability

22
Q

Measurement of the AMOUNT of drug that has been ABSORBED at a GIVEN TIME after administration

A

Area under the Curve

23
Q

The MAXIMUM level of drug achieved in the BLOODSTREAM

A

Peak serum drug concentration

24
Q

The TIME it takes for the concentration of the drug in the bloodstream to fall to half of its peak value.

A

Half Life

25
Q

The metabolism of drugs the FIRST TIME they pass through the LIVER, before they have the chance to circulate to other body tissues. May reduce bioavailability and so affect dosage.

A

First-Pass Effect

26
Q

The affinity of a drug to bind with proteins, chiefly ALBUMIN, in the blood stream

A

Blood Protein Binding

27
Q

True of false.
Protein bound proportion of a drug may be pharmacologically inactive, leaving only the unbound drug being available to the tissues.

A

True

28
Q

What are the two pharmacodynamic parameters?

A

MIC - minimum inhibitory concentration

MBC - minimum bactericidal concentration

29
Q

Lowest drug concentration needed to inhibit the growth of the bacteria

A

Minimum Inhibitory Concentration

30
Q

Lowest drug concentration needed to kill a particular bacteria strain

A

Minimum Bactericidal Concentration

31
Q

Length of time that the serum concentrations of the antibiotic remains higher than the MIC.

A

T>MIC

Time above MIC

32
Q

3 Pharmacodynamic Properties

A

Drug Action
Drug Effects
Drug Response Curves

33
Q

The initial INTERACTION of the drug with its receptor/target molecule

A

Drug Action

34
Q

Physiological Effects that result from the binding of the drug with its receptor.

A

Drug Effects

35
Q

Efficacy of the drug at different DOSES.

A

Drug Response Curves

36
Q

Used to designate a quantitative statement of the selectivity of the drug when a therapeutic and an untoward effect are being compared.

A

Therapeutic Index
TD50
____
ED50

37
Q

Has therapeutic effects at a dose that is unlikely to cause toxic effects

A

Wide therapeutic index

38
Q

Has therapeutic effects at a dose that is close to the toxic dose

A

Narrow therapeutic Index

39
Q

Unwanted effects that occur when the drug is used within its normal dosage range

A

Side Effect

40
Q

Potentially dangerous effect that occur at doses higher than the normal therapeutic range

A

Toxic effect

41
Q

The ability to cause developmental defects in the fetus

A

Teratogenicity

42
Q

The ability to cause toxic effects in the fetus

A

Fetotoxicity

43
Q

Patient Factors Influencing Risk of Adverse Reactions

A
Body Weight
Age and Sex
Allergy
Route of Administration
Time of Administration
44
Q

The science and art of using drugs in the treatment of disease

A

Pharmacotherapeutics