Pharm 1 Flashcards

1
Q

Drug

A

Any substance that – through its chemical action – brings about a change in function.

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2
Q

Formulation

A

process by which different chemicals are combined to make a final product.

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3
Q

Solution

A

a homogeneous mixture of a solid, liquid or gas usually with a liquid.

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4
Q

Suspension

A

a mixture of a drug(s) with a liquid where the drug particles do not dissolve in the liquid.

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5
Q

Colloid

A

a homogeneous, noncrystalline substance consisting of large molecules or ultramicroscopic particles of one substance dispersed through a second substance. Colloids include gels, sols, and emulsions; the particles do not settle and cannot be separated out by ordinary filtering or centrifuging like those in a suspension.

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6
Q

Tincure

A

a preparation made by dissolving a drug in alcohol.

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7
Q

Syrup

A

a sugary liquid preparation that could be a solution, suspension or other and may contain alcohol.

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8
Q

Oral formation: capsule

A

drug formulation in which a shell, usually made of gelatin, is used to package the drug.

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9
Q

Oral formation: tablet

A

a hardened (often pressed under high pressure) condensed mass of drug.

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10
Q

Oral formation: sublingual tablet

A

tablet that is specifically designed to rapidly dissolve beneath the tongue and be absorbed under the tongue.

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11
Q

Oral formation: Troche/lozenge

A

a small, usually sweetened, hardened medicated mixture that is designed to be held in the mouth and slowly dissolve.

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12
Q

Oral formulation: immediate-release (IR)

A

A formulation of a drug that allows for the the standard release of medication from the dosage form right after administration. (i.e., is NOT extended release).

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13
Q

Oral formulation: extended-release (ER)

A

A dosage form that allows for at least a two-fold reduction in dosing frequency as compared to immediate release form; drug releases slowly over time ex. 12 or 24 hr dosing.
Also known as SR, XR, CR, LA, XT, CD.

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14
Q

Mechanism of action (MOA)

A

explanation of which specific molecular target(s) a drug binds to in order to cause a pharmacological effect

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15
Q

Agonist

A

chemical compound that binds to a receptor and causes the same response as the body’s endogenous chemical

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16
Q

Antagonist

A

a chemical compound that binds to a receptor and blocks the response that the endogenous chemicals would cause.

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17
Q

Poison

A

a chemical compound that binds to a receptor and blocks the response that the endogenous chemicals would cause.

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18
Q

Toxin

A

a poisonous substance that is a specific product of the metabolic activities of a living organism.

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19
Q

Toxicity

A

the degree to which a substance (toxin or poison) can harm an organism.

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20
Q

Antidote

A

a drug that counteracts the effects of a poison.

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21
Q

Pharmacokinetics

A

study of how the body absorbs, distributes, metabolizes and excretes a drug (what the body does to the drug).

22
Q

Pharmacodynamics

A

study of the biochemical and physiological effects of a drug on the body (what the drug does to the body).

23
Q

Concentration gradient

A

measurement of how the concentration of a chemical changes from one side of a permeable barrier to the other side.

24
Q

Passive diffusion

A

movement of molecules across a semipermeable membrane without the use of energy. Always down a concentration gradient (from higher concentration to lower concentration).

25
Active transport
movement of ions or molecules across a membrane against the electrochemical or concentration gradient with the use of energy.
26
Hydrophilic
having high affinity for water, readily absorbs or dissolves in water.
27
Hydrophobic/lipophilic
repels/unable to dissolve in water. Readily dissolves/absorbs into lipids.
28
Effectiveness
measurement of efficacy, tolerability and ease of use.
29
Efficacy
the ability of a drug to produces a desired and measurable effect.
30
Potency
measure of dose vs effect. Low dose with high effect is more potent than a high dose to get the same effect.
31
Placebo
an inert preparation that is typically used to compare an active drug.
32
Area under the curve
amount of drug present in circulation over a specific time frame.
33
Bioavailability
amount of drug systemically absorbed, available to the body after a dose.
34
Bioequivalence
two drugs with the same active ingredient(s) and the same formulation that have similar bioavailability.
35
ED50
effective dose in 50% of the population
36
ED 99
effective dose in 99% of the population.
37
TD 50
toxic dose in 50% of the population.
38
LD 50
lethal dose in 50% of the population.
39
Route of administration
the location/method that the drug is introduced to the body.
40
Route of administration: Enteral
Drug delivery via the digestive tract (stomach, duodenum, jejunum)
41
PO
by mouth-swallowed, sublingual (SL): under the tongue, etc.
42
Route of administration: Parenteral
Delivery that is not via the digestive tract (IV, IM, Sub-Q)
43
Intravenous (IV) injection
Directly into a vein
44
Intramuscular (IM) injection
Directly into the muscle
45
Subcutaneous (Sub-Q) injection
Directly into fatty tissue
46
Transdermal
Across the dermis
47
Route of administration: Topical
Onto a surface
48
Route of administration: Opthalmic
Into the eyes
49
Route of administration: Otic
Into the ears
50
Route of administration: Buccal
Between the cheeks and the gums