Pharmacology Flashcards

(43 cards)

1
Q

Drug Classes to treat Stroke

A

anti-thrombotics

thrombolytics

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2
Q

“prolol” endings

A

beta-blockers

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3
Q

“sartan” ending

A

angiotensin II receptor blockers

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4
Q

“pril” ending

A

ACE inhibitors

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5
Q

“actone” ending

A

potassium sparking diuretics

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6
Q

Factors affecting drug absorption

A

food –> increases stomach pH
lipid solubility of drug
polarity of drug
route of administration

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7
Q

Pharmacodynamics Definition

A

how drug impacts the body

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8
Q

Pharmacokinetics Definition

A

how the body processes a drug

“ADME”

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9
Q

ADME Definition

A

Absorption
Distribution
Metabolism
Excretion

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10
Q

How drugs work

A

1) replace or act as substitute for missing chemicals (insulin)
2) increase or stimulate cellular activity (cocaine)
3) decrease or depress cellular activity (fentanyl)
4) interfere with cellular functioning (invading neoplasms)

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11
Q

Agonist

A

a drug that causes a reaction (usually activity typical of that cell)

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12
Q

Antagonist

A

a drug that inhibits a cellular an effect. blocks cellular receptors or normal activity

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13
Q

Competitive antagonist

A

competes for receptors on cell membrane. blocks chemicals from binding with that receptor site and causing a reaction

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14
Q

Non-competitive antagonist

A

can be functional or allosteric.
functional = prevents agonist from causing a reaction
allosteric = binds to a non-agonist site on cell to inhibit receptor activation

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15
Q

Selective Toxicity

A

ability of drug to only target systems of foreign cells

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16
Q

Critical concentration

A

amount of drug required to induce a therapeutic effect

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17
Q

Loading dose

A

larger than normal dose of drug to accelerate a therapeutic reaction
preloading dose

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18
Q

Absorption

A

time period between administration of drug and drug reaching the circulatory system

19
Q

Parenteral

A

outside the GI tract

20
Q

Types of drug administration

A
PO
IV
IM
SC
Inhaled
Rectal
Transdermal
Mucous membranes
21
Q

Fastest drug route

22
Q

Factors impacting PO drugs

A

food increases stomach acidity

fatty food causes stomach to empty more slowly, affecting distribution

23
Q

Absorption processes

A

passive diffusion
active transport
filtration

24
Q

Distribution

A

movement of drug from circulation to bodily tissues

25
Factors affecting distribution
lipid solubility --> water-soluble particles unable to cross plasma membrane polarity perfusion of target tissue protein transport
26
Which drugs can cross the BBB
lipid-soluble drugs | most antibiotic drugs are not lipid-soluble
27
Metabolism
aka biotransformation | detoxifying enzymes inactivate drugs and make them more water-soluble for excretion
28
Liver enzymes
cytochrome P450 enzymes
29
First-pass effect
PO drugs pass through GI tract --> hepatic portal vein --> liver where they get metabolized. less active drug available before it reaches circulation
30
Stages of Metabolism
Phase 1: biotransformation (inactivate drug) occurs via oxidation, reduction, hydrolysis Phase 2: conjugation (water-soluble)
31
Enzyme Induction
enzymatic activity increases during drug metabolism | mixing drugs can cause a decrease the therapeutic effect by increasing metabolism of a particular drug
32
Organ responsible for metabolism
liver
33
Organ responsible for excretion
kidney
34
Routes of excretion
``` urine saliva bile feces sweat respiration ```
35
Factors affecting excretion
GFR (normally 50-60) kidney disease urine acidity
36
Half-life
time it takes for a drug to decrease by half of its peak amount
37
Accumulation
drugs can build up in the body. can be toxic if drug doses are not spaced out properly (think of half-life)
38
Types of drug interactions
absorption site --> prevents absorption distribution --> compete for protein transport decreased metabolism --> toxicity excretion --> accumulation & toxicity site of action --> reduced therapeutic effect
39
Areas of drug interactions
absorption site --> prevents absorption distribution --> compete for protein transport decreased metabolism --> toxicity excretion --> accumulation & toxicity site of action --> reduced therapeutic effect
40
Prodrugs
drugs that are inactive upon administration and activated by liver metabolism
41
Types of drug interactions
synergistic (drugs amplify effect) antagonistic (drug blocks/inhibits effect of another) potentiation (drug that has no effect, amplifies another)
42
First Order Kinetics
drug elimination is proportional to concentration of drug in blood plasma
43
Zero Order Kinetics
drug elimination is independent of plasma concentration --> constant rate of excretion higher risk for toxicity