Pharm Chapters 1-4 Flashcards

1
Q

Pharmacology (Pharmacotherapeutics)

A

area of pharmacy that refers to use of specific drugs to prevent, treat, and diagnose disease

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2
Q

Pharmacokinetics

A

study of how body deals with the drug in terms of ADME

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3
Q

ADME

A

absorption, distribution, metabolism, excretion

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4
Q

Pharmacodynamics

A

what drug does in body including its excretion

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5
Q

Types of Drug nomenclature

A

Chemical Name
Generic Name
Brand Name

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6
Q

Chemical Name

A

Organic Chemistry Name

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7
Q

Generic name

A

like acetaminophen

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8
Q

Brand name

A

like “Tylenol”

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9
Q

FDA Therapeutic Equivalency Standards

A

Drug products are considered to be therapeutic equivalents only if they are pharmaceutical equivalents and if they can be expected to have the same clinical effect and safety profile when administered to patients under the conditions specified in the labeling.

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10
Q

Preclinical Testing

A

Animal trials for safety and efficacy

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11
Q

Human Studies Phase 1

A

safe dose, effect, kinetics (mostly tested on rats)

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12
Q

Human Studies Phase 2

A

effectiveness in disorder

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13
Q

Human Studies Phase 3

A

large scale safety and efficacy (used to determine safe dosages)

  • phase where papers to FDA for drug approval are submitted and rejected/accepted
  • highly controlled patient studies conducted (minimal medical conditions and other currently taken meds present - potentially poses future problems)
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14
Q

Human Studies Phase 4

A
post marketing (approved by FDA, but still need to keep track for 3 years minimum of how the general public responds to the drug)
**this is where hc community really finds out if drug is safe or not
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15
Q

OTC (over the counter) vs Prescription Medications

A

OTCs are safe for use by the general population without guidance of a health professional
Prescription meds are for those that have seen a Dr. first, not always safe for the general population

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16
Q

Classes of controlled substances

A

C1- are illegal (like LSD and cocaine= the good stuff)
C2- major pain meds, like morphine
C3- hydrocodone
C4
C5
**The Lower the class, the higher the potential for abuse

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17
Q

Threshold Effect

A

the start of efficacy

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18
Q

Ceiling Effect

A

max effect of a drug

19
Q

Potency

A

related to the dose that produces a given response in a specific amplitude
Ex: One drug may take 1mg to have the SAME effect as 10mg of another drug
So the 1mg drug is more potent than the 10mg drug

20
Q

Efficacy

A

How effective a drug is at it’s intended purpose

21
Q

ED-50

A

The dose at which 50% of the population respond to the drug in a specified manner (Median effective dose)

22
Q

TD-50

A

The dose that causes death in 50% of the animals studied (Median lethal dose) ie. Toxic Dose

23
Q

Therapeutic Index (TI)

A

TI = TD50/ED50

Used to as an indicator of the drug’s safety. The greater the value of TI the safe the drug is considered

24
Q

Enteral administration and examples

A

These are preferred and use the gut to absorb the medication (you want to utilize the gut)
Ex: Oral, sublingual, buccal, rectal

25
Q

Parenteral administration and examples

A

bypasses the gut

Ex: Inhalation & Injection

26
Q

Types of injection administration

A

IV, SC (subcutaneous), IM (intramuscular), & Intrathecal

27
Q

Transdermal administration

A

slow release concentration. Must be able to penetrate skin, must not be degraded by enzymes of dermis

28
Q

Bioavailability (F)

A

% of drug administered that enters bloodstream

29
Q

passive vs active transport

A

initially you want active to get through plasma membrane; when dealing with excretion, usually passive

30
Q

Acid vs basic drugs

A

acid get through in stomach; basic get through in intestine wall

31
Q

What determines distribution of drugs within the body?

A

Tissue permeability
Blood flow = bad circulation means they might not be able to metabolize drugs as well
Binding to plasma proteins

32
Q

Where are reservoirs for drug storage?

A

adipose, bone, and muscle

33
Q

4 examples of biotransformation

A

Oxidation, reduction, hydrolysis, conjugation

34
Q

Cytochrome P450

A

Enzymes responsible for drug metabolism

35
Q

Cytochrome P450 induction

A

increases metabolism

36
Q

Cytochrome P450 Inhibition

A

blocks metabolism

37
Q

Substrates

A

med the uses pathway but does not have any positive/negative effect

38
Q

Most dominant isoenzyme?

A

CYP3A4

39
Q

Where is the distribution of 3A4 located in the body?

A

70% in intestines, 60% in Liver

40
Q

Creatine Clearance

A

way to measure how well kidney is working

41
Q

Half Life

A

The time it takes for 1/2 a drug to disappear from the body

42
Q

Dosing Regimes

A

designed to keep body at a steady state (5x to take to get to steady state)

43
Q

Variables in Drug Response include:

A
Genetics
Disease
Drug interactions
Age= very young and very old T
Race
Sex= females have higher risk 
Diet