Intro to Pharmacology Flashcards

(54 cards)

1
Q

How can drugs affect PT

A
  • Hindering therapy (decrease exercise tolerance)
  • Facilitating therapy (decrease pain or attention )
  • Contributes to pt safety
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2
Q

what is a schedule 1 drug classification definition

A

Drugs that are not currently accepted in medical use and have the highest potential for abuse

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3
Q

what is a schedule 2 drug classification definition

A

drugs that are accepted for medical use however they tend to have a high potential for abuse

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4
Q

what is a schedule 3 drug classification definition

A

Moderate or lower abuse potential then schedule 2 drugs

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5
Q

what is a schedule 4 drug classification definition

A

Lower abuse potential then schedule 3 drugs

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6
Q

what is a schedule 5 drug classification definition

A

the lowest abuse potential

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7
Q

what is an example of a schedule 1 drug classification

A

weed

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8
Q

what is an example of a schedule 2 drug classification

A

Fentanyl

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9
Q

what is an example of a schedule 3 drug classification

A

Ketamine

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10
Q

what is an example of a schedule 4 drug classification

A

Lorazepam

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11
Q

what is an example of a schedule 5 drug classification

A

Pregabalin

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12
Q

what are examples of natural sources of drugs

A

plants, animals, marine organisms, minerals, microorganisms

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13
Q

what are examples of chemical sources of drugs

A

Semi-synthetic and Fully synthetic

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14
Q

what are examples of biotechnological sources of drugs

A

monoclonal antibodies, recombinant proteins , gene therapy

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15
Q

when is it safe to substitute generic Ds for Brand name

A

it has the same type and amount of active ingredients, same pharmacokinetic profile, same administration route, and same therapeutic effects

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16
Q

what is off label prescribing

A

using a drug to treat a condition that it is was not originally approved to treat. Ex: anti-seizure medication (gabapentin) for chronic pain

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17
Q

what is pharmacokinetics (PK)

A

“what the body does to the drug”; the movement of the drug through the body (absorption, distribution, metabolism, and excretion)

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18
Q

what is pharmacodynamics (PD)

A

” what the drug does to the body” ; how the drug effects the body. Cellular and systemic effects of the drug.

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19
Q

Toxicology

A

the study of the toxic effect of medication

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20
Q

what is pharmacotherapeutics

A

the pharmacokinetics and pharmacodynamics of the drug

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21
Q

what is the main organ for metabolism of a drug

A

the liver

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22
Q

what is the main organ for excretion of a drug

23
Q

what is the bioavailability of a drug

A

the amount that the drug can gain access to the systemic circuit through absorption. the percentage of blood that enters the blood stream.

24
Q

what are some things that can impact absorption

A
  • Stomach acidity
  • Gastric emptying
  • Surface Area
  • GI enzymes
  • Developmental changes
25
what is one way to achieve 100% bioavailability?
through IV administering of the medication
26
what is passive diffusion
the movement of molecules through the concentration gradient. Usually smaller molecules
27
what is active transport
the movement of molecules against their concentration gradient. Uses ATP
28
what does bioavailability/ absorption depend on
- the route of administration - the drugs ability to cross membrane barriers
29
what are some things that can impact drug distribution?
- tissue permeability - blood flow - binding to plasma proteins - binding to sub cellular components
30
what are the tissues that drugs can be stored in?
- adipose - bone - muscle - bones
31
what is the definition of volume of distribution (Vd)
ratio expressing the amount of drug administered divided by the concentration of drug in plasma.
32
what does the increase in drug bond to plasma proteins or subcellular components due
decrease the volume of distribution
33
what are the 2 mechanisms of filtration
- glomerular filtration - tubular secretion
34
what are the family of enzymes in the liver that are responsible for biotransformation?
Cytochrome P450 (CYP)
35
what does CYP-inhibition (Valproic acid Fluoxetine) do
decrease the metabolism of a drug and lead to toxicity
36
what does CYP-inductions (Rifampin Carbamazepine) do
increase the metabolism of a drug
37
what is phase 1 of drug metabolism
oxidation reduction (breakdown of the molecule) using CYP450
38
what kind of drugs are reabsorbed in the kidney?
lipid soluble drugs
39
what is phase 2 of drug metabolism
make the molecule more water soluble
40
what is the definition of drug clearance
the ability of all organs and tissues to eliminate the drug or the ability of a single organ or tissue to eliminate the drug
41
what is the definition of drug half life
the amount of time required for 50% of the drug remaining in the body to be eliminated
42
what are some things that can impact the bodies response to drugs
- genetics - disease especially liver or kidneys - age - diet - gender - drug interactions
43
drug absorption in infants
- less acidic stomachs (increases bioavailability of acid labile drugs) - delayed gastric emptying (increases time to reach therapeutic concentrations) - larger relative skin surface area - thinner stratum corneum (increased absorption of topicals)
44
drug metabolism in infants
hepatic enzyme activity 50-70% of adults
45
drug excretion in infants
glomerular filtration and tubular secretion decreased
46
drug absorption in elderly
- increased gastric pH versus adult - delayed gastric emptying
47
drug distribution in elderly
- increase adipose tissue - decreased serum albumin binding
48
drug excretion in elderly
decreased glomerular filtration and tubular secretion
49
what is the therapeutic window
the area/ dosage between the minimal effective dose and the dose of adverse response/toxicity
50
Median Effective Dose (E50)
the dose at which 50% of the population responds to the drug in a specific manner
51
median toxic dose (T50)
the dose at which 50% of the group exhibits the adverse reaction
52
median lethal dose (L50)
dose that causes death in 50% of the group
53
what is the equation for therapeutic index (TI)
TI = TD50/ED50
54
what is the definition of Therapeutic Index (TI)
an indicator of the drugs safety. The greater the Ti the safer the drug is