Intro to Pharmacology Lecture Flashcards

5/31/19

1
Q

Pharmacology

A

Study of drugs

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2
Q

Drug

A

Chemical utilized for a diagnosis, prevention, cure, or amelioration of an unwanted health condition, any chemical, excluding food, that interacts with living organisms to produce a response (beneficial or harmful)

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3
Q

Branches of pharmacology

A
  • Therapeutics ***we will mainly focus here
  • Toxicology
  • Pharmacodynamics
  • Pharmacokinetics
  • Pharmacogenomics: personalized/precision medicine
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4
Q

Example of pharmacogenetics

A

Some patients have variants in liver enzyme CYP2D9 that degrades the anticoagulent warfarin, if it metabolizes warfarin slowly, it accumulates and increases bleeding - now we can genetically test to determine this variation and respond with specific drugs accordingly

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5
Q

Pharmacology vs pharmacy

A

Pharmacology is the science of interaction of chemicals with living organisms or systems to develop and use medicines to cure, prevent, or ease disease
Pharmacy is a health profession concerned with appropriate use of medications, devices, and services, largely concerned with art of preparing and dispensing drugs, link between pharmacology and the patient

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6
Q

Major drug legislation in the US

A
  • 1906 pure food and drug act
  • 1938 federal food, drug, and cosmetic act established the FDA
  • 1951 Durham humphrey amendments create prescription and OTCs
  • 1962 thalidomide crisis in UK caused limbless babies, amendment established that before drugs be marketed must be shown to be safe and efficacious
  • 1970 Controlled substance act established DEA to monitor drugs with potential for abuse (schedule1-5 drugs)
  • 1983 Orphan Drug Amendments creates incentives development of drugs that treat rare diseases
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7
Q

Phases of drug development

A
  • Preclinical testing on laboratory animals
  • Phase I small # of volunteers
  • Phase II assess effectiveness of treating target disorder
  • Phase III assess larger patient population
  • NDA approval
  • Phase IV postmarketing surveillance to monitor problems occurring after NDA approval
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8
Q

Cost of drug development

A

Very expensive and time consuming, for every 5000 compounds 1 will be approved by the FDA after 12 years and $800 million dollars

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9
Q

Drug naming convention

A

Chemical name: organic chemistry structure
Generic name: shortened name
Trade name: license name by drug company

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10
Q

Advantages of OTC’s

A
  • Effective
  • Freely available
  • Inexpensive
  • Save consumer money/physician time
  • Relatively safe, dosage fairly universal
  • instructions simple
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11
Q

Disadvantages of OTC’s

A
  • Have to lower strength when going from prescription to OTC
  • Greatly overused
  • Greatly misused
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12
Q

Sources of drugs

A
  • plant products
  • minerals
  • animals
  • synthetic
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13
Q

a.c.

A

Before meals

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14
Q

b.i.d.

A

twice a day

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15
Q

p.o.

A

orally

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16
Q

h.s.

A

at bed time

17
Q

o.l. or o.s.

A

left eye

18
Q

o.d.

A

right eye

19
Q

s.s.

A

one half

20
Q

Herbal medicinal and dietary supplements differ from traditional medicine in that…

A

…they are assumed safe unless disproven by the FDA, cannot put labels making medical claims - restricted to general statements about how the product affects people