Intro Flashcards

1
Q

Autonomic Nervous System

A

Basic Life Functions; subconsciously…NOT muscular movements.

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2
Q

Sympathetic Nervous System

A

STRESS response, fight or flight (i.e. beta ablockers block this to decrease htn)

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3
Q

Pharmacology

A

Late 1600s and then 1800s is when drug regulations began… “A science that draws on information from multiple disciplines.

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4
Q

Nursing Process

A

Assess, diagnose, plan, Intervention, Evaluate.

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5
Q

Two most important properties of an ideal drug…

A

Safety and Efficacy.

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6
Q

…additional Properties of an Ideal Drug

A
  • Rapid predictable response
  • Convenient Administration (po)
  • Once a day (short term…b/c more compliance)
  • Inexpensive
  • Eliminated quickly
  • Few drug-drug interactions
  • Specificity
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7
Q

Goal of drugs?

A

Maximum benefit with minimum harm. *Risk Benefit

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8
Q

Anticoagulants

A

Blood Clotting

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9
Q

Antihyperlipidemics

A

Lower blood cholesterol

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10
Q

Antihypertensives

A

Lower blood pressure

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11
Q

Antidysrhythmics

A

Restore normal cardiac rhythm

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12
Q

Antianginals

A

Treat Angina (chest pain caused by reduced blood flow to the heart)

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13
Q

Diuretic

A

Lowers plasma volume

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14
Q

Calcium Channel Blocker

A

Blocks heart calcium channels (dec. how hard heart squeezes)

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15
Q

Angiotensin-converting enzyme inhibitor

A

Blocks hormonal activity

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16
Q

Adrenergic antagonist (blocker)

A

Blocks physiological reactions to stress

17
Q

Vasodilator

A

Dilates peripheral blood vessels

18
Q

Therapeutic vs. Pharmacologic

A

WHY vs. HOW

19
Q

Bioavailability

A

Amount of drug that body has to use and how quickly body can use that. This can be affected by generic vs. trade.

20
Q

Drug Standards

A

**Purity and Strength.

21
Q

FDA

A

medical devices, herbal products, cosmetics….medications, vet drugs, radiation, tobacco products… BUT NOT AS STRICT AS MEDICATION.

22
Q

Drug Development

A

KNOW….phases.

23
Q

Preclinical research

A

Non-human lab research…in order to get “investigative new drug” (IND) approval.

24
Q

Phase 1

A

SAFETY. (days-weeks and 30-50 people) Healthy males, 150-180 lbs, no medical history. Not if drug works, checking SAFETY.

25
Q

Phase 2

A

EFFICACY & safety. (weeks-months and hundreds of people) Tight group but perfect pts - LOTS of restrictions with specific people… “perfect” pts.

26
Q

Phase 3

A

Clinical Trials. (several years, and thousands of patients) Typical patients, but not extreme cases. Pt’s have co-morbidities but not terrible. “New Drug Application” = NDA accepted… NDA approved.

27
Q

Postmarketing Surveillance

A

Last phase - where COVID vaccine is right now. Lots of maybes and continuing to test. Longest period. Still don’t know all risks.