Pharmacology Flashcards

1
Q

Pharmacokinetics

A

The metabolism and excretion out of the body

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Pharmacodynamics

A

Cellular and systemic effects on the body

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Medication Benefits

A

Helps with controlling seizures, controlling arterial pressure, blood sugar, decrease heart events, helps people sleep, relax spastic muscles, and most importantly for you control pain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Medication Challenges/Adverse Affects

A

Side Effects: makes people dizzy, slows dow reflexes, increase risk of falls, lowers BP to potenially dangerous levels, DEPENDENCE, bone deterioration, liver and kidney deterioration (putting people at risk for other diseases)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Over the Counter (OTC) Medications Impact on Prescription Drugs

A

Adds complexity that develops in their body creating other unexpected side effects

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Herbal/Vitamins Effect with Prescription Drugs

A

Interferes with Metabolism and half life of the medications in the body and the way they are excreted (in turn, affects the therapeutic levels of medication in the blood)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Illicit Drugs/Alcohol/Caffeine/Nicotine

A

Compounds the overall picture of the exposure to chemicals with therapeutic and potentially toxic effects and the accompanying symptoms displayed as a result of that

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Agonist

A

Drugs that occupy receptors and activate them

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Antagonists

A

Drugs that occupy receptors but do not activate them. Antagonist block receptor activation by agonists

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Drug Impact

A
  • Drugs can affect/change vision, hearing, olfaction/taste, touch sensation, and bring about a state of sensory senescence (aging)
  • Age is an impact
  • Drugs can make your bodies over sensitive or under sensitive to sensation, thirst, sleep, etc
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

FDA Pregnancy Category A

A

Studies have not demonstrated risk to fetus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

FDA Pregnancy Category B

A

Studies have not been done on humans, but in animal studies there was no risk to the fetus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

FDA Pregnancy Category C

A

Studies have not been done on humans or animals, or studies done on animals have shown teratogenic effects

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

FDA Pregnancy Category D

A

Studies have revealed adverse risk to the fetus, so benefit-to-risk ratio must be established before use in pregnancy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

FDA Pregnancy Category X

A

Studies have revealed teratogenic effects in women and/or animals; fetal risk clearly outweighs benefit, and drug is contraindicated in pregnancy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Teratogenic Effect

A

Anything that produces nonheritable birth defects is said to be teratogenic (chemicals/radiation can cause abnormal defects in embryo)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Pharmokinetic Phases

ADME

A
  1. Absorption
  2. Distribution
  3. Metabolism
  4. Excretion
  • occurs after the pharmaceutic phase
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Pharmaceutic Phase

A
  • the dissolution of the drug (a pill or capsule)
  • Drugs must be in solution to be absorbed.
  • Drugs that are liquid or drugs given by injection do not go through the pharmaceutic phase because they are already in solution
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Absorption

A

Drug passes into the circulating body fluids or tissue via the capillaries/blood vessels

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Distribution

A

Transportation of the drug to site of action

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Metabolism

A

Drugs are converted into harmless substances (biotransformation)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Excretion

A

Elimination of the drug from the body

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Absorption Methods

A
  • Active absorption
  • Passive absorption
  • Pinocytosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Absorption Factors

A
  • Route of administration
  • Solubility of the drug
  • Body conditions (anything that slows the blood flow in the body)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

Bioavailability (Absorption)

A

Fraction of the drug that reaches circulation unchanged

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

Drug Distribution (Absorption)

A

Amount of drug that reaches the site of action

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

Biotransformation (Metabolism)

A
  • Process of chemical reactions in the liver that convert the drug to an inactive compound
  • Helps drugs to more easily diffuse ad more easily be eliminated
28
Q

First-pass effect

Metabolism

A
  • All oral drugs undergo first-pass effect in the liver before going into systemic circulation
  • Parenteral drugs bypass the first-pass effect
29
Q

Parenteral Drugs

A

Administered drugs through the skin (usually via injection)

30
Q

Loading Dose

A

An initial higher dose of a drug that may be given at the beginning of a course of treatment before dropping down to a lower maintenance dose

31
Q

Liver

A
  • primary organ for the METABOLIC phase
  • also partially assists in excretion
  • tylenol is responsible for half of liver disease in the U.S.
32
Q

clearance

A
  • elimination of drugs from the body

- good clearance PREVENTS TOXICITY

33
Q

Kidney

A
  • primary organ for EXCRETION (URINE)

- poor kidney function = poor clearance

34
Q

Other methods of excretion

A
  • sweat
  • breast milk
  • breathing
  • feces
  • bile
35
Q

Half-Life

A

Measure of the rate at which the drug is removed from the body (hours, days, weeks, etc.)

36
Q

Drug Dosage

A
  • how often the drug is taken
  • can affect the half-life
  • too low will cause there to be no affect
  • too high will cause overdose (adverse effects)
37
Q

Therapeutic Effect/Response

A

the intended effect of the drug on the body

38
Q

Alteration in the Cellular Environment by a Drug (Pharmacodynamic)

A
  • Osmotic pressure
  • Lubrication
  • Absorption
39
Q

Alteration in the Cellular Function by a Drug (Pharmacodynamic)

A

Can increase or decrease physiologic function as a result

40
Q

Types of Drug Reactions

A
  • Adverse drug reactions
  • Allergic drug reactions
  • Drug idiosyncrasy
  • Drug tolerance
  • Cumulative drug effect
  • Toxic reactions
41
Q

Adverse reactions

A
  • undesirable drug effects

- often called side effects when they are mild

42
Q

Allergic reactions

A

called hypersensitivity reactions and may prompt body to produce antibodies against what it perceives as an antigen

43
Q

Anaphylactic shock

A

an extremely serious allergic reaction and can be life-threatening if not recognized and treated immediately.

44
Q

Drug Idiosyncrasy

A
  • Any abnormal or unusual reaction to a drug

- Unknown cause and no predictability

45
Q

Drug Tolerance

A
  • Decreased response to drug requiring increase in dosage; a sign of drug dependence
  • Different than dependence (dependence causes withdrawal)
  • decreased receptor sensitivity after repeated drug exposure
46
Q

Up-Regulate

A

bumping up the ability to metabolize a drug faster

47
Q

Cumulative effect

A

Increased response to drug because of decreased metabolism and excretion (usually secondary to liver or kidney disease)

48
Q

Toxic reaction

A

Poisoning of the system secondary to overdose of chemical in the blood concentration

49
Q

Pharmacogenetic reaction

A

Genetically caused abnormal response to drug

50
Q

Drug-drug Interaction

A

occurs when one drug interacts with or interferes with the action of another drug

51
Q

Additive Drug Reaction

A

Occurs when the combined effect of two drugs is equal to the sum of each drug given alone

52
Q

Synergistic Drug Reaction

A

Occurs when drugs interact with each other and produce an effect that is greater than the sum of their separate actions

53
Q

Antagonistic Drug Reaction

A

occurs when one drug interferes with the action of another, causing neutralization or a decrease in the effect of one drug

54
Q

Factors Influencing Drug Response

A
  • Age (Elderly, Infants)
  • Weight
  • Gender
  • Disease
  • Route of administration
55
Q

Polypharmacy

A
  • Taking of multiple drugs
  • Potential for interactions
  • Often practiced by the elderly who have more conditions for which to be medicated
  • Increases possibility of adverse reactions
56
Q

Sedative Hypnotics and Antianxiety Agents

A
  • Decrease internal stress and facilitate sleep
  • in higher doses, depresses CNS activity
  • concerns: drowsiness, low motor function, hang over effect, tolerance/dependence issues
57
Q

Antidepressants

A
  • Mood (affective) Disorders
  • Depression is most prevalent med condition in the U.S.
  • Widely prescribed meds
58
Q

Antipsychotics

A
  • For psychosis and impaired perception of reality and thought disturbances (schizophrenia and paranoia)
  • side effects: torticollis (head becomes persistently turned to one side/muscle spasm), Akatisia (restlessness), pseudo parkinsonism, and other MOVEMENT DISORDERS)
59
Q

Anti-Epileptic Medication

A
  • Prevents seizures due to trauma, infection, CNS issues

- side effects: sedation, fatigue, dizziness

60
Q

Parkinson’s Medications

A
  • For rigidity, resting tremors, bradykinesia

- Side effects: dyinesia, akinesia, dry mouth/eyes, cognitive decline

61
Q

Anesthetics

A
  • a substance that induces insensitivity to pain
  • mixed in to many OTC drugs
  • combination of drugs, rapid onset
  • recovery may effect rehab for days after (could lower BP over next few days or even week)
62
Q

Muscle Relaxants

A
  • drugs for spasticity of the muscles from CNS trauma, infection, metabolic
  • side effects: fatigue, hypotension, headache, nausea, confusion, dizziness, insomnia
63
Q

Opioid Analgesics

A
  • used for treating moderate to severe pain
  • side effects: seizures, dizziness, visual disturbances, constipation, nausea, itching, hypertonia, mood swings
  • avoid alcohol (increases chance for prolonged sedation)
  • peak in 2-3 hours and last 4-6 hours
64
Q

NSAIDS

A
  • non-steroidal anti-inflammatory drugs that widen capillary pores and migration of the activated immune system cells into tissue causing small local swelling and l pain activation (nociceptive pain)
  • increased risk of bleeding when used with anticoagulants
65
Q

Rheumatoid Arthritis Drugs

A
  • Disease modifying anti-rheumatic drugs (DMARDs) that assist in reducing advancement of disease processes
  • side effects: stomach and liver toxicity, birth defects
66
Q

Osteoarthritis drugs

A
  • use regimes containing NSAIDS, opioids, hyaluronic acid, corticosteroids