Pharmacology Basics Flashcards

1
Q

What are the six rules before administering medication that must be present?

A
  1. Patient name
  2. Date of order
  3. Drug(s) need to be named
  4. Dosage amount and frequency
  5. Root of administration
  6. Signature from prescriber
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2
Q

What part of the nursing process do the ten rights fall under?

A

Implementation

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3
Q

Describe the difference between critical thinking and critical reasoning

A

Thinking - providing best possible patient care using best practice informed by evidence

Reasoning - Critical thinking leads to critical reasoning. Analyzing and understanding patient issues, making timely and effective patient-centred decisions, and it is holistic

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4
Q

List the 10 rights of drug administration

A
  1. Drug
  2. Dose
  3. Time
  4. Route
  5. Patient
  6. Reason
  7. Documentation
  8. Evaluation/assessment
  9. Education
  10. To refuse
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5
Q

What is the magic window for a time critical medication? What constitutes a time critical medication? What happens if it is not given in this window?

A

30 minutes either way

q4h or more frequent

When we pass this, the patient will not have the therapeutic response to the medication as needed (i.e., can develop antibiotic resistance)

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6
Q

What is the non-critical magic window?

A

1 hour either way

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7
Q

Define pharmaceutics

A

Study of how various dosage forms influence the way in which a drug affects the body

i.e., pill, tablet, liquid, controlled release, sustained release, crushable

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8
Q

Define pharmacokinetics

A

Study of what the body does to the drug (absorption, distribution, metabolism, and excretion)

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9
Q

Define absorption

A

the drug moves from its site of administration into the blood stream

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10
Q

Define distribution

A

transport of the blood by the blood stream to the site of action

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11
Q

Would dosage of an oral medication or IV medication be higher? Why?

A

Oral because they work through the liver and some may be lost/excreted

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12
Q

Define metabolism

A

medication is broken down into its active components

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13
Q

Define excretion. What organs excrete medications?

A

ensure that the kidneys are excreting what they should be to ensure the patient is not going into toxicity

Excreted through the kidneys, skin, lungs, and GI tract/colon

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14
Q

Define pharmacodynamics

A

Relationship between drug concentrations and pharmacological response (mechanism of action) - how does the drug work?

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15
Q

Define pharmacotherapeutics

A

Clinical use of drugs to prevent or treat (acute, maintenance, supplemental, palliative, supportive, prophylactic & empirical)

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16
Q

Match the following medications to the purpose

Supportive, Acute, Prophylactic/empirical, Supplemental, Maintenance, Palliative

Insulin, Electrolytes, BP medications, Vaccines, Analagesics, Vasopressors

A

Acute - Vasopressors
Maintenance - BP medications
Supplemental - Insulin
Palliative - Analgesics
Supportive - Electrolytes
Prophylactic/empirical - Vaccines

17
Q

Define the difference between an adverse event and reaction

A

Event - any undesirable occurrence involving medications

Reaction - anaphylaxis or hypersensitivity to a drug administered

18
Q

Are adverse events or reactions more common?

A

Events

19
Q

What is an idiosyncratic reaction?

A

Rare, not understood completely, occur unexpectedly, evidence suggests a genetic component

20
Q

What is teratogenic reaction?

A

negatively impacts the developing fetus (i.e., thalidomide)

21
Q

What is carcinogenic reaction?

A

medications that can cause cancer (i.e., immunotherapy or hormone therapy can cause structural differences to DNA)

22
Q

Describe phase one of new drug development. How many people are involved?

A

trial in a clinical setting, small numbers of individuals (<100), lasts a couple of days to a couple weeks, and they are healthy individuals

23
Q

What phase of a new drug trial is pharmacokinetics being tracked?

A

Phase one

24
Q

Describe phase two of new drug development. How many people are involved?

A

100-300 individuals who have the disease, clinical trial, adverse reaction and events are monitored

25
Q

Describe phase three of new drug development. How many people are involved?

A

larger numbers (1000-3000), reaching out to medical research centre

26
Q

What phase is placebo introduced in new drug development?

A

Phase 3

27
Q

Describe phase four of new drug development. How long is the drug followed for?

A

medication is deemed safe, distributed by pharmaceutical companies that follow the medication for two years

28
Q

List and describe the three classes of recalls

A

Class I - serious issues or reasonable probability of adverse effects/death - Medication will be terminated completely

Class II - adverse events are temporary or reversible - will have a black box warning but won’t be pulled

Class III - Not much will happen, but a warning label – onus is on the person taking the medication to read warning guide

29
Q

Describe some considerations for older adults in pharmacology

A

Decline in total organ function, lower GI absorption function, take four times more over the counter medication than any other group, often on four to five prescription medications and two over the counter (medications could interact with one another), most common medications used by older adults are statins, unintentional self-medication errors can occur (writing too small, timing errors, dosing errors), may be taking natural products, issues with polypharmacy (have seen many health professionals and have been prescribed multiple different drugs because the professionals don’t check what they are currently already taking), prescribing cascade (one prescription often leads to multiple others to supplement issues/changes with the initial medication needing to be prescribed), non-adherence