Intro to Pharmacology Flashcards

1
Q

Why should we study pharmacology?

A

Vet tech must understand why a drug was prescribed and how this will affect the patient

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2
Q

Chemical name describes…

A

Chemical composition

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3
Q

Generic name is…

A
  • The common, concise name.
  • Usually listed as active ingredient
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4
Q

Trade name is…

A

The name of a product from a specific company

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5
Q

Generic equivalent is…

A

After the patent expires on a drug, companies other than the original developer may produce that drug.
- Theoretically, the generic equivalent is equal to the OG drug in effectiveness. Although, occasionally, differences in manufacturing produce difference in bioavailability.

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6
Q

T/F: Patients on chronic medication should be kept on the same brand long term

A

True!
If this isn’t possible, O must be informed of brand changes

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7
Q

Dose is…

A

The amount of drug given to a patient at one treatment

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8
Q

Dosage is…

A

How the drug is to be administered as the total plan

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9
Q

Sugar coated tablets help improve ___ and it’s important to prevent ___ during administration.
Enteric coated tablets protect the drug from ___ acid or protect ___ from drug. These tablets should not be ___.
Blister packs & foils protect the drug from ___, moisture, or ___. Do not remove them from containers until right before ___.

A
  1. Taste
  2. Melting
  3. Stomach
  4. Stomach
  5. Split
  6. Air
  7. Light
  8. Administration
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10
Q

For injectables, always read the label!! Why is this? (2)

A
  1. Determining the appropriate route (IM, SQ, IV). Routes are not always interchangeable!
  2. Packing
    - Single dose vial: use entire contents for one dose.
    - Multidose vial: clean rubber top with alcohol
    - Ampules: use special filter tip needles
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11
Q

Drug label must contain (7)

A
  1. Name (generic & trade)
  2. Concentration & quantity
  3. Name & address of manufacturer
  4. Manufacturer’s control or lot number
  5. Expiration date of drug
  6. Withdrawal time (if warranted)
  7. Controlled substance status of drug (“)
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12
Q

Package inserts

A
  • Most up to date info regarding specific product
  • Extra label use will not be provided
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13
Q

Formularies

A
  • Excellent sources of info, anew one should be purchased every 3-4 years
  • Careful of “digest versions” with minimal details
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14
Q

PDR (physician’s desk reference)

A

Ideal source of info as it relates to humans. However, animal testing info & side effect info may be applicable

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15
Q

What does a package insert include? (11)

A
  1. Registered trade name, generic name, controlled substance notation
  2. Description of composition statement
  3. Clinical pharmacology, actions, or mode of action
  4. Indications & usage
  5. Contraindications
  6. Precautions
  7. Warnings
  8. OD info
  9. Dosage administration
  10. Storage
  11. How supplied
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16
Q

Expiration date is the date before which a drug meets all ___ & after which the drug can no longer be ___. These are assigned based on the ___ of the drug.
Drugs that are reconstituted have an expiration date ___ reconstitution, and another ___.

A
  1. Specifications
  2. Used
  3. Stability
  4. Before
  5. Afterwards
17
Q

Veterinary drugs vs Human drugs

A
  • Vet drugs: Those approved only for use in animals.
  • Human: Approved by the FDA and guidelines for the use in food-producing animals is provided in the Compliance Policy Guide.
18
Q

What is the veterinarian/client/patient relationship?

A

This means the vet needs to have seen that patient for that problem within appropriate amount of time (no longer than a year). This must be established before any medication is prescribed to the patient.

19
Q

What is “extra-label use”?

A

Any use of a drug that is different than what is described on the label
- Use in a species not listed on label
- Use for indication (disease) not listed
- Use of a different dose, route, or freq
- Deviation from label withdrawal time

20
Q

What are reasons a vet may use extra-label use? (4)

A
  1. No approved drug exists that specifically meets the animal need
  2. A careful medical Dx has been made by a DVM
  3. The treated animal is carefully identified & an extended withdrawal time is assigned
  4. Prescribed drug is properly labeled according to guidelines
21
Q

Withdrawal times (witholding times)

A

Time period after a drug is discontinued when it’s safe to use a product from that animal for human use
- Failure to meet could result in fines &/or prison

22
Q

Six rights of the patient!

A

The right…
1. Patient
2. Drug
3. Dose
4. Route
5. Time & frequency
6. Documentation