ACT 2 Flashcards

1
Q

used for outpatient care

A

prescription

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2
Q

used in institutional care (hospitals, nursing homes, other institutions)

A

medication

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3
Q

drug substance responsible for the pharmacologic activity of the drug product

A

active pharmaceutical ingredient

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4
Q

inactive ingredient that may contribute to the pharmaceutic activity of the drug product

A

excipient

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5
Q

formulation containing a specific quantity of active ingredients in combination with one or more excipients

A

dosage form

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6
Q

includes the quantities of active and inactive ingredients to be used in compounding of prescription or medication order

A

compounding

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7
Q

predetermined amount of the drug administered at one time to produce a certain degree of biological response

A

dose

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8
Q

predetermined amount and rate of administration of a drug for a patient

A

dosage

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9
Q

frequency and duration of a prescribed drug or recommended use

A

dosage regimen

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10
Q

quantity of an active ingredient used to achieve the desired drug concentration

A

drug concentration

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11
Q

quantity of drug administered per unit of time to meet prescribed dosing schedule

A

rate of drug administration

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12
Q

usual time format to record patient’s admission, time of drug administration, and time of medical procedures

A

military time

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13
Q

degree to which the person’s behavior corresponds with the agreed recommendation from a health care provider

A

medication compliance

number of days supply of medication/number of days since last refill x 100 = compliance rate

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14
Q
  • responsibility of the pharmacist to help minimize errors and ensure the safety and well-being of patients
  • incorrect medication administration can result in severe complications, including allergic reactions, overdose and even death
  • _______, ________, and ________ are some technological advancements that help reduce medication error and document medication administration

it involves 5 steps:

A

MEDICATION VERIFICATION

  • barcoding, electronic medical records (EMR), and automated dispensing systems

5 steps:
1. prescription review
2. preparation
3. double-check
4. patient identification
5. documentation

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15
Q

5 principles of medication administration

A
  1. right patient
  2. right medication
  3. right dose
  4. right route
  5. right time
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16
Q

parts of prescription

A
  1. Date (and time)
  2. Patient information
  3. Superscription
  4. Inscription
  5. Subscription
  6. Signatura (aka signa)
  7. Auxillary label (aka special instructions)
  8. Prescriber’s information
17
Q
  • derived from latin phrase ________, meaning before writing
  • orders for medication, non-drug products and services that are written by a licensed or mid-level practitioner who is authorized by stature to prescribe
  • means of communication (written, verbal, or electronic) from the prescriber to the pharmacist
A

PRESCRIPTION
- praescriptus

18
Q
  • for verification purposes, establishing the medication record of the patient and protects patient from medication abuse
  • may include date prescribed and date filled in the pharmacy
A

date (and time)

19
Q
  • for identification purposes, which should include the legible full name, address, gender, age, height, and weight of the patient
A

patient information

20
Q
  • beginning of a direct order from the prescriber to the pharmacist
  • symbolized by Rx symbol, which means “take thou” or “you take” in Latin
A

superscription

21
Q
  • principal part of the prescription order that contains the medication information
A

inscription

22
Q
  • directions to the pharmacist for the preparation of the prescription
  • may serve to designate the DF or # of units
A

subscription

23
Q
  • directions to the patient that is transcribed by the pharmacist
  • symbolized by “___,” which means “______” in latin
A

SIGNATURA (signa)
- sig
-mark thou

24
Q
  • used to emphasize the important aspects of the dispensed medication including proper use, handling, storage, refill status and necessary warning or precautions
  • must have aesthetic and professional appeal
  • color coded as:
A

auxillary label (special instructions)

25
Q
  • for verification purposes, which should include the legible full name, address, contact and registration number
A

prescriber’s information

26
Q

PROPER HANDLING OF PRESCRIPTION

A
  • receiving
  • reading and checking
  • numbering and dating
  • labelling
  • preparing
  • packaging
  • recording and filling
  • pricing
27
Q

KINDS OF PRESCRIPTION

A
  1. ORDINARY
    - medication order
    - tamper resistant prescription pads
    - E-prescription
  2. CONTROLLED
    - dangerous drug (DD)
    - exempt dangerous drug (EDD)
  3. COMPOUNDING
  4. INCORRECT PRESCRIPTIONS
    - erroneous
    - violative
    - impossible
28
Q

printed or handwritten order not requiring control

A

ordinary prescription

29
Q

prescriptions ordered within the clinical practice

A

medication order

30
Q

used to prevent unauthorized copying, modification, or counterfeiting of prescriptions

A

tamper resistant prescription pads

31
Q

for efficiency of both the prescriber and pharmacist, convenience to the patient

A

E-prescription

32
Q

used for medications that have high potential for abuse

A

controlled

33
Q
  • medications listed in the Comprehensive Dangerous Drugs Act of 2002
  • supplied only on Yellow Rx by a licensed PDEA prescribing physician
A

dangerous drug (DD)

34
Q
  • medication containing any amount of prohibited or regulated drug
  • supplied on ordinary prescription form with S2 license number by a licensed PDEA prescribing physician
A

exempt dangerous drug (EDD)

35
Q

requiring the pharmacist to prepare a patient-specific medication

A

compounding

36
Q
  • where the brand name precedes the generic name
  • where the generic name is the one in parenthesis
  • where the brand name is not in parenthesis
37
Q
  • where the brand name is not written
  • generic name is not legible and the brand name which is legible is written
  • brand name is indicated and instructions added “no substitution”
38
Q
  • when only the generic name is written but is not legible
  • when the generic name does not correspond to the brand name
  • when both the brand name and generic name are not legible
  • when the product prescribed are not registered with the BFAD/FDA
A

impossible