pharma quiz 1 Flashcards

1
Q

drug stages after administration LADME

A

Liberation
absorption
distribution
metabolism
excretion

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2
Q

How long does it take a drug to develop & pass ?

A

8-15 years

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3
Q

pharmacology

A

Deals with the study of drugs and their actions or effects.

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4
Q

Therapeutic methods are approaches to treating illnesses

A
  • Diet therapy
  • Drug therapy
  • Physiotherapy
  • Psychotherapy
  • Therapeutic methods are often used in combination
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5
Q

what metabolizes drugs?

A

liver metabolizes drugs

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6
Q

a pt with poor kidney function ?

A

A pt with poor kidney function will have an increased action and duration of a drug.

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7
Q

displacement

A

warfarin + valproic acid = increased anticoagulant effect.

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8
Q

infants and elderly

A

infants and elderly tend to be the most sensitive to drug effects.

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9
Q

organs with larger blood supply

A

Organs with larger blood supply receive the distributed drug most rapidly.

drug protein is a way of transportation.

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10
Q

FDA

A

Food and drug administration

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11
Q

Chemical Name: Generic/Brand Names:

A
  • Most meaningful to the
    chemist
  • Chemist understands the
    exact chemical constitution
    of the drug and the exact
    placement of its atoms or
    molecular groupings
  • Generic name: Important to
    know because formularies
    use them; not capitalized
  • Official name: Listed by FDA
  • Brand or trademark:
    Registered by manufacturer;
    capitalize
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12
Q

Which name(s) of a drug should the nurse use when
teaching a patient about a new prescription?

A

Generic and trade

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13
Q

Drug
Classifications

A
  • Body system classification
    (e.g., cardiovascular,
    gastrointestinal)
  • Therapeutic use or clinical
    indications (e.g., antacids,
    antibiotics)
  • Physiologic or chemical
    action (e.g.,
    anticholinergics, calcium
    channel blockers)
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14
Q

Prescription:

A

Requires an order by a health professional
licensed to prescribe drugs

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15
Q

Nonprescription

A

Over-the-counter (OTC) drugs sold without a prescription.

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16
Q

Illegal or recreational drugs

A

Used for nontherapeutic
purposes; obtained illegally

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17
Q

Biosimilar:

A

Biologic product that is close in
structure/function to an existing approved biologic product

18
Q

Resources for
Drug
Information

A
  • Official source for American drug
    standards
  • The United States
    Pharmacopeia (USP)/National
    Formulary (NF)
  • USP Dictionary of USAN and
    International Drug Names
  • Sources for prescription and
    nonprescription drugs
  • Package inserts
  • Nursing journals
  • Electronic database
19
Q

Controlled Substances Act
(1970): Defined five
classifications or schedules of
controlled substances

A
  • Schedule I : These drugs have high potential for abuse.
    ex: heroin, ecstasy, LSD, weed, pcp
  • Schedule II : HIgh potential for abuse . Has accepted medical use for treatment.
    ex: oxycodone, morphine, methamphetamine
  • Schedule III: less abuse potential then cII drugs. accepted medical use.
    ex: anabolic steroids, hydrocodone
  • Schedule IV: less abuse then cIII drugs. accepted medical use.
    ex: valium,xanax,darvon,phentermine
  • Schedule V: less abuse potential then cIv drugs. accepted medical use.
    ex: cough medicine with codeine
20
Q

Which entity is responsible for monitoring drug safety in the
United States?

A

Drug Enforcement Agency (DEA)

21
Q

Which drug schedule indicates drugs with the highest risk for
abuse?

A

Schedule I

22
Q

Orphan drugs

A

Medicines developed for rare disorders.
Orphan Drug Act, 1983: Promotes development of products
that demonstrate promise for diagnosis or treatment of rare
diseases or conditions
* Examples of rare diseases include cystic fibrosis, Hansen’s
disease (leprosy), sickle cell anemia, infant botulism.

23
Q

Drug receptors

A

Specific sites where drugs form
chemical bonds
The drug and the receptor must have similar shape
* similar to a key and lock. The better the fit, the better the
response
 The drug must have a chemical affinity for the
receptor

24
Q

Pharmacodynamics:

A

Study of interactions between
drugs and their receptors and the series of events that
result in a pharmacologic response

25
Q

Agonists:

A

Drugs that interact with a receptor to
stimulate a response

26
Q

Antagonist:

A

Drugs that attach to a receptor but do not stimulate a response

27
Q

Partial Agonists:

A

Drugs that attach and elicit a small
response but also block other responses

28
Q

Routes of Drug Administration
Enteral:

A

Via the gastrointestinal tract by the oral,rectal, or nasogastric routes.

29
Q

Routes of Drug Administration
Parenteral

A

Bypasses the GI tract by using
subcutaneous, intramuscular, and intravenous
injection.

30
Q

Routes of Drug Administration
Percutaneous:

A

Absorbed through the skin and
mucous membranes
Inhalation, sublingual, or topical

31
Q

Drug Stages After Administration
LADME

A

Liberation: Drug released from dosage form
Absorption: Depends on route of administration
Distribution: Depends on circulation to be transported throughout body
Metabolism: Depends on enzyme systems
Excretion: Depends on GI tract and kidneys

32
Q

Liberation

A

Drug released from dosage form and is dissolved in body fluid.
Process of converting oral drug can be influenced by food and water in the stomach.

33
Q

All drugs are processed in the body through
pharmacokinetics. What is the correct order
that drugs pass through the body?

A

Liberation, absorption, distribution, metabolism, excretion.

34
Q

Absorption

A

-Drug is transferred from entry site into the body’s circulating fluids.
-Absorption rate depends on route, blood flow, and solubility of the drug.
-Subcutaneous and intramuscular injection absorption is affected by circulation.
Intravenous medications are absorbed fastest.
-Topical medications applied to the skin can be influenced by skin thickness and hydration.

35
Q

Which route of administration has the fastest rate of distribution?

A

Intravenous

36
Q

Distribution

A

-Drugs are transported throughout the body by body fluids to the sites of action.
-Protein binding and fat solubility affect distribution.
-Organs with largest blood supply receive the distributed drug most rapidly.
-Some drugs cannot pass through the blood-brain barrier or the placental barrier

37
Q

Metabolism

A

-The process whereby the body inactivates drugs
-Primary organ of metabolism is the liver; other sites are GI tract and lungs

38
Q

Excretion

A

-Elimination of drug metabolites and some of the active
drug from the body
-Kidneys are the major organ of excretion; some excreted
in feces
-A patient with poor kidney function will have an increased action and duration of a drug

39
Q

Half-Life of Drugs

A

-Factors modifying the quantity of drug reaching a site of action after a single oral dose.
-When the half-life of a drug is known, dosages and frequency of administration can be calculated.
-Drugs with long half-lives (digoxin is 36 hours) need to be administered once daily.

40
Q

Idiosyncratic reactions:

A

Occur when something unusual/abnormal happens when drug is first administered

41
Q

Allergic reactions:

A

Occur among patients who have previously been exposed to a drug and whose immune systems have developed antibodies to the drug