Unit 1 - Introduction Flashcards

1
Q
A
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1
Q

in regards to the sask vet act, 1987, what ability do the vet and vet techs have

A

vet have ability to prescribe and dispense/administer prescribed drug
Vet techs have ability to dispense and administer prescribed drug under direction of the vet
MUST have valid VCPR to carry out role

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2
Q

What is the difference btw pharmacology and pharmacy

A

pharmacology - science of how drugs work; chem, effects in body, uses/indications, how the body responds to drugs, what happens to the drug in the body
Pharmacy - preparation, dispensing and proper utilization of drugs

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3
Q

What are the 4 rules to live by for safe drug usage?

A

1 - all drugs are poisons
2 - no drug is a silver bullet
3 - all doses are guesses
4 - complacency kills

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4
Q

What names a name a generic name for a drug?

A

common name
refers to the active pharmaceutical ingredient
generic name never changes btw human, vet or diff countries
does not indicate the dose format or formulation
starts with “small case” not capitalized, ex meloxicam

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5
Q

How do you know which name is a trade name or proprietary name?

A

capitalized; followed by a registered or TM trademarked symbol
proprietary names are licensed by a specific drug manufacturer
refers to a specific drug that had been formulated in a specific manner
names will change by country

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6
Q

What are some generic equivalents in drugs?

A

“generics”
do not appear until original patent on the licensed trade name drug has expired
contains the same active drug as the original licensed drug (same as the original tradename product)
but may not work exactly the same due non-medicinal components that may affect the kinetics/dynamics of the drug

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7
Q

Where can you look for sources of drug information?

A
  1. label or package insert
  2. compendium
  3. vet drug formularies
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8
Q

What is an on label drug use?

A

Using a drug according to the directions on the drug label without deviation.
Advantages
drug more likely to be effective, known outcome, decreases risk of side effects, in the events of adverse side effects, the manufacturer will stand behind the product
professional safety net in the event of adverse effects occurring
known withdrawal time for food animals
ALWAYS preferred method

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9
Q

What is extra-label drug use? AKA off label

A

use of a druge in a manner not consistent w/ what is indicated on the label, package insert or product monograph of any drug product approved by health canada
use in a species not listed, use for an indication not listed, use of a diff dose, frequency of administration or brought of administration

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10
Q

WHat are the responsibilities of ELDU?

A

Always require a prescription and a valid VCPR
responsibility for all aspects, including safety, adverse reactions, withdrawal times lie with the prescribing vet
Applies to all prescription drugs and OTC meds used off-label
not permitted for insecticides, pesticides and biologicals (including vx’s)
best to avoid ELDU in ALL food producing animals due to questionable WT

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11
Q

What is compounding drugs?

A

is considered ELDU extra label drug use
a process of combining, mixing, or altering ingredients to create a med tailored to needs of individual anim or a sm group of anims”
ex. having a pharmacist compound a drug into a dosage form to ease administration (ex. methimazole topical gel for cats)
mixing penicillin with dexamethasone into ointment in your clinit to make “scratches ointment” for a horse

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12
Q

What SVMA policy allows vets to compound drugs?

A

“When no appropriate approved products (veterinary or human) exist, veterinarians may prescribe drugs to be compounded for
use for a specific animal or group of animals provided the veterinarian has adequate medical justification for the prescription.”

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13
Q

All drugs are poisonous, when selecting a drug, why does concentration matter?

A

The conc of drug inside the animal determines whether drug will be beneficial or toxic

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14
Q

What is drug toxicity, why might it happen?

A

Outright or relative overdose, side effects, accidental exposure, drug interactions or incorrect tx

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15
Q

What are some acute adverse effects of drug toxicity?

A

Immediatel often no further damage once drug is removed
Effects on CV/resp system/muscles/GI/nervous/endocrine/ repro

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16
Q

What are some chronic adverse effects of drug toxicity?

A

May not be revealed for years or generations
dec repro, teratogenicity and cancer
long-term liver damage

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17
Q

In terms of drug toxicity, explain what might happen with cats and enrofloxacin?

A

At label doses may cause retinal degernation/detachment = blindness
May show up days-12wks of tx starting
recovery is guarded
discovered after trials and approved for market

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18
Q

What is a lethal dose?

A

LD50 (medial lethal dose)
A measure of toxicity
Definition: Dose of a drug (mg/kg) that kills 50% of the animals that receive it
Drugs with high LD50 are safer than drugs with low LD 50
Alters with species, age, health status of patient
Chemicals with LD50 values less than 300mg/kg are considered highly toxic
300-1000mg/kg are moderately toxic
1000-5000mg/kg are slightly toxic

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19
Q

In terms of LD50, which chemical is more toxic?

A: LD50 = 3.2 mg/kg
B: LD50 = 48 mg/kg

A

A, because only a small amount is required to be a toxic dose compared to B

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20
Q

What is an effective dose?

A

The amount of drug required to reach this therapeutic effect.
ED50 or median effective dose
Amount of drug (mg/kg) required to produce a desired effect in 50% of animals that receive it
May be different for each indication and individual patients may require a slightly higher/lower dose

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21
Q

What are some examples where ED50 may be different for each indication?

A

ED50 is higher for septic peritonitis than for a skin infection
Lower doses of pred are used to dec inflam; at higher dose, is immunosuppressive
A low dose of pentobarbital can be anti-convulsant; higher dose for unconsciousness and 2x the dose is euthanasia

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22
Q

What is a therapeutic Index?

A

A measure of drug safety
The difference btw the effective dose and the lethal dose or TI = LD50/ED50

23
Q

What does it mean if TI is high, TI is low, TI is 1, or TI is <1?

A

If TI is high (»1), the drug is safe to use
if TI is low, (>1) the drug is less safe to use
If TI is 1, the tx or death are equally likely to occur
If TI is <1, the indication for the drug is death

24
Q

How do drugs in the plasma work?

A

Even administered locally, it may eventually absorb (at lower lvls) into the blood stream
For a drug to work, it must get to the target tissue via the plasma - must be a conc of drug in plasma to have an effect
Once in plasma, drugs can go to ANY tissue and could have adverse side effects

25
Q

What is definition of a plasma drug concentration?

A

The amount of drug present in the blood (μg/dl)

26
Q

What is a therapeutic range for plasma drugs?

A

conc of drug in the blood that will provide an effect with the least adverse effects
dosage goal

27
Q

What is the toxic range?

A

Higher than desired conc of drug in the blood
may be therapeutic, but adverse side effects will occur

28
Q

What is the subtherapeutic range?

A

Lower than desired conc of drug in blood
drug has no beneficial effects, but may experience side effects
when referring to antimicrobial use, high risk of creating drug resistance

29
Q

What is the maximum effective concentration? (MEC)

A

border btw conc’s that are beneficial and concs when adverse reactions are first noted
Highest desired drug conc, if higher, adverse side effects will occur

30
Q

What is the minimum effective concentration (MEC)

A

Lowest drug conc in blood to obtain desired effect
below the MEC, drug has no beneficial effects (may have side effects)

31
Q

What is the goal of any dosage?

A

To maintai the conc of drug in the therapeutic range
Smler, more frequent doses are more likely to stay within range
Less frequent dosing req lg doses that are more likely to exceed MEC; also a greater chance of dropping below the min EC

32
Q

What is a narrow therapeutic range? What is a narrow therapeutic range = narrow therapeutic index?

A

Drugs that have a max effective dose and the minimal effective dose close to each other
Range = index: dose that prods the minimal beneficial effect not far from dose that prods toxicity. Shot not be dosed in such a way that causes wide swings btw peak and the trough concentrations

33
Q

What are loading and maintenance doses?

A

Initial lger dose to load the body
A smaller ‘maintentance’ dose to match the bodies rate of elimination to maintain body lvls

34
Q

What is a total daily dose?

A

A combined amount of drug (mass) times the # of doses administered in a give day

Peak conc highest drug conc
Trough conc lowest drug conc

35
Q

What is the parenteral route administration?

A

Para - beside; enteron - intestines
Not by the intestines or not orally

EX> IV, SQ, IM

36
Q

What is the non-parenteral route administered?

A

We are giving it by the intestines
Includes topical drugs (applied to a particular place on or in the body. Most often body surface of mucous membranes

37
Q

Explain the effects of rapid IV bolus’ and what to keep in mind

A

A single dose given over approx. 30s; CPR drugs can be faster
Immediate onset of action
All the drug enters the plasma
Higher initial plasma lvls of drug results in fastest therapeutic effect
highest peak drug conc = highest risk
shorter duration of activity

38
Q

What is a slow IV bolus and what are some things to keep in mind

A

Single dose given over 10-20 mins
Onset of action not as rapid as IV bolus
Slower time to peak conc and lowers peak conc
Still immediate
all the drug enters the plasma
decrease peak conc

39
Q

What is a constant infusion rate?

A

A CRI, a very small dose of a drug given at very short intervals
Can be for a short or extended period
EX. mc/s
BEST for maintaining therapeutic range w/ minimal deviation in blood plasma concentration
Amount in equals the amount metabolized in that same period of time

40
Q

How is IM administered and what are some things to keep in mind?

A

Muscle has great blood supply
In general; relatively rapid onset of action and the 2nd fastest absorption and onset of action
Longer duration of effect than IV routes
Close to 100% of drug absorbed
% drug absorbed and rate of absorption can be affected by drug formulation - repositories or depot preparations delay drug release

41
Q

Why is it important that drugs with specific routes are given that specific route?

A

Improperly, it can cause severe inflam or tissue necrosis, pain, sloughing of skin

EX. Clostridial myositis caused by IM injection with banamine

42
Q

What is intradermal injections an dwhat are some things to keep in mind?

A

JUST under the skin, makes a lil blep
Skin has excellent blood supply to has a very similar curve to IM delivery in which is has a fairly rapid absorption and onset of action with an almost 100% drug absorbed

Temp will affect drugs bc heat -> vasodilation -> speeds up absorption + inc toxicity risk
Cold -> vasoconstriction -> slows absorption and lower tox risk
Limited V of drug can be delivered and excess V are painful

43
Q

What are SQ injections and what are some things to keep in mind with them

A

Under the skin and into subcutaneous fat
Slower absorption and onset of action than IV/IM/ID routes due to slower vascularity
Even slower if injected into fat layer - fat not well vascularized. Lipophilic drugs may have delayed absorption as fat will act as as ink and bind drug
Rate of absorption affected by temp so heat = faster, cold = slower
Can give larger V by IM/ID

44
Q

What is intraperitoneal administration and what are some things to keep in mind?

A

Drug absorbed via mesenteric vessels and ultimately ends up in liver (shares properties of non-parenteral routes)
Can give very lg V
Slower absorption than SC

45
Q

What is intraarterial and intracardiac administration and what are some things to keep in mind?

A

Very rapid onset and highest peak plasma concentration in all tissues, especially the heart and brain
Very high risk of toxicity - AVOID

46
Q

What does non-parenteral administration include? What is the advantages of it?

A

Oral, sublingual, rectal
Absorption rates, onset of action and % of drug absorbed all depend on which of the above is used
Advan: lowest cost, easier routes of delivery for owner to manage, can give lg amounts if PO/rectal

47
Q

What is PO/per os? What should we keep in mind with it?

A

Drugs given by mouth or ingested. Must travel the digestive tract which it can then be
- Digested/broken down by digestive enzymes in saliva, the intestines or stomach acid
Stay in the intestines and act locally (not absorbed and act on the lumen of the digestive tract) ex ant-acids, pre/probiotics/soothers
Absorbed into the plasma

48
Q

What are the limitations of giving drugs PO?

A

Long onset of action
Always some loss of drugs due to stomach avid, digestive enzymes in saliva + intestines, microbial digestion
Must be formulated in a way to withstand the above
Drug that is absorbed may be metabolized in the liver (AKA 1st pass effect), ergo, eliminated from body
Side effects: GI upset
Doesn’t work well in ruminents or if GI dz

49
Q

What are sublingual drugs? What to keep in mind?

A

The oral mucose in some animals is easily crossed by small molecules (especially cats/neonates)
Most permeable areas are under tongue and buccal pouch (cheek)
drug placed in these areas -> rapidly crosses mucose -> very vascular
Rate of absorption/onset of action similar to IM/ID
Some drug lost bc enzymes in saliva/swallow - any drug that is swallowed is not absorbed, does not avoid the 1st pass effect and intestinal digestion

50
Q

What are rectal drugs? What are some things to keep in mind?

A

Preferred method for unconscious or seizuring patients
bypasses all digestive functions
drug is absorbed with the rectal mucose
disadvan: inconsistent absorption

51
Q

What is a topical drug delivery and what are some things to keep in mind?

A

Admin of a drug directly to target tissue
Preferred fro drugs w/ severe systemic side effects, drugs w/ poor absorption and/or distribution; hard time getting to intended target
Drugs with a high cost
target tissues that are easily accessible (skin wounds, ear canal, eyes)

52
Q

What is an example of topical drugs?

A

Ointments, creams, eye and ear drops
May not be delivered locally! Might be applied to skin and absorbed into the blood stream like anti-parasitics

Aerosols - nebulizers, metered dose inhalers

53
Q

What are the advantages of topical drug delivery?

A
  1. faster onset of action 0 peak conc of drug in target tissue reached faster
  2. inc conc of drug @ target tissue
  3. Specifically dec systemic side effects. Still has some risk of systemic toxicity as drug is absorbed, just less absorbed. Also depends on drug/patient
  4. can use a lower dose of drug = lowering cost
54
Q

How can we counteract drug toxicitites?

A

Tell someone!!
Remove drug if possible - may induce vomiting
give antidote/reversal
enhand elimination (diuresis, ventilate)
dilute/constrict; cool/heat
treat symptomatically
know drugs and drug labels!!
report adverse reactions

55
Q

What are the 6 rights of proper drug administration?

A

1 right drug
2 right dose
3 right time
4 right route/technique
5 right patient
6 right documentation