Labtest Flashcards

(44 cards)

1
Q

Give the three different drug name categories and when they’re used

A
  1. chemical name (rarely used on prescriptions)
  2. approved name (used for official/prepared medicines in prescription and pharmacopea)
  3. licensed/brand name (used for prescribing authorized medicines)
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2
Q

When do you have to write inscription and subscription in numbers AND letters?

A

When prescribing schedule 2 or 3 drugs

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3
Q

What was decided since 2015 for special requirements?

A

It must be written indelible or computer generated and the signature must be in ink or electronic prescription form

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4
Q

What is not allowed for prescription of schedule 2 and 3 drugs?

A

“Take as required”

No latinization or abbreviation is allowed

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5
Q

What happens if the S2/S3 prescription does not follow the requirements?

A

The pharmacist is not allowed to dispense the medication, as it is not valid

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6
Q

How long is the S2/S3 prescription valid?

A

28 days

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7
Q

How many repeats of S2/S3 drugs?

A

Zero repeats

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8
Q

How long is S4 prescriptions valid?

A

28 days

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9
Q

How long are S5 prescriptions valid?

A

6 months

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10
Q

Which S3 drug differs from the others concerning the rules?

A

Buphrenorphine

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11
Q

What must the label of dispensed medicines contain?

A

Name and address of owner and veterinarian
Date of dispensing
Topical use only
Relevant WP
Whether the product contains hexachlorophene, aspirin

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12
Q

What is MFS (2013) and who do they apply to?

A

Medicated feeding stuff prescriptions
They apply to anyone who incorporates a medicated product in an animal feeding stuff

Any mixture of a VMP/s and feedingstuff which is ready prepared for supply and
intended to be fed to animals without further processing.

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13
Q

Who do MFS not apply to?

A

Companion animal owners administering a medicinal product mixed in the feed or a farmer ‘top dressing’ feed or medicating via drinking water.

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14
Q

What do all manufacturers and distributors who add medicines to feed have to do?

A

Register with the royal pharmaceutical society of GB (RPSGB) or DARD for NI

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15
Q

Basic requirements for MFS prescription

A

Three copies: compounder, farmer and veterinarian

Valid for 3 months or shorter

According to data sheet recommendations

May be incorporated into feed by a registered person only if product has relevant product license or animal test certificate (ATC)

Medicinal products must be licensed for in-feed use

Must be sufficient for only one course of treatment

An MFS is required if they are to be incorporated in any way not in accordance with the product license

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16
Q

MFS prescription should include:

A

• the name and address of the person prescribing the product
• the qualifications enabling the person to prescribe the
product
• the name and address of the keeper of the animals to be treated
• the species of animal, identification and number of the animals
• the premises at which the animals are kept if this is different from the address of the keeper
• the date of the prescription
• the signature or other authentication of the person
prescribing the product
• the name and amount of the product prescribed
• the dosage and administration instructions
any necessary warnings;
• the withdrawal period;
• the manufacturer or the distributor of the feedingstuffs (who must be approved for the purpose);
• if the validity exceeds one month, a statement that not more than 31 days’ supply may be provided at any time;
• the name, type and quantity of feedingstuffs to be used;
• the inclusion rate of the veterinary medicinal product and
the resulting inclusion rate of the active substance;
• any special instructions;
• the percentage of the prescribed feedingstuffs to be added to the daily ration; and
• if it is prescribed under the cascade, a statement to that effect.

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17
Q

Dosage form: powder for external use

A

Talcum powder, sparsorium
Usage reduced

Active substances: ab, antiseptics, antimycotics, ectoparasiticides

Binders: talcum, zinc oxide etc.

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18
Q

What is negative about powder for external use

A

Watery wounds can give granulation/Fibrosis etc

May cause overstimulation of the wound

19
Q

Dosage form: powder for internal use

Administration and categories

A
Pulvis, -eris
Administration: per os (oral)
Categories:
Water-soluble powder (drinking water)
Powder for in-feed use
Powder for oral solution and suspension
For direct administration: capsule
20
Q

Dosage form: powder for internal use

Composition

A

Active substance

Binder: lactose, sorbit, glucose, bran/cereal flour (all water-soluble)

21
Q

Dosage form: powder for internal use

Powder division

A

Small animal medicine, drugs with low therapeutic index

Dividation: a+b+c = abc then divide into doses
Dispension: a+b+c= one dose

22
Q

Dosage form: granules usage

A

Granulatum
Usage:
farm animals: mixed in feed or drinking water
small animals, human: for solution or mixed in feed

23
Q

Dosage form: granules

Composition

A

Active substance
Binder (saccharose, lactose)
Adhesive (purified water, ethanol, methylcellulose (GEL)
Coating if needed (biphasic formulation)

24
Q

Medicated premix

25
Feed supplements
Microelements, vitamins, prebiotics
26
Medicated premix/feed supplement usage
Per os (small and large scale) Powder, granulated (microencapsulated), liquid Homogenous mixing: large scale Always added to feed
27
Premix composition
Active substance: medicated: drugs (ab, antiparasitic etc) Feed suookement: microelements, vitamins, prebiotics, probiotics etc Binder: similar to feed Nutritional value: flour, bran Indifferent: silicates
28
Dosage form: capsule | Usage
Per os, no chewing | Only individual treatment: SMALL ANIMAL MED
29
Soft capsule
Before: gelatine, sugar, glycerol, water Not anymore - animal origin Now: synthetic polymers
30
Hard capsule
Before: gelatine, sugar, water (NO glycerol) Dissolves in gastric fluid (15min) Hydroxypropyl methylcellulose
31
Gastro-resistant capsule (soft and hard)
``` E.g. methacrylate coating Capsula intestinosolvens (film coated tablets) ```
32
Tablet, dragee
Most precise divided form | Per os, intrauterine, intravaginal, for preparing solutions
33
Tablet composition
``` Active substance Binder Adhesive Lubricant Colouring, flavouring agents etc. Coating (TiO2: protection from light) ```
34
Controlled release tablet two types
``` Insoluble matrix (citrate, potassium) Soluble matrix (polymer) ``` Less frequent administration needed
35
Intraruminal bolus
Large tablets for ruminants, modified release | Sustained or pulse
36
Sustained release intraruminal bolus
Best for food consumption (MRL)
37
Pulse release intraruminal bolus
6 month WP
38
Packaging of tablets
Usually plastic or aluminium foil (blister) and paper box - authorized products
39
Herbal tea usage and forms
Per os or topically (wound) Infusion: essential oils, substances that are easily diffolved - inactivation when expressed to permanently hot temperature Decoction: substances that are difficult to extract (tannic acid) Maceration: soaking
40
Herbal tea composition
Active substance with mild effect + herbal parts + occasionally: effect enhancer chemicals
41
Transdermal patch, implant
Continous, prolonged release | Dermal absorption - systemic effect (synthetic opioids)
42
Subdermal implants
Frequently used | Oestrus synchronisation, progestagens, deslorelin
43
Antiparasitic collars and ear tags
Usually prescription is not needed
44
Vaginal delivery systems
Oestrus synchronization (progestagens) Not tolerated by horses