LAISHA
Open Laisha

Veterinary Council of Ireland registration exam Veterinary Pharmacy, Prescribing Law & Medicines Regulation: practice questions

Veterinary Council of Ireland registration exam · Ireland · Veterinary Council of Ireland

Original practice questions written to the published syllabus · not past papers
10worked here, free
32written to this exam in this subject
9syllabus units

What this subject covers

Writing a lawful prescription and dispensing safely: who may prescribe, extra-label use and the cascade, withdrawal periods and MRLs, drugs prohibited in food animals, pharmacovigilance, controlled drugs and records.

In the exams: EAEVE Day One competences on prescribing, dispensing and reporting adverse reactions; WOAH Day 1 veterinary products; RCVS Day One competences (the cascade)

What Veterinary Council of Ireland registration exam asks from it

RCVS Statutory Membership Examination (UK) and Veterinary Council of Ireland registration exam

Legal categories (POM-V, POM-VPS, NFA-VPS, AVM-GSL), animals under care, the cascade steps and conditions, minimum withdrawal periods for off-label use in food animals, horse passports and the food chain, controlled-drug schedules, registers and prescriptions, and reporting suspected adverse events to the VMD.

Where the 32 questions fall

How our questions for Veterinary Council of Ireland registration exam spread across the units of Veterinary Pharmacy, Prescribing Law & Medicines Regulation. Difficulty: 11 easy, 12 medium, 9 hard.

Withdrawal periods8
Extra-label use: US AMDUCA and the UK cascade5
Controlled drugs4
Record keeping4
Prescription writing3
Who may prescribe: IVC Act s.30, the US VCPR and UK POM-V3
Drugs prohibited in food-producing animals2
Pharmacovigilance and adverse-event reporting2
Maximum residue limits1

10 practice questions, worked

Choose an answer, then open the working. Each explanation says why the right answer is right and why the others are not.

1 · Extra-label use: US AMDUCA and the UK cascade · hard

Under the EU cascade, a vet wants to give a dairy cow a human medicine. Which condition concerning the active substance must be met?

  1. It must be listed in Table 2 of Regulation 37/2010
  2. It must be listed in Table 1 of Regulation 37/2010 as an allowed substance
  3. It must have been used safely in cattle in another country for 5 years
  4. It must have a human marketing authorisation in at least two member states
Answer and working

B. It must be listed in Table 1 of Regulation 37/2010 as an allowed substance

Any substance given to a food-producing animal, even under the cascade, must be an allowed substance in Table 1 of Regulation 37/2010. Table 2 lists prohibited substances for which no MRL can be set.

Further reading: Regulation (EU) 2019/6, Art 113; Regulation (EU) 37/2010

2 · Withdrawal periods · medium

Under Article 115 of Regulation (EU) 2019/6, a product authorised for cattle with a 10-day meat withdrawal is used under the cascade in sheep. What is the minimum meat withdrawal?

  1. 28 days
  2. 15 days
  3. 10 days
  4. 20 days
Answer and working

B. 15 days

When the product is authorised for a food species, the minimum is the longest SPC meat withdrawal × 1.5 = 15 days. 28 days applies only when the product is not authorised for any food-producing animal; 10 days ignores the multiplier; 20 days doubles instead of × 1.5.

Further reading: Regulation (EU) 2019/6, Article 115

3 · Withdrawal periods · hard

Under the EU cascade rule (longest fish withdrawal × 1.5), a product authorised for salmon with a 300 degree-day withdrawal is used in rainbow trout kept at 9 °C. What is the minimum withdrawal in calendar days?

  1. 33.3 days
  2. 50 days
  3. 55.6 days
  4. 450 days
Answer and working

B. 50 days

Minimum = 300 × 1.5 = 450 degree-days; at 9 °C that is 450 ÷ 9 = 50 days. 33.3 days forgets the multiplier; 450 days treats degree-days as calendar days; 55.6 days applies the 500 degree-day minimum meant for products not authorised in any food species.

Further reading: Regulation (EU) 2019/6, Article 115

4 · Withdrawal periods · medium

Under Article 115 of Regulation (EU) 2019/6, a product authorised for cattle with a zero meat withdrawal is used under the cascade in turkeys. What is the minimum meat withdrawal?

  1. 1 day
  2. 7 days
  3. Zero days
  4. 28 days
Answer and working

A. 1 day

When a product with a zero withdrawal period is used in a different taxonomic family, the EU minimum is 1 day for meat. Zero is the label figure for the authorised species only; 28 days is for products not authorised in food animals.

Further reading: Regulation (EU) 2019/6, Article 115

5 · Withdrawal periods · hard

A UK horse's passport has not been signed out of the food chain. The vet wants to treat chronic lameness with phenylbutazone. What is the legal position?

  1. Not allowed: phenylbutazone has no MRL and the horse is in the food chain
  2. It may be given because horses are never classed as food-producing animals
  3. It may be given with a 6-month withdrawal as an essential substance
  4. It may be given with a standard 28-day meat withdrawal under the cascade
Answer and working

A. Not allowed: phenylbutazone has no MRL and the horse is in the food chain

In the UK and EU every horse is a food animal unless its passport declaration excludes it. Phenylbutazone has no MRL and is not on the essential substances list, so it may not be used in a food-chain horse. The 6-month withdrawal applies only to listed essential substances.

Further reading: Commission Regulation (EU) 122/2013; VMD guidance on horse medicines

6 · Pharmacovigilance and adverse-event reporting · hard

Milk from a cow tests positive for residues above the MRL even though the farmer observed the label withdrawal period exactly. How should this be treated?

  1. As the farmer's fault, so no report to the regulator is needed
  2. As an adverse event suggesting the label withdrawal is too short
  3. As normal biological variation that needs no further action
  4. As a laboratory error, so the positive result can safely be ignored
Answer and working

B. As an adverse event suggesting the label withdrawal is too short

A residue violation after the correct withdrawal is part of the scope of pharmacovigilance in the EU and GB. Reports can lead to a review of the withdrawal period.

7 · Controlled drugs · medium

Under the UK Misuse of Drugs (Safe Custody) Regulations 1973, which of these veterinary drugs must be kept in a locked controlled-drug cabinet?

  1. Buprenorphine
  2. Furosemide
  3. Meloxicam
  4. Amoxicillin
Answer and working

A. Buprenorphine

Schedule 2 drugs and certain Schedule 3 drugs, including buprenorphine, are subject to safe custody. Meloxicam, amoxicillin and furosemide are not controlled drugs.

Further reading: Misuse of Drugs (Safe Custody) Regulations 1973

8 · Record keeping · medium

Under the GB Veterinary Medicines Regulations, how often must a practice carry out a detailed audit of its incoming and outgoing medicines against stock held?

  1. Every week
  2. At least once a year
  3. Only when inspected
  4. Every five years
Answer and working

B. At least once a year

A detailed audit reconciling incoming and outgoing medicines with stock must be done at least annually. Controlled drugs are checked far more often in good practice.

Further reading: Veterinary Medicines Regulations 2013

9 · Record keeping · easy

Under EU rules, keepers of food-producing animals must keep records of medicines bought and given. For how long at minimum?

  1. 6 months
  2. 2 years
  3. Until the animal is slaughtered
  4. 5 years
Answer and working

D. 5 years

Regulation 2019/6 requires keepers of food-producing animals to keep medicine records for at least five years, so residue investigations can trace treatments after the animal has gone.

Further reading: Regulation (EU) 2019/6, Article 108

10 · Record keeping · hard

When a GB vet uses a medicine under the cascade, what should the clinical record show besides the drug and dose?

  1. Only the price charged, because cascade drugs are invoiced differently
  2. The pharmacist's view, which must be obtained for every case
  3. The reason no authorised product suited, the step used and consent
  4. Nothing extra, because cascade use is recorded only by the VMD
Answer and working

C. The reason no authorised product suited, the step used and consent

Good practice, and the RCVS guidance, expect the record to justify cascade use: the clinical reason, why authorised products were unsuitable, the cascade step, consent and, for food animals, the withdrawal period. GB cascade records for food-producing animals must be kept for five years.

Further reading: RCVS supporting guidance; VMD cascade guidance

Ten here, 32 in the app. The Laisha app has every practice question we have written to Veterinary Council of Ireland registration exam in this subject, marked as you go, with timed papers, a jump-to-unanswered list and a certificate when you pass at 70 per cent.

Free for ten days, then one subscription of US$10 a month. We would rather say so here than have you find it later.

Practise the full set in Laisha →

Read the subject

Veterinary Pharmacy, Prescribing Law & Medicines RegulationThe full study manual, free Veterinary Council of Ireland registration examFormat, sections and how it has changed

Veterinary Pharmacy, Prescribing Law & Medicines Regulation for other exams

RCVS Statutory Membership Examination · UKNAVLE · USA / CanadaAustralasian Veterinary Examination, formerly the National Veterinary Examination · Australia / New ZealandSAVC Registration Examination · South AfricaNational Licensure Examination for Veterinarians · NepalKenya Veterinary Board pre-registration exam · Kenya

Ask Laisha about this

Opens Laisha's chat with your question ready to send. Sign in or start free.