Misuse of drugs 1 Flashcards

1
Q

List 5 relevant legislation to CDs

A
  • misuse of drug regulations 2017
  • persons authorised to witness destruction of controlled drugs
  • misuse of drugs (safe custody) regulations 1982
  • misuse of drugs (supervision of prescription and supply of methadone and medicinal products containing buprenorphine authorised for opioid substitution treatment) regulations 2019
  • misuse of drugs (prescription and control of supply of cannabis for medical use) regulations 2019
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2
Q

What is part 1 of misuse of drug regulations 2017-2020 and list the regulations of it

A

Part 1 - Preliminary and General
1. Citation and commencement
2. Interpretation

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3
Q

What is part 2 of misuse of drug regulations 2017-2020 and list the regulations of it

A

Part 2 - Issuing of prescriptions by registered nurses and registered midwives
3. Provisions applicable to practitioners who are registered nurses or registered midwives
4. Person may refuse to supply drug if reasonable cause to believe
conditions referred to in regulation 3 have not been satisfied.

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4
Q

What is part 3 of misuse of drug regulations 2017-2020 and list the regulations of it

A

PART 3 = Production, Supply, Importation and Exportation of Controlled Drugs
5. General prohibition.
6. Licences.
7. Administration.
8. Exemption for practitioners, pharmacists, etc.
9. Supply.

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4
Q

What is part 4 of misuse of drug regulations 2017-2020 and list the regulations of it

A

PART 4 = Possession of Controlled Drugs
10. General exemptions.
11. Exemption to possess butan-1,4-diol or dihydrofuran-2(3H)-one.
12. Exemption for midwives in respect of pentazocine and pethidine.
13. General authorities.

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5
Q

What is part 5 of misuse of drug regulations 2017-2020 and list the regulations of it

A

PART 5 = Documentation and Record-Keeping
14. Documents to be obtained by a supplier.
15. Form of prescriptions.
16. Supply on prescription.
17. Marking of containers.
18. Documents required for export of controlled drugs.
19. Keeping of registers for drugs in Schedules 1 and 2.
20. Record-keeping in particular cases for drugs in Schedule 2.
21. Keeping of records for drugs in Schedules 3 and 4.
22. Preservation of registers, etc.
23. Preservation of records for drugs in Schedules 3, Part 1 of Schedule 4, and Schedule 5
24. Furnishing of information with respect to controlled drugs.

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6
Q

What is part 6 of misuse of drug regulations 2017-2020 and list the regulations of it

A

PART 6 = Miscellaneous
25. Destruction of certain drugs.
26. Disposal of certain drugs on cessation of business.
27. Forged, etc. prescriptions.
28. Publication, sale etc. of certain books, periodicals and other publications.
29. References to the revoked Regulations of 1988 in other enactments.
30. Transitional provisions

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7
Q

How many regulations and parts in total

A

6 parts and 30 regulations

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8
Q

What does paragraph (1) of regulation 3 state

A

any references in the regulations to schedule 2/3 should be understood as a reference to schedule 8

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9
Q

What does paragraph (2) of regulation 3 state

A

registered nurses cannot prescribe drugs listed in schedules 4,5,8 unless the following conditions are met

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10
Q

What do part 1 - part 5 of schedule 8 refer to

A

Part 1 - (i) relief of pain
(ii) immediately prior to medical or surgical procedure
(iii) post operative pain relief
Part 2 - palliative care
Part 3 - midwifery
Part 4 - neonatal care
Part 5 - mental health or intellectual disability

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11
Q

What does paragraph (3) of regulation 3 state

A

the regulation doesn’t limit a health service provider from preventing a nurse from prescribing, or setting additional conditions
the nursing and midwifery board of ireland from carrying out any duties assigned to them by the nurses and midwifes act

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12
Q

What is regulation 4

A

Person may refuse to supply drug if reasonable cause to believe conditions referred to in Regulation 3 have not been satisfied.

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13
Q

What does the Paragraph (1) of regulation 5 refer to

A

Subject to the provisions of these Regulations, a person shall not—
(a) produce a controlled drug,
(b) supply or offer to supply a controlled drug, or
(c) import or export a controlled drug.

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14
Q

What does paragraph (2) of regulation 5 refer to

A

(a) Paragraph (1)(b) shall not apply to poppy straw. (can supply poppy straw)
(b) Paragraph (1)(c) shall not apply to any drug specified in—
* (i) Part 2 of Schedule 4, or
* (ii) Schedule 5
(import or export)

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15
Q

What does regulation 7 refer to

A

Administration - it is okay for anyone to give drugs from schedule 5 to someone else
a practitioner except vet to give patient schedule 2,3,4
non-medical professional to give patients drugs from schedule 2,3,4 as long as they follow instructions from a dentist, nurse, midwife

16
Q

What does regulation 8 refer to?

A

exemptions of pharmacist, practitioner
they can:
(a) supply or offer to supply S 2,3,4 to authorised persons
(b) make or prepare CD

(2) Registered nurses can’t make or prepare CD

(3) a person who runs a retail pharmacy can supply/ offer to supply S2,3,4 to individuals who are allowed to have them at the location where their business operates

17
Q

What does regulation 9 refer to?

A

Supply
- list of people who can supply
- director of nursing can’t if there is a pharmacist in charge of dispensing
- nurses can only supply CDs as directed by medical practitioners

18
Q

What does paragraph (3) of regulation 9 refer to

A

owner of ship/ master of ship

19
Q

What does paragraph (4) of regulation 9 refer to

A

installation manager of an offshore installation

20
Q

What does regulation 12 refer to

A

exemption for midwives in respect of pentazocine and
pethidine.
(1) they are allowed to possess pentazocine/ pethidine as necessary for their practice
(2) specific conditions for allowing them to possess pethidine/pentazocine as mentioned in paragraph (1)

21
Q

Regulation 13?

A

General authorities - people who may have a controlled drug in their possession

22
Q

Regulation 14?

A

Documents to be obtained by supplier
(7) - must furnish a receipt
(8) - pharmacist must check and return receipt not later than 3 working days

23
Q

Regulation 15

A

forms of a prescription
(1) must know identity and must comply with requirements in (2)
(2) requirements