S.I. No. 173/2017 - Misuse of Drugs Regulations 2017
This is the act as published. Later amendments are not folded into the text below: each one is a separate act in this repository and an entry in this law's history.
13 amending acts · 2026-08-25, S.I. No. 438/2026 - Misuse of Drugs (Amendment) (No. 2) Regulations 2026
- (b) the prescription complies with the requirements of Regulations 7(1) or 7A(1) of the Medicinal Products (Prescription and Control of Supply) Regulations 2003 (as amended and inserted by Regulations 4 and 5 of the Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 2) Regulations 2014 ( S.I. No. 504 of 2014 ) res-pectively), as appropriate, or, in the case of an animal remedy, Regulation 43 of the European Communities (Animal Remedies) (No. 2) Regulations 2007 ( S.I. No. 786 of 2007 ) (as amended by Regulation 2(c) and (d) of the European Communities (Animal Remedies) (Amendment) Regulations 2014 ( S.I. No. 162 of 2014 )), and
- (c) the supply is made not later than the date specified in Regulation 7(5)(a) of the Medicinal Products (Prescription and Control of Supply) Regulations 2003 or, in the case of an animal remedy, the date specified in Regulation 43(7)(c) of the European Communities (Animal Remedies) (No. 2) Regulations 2007.
- (3) Notwithstanding Regulations 15 and 16, a prescription for a controlled drug specified in Schedule 2 or 3, written and issued before the commencement of these Regulations in accordance with Regulation 13 of the Regulations of 1988, shall be deemed to be written and issued in accordance with Regulation 15 for the purpose of supply in accordance with Regulation 16 of these Regulations.
SCHEDULE 1
The following substances and products, namely:—
- (a) N-(Adamantan-1-yl)-1-(5-fluoropentyl)-1H-indazole-3-carboxamide (otherwise known as Clockwork Orange, 5F AKB48)
5-(2-Aminopropyl) indole (otherwise known as 5-IT)
1-(1,3-Benzodioxol-5-yl)-2-(1-pyrrolidinyl)-1-pentanone
N-(1-Benzyl-4-piperidyl) propionanilide
2-(4-Bromo-2,5-dimethoxyphenyl)-N-[(2-methoxyphenyl) methyl]ethanamine (otherwise known as 25B-NBOMe)
1-(4-Bromofuro[2,3-f][1]benzofuran-8-yl) propan-2-amine (otherwise known as BromodragonFLY)
Bufotenine
Cannabinol, except where contained in Cannabis or cannabis resin
Cannabinol derivatives
Cannabis (not being a preparation specified in paragraph 5 of Schedule 4 Part 1)
Cannabis resin
Cathinone
2-(4-Chloro-2,5-dimethoxyphenyl)-N-[(2-methoxyphenyl) methyl]ethanamine (otherwise known as 25C-NBOMe)
1-Cyclohexyl-4-(1,2-diphenylethyl) piperazine (otherwise known as MT-45)
Coca leaf
Concentrate of poppy straw
3,4-Dichloro-N-[[1-(dimethylamino) cyclohexyl]methyl]benzamide (otherwise known as AH-7921)
[2,3–Dihydro-5-methyl-3-(4-morpholinylmethyl) pyrrolo[1,2,3-de]-1,4-benzoxazin-6-yl]-1-naphthalenylmethanone
N,N-Diethyltryptamine
2,5-Dimethoxy-α,4-dimethylphenethylamine
N,N-Dimethyltryptamine
3-Dimethylheptyl-11-hydroxyhexahydrocannabinol
Eticyclidine
Etryptamine
1-(2-Fluorophenyl)-2-methylaminopropan-1-one
1-(3-Fluorophenyl)-2-methylaminopropan-1-one
1-(4-Fluorophenyl)-2-methylaminopropan-1-one
9-(Hydroxymethyl)-6,6-dimethyl-3-(2-methyloctan-2-yl)-6a,7,10,10a-tetrahydrobenzo[c]chromen-1-ol
[9-Hydroxy-6-methyl-3-[5-phenylpentan-2-yl]oxy-5,6,6a,7,8,9,10,10a-octahydrophenanthridin-1-yl]acetate
N-Hydroxy-tenamphetamine
2-(4-Iodo-2,5-dimethoxyphenyl)-N-[(2-methoxyphenyl) methyl]ethanamine (otherwise known as 25I-NBOMe)
Khat (being the leaves of Catha edulis (Celastraceae))
Lysergamide
Lysergide and other N-alkyl derivatives of lysergamide
Mescaline
Methcathinone
2-(3-Methoxyphenyl)-2-(ethylamino) cyclohexanone (otherwise known asmethoxetamine)
1-(4-Methoxyphenyl)-2-(methylamino) propan-1-one
Methyl (2S,4aR,6aR,7R,10aS,10bR)-9-acetyloxy-2-(furan-3-yl)-6a,10b-dimethyl-4,10-dioxo-2,4a,5,6,7,8,9,10a-octahydro-1H-benzo[f]isochromene-7-carboxylate (otherwise known as Salvinorin A) and any product, whether natural or otherwise, including any plant or plant material of any kind or description, which contains any proportion of the said substance
2-Methylamino-1-(3,4-methylenedioxyphenyl) butan-1-one
2-Methylamino-1-(3,4-methylenedioxyphenyl) propan-1-one
4-Methyl-aminorex
Methyl 2-[[1-(cyclohexylmethyl) indole-3-carbonyl]amino]-3,3-dimethylbutanoate (otherwise known as MDMB CHMICA)
Methyl (E)-2-[(2S,3S,7aS,12bS)-3-ethyl-7a-hydroxy-8-methoxy-2,3,4,6,7,12b-hexahydro-1H-indolo[2,3a]quinolizin-2-yl]-3-methoxyprop-2-enoate (otherwise known as 7-Hydroxymitragynine) and any product, whether natural or otherwise, including any plant or plant material of any kind or description, which contains any proportion of the said substance
Methyl (E)-2-[(2S,3S,12bS)-3-ethyl-8-methoxy-1,2,3,4,6,7,12,12b- octahydroindolo[2,3a]quinolizin-2-yl]-3-methoxyprop-2-enoate(otherwise known as Mitragynine) and any product, whether natural or otherwise, including any plant or plant material of any kind or description, which contains any proportion of the said substance
4-Methyl-5-(4-methylphenyl)-4,5-dihydro-1,3-oxazol-2-amine(otherwise known as 4,4’-DMAR)
α-Methyl-4-(methylthio) phenethylamine
1-(4-Methylphenyl)-2-methylaminopropan-1-one
Psilocin
Quinolin-8-yl 1-(5-fluoropentyl)-1H-indole-3-carboxylate (otherwiseknown as Clockwork Orange, PB22)
Raw opium
Rolicyclidine
Tenocyclidine
N-[1-(2-Thenyl)-4-piperidyl]propionanilide
- (b) Any substance (not being bupropion, diethylpropion or pyrovalerone) structurally derived from 2-amino-1-phenyl-1-propanone by modification in any of the following ways:
- (i) by substitution in the phenyl ring to any extent with alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylenedioxy, haloalkyl or halo substituents, whether or not further substituted in the phenyl ring by one or more other univalent substituents;
- (ii) by substitution at the 2- or 3-position of the propanone side-chain with an alkyl substituent;
- (iii) by substitution at the nitrogen atom with one or more alkyl or dialkyl groups, or by inclusion of the nitrogen atom in a cyclic structure.
- (c) Any substance structurally derived from 2-amino-1-propanone by substitution at the 1-position with any monocyclic, or fused-polycyclic ring system (not being a phenyl ring or alkylenedioxyphenyl ring system), whether or not the substance is further modified in any of the following ways:
- (i) by substitution in the ring system to any extent with alkyl, alkenyl, alkynyl, alkoxy, alkylthio, haloalkyl or halo substituents, whether or not further substituted in the ring system by one or more other univalent substituents;
- (ii) by substitution at the 3-position with an alkyl substituent;
- (iii) by substitution at the 2-amino nitrogen atom with one or more alkyl or dialkyl groups, or by inclusion of the 2-amino nitrogen atom in a cyclic structure.
- (d) Any substance structurally derived from 3-(1-benzoyl) indole or 3-(1-naphthoyl) indole by modification in any of the following ways:
- (i) by substitution at the nitrogen atom of the indole ring by alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2-(4-morpholinyl) ethyl;
- (ii) by replacement of one or more hydrogen atoms of any of the substituents referred to in clause (i), with a halo substituent;
whether or not further substituted in the indole ring to any extent and whether or not substituted in the phenyl or naphthyl ring to any extent.
- (e) 1-Benzylpiperazine or any substance (not being a substance specified in Schedule 3) structurally derived from 1-benzylpiperazine or 1-phenylpiperazine by modification in any of the following ways:
- (i) by substitution at the second nitrogen atom of the piperazine ring with alkyl, benzyl, haloalkyl or phenyl groups;
- (ii) by substitution in the aromatic ring to any extent with alkyl, alkoxy, alkylenedioxy, halo or haloalkyl groups.
- (f) Any substance (not being a substance specified in Schedule 2) structurally derived from fentanyl by modification in one or more of the following ways, that is to say:
- (i) by replacement of the phenyl portion of the phenethyl group by any heteromonocycle whether or not further substituted in the heterocycle;
- (ii) by substitution in the phenethyl group with alkyl, alkenyl, alkoxy, hydroxy, halo, haloalkyl, amino or nitro groups;
- (iii) by substitution in the piperidine ring with alkyl or alkenyl groups;
- (iv) by substitution in the aniline ring with alkyl, alkoxy, alkylenedioxy, halo or haloalkyl groups;
- (v) by substitution at the 4-position of the piperidine ring with any alkoxycarbonyl or alkoxyalkyl or acyloxy group;
- (vi) by replacement of the N-propionyl group by another acyl group.
- (g) Any substance structurally derived from 2-(3-hydroxycyclohexyl) phenol by substitution at the 5-position of the phenolic ring by alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2-(4-morpholinyl) ethyl, whether or not further substituted in the cyclohexyl ring to any extent.
- (h) Any substance structurally derived from 3-(1-naphthoyl) indole or 1H-indol-3-yl-(1-naphthyl) methane by substitution at the nitrogen atom of the indole ring by alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2-(4-morpholinyl) ethyl, whether or not further substituted in the indole ring to any extent and whether or not substituted in the naphthyl ring to any extent.
- (i) Any substance structurally derived from 3-(1-naphthoyl) pyrrole by substitution at the nitrogen atom of the pyrrole ring by alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2-(4-morpholinyl) ethyl, whether or not further substituted in the pyrrole ring to any extent and whether or not substituted in the naphthyl ring to any extent.
- (j) Any substance structurally derived from 1-(1-naphthylmethyl) indene by substitution at the 3-position of the indene ring by alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2-(4-morpholinyl) ethyl, whether or not further substituted in the indene ring to any extent and whether or not substituted in the naphthyl ring to any extent.
- (k) Any substance (not being a substance specified in Schedule 2) structurally derived from pethidine by modification in one or more of the following ways, that is to say:
- (i) by replacement of the 1-methyl group by an acyl, alkyl (whether or not unsaturated), benzyl or phenethyl group, whether or not further substituted;
- (ii) by substitution in the piperidine ring with alkyl or alkenyl groups or with a propano bridge, whether or not further substituted;
- (iii) by substitution in the 4-phenyl ring with alkyl, alkoxy, aryloxy, halo or haloalkyl groups;
- (iv) by replacement of the 4-ethoxycarbonyl by any other alkoxycarbonyl or any alkoxyalkyl or acyloxy group;
- (v) by formation of an N-oxide or of a quaternary base.
- (l) Any substance (not being methoxyphenamine) structurally derived from phenethylamine, an N-alkyl-phenethylamine, α-methylphenethylamine, an N-alkyl-α-methylphenethylamine, α-ethylphenethylamine, or an N-alkyl-α-ethylphenethylamine by substitution in the ring to any extent with alkyl, alkoxy, alkylenedioxy or halo substituents, whether or not further substituted in the ring by one or more other univalent substituents.
- (m) Any substance structurally derived from 3-phenylacetylindole by substitution at the nitrogen atom of the indole ring with alkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl or 2-(4-morpholinyl) ethyl, whether or not further substituted in the indole ring to any extent and whether or not substituted in the phenyl ring to any extent.
- (n) Any fungus containing any proportion of Psilocin or of an ester of Psilocin.
- (o) 1,2,3,4-Tetrahydronaphthalen-2-amine, 1,2-dihydronaphthalen-2-amine or 2,3-dihydro-1H-inden-2-amine or any substance structurally derived from 1,2,3,4-tetrahydronaphthalen-2-amine, 1,2-dihydronaphthalen-2-amine or 2,3-dihydro-1H-inden-2-amine by modification in any of the following ways:
- (i) by substitution in the phenyl ring to any extent with alkyl, alkoxy, alkenyl, alkynyl, alkylthio, alkylenedioxy, haloalkyl, hydroxy or halo substituents, whether or not further substituted by one or more other univalent substituents;
- (ii) by mono- or di-substitution at the nitrogen atom with alkyl, alkenyl, alkynyl or haloalkyl groups or by inclusion of the nitrogen atom in a cyclic structure.
- (p) Any substance structurally derived from tryptamine or from a ring-hydroxy tryptamine by substitution at the nitrogen atom of the side-chain with one or more alkyl substituents but no other substituent.
Any stereoisomeric form of a substance specified in paragraph 1.
Any ester or ether of a substance specified in paragraph 1 or 2.
Any salt of a substance specified in any of paragraphs 1, 2 or 3.
Any preparation or other product containing any proportion of a substance or product specified in any of paragraphs 1, 2, 3 or 4, not being a preparation specified in Schedule 5.
SCHEDULE 2
The following substances and products, namely:—
Acetorphine
Acetylmethadol
Alfentanil
Allylprodine
Alphacetylmethadol
Alphameprodine
Alphamethadol
Alphaprodine
(3-Amino-2,2-dimethylpropyl)4-aminobenzoate (otherwise known as desethyl dimethocaine)
Anileridine
Benzethidine
Benzylmorphine (3-benzylmorphine)
Betacetylmethadol
Betameprodine
Betamethadol
Betaprodine
Bezitramide
Carfentanil
Clonitazene
Cocaine
Codoxime
4-Cyano-2-dimethylamino-4,4-diphenylbutane
4-Cyano-1-methyl-4-phenylpiperidine
Desomorphine
Dextromoramide
Diamorphine
Diampromide
Diethylthiambutene
Difenoxin
Dihydroetorphine
Dihydromorphine
Dimenoxadole
Dimepheptanol
Dimethocaine
Dimethylthiambutene
Dioxaphetyl butyrate
Diphenoxylate
Dipipanone
Drotebanol
Ecgonine, and any derivative of ecgonine which is convertible to ecgonine or to cocaine
Ethylmethylthiambutene
Etonitazene
Etorphine
Etoxeridine
Fentanyl
Furethidine
Hydrocodone
Hydromorphinol
Hydromorphone
Hydroxypethidine
Isomethadone
Ketobemidone
Levomethorphan
Levomoramide
Levophenacylmorphan
Levorphanol
Lofentanil
Medicinal opium
Metazocine
Methadone
(8-Methyl-8-azabicyclo[3.2.1]octan-3-yl)-4-fluorobenzoate (otherwise known as fluorotropacocaine)
Methyldesorphine
Methyldihydromorphine (6-methyldihydromorphine)
2-Methyl-3-morpholino-1,1-diphenylpropane carboxylic acid
1-Methyl-4-phenylpiperidine-4-carboxylic acid
Metopon
Morpheridine
Morphine
Morphine methobromide, morphine N-oxide and other pentavalent nitrogen morphine derivatives
Myrophine
Nabilone
Nicomorphine
Noracymethadol
Norlevorphanol
Normethadone
Normorphine
Norpipanone
Oripavine
Oxycodone
Oxymorphone
Pethidine
Phenadoxone
Phenampromide
Phenazocine
Phencyclidine
Phenomorphan
Phenoperidine
1-Phenylcyclohexylamine
4-(1-Phenylcyclohexyl) morpholine
4-Phenylpiperidine-4-carboxylic acid ethyl ester
1-Piperidinocyclohexanecarbonitrile.
Piminodine
Piritramide
Proheptazine
Properidine
Racemethorphan
Racemoramide
Racemorphan
Remifentanil
Sufentanil
Tapentadol
Thebacon
Thebaine
4-[1-(2-Thienyl) cyclohexyl]morpholine.
1-[1-(2-Thienyl) cyclohexyl]pyrrolidine
Tilidine
Trimeperidine.
Any stereoisomeric form of a substance specified in paragraph 1 not being dextromethorphan or dextrorphan.
Any ester or ether of a substance specified in paragraph 1 or 2, not being a substance specified in paragraph 6.
Any salt of a substance specified in any of paragraphs 1, 2 or 3.
Any preparation or other product containing any proportion of a substance or product specified in any of paragraphs 1, 2, 3 or 4, not being a preparation specified in Schedule 5.
The following substances and products, namely:
Acetyldihydrocodeine
Amineptine
Amphetamine
Amphetaminil
Benzphetamine
Buprenorphine
Butorphanol
Codeine
Dexamphetamine
Dextropropoxyphene
Dihydrocodeine
N-Ethylamphetamine
Ethylmorphine (3-ethylmorphine)
Fenethylline
Glutethimide
4-Hydroxybutanoic acid
Lefetamine
Lisdexamphetamine
Mecloqualone
Methaqualone
Methylamphetamine
Methylphenidate
Nalbuphine
Nicocodine
Nicodicodine (6-nicotinoyldihydrocodeine)
Norcodeine
Phendimetrazine
Phenmetrazine
Pholcodine
Propiram
Quinalbarbitone
Zipeprol.
Any stereoisomeric form of a substance specified in paragraph 6.
Any salt of a substance specified in paragraph 6 or 7.
Any preparation or other product containing any proportion of a substance or product specified in any of paragraphs 6, 7 or 8 not being a preparation specified in Schedule 5.
SCHEDULE 3
The following substances, namely:—
- (a) 2-Benzhydrylpiperidine (otherwise known as desoxypipradrol)
Cathine
1-(3-Chlorophenyl)-4-(3-chloropropyl) piperazine
1-(3-Chlorophenyl) piperazine
Chlorphentermine
Diethylpropion
Ethchlorvynol
Ethinamate
Flunitrazepam
Ketamine
Mazindol
Mephentermine
Meprobamate
Methyprylone
Pemoline
Pentazocine
Phentermine
Pipradrol
Temazepam
- (b) any substance (not being quinalbarbitone) structurally derived from barbituric acid by disubstitution at the 5,5 positions, whether or not there is also substitution at the 1-position by a methyl substituent.
Any stereoisomeric form of a substance specified in paragraph 1, not being phenylpropanolamine.
Any salt of a substance specified in paragraphs 1 or 2.
Any preparation or other product containing any proportion of a substance or product specified in paragraphs 1, 2 or 3, not being a preparation specified in Part 2 of Schedule 4 or in Schedule 5.
SCHEDULE 4
PART 1
The following substances, namely:—
Alprazolam
Bromazepam
Brotizolam
Camazepam
Chlordiazepoxide
Clobazam
Clonazepam
Clorazepic Acid (clorazepate)
Clotiazepam
Cloxazolam
Delorazepam
Diazepam
Estazolam
Ethyl loflazepate
Fludiazepam
Flurazepam
Halazepam
Haloxazolam
Ketazolam
Loprazolam
Lorazepam
Lormetazepam
Medazepam
Midazolam
Nimetazepam
Nitrazepam
Nordazepam
Oxazepam
Oxazolam
Phenazepam
Pinazepam
Prazepam
Tetrazepam
Triazolam
Zaleplon
Zolpidem
Zopiclone.
Any stereoisomeric form of a substance specified in paragraph 1.
Any salt of a substance specified in paragraphs 1 or 2.
Any preparation or other product containing any proportion of a substance or product specified in any of paragraphs 1 to 3, not being a preparation specified in Schedule 5.
An extract of Cannabis which—
- (a) is a medicinal product for human use which has been granted a marketing authorisation and which is presented as a liquid formulation for administration to a person through a meter dose pump as a mucosal mouth spray, and
- (b) has a concentration of not more than 30 milligrams of cannabidiol per millilitre, and not more than 30 milligrams of delta-9-tetrahydrocannabinol per millilitre, where the ratio of cannabidiol to delta-9-tetrahydrocannabinol is between 0.7 to 1.3.
Any stereoisomeric form of a substance specified in paragraph 5.
Any preparation or other product containing any proportion of a substance or product specified in any of paragraphs 5 or 6, not being a preparation specified in Schedule 5.
PART 2
The following substances namely:-
Aminorex
Fencamfamin
Fenproporex
Mefenorex
Mesocarb
Propylhexedrine
Pyrovalerone
Selegiline
Any stereoisomeric form of a substance specified in paragraph 1.
Any salt of a substance specified in paragraphs 1 or 2.
Any preparation or other product containing any proportion of a substance or product specified in any of paragraphs 1 to 3, not being a preparation specified in Schedule 5.
Any preparation containing not more than 100 milligrams of methylphenobarbitone or of phenobarbitone (calculated in either case in terms of base) per dosage unit and no other controlled drug and which in the case of an undivided preparation has a concentration of not more than 0.5 per cent of phenobarbitone (calculated as base) and no other controlled drug.
SCHEDULE 5
(a) Any preparation of one or more of the substances to which this paragraph applies (not being a preparation designed for administration by injection) when compounded with one or more other ingredients and which contains a total of not more than 100 milligrams of the substance or substances (calculated as base) per dosage unit and which in the case of an undivided preparation has a total concentration of not more than 2.5 per cent of the substance or substances (calculated as base).
- (b) The substances to which this paragraph applies are acetyldihydrocodeine, codeine, ethylmorphine (3-ethylmorphine), nicocodine, nicodicodine (6-nicotinoyldihydrocodeine), norcodeine, pholcodine and their respective salts.
Any preparation of dihydrocodeine (not being a preparation designed for administration by injection) containing, per dosage unit, not more than 10 milligrams of dihydrocodeine (calculated as base) and which in the case of an undivided preparation has a concentration of not more than 1.5 per cent of dihydrocodeine (calculated as base).
Any preparation of cocaine containing not more than 0.1 per cent of cocaine (calculated as cocaine base), being a preparation which is compounded with one or more other ingredients in such a way that the cocaine cannot be readily recovered.
Any preparation of medicinal opium or of morphine (not being a preparation designed for administration by injection) containing, in either case, not more than 0.2 per cent of morphine (calculated as anhydrous morphine base), being a preparation which is compounded with one or more other ingredients in such a way that the opium or morphine cannot be readily recovered.
Any preparation of dextropropoxyphene, being a preparation designed for oral administration, containing not more than 135 milligrams of dextropropoxyphene (calculated as base) per dosage unit or with a total concentration of not more than 2.5 per cent, (calculated as base) in undivided preparations.
Any preparation of difenoxin containing, per dosage unit, not more than 0.5 milligrams of difenoxin and a quantity of atropine sulphate equivalent to at least 5 per cent of the dose of difenoxin.
Any preparation of diphenoxylate containing, per dosage unit, not more than 2.5 milligrams of diphenoxylate (calculated as base), and a quantity of atropine sulphate equivalent to at least 1 per cent of the dose of diphenoxylate.
Any preparation of propiram containing, per dosage unit, not more than 100 milligrams of propiram (calculated as base) and which is compounded with at least the same amount, by weight, of methylcellulose.
Any powder of ipecacuanha and opium comprising 10 per cent powdered opium, 10 per cent powdered ipecacuanha root, both well mixed with the remaining 80 per cent consisting of any other powdered ingredient which contains no controlled drug.
Any mixture containing one or more of the preparations specified in this Schedule, being a mixture of which none of the other ingredients is a controlled drug.
SCHEDULE 6 Form of Register
Class of Drug
Product
(Insert name, form, strength and pack size as necessary)
Date on which supply received or transaction effected
Name and address of person from whom obtained or to whom supplied
Authority of person supplied to be in possession
Amount
Stock Balance
Obtained
Supplied
SCHEDULE 7 Form of Register
PART 1 Entries to be made in case of obtaining.
Date on which supply received
Name
Address
Amount obtained
Form in which obtained
Of person or firm from whom
PART 2 Entries to be made in case of supply
Date on which the transaction was effected
Name
Address
Particulars as to licence or authority of person or firm supplied to be in possession
Amount supplied
Form in which supplied
Stock Balance
Of person or firm supplied
SCHEDULE 8 DRUGS WHICH PRACTITIONERS WHO ARE REGISTERED NURSES OR REGISTERED MIDWIVES MAY PRESCRIBE WITHIN SCHEDULES 2 AND 3
PART 1 Drugs for pain relief in hospital
| Drug | Route of administration |
| Buprenorphine | Transdermal |
| Codeine phosphate | Oral |
| Dihydrocodeine | Oral |
| Fentanyl | Intranasal, intravenous, transdermal, transmucosal, subcutaneous, sublingual/buccal |
| Morphine sulphate | Intramuscular, intravenous, oral, subcutaneous |
| Morphine tartrate | Intramuscular, intravenous, subcutaneous |
| Oxycodone | Oral, subcutaneous, intravenous |
| Pethidine | Intramuscular, intravenous, subcutaneous |
PART 2 Drugs for palliative care
| Drug | Route of administration |
| Buprenorphine | Transdermal |
| Codeine phosphate | Oral |
| Fentanyl | Intranasal, Intravenous, transdermal, transmucosal, subcutaneous, sublingual/buccal |
| Hydromorphone | Oral, subcutaneous |
| Methylphenidate | Oral |
| Morphine sulphate | Intramuscular, oral, subcutaneous |
| Morphine tartrate | Intramuscular, subcutaneous |
| Oxycodone | Oral, subcutaneous |
PART 3 Drugs for purposes of midwifery
| Drug | Route of administration |
| Pethidine | Intramuscular |
PART 4 Drugs for neonatal care
| Drug | Route of administration |
| Fentanyl | Intravenous, transdermal, transmucosal |
| Morphine sulphate | Intramuscular, intranasal, intravenous, oral, subcutaneous |
| Morphine tartrate | Intramuscular, intravenous, subcutaneous |
PART 5 Drugs for use in mental health or intellectual disability
| Drug | Route of administration |
| Methylphenidate | Oral |
SCHEDULE 9 Provisions of revoked Regulations of 1988 and corresponding provisions in these Regulations
| Column 1 | Column 2 | Column 3 | Column 4 |
| Old Number | Old Title | New Number | New Title |
| 1 | Citation | 1 | Citation and Commencement |
| 2 | Revocations | ||
| 3 | Interpretation | 2 | Interpretation |
| 3A | Provisions applicable to practitioners who are registered nurses | 3 | Provisions applicable to practitioners who are registered nurses or registered midwives |
| 3B | Person may refuse to supply drug if reasonable cause to believe conditions referred to in article 3A have not been satisfied | 4 | Person may refuse to supply drug if reasonable cause to believe conditions referred to in regulation 3 have not been satisfied |
| 4 | General prohibition | 5 | General prohibition |
| 5 | Licences | 6 | Licences |
| 6 | Administration | 7 | Administration |
| 7 | Exemption for practitioners, pharmacists etc. | 8 | Exemption for practitioners, pharmacists etc. |
| 8 | Supply in hospitals etc. | 9 | Supply |
| 9 | General Exemptions | 10 | General Exemptions |
| 11 | Exemption to possess butan-1,4-diol or dihydrofuran-2(3H)-one | ||
| 10 | Exemption for midwives in respect of pentazocine and pethidine. | 12 | Exemption for midwives in respect of pentazocine and pethidine. |
| 11 | General authorities | 13 | General authorities |
| 12 | Documents to be obtained by a supplier | 14 | Documents to be obtained by a supplier |
| 13 | Form of prescriptions | 15 | Form of prescriptions |
| 14 | Supply on prescriptions | 16 | Supply on prescription |
| 15 | Marking of containers | 17 | Marking of containers |
| 15A | 18 | Documents required for export of controlled drugs | |
| 16 | Keeping of registers for drugs in Schedules 1 and 2 | 19 | Keeping of registers for drugs in Schedules 1 and 2 |
| 17 | Record-keeping in particular cases for drugs in Schedule 2 | 20 | Record-keeping in particular cases for drugs in Schedule 2 |
| 18 | Keeping of records for drugs in Schedules 3 and 4 | 21 | Keeping of records for drugs in Schedules 3 and 4 |
| 19 | Preservation of registers, etc. | 22 | Preservation of registers, etc. |
| 20 | Preservation of records for drugs in schedules 3 and 5 | 23 | Preservation of records for drugs in schedules 3, Part 1 of Schedule 4, and Schedule 5 |
| 21 | Furnishing of information with respect to controlled drugs | 24 | Furnishing of information with respect to controlled drugs |
| 22 | Destruction of certain drugs | 25 | Destruction of certain drugs |
| 23 | Disposal of certain drugs on cessation of business | 26 | Disposal of certain drugs on cessation of business |
| 24 | Forged, etc. prescriptions | 27 | Forged, etc. prescriptions |
| 25 | Publication, sale, etc. of certain books, periodicals and other publications | 28 | Publication, sale etc. of certain books, periodicals and other publications |
| 26 | Amendment of the Misuse of Drugs (safe Custody) Regulations 1982 ( S.I. No. 321 of 1982 ) | ||
| 29 | References to revoked Regulations of 1988 in other enactments | ||
| 27 | Transitional provisions | 30 | Transitional provisions |
GIVEN under my Hand,
4 May 2017.
CATHERINE BYRNE,
Minister of State at the Department of Health.
EXPLANATORY NOTE
(This note is not part of the Instrument and does not purport to be a legal interpretation.)
These Regulations apply controls to the groups of drugs specified in Schedules 1 to 5 of the Regulations (being drugs to which the Misuse of Drugs Acts 1977 to 2016 apply). The effect of the Regulations is to impose restrictions on the production, supply, importation and exportation of the drugs in question, which vary according to the extent to which these drugs are used for medical or scientific purposes and having regard to the likelihood of their being abused. Appropriate exemptions are provided to cover legitimate use for professional purposes by doctors, pharmacists, nurses and midwives, veterinary practitioners, prison officers, etc. and in other specified circumstances.
In addition to these controls the Regulations specify the classes of persons who may have controlled drugs in their possession and the circumstances in which such possession would not be in contravention of the Act.
The Regulations contain other miscellaneous provisions such as requirements as to the form of prescriptions for controlled drugs, the keeping of books and records, proper documentation relating to export of controlled drugs, arrangements for destruction or disposal of such drugs, and provisions regarding possession of forged prescriptions.
The Regulations also prescribe certain controlled drugs for the purposes of section 5 of the Misuse of Drugs Act 1984 .
The Regulations confer authority on certain inspectors, in the Department of Agriculture, Food and the Marine, to lawfully possess Cannabis (hemp) in the course of their duties while monitoring and sampling for the purpose of the relevant EU scheme involving the grant of aid for the production of hemp fibre.
Footnotes
OJ No. L 311, 28.11.2001, p. 67.
OJ. No. L 136, 30.4.2004, p. 1.
OJ No. L 1, 3.1.1994, p. 572.
OJ No. L 311, 28.11.2001, p. 1.
OJ No. L. 227, 31.7.2014, p. 69.
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