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Statutory Instruments

2005 No. 765

MEDICINES

The Medicines for Human Use (Prescribing) Order 2005

Made

16th March 2005

Laid before Parliament

17th March 2005

Coming into force

7th April 2005

As respects England, Scotland and Wales, the Secretary of State in England, and , as respects Northern Ireland, the Department of Health, Social Services and Public Safety and the Department of Agriculture and Rural Development, acting jointly in exercise of the powers conferred upon them by sections 15(1), 58(1), (4), (4A), (4B) and (5) and 129(4) of the Medicines Act 1968( 1 ), or, as the case may be, those powers conferred by the said provisions and now vested in them( 2 ), and of all other powers enabling them in that behalf, after consulting such organisations as appear to them to be representative of interests likely to be substantially affected by this Order, pursuant to section 129(6) of that Act, and after consulting and taking into account the advice of the Committee on Safety of Medicines, pursuant to sections 58(6) and 129(7) of that Act, and taking into account the advice of the Medicines Commission, pursuant to section 129(7) of that Act, hereby make the following Order:—

Citation, commencement, extent and interpretation

1. —(1) This Order may be cited as the Medicines for Human Use (Prescribing) Order 2005 and shall come into force on 7th April 2005.

(2) Subject to paragraph (3), this Order applies to the whole of the United Kingdom.

(3) Paragraphs (2) and (3) of article 2 extend to Scotland only.

(4) In this Order—

the Act” means the Medicines Act 1968;

first level nurse” means a person registered in Sub-Part 1 of the Nurses' Part of the professional register;

medicinal product” includes any article or substance in respect of which section 58 of the Act has effect by virtue of an order made under section 104 of the Act, but does not include—

(a)

a medicinal product which is a veterinary drug as defined in section 132(1) of the Act; or

(b)

an article or substance in respect of which section 58 has such effect where that article or substance is only to be administered to animals;

the POM Order” means the Prescription Only Medicines (Human Use) Order 1997( 3 );

professional register” means the register maintained by the Nursing and Midwifery Council under article 5 of the Nursing and Midwifery Order 2001( 4 );

registered midwife” means a person registered in the Midwives' Part of the professional register;

relevant register” means —

(a)

in relation to a first level nurse or registered midwife, the professional register;

(b)

in relation to a pharmacist, the register maintained in pursuance of section 2(1) of the Pharmacy Act 1954( 5 ) or the register maintained in pursuance of Articles 6 and 9 of the Pharmacy (Northern Ireland) Order 1976( 6 ); and

(c)

in relation to a person whose name is registered in the part of the register maintained by the Health Professions Council in pursuance of article 5 of the Health Professions Order 2001( 7 ) relating to—

(i)

chiropodists and podiatrists;

(ii)

physiotherapists;

(iii)

radiographers: diagnostic or therapeutic,

that register;

supplementary prescriber” means—

(a)

a first level nurse;

(b)

a pharmacist;

(c)

a registered midwife; or

(d)

a person whose name is registered in the part of the register maintained by the Health Professions Council in pursuance of article 5 of the Health Professions Order 2001 relating to—

(i)

chiropodists and podiatrists;

(ii)

physiotherapists; or

(iii)

radiographers: diagnostic or therapeutic,

against whose name is recorded in the relevant register an annotation or entry signifying that he is qualified to order drugs, medicines and appliances as a supplementary prescriber.

Exemption to the restrictions imposed by sections 7 and 8 of the Medicines Act 1968

2. —(1) The restrictions imposed by sections 7 and 8 of the Medicines Act 1968 do not apply to anything which is done in a registered pharmacy, a hospital or a health centre and is done there by or under the supervision of a pharmacist and consists of—

(a) preparing or dispensing a medicinal product in accordance with a prescription given by a supplementary prescriber; or

(b) procuring the preparation or dispensing of a medicinal product in accordance with a prescription given by a supplementary prescriber.

(2) The restrictions imposed by sections 7 and 8 of the Medicines Act 1968 do not apply to anything which is done in a care home service and is done there by or under the supervision of a pharmacist and consists of—

(a) preparing or dispensing a medicinal product in accordance with a prescription given by a supplementary prescriber; or

(b) procuring the preparation or dispensing of a medicinal product in accordance with a prescription given by a supplementary prescriber.

(3) In paragraph (2), “a care home service” has the meaning given by section 2(3) of the Regulation of Care (Scotland) Act 2001( 8 ).

Amendment of article 1 of the POM Order

3. In article 1 of the POM Order (citation, commencement and interpretation), in paragraph (2)—

(a) in the definition of “relevant register”—

(i) in paragraph (a) omit “and”;

(ii) in paragraph (b), after “the Pharmacy (Northern Ireland) Order 1976;” insert “and”; and

(iii) after paragraph (b), insert—

(c) in relation to a person whose name is registered in the part of the register maintained by the Health Professions Council in pursuance of article 5 of the Health Professions Order 2001 relating to—

(i) chiropodists and podiatrists;

(ii) physiotherapists; or

(iii) radiographers: diagnostic or therapeutic;

that register ;

(b) in the definition of “supplementary prescriber”( 9 )—

(i) in paragraph (b), omit “or”;

(ii) in paragraph (c), after “a registered midwife,” insert “or”;

(iii) after paragraph (c), insert—

(d) a person whose name is registered in the part of the register maintained by the Health Professions Council in pursuance of article 5 of the Health Professions Order 2001 relating to—

(i) chiropodists and podiatrists;

(ii) physiotherapists; or

(iii) radiographers: diagnostic or therapeutic; ; and

(c) after “an annotation”, insert “or entry”.

Amendment of article 3B of the POM Order

4. In article 3B( 10 ) of the POM Order (prescribing and administration by supplementary prescribers), in paragraph (3), omit sub-paragraph (b).

Amendment of article 13A of the POM Order

5. In article 13A( 11 ) of the POM Order (exemptions relating to prescriptions given by nurses), in paragraph (1)—

(a) in paragraph (b), omit “or”;

(b) in paragraph (c), after “a registered midwife;”, insert “or”;

(c) after paragraph (c), insert—

(d) a person whose name is registered in the part of the register maintained by the Health Professions Council in pursuance of article 5 of the Health Professions Order 2001 relating to—

(i) chiropodists and podiatrists;

(ii) physiotherapists; or

(iii) radiographers: diagnostic or therapeutic, .

Amendment of article 15 of the POM Order

6. For Article 15 of the POM Order (prescriptions)( 12 ), substitute the following article —

15. —(1) For the purposes of section 58(2)(a), and subject to paragraph (3), a prescription only medicine shall not be taken to be sold or supplied in accordance with a prescription given by an appropriate practitioner unless the conditions specified in paragraph (2) are fulfilled.

(2) The conditions referred to in paragraph (1) are that the prescription—

(a) shall be signed in ink with his own name by the appropriate practitioner giving it;

(b) shall, without prejudice to sub-paragraph (a), be written in ink or otherwise so as to be indelible, unless it is a health prescription which is not for a controlled drug specified in Schedule 1, 2 or 3 to the Misuse of Drugs Regulations ( 13 ) , in which case it may be written by means of carbon paper or similar material;

(c) shall contain the following particulars—

(i) the address of the appropriate practitioner giving it,

(ii) the appropriate date,

(iii) such particulars as indicate whether the appropriate practitioner giving it is a doctor, a dentist, a supplementary prescriber, a district nurse/health visitor prescriber,an extended formulary nurse prescriber, a veterinary surgeon or a veterinary practitioner,

(iv) where the appropriate practitioner giving it is a doctor, dentist, a supplementary prescriber, a district nurse/health visitor prescriber, or an extended formulary nurse prescriber, the name, address and the age, if under 12, of the person for whose treatment it is given, and

(v) where the appropriate practitioner giving it is a veterinary surgeon or a veterinary practitioner, the name and the address of the person to whom the prescription only medicine is to be delivered and a declaration by the veterinary surgeon or veterinary practitioner giving it that the prescription only medicine is prescribed for an animal or herd under his care;

(d) shall not be dispensed after the end of the period of 6 months from the appropriate date, unless it is a repeatable prescription in which case it shall not be dispensed for the first time after the end of that period nor otherwise than in accordance with the directions contained in the repeatable prescription;

(e) in the case of a repeatable prescription which does not specify the number of times it may be dispensed, shall not be dispensed on more than two occasions unless it is a prescription for an oral contraceptive in which case it may be dispensed 6 times before the end of the period of 6 months from the appropriate date.

(3) For the purposes of paragraph (1) the prescription may, as an alternative to fulfilling the conditions specified in paragraph (2)(a) and (b), fulfil instead the conditions specified in paragraph (4), unless the prescription is a health prescription for a controlled drug specified in Schedule 1, 2 or 3 to the Misuse of Drugs Regulations or is given by a veterinary surgeon or a veterinary practitioner.

(4) The conditions referred to in paragraph (3) are that the prescription shall be created in electronic form and signed with an advanced electronic signature and transferred to the person by whom it is dispensed as an electronic communication (including where it is so transferred through one or more intermediaries).

(5) The prohibition on sale or supply imposed by section 58(2)(a) shall not apply where a prescription only medicine is sold or supplied other than in accordance with a prescription given by an appropriate practitioner and –

(a) the reason the sale or supply is not in accordance with such a prescription is that a condition specified in paragraph (2) or (4) is not fulfilled; and

(b) the person selling or supplying the prescription only medicine has exercised all due diligence and believes on reasonable grounds that the condition is fulfilled.

(6) In paragraph (2) “appropriate date” means—

(a) in the case of a health prescription, the date on which it was signed by the appropriate practitioner giving it or a date indicated by him as being the date before which it shall not be dispensed; and

(b) in every other case, the date on which the prescription was signed by the appropriate practitioner giving it,

and, for the purposes of sub-paragraphs (d) and (e) of that paragraph, where the health prescription bears both the date on which it was signed and a date indicated as being that before which it shall not be dispensed, the appropriate date is the later of those dates.

(7) In this Article—

“advanced electronic signature” means an electronic signature which is—

(a)

uniquely linked to the signatory,

(b)

capable of identifying the signatory,

(c)

created using means that the signatory can maintain under his sole control, and

(d)

which is linked to the data to which it relates in such a manner that any subsequent change of data is detectable;

“electronic communication” means a communication transmitted (whether from one person to another, from one device to another or from a person to a device or vice versa)—

(a)

by means of a telecommunication system (within the meaning of the Telecommunications Act 1984 ( 14 ) , or

(b)

by other means but while in an electronic form; and

“signatory” means the appropriate practitioner giving the prescription. .

Amendment of Schedule 3A to the POM Order

7. In the table in Schedule 3A to the POM Order( 15 ), (substances which may be prescribed, administered or directed for administration by extended formulary nurse prescribers)—

(a) in column 1 insert, at the appropriate place in the alphabetical order of the entries as they appear in that column, the entry set out in column 1 below, and in column 2, insert, against that entry, the corresponding entry in column 2 below—

Column 1 Column 2
Acetylcysteine Parenteral
Adrenaline Parenteral
Alteplase Parenteral
Amiodarone Parenteral
Bemiparin sodium Parenteral
Benzatropine mesilate Parenteral
Calcipotriol External
Calcitriol External
Cefotaxime sodium Parenteral
Ceftriaxone Sodium Parenteral
Certoparin sodium Parenteral
Chlorphenamine maleate Parenteral
Cimetidine Parenteral
Cyclizine hydrochloride Oral
Cyclizine lactate Parenteral
Dalteparin sodicum Parenteral
Dexamethasone sodium phosphate Oral
Dextran 70 Parenteral
Dolesetron mesilate Oral and parenteral
Enoxaparin Parenteral
Furosemide Oral and parenteral
Gelatin 3.5 – 4% Parenteral
Glucose 5% Parenteral
Glucose 5% with Potassium (K + 40 mmol/L) ready made infusion bag Parenteral
Granisetron hydrochloride Parenteral
Heparin sodium Parenteral for the purpose of cannulae flushing
Hexastarch Parenteral
Human soluble insulin Parenteral
Hydroxyethl starch Parenteral
Levomepromazine Oral and parenteral
Naloxone Parenteral
Omeprazole Oral
Omeprazole sodium Parenteral
Ondansetron Hydrochloride Oral and parenteral
Oxbuprocaine hydrochloride Ophalmic
Pentastarch Parenteral
Prilocaine External and parenteral
Prochlorperazine mesilate Oral and rectal
Prochlorperazine maleate Oral, rectal and buccal
Proxymetacaine hydrochloride Ophthalmic
Reteplase Parenteral
Sodium chloride 0.9% Parental, for reconstitution of injections and for the purpose of cannulae flushing
Sodium chloride 0.9% & Glucose 5% ready made infusion bag Parenteral
Sodium chloride 0.45% & Glucose 5% ready made infusion bag Parenteral
Sodium chloride 0.9% with Potassium (K + 40 mmol/L) ready made infusion bag Parenteral
Sodium chloride 0.45% and Glucose 5% with Potassium 20mmol per 500 ml ready made infusion bag Parenteral
Streptokinase Parenteral
Tacalcitol External
Tenecteplase Parenteral
Tetanus immunoglobulin Parenteral
Tetracaine External
Tinzaparin sodium Parenteral
Tropicamide Ophthalmic
Tropisetron hydrochloride Parenteral
Unfractionated Heparin Parenteral
Vaccine – Combined Tetanus, diphtheria, acullular pertussis, inactivated poliomyelitis and haemophilus influenza type B Parenteral
Vaccine – Inactivated Poliomyelitis Parenteral
Vaccine – Meningococcal Polysaccharide A, C, W135 and Y Parenteral

(b) in the entry for “Beclometasone dipropionate”, in column 2, after “nasal” add “inhalation”;

(c) in the entry for “Budesonide”, in column 2, after “Nasal” add “inhalation”;

(d) omit the entry for “Cyclizine”;

(e) in the entry for “Diazepam”( 16 ), in column 2, omit “in palliative care”;

(f) in the entry for “Diclofenac sodium”( 17 ), in column 2, after “oral” omit “or” and after “rectal” add “or ophthalmic”;

(g) in the entry for “Domperidone”, in column 2, omit “in palliative care”;

(h) in the entry for “Domperidone maleate”, in column 2, omit “in palliative care”;

(i) in the entry for “Flucloxacillin sodium”, in column 2, after “oral” add “or parenteral”;

(j) in the entry for “Hydrocortisone sodium succinate”, in column 2, after “lozenges” add “or parenteral”;

(k) in the entry for “Ipratropium bromide”, in column 2, after “nasal” add “inhalation”;

(l) in the entry for “Lorazepam”( 18 ), in column 2, omit “in palliative care”;

(m) in the entry for “metoclopramide hydrochloride”, in column 2, omit “in palliative care”;

(n) in the entry for “Midazolam”( 19 ), in column 2, omit “in palliative care”;

(o) in the entry for “Ranitidine hydrochloride”, in column 2, after “Oral” insert “or parenteral”.

Amendment of Schedule 5 of the POM Order

8. In the table in Schedule 5 to the POM Order (exemption from restrictions on sale or supply), in paragraph 5 of Part I, in column 2, in sub-paragraph (c)—

(a) omit “Atropine sulphate”, “Bethanecol chloride”, and “Carbachol”;

(b) after “Cyclopentolate hydrochloride” insert “Fusidic Acid”; and

(c) omit “Homatrophine hydrobromide”, “Naphazoline hydrochloride”, “Naphazoline Nitrate”, “Physostigmine salicylate”, “Philocarpine hydrochloride”, and Philocarpine nitrate”.

Signed by authority of the Secretary of State for Health

Warner

Parliamentary Under Secretary of State,

Department of Health

16th March 2005

Sealed with the Official Seal of the Department of Health, Social Services and Public Safety

Deirdre Kenny

A Senior Officer of the,

Department of Health, Social Services and Public Safety

15th March 2005

Sealed with the Official Seal of the Department of Agriculture and Rural Development

Gerald Lavery

A Senior Officer of the

Department of Agriculture and Rural Development

15th March 2005

( 1 )

1968 (c. 67) . The expression “the appropriate Ministers” and the expression “the Ministers”, which are relevant to the powers being exercised in the making of this Order, are defined in section 1 of that Act as amended by article 2(2) of, and Schedule 1 to, S.I. 1969/388 , by article 5 of, and paragraph 1(1) of the Schedule to, S.I. 1999/3142 , and by article 5(1) of, and paragraph 15 of Schedule 1 to, S.I. 2002/794 ; section 58 of that Act was amended by section 1 of the Prescription by Nurses etc. Act 1992 (c. 28) and by section 63 of the Health and Social Care Act 2001 (c. 15) and by article 54(3) of, and paragraph 2(b) of Schedule 5 to, S.I. 2002/253 .

( 2 )

In the case of the Secretary of State concerned with health in England, by virtue of article 2(2) of, and Schedule 1 to S.I. 1969/388 , and articles 2(1) and 5 of, and paragraph 1(1) of the Schedule to, S.I. 1999/3142 ; and in the case of the Department of Health, Social Services and Public Safety and the Department of Agriculture and Rural Development, by virtue of the powers vested in the Ministers in charge of those Departments by virtue of section 95(5) of, and paragraph 10 of Schedule 12 to, the Northern Ireland Act 1998 (c. 47) which may now be exercised by the Departments by virtue of section 1(8) of, and paragraph 4(1)(b) of the Schedule to, the Northern Ireland Act 2000 (c. 1) ; the Departments were renamed by virtue of Article 3(4) and (6) of S.I. 1999/283 (N.I.I.) .

( 3 )

S.I. 1997/1830 ; relevant amending instruments are S.I. 1998/1178 , 2000/2899 , 2001/2889 , 2002/549 , 2003/696 and 2915 , and 2004/2 , 696 , 1031 , 1189 , 1771 and 2693 .

( 4 )

S.I. 2002/253 .

( 7 )

S.I. 2002/254 .

( 8 )

2001 asp8 .

( 9 )

The definition of “supplementary prescriber” was inserted by S.I. 2003/696 and amended by S.I. 2004/1771 .

( 10 )

Article 3B was inserted by S.I. 2003/696 and amended by S.I. 2004/1031 .

( 11 )

Article 13A was inserted by S.I. 2002/549 and amended by S.I. 2003/696 .

( 12 )

Relevant amending instruments are S.I. 2001/2889 , 2002/549 , 2003/696 .

( 13 )

S.I. 2001/3998 .

( 15 )

Schedule 3A was inserted by S.I. 2002/549 , and amended by S.I. 2003/696 and 2915 , and 2004/2 , 1189 and 2693 .

( 16 )

The entry for “Diazepam” was inserted by S.I. 2003/2915 .

( 17 )

The entry for “Diclofenac Sodium” was inserted by S.I. 2004/2 .

( 18 )

The entry for “Lorazepam” was inserted by S.I. 2003/2915 .

( 19 )

The entry for “Midazolam” was inserted by S.I. 2003/2915 .

( 20 )

S.I.. 2001/2889 .

Status: This is the original version (as it was originally made). This item of legislation is currently only available in its original format.
The Medicines for Human Use (Prescribing) Order 2005 (2005/765)

Displaying information

Status of this instrument

footnotecommentarytransitional and savingsin force statusrelated provisionsgeo extentinsert/omitsource countin force adj
Defined TermSection/ArticleIDScope of Application
a care home serviceart. 2.a_care_hom_rtdpjDh
Beclometasone dipropionateart. 7.Beclometas_rtN1Zb4
Budesonideart. 7.Budesonide_rtcMpuO
first level nurseart. 1.first_leve_rttlgSN
Flucloxacillin sodiumart. 7.Flucloxaci_rt4Q1mm
Hydrocortisone sodium succinateart. 7.Hydrocorti_rtGGJrp
inhalationart. 7.inhalation_rtPStev
inhalationart. 7.inhalation_rtseNM2
inhalationart. 7.inhalation_rtx0wPB
Ipratropium bromideart. 7.Ipratropiu_rtlPXaA
lozengesart. 7.lozenges_rtmGVmK
medicinal productart. 1.medicinal__rtQKGA5
nasalart. 7.nasal_rt0fzJC
Nasalart. 7.Nasal_rtQ9BS3
nasalart. 7.nasal_rtPRCuF
or parenteralart. 7.or_parente_rty5DW4
or parenteralart. 7.or_parente_rtK1NKI
oralart. 7.oral_rtkRkWZ
Philocarpine hydrochlorideart. 8.Philocarpi_rtD3Dah
Physostigmine salicylateart. 8.Physostigm_rtcStE9
professional registerart. 1.profession_rtEsV3Z
registered midwifeart. 1.registered_rtrUn4u
relevant registerart. 1.relevant_r_rt7vOLQ
supplementary prescriberart. 1.supplement_rtAYNL0
the Actart. 1.the_Act_rtPuUKu
the POM Orderart. 1.the_POM_Or_rtWmeNj
Changes that affect Made by
Sort descending by Changed Legislation Sort descending by Year and Number Changed Provision Type of effect Sort descending by Affecting Legislation Title Sort descending by Year and Number Affecting Provision Sort descending by Changes made to website text Note
The Medicines for Human Use (Prescribing) Order 2005 2005 No. 765 Order revoked The Human Medicines Regulations 2012 2012 No. 1916 Sch. 35 Not yet
The Medicines for Human Use (Prescribing) Order 2005 2005 No. 765 art. 1(4) words substituted The Health and Social Care Act 2012 (Consequential Provision—Social Workers) Order 2012 2012 No. 1479 Sch. para. 45(a) Not yet
The Medicines for Human Use (Prescribing) Order 2005 2005 No. 765 art. 1(4) words substituted The Health and Social Care Act 2012 (Consequential Provision—Social Workers) Order 2012 2012 No. 1479 Sch. para. 45(b) Not yet
The Medicines for Human Use (Prescribing) Order 2005 2005 No. 765 art. 2(3) words substituted The Public Services Reform (Scotland) Act 2010 (Consequential Modifications of Enactments) Order 2011 2011 No. 2581 Sch. 2 para. 46 Not yet
The Medicines for Human Use (Prescribing) Order 2005 2005 No. 765 art. 1(4) words substituted The Pharmacy Order 2010 2010 No. 231 Sch. 4 para. 48 Not yet
The Medicines for Human Use (Prescribing) Order 2005 2005 No. 765 art. 1(4) words substituted The Pharmacists and Pharmacy Technicians Order 2007 2007 No. 289 Sch. 1 para. 43 Not yet
The Medicines for Human Use (Prescribing) Order 2005 2005 No. 765 art. 1(4) words inserted The Medicines for Human Use (Prescribing) (Miscellaneous Amendments) Order 2005 2005 No. 1507 art. 2(a) Not yet
The Medicines for Human Use (Prescribing) Order 2005 2005 No. 765 art. 1(4)(b) word omitted The Medicines for Human Use (Prescribing) (Miscellaneous Amendments) Order 2005 2005 No. 1507 art. 2(b)(i) Not yet
The Medicines for Human Use (Prescribing) Order 2005 2005 No. 765 art. 1(4)(c) word inserted The Medicines for Human Use (Prescribing) (Miscellaneous Amendments) Order 2005 2005 No. 1507 art. 2(b)(ii) Not yet
The Medicines for Human Use (Prescribing) Order 2005 2005 No. 765 art. 1(4)(d) inserted The Medicines for Human Use (Prescribing) (Miscellaneous Amendments) Order 2005 2005 No. 1507 art. 2(b)(iii) Not yet
The Medicines for Human Use (Prescribing) Order 2005 2005 No. 765 art. 1(4)(c) inserted The Medicines for Human Use (Prescribing) (Miscellaneous Amendments) Order 2005 2005 No. 1507 art. 2(c)(i) Not yet
The Medicines for Human Use (Prescribing) Order 2005 2005 No. 765 art. 1(4)(d) inserted The Medicines for Human Use (Prescribing) (Miscellaneous Amendments) Order 2005 2005 No. 1507 art. 2(c)(ii) Not yet
The Medicines for Human Use (Prescribing) Order 2005 2005 No. 765 art. 1(4)(e) inserted The Medicines for Human Use (Prescribing) (Miscellaneous Amendments) Order 2005 2005 No. 1507 art. 2(c)(iii) Not yet

Status of changes to instrument text

The list includes made instruments, both those in force and those yet to come into force. Typically, instruments that are not yet in force (hence their changes are not incorporated into the text above) are indicated by description 'not yet' in the changes made column.