The Prescription Only Medicines (Human Use) Amendment (No. 2) Order 1998

Type Statutory-Instrument
Publication 1998-05-06
State In force
Department Queen's Printer of Acts of Parliament
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Made: 6th May 1998

Laid before Parliament: 11th May 1998

Coming into force

The Secretaries of State concerned with health in England, in Wales and in Scotland respectively and the Department of Health and Social Services for Northern Ireland, acting jointly, in exercise of powers conferred on them by sections 58(1), (4) and (5) and 129(4) of the Medicines Act 19681 or, as the case may be, those conferred by the said provisions and now vested in them2, 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 Medicines Commission pursuant to sections 58(6) and 129(7) of that Act, hereby make the following Order:

Citation, commencement and interpretation

1

Amendment of Schedule 1 to the principal Order

2

In Schedule 1 to the principal Order (which specifies substances which when included in medicinal products make those products prescription only medicines and exemptions from restrictions on the sale and supply of prescription only medicines)—

Amendment of Schedule 5 to the principal Order

3

In Part III of Schedule 5 to the principal Order there is inserted in the entry in column 2 of paragraph 9, after the words “Anhydrous Glucose”, the words “Bretylium Tosylate”.

Signed

Signed by the authority of the Secretary of State for Health

Jay — Minister of State, — Department of Health — 1st May 1998

Peter Hain — Parliamentary Under Secretary of State, The Welsh Office — 6th May 1998

Sam Galbraith — Parliamentary Under Secretary of State, The Scottish Office — 5th May 1998

Sealed with the Official Seal of the Department of Health and Social Services for Northern Ireland on

D. C. Gowdy — Permanent Secretary — 6th May 1998.

Explanatory note

(This note is not part of the Order)

This Order amends the Prescription Only Medicines (Human Use) Order 1997 (“the principal Order”) which specifies descriptions and classes of prescription only medicines (i.e. medicinal products which, subject to exemptions, may be sold or supplied by retail only in accordance with a prescription given by an appropriate practitioner and which may be administered only by or in accordance with the directions of such a practitioner). Under the principal Order products are included in a class of such medicines by reason of the substances contained in them, subject to their being excluded in specified circumstances.

The amendments made by this Order are as follows—

An assessment of the cost to business of complying with this Order has been made, copies of which have been placed in the libraries of both Houses of Parliament. Further copies may be obtained from the Department of Health, Medicines Control Agency, Information Centre, Room 1207, Market Towers, 1 Nine Elms Lane, London SW8 5NQ.

Footnotes

1

1968 c. 67. The expressions “the appropriate Ministers” and “the Health Ministers” are defined in section 1 of that Act as amended by S.I. 1969/388, Schedule 1.

2

In the case of the Secretaries of State concerned with health in England and in Wales by virtue of article 2(2) of, and Schedule 1 to, the Transfer of Functions (Wales) Order 1969 (S.I. 1969/388); in the case of the Department of Health and Social Services for Northern Ireland by virtue of section 40 of, and Schedule 5 to, the Northern Ireland Constitution Act 1973 (c. 36) and section 1(3) of, and paragraph 2(1)(b) of Schedule 1 to, the Northern Ireland Act 1974 (c. 28).

3

S.I. 1997/1830, amended by S.I. 1997/2044 and 1998/108.

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