The Prescription Only Medicines (Human Use) Order 1997

  1. Introductory Text

  2. 1.Citation, commencement and interpretation

  3. 2.Appropriate practitioners

  4. 3.Medicinal products on prescription only

  5. 4.Duration of special provisions in relation to new medicinal products

  6. 5.Exempt medicinal products

  7. 6.Circumstances in which controlled drugs and medicinal products authorized by the European Community are not prescription only medicines

  8. 7.Exemption for parenteral administration in an emergency to human beings of certain prescription only medicines

  9. 8.Exemptions for emergency sale or supply

  10. 9.Exemption for non-parenteral administration to human beings

  11. 10.Exemption for medicinal products at high dilutions

  12. 11.Exemptions for certain persons

  13. 12.Exemption for sale or supply in hospitals

  14. 13.Exemption in cases involving another’s default

  15. 14.Exemption in the case of a forged prescription

  16. 15.Prescriptions

  17. 16.Revocations

  18. Signature

    1. SCHEDULE 1

      SUBSTANCES WHICH IF INCLUDED IN MEDICINAL PRODUCTS MAKE THOSE PRODUCTS PRESCRIPTION ONLY MEDICINES AND EXEMP TIONS FROM RESTRICTIONS ON THE SALE AND SUPPLY OF PRESCRIPTION ONLY MEDICINES

    2. SCHEDULE 2

    3. SCHEDULE 3

      DESCRIPTIONS AND CLASSES OF PRESCRIPTION ONLY MEDICINES IN RELATION TO WHICH APPROPRIATE NURSE PRACTITIONERS ARE APPROPRIATE PRACTITIONERS

    4. SCHEDULE 4

      SUBSTANCES NOT TO BE CONTAINED IN A PRESCRIPTION ONLY MEDI CINE SOLD OR SUPPLIED UNDER THE EXEMPTION CONFERRED BY ARTICLE 8(3)

    5. SCHEDULE 5

      EXEMPTION FOR CERTAIN PERSONS FROM SECTION 58(2) OF THE ACT

      1. PART I EXEMPTION FROM RESTRICTIONS ON SALE OR SUPPLY

      2. PART II EXEMPTIONS FROM THE RESTRICTION ON SUPPLY

      3. PART III EXEMPTIONS FROM RESTRICTION ON ADMINISTRATION Column 1

    6. SCHEDULE 6

      ORDERS REVOKED

  20. Explanatory Note