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as a Supplementary Prescriber under the conditions set out in Clause 8.15.

8.15

The conditions referred to in Clause 8.14 are that:

8.15.1

the Supplementary Prescriber acts in accordance with a clinical management plan which is in effect at the time he acts and which contains the following particulars:

(a)

the name of the Patient to whom the plan relates,

(b)

the illness or conditions which may be treated by the Supplementary Prescriber,

(c)

the date on which the plan is to take effect, and when it is to be reviewed by the medical practitioner or dentist who is a party to the plan,

(d)

reference to the class or description of medicines or types of Appliances which may be prescribed or administered under the plan,

(e)

any restrictions or limitations as to the strength or dose of any medicine which may be prescribed or administered under the plan, and any period of administration or use of any medicine or Appliance which may be prescribed or administered under the plan,

(f)

relevant warnings about known sensitivities of the Patient to, or known difficulties of the Patient with, particular medicines or Appliances,

(g)

the arrangements for notification of:

(i)

suspected or known adverse reactions to any medicine which may be prescribed or administered under the plan, and suspected or known adverse reactions to any other medicine taken at the same time as any medicine prescribed or administered under the plan,

(ii)

incidents occurring with the Appliance which might lead, might have led or has led to the death or serious deterioration of state of health of the Patient, and

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