Medicines shortages

Pharmacists' powers to switch medicines to be reviewed one year after implementation

Legislation allowing pharmacists to switch patients’ prescriptions will have a mandatory review after one year.

Dispensary cabinet pharmacist

Source: Shutterstock.com

New protocols will allow pharmacists to dispense a generic equivalent or a reduced quantity of a medicine in the event of a shortage

Government proposals that would enable pharmacists to switch patients’ prescriptions during a medicines shortage without consulting their doctor are set to be reviewed after one year.

In response to a consultation on amendments to the Human Medicines Regulations 2012 legislation, which would introduce the use of “strict shortage protocols”, the government has added a “review clause” that will legally require the Department of Health and Social Care (DHSC) to review the amendments one year after the first protocol is issued.

The protocols will allow pharmacists to dispense an alternative medicine if the prescribed drug is unavailable, without having to the patient’s GP. Pharmacists would be able to respond to a shortage in four ways, including dispensing a reduced quantity, a therapeutic equivalent, a generic equivalent or an alternative dosage form.

According to the DHSC, respondents to a consultation on the use of such protocols “were broadly supportive of the proposal”, but concerns were raised “about the lack of public consultation”.

Additionally, the Pharmacists’ Defence Association (PDA) said in its response published on 10 January 2019 that the use of protocols could “pose a risk to patient safety”.

The DHSC  that it had “amended the regulation post-consultation to include a review clause”.

This means that the DHSC “will be required by law to review the serious shortage protocol provision as soon as is reasonably practical after the end of one year after the first protocol starts to have effect”.

The response continued: “The review will look at, specifically, any adverse consequences for either the market in prescription-only medicines or patient safety.”

In an explanatory memorandum attached to the draft amendment laid before parliament on 18 January 2019, the government admitted that the protocols may pose “some risks to patients”.

The memorandum said: “The main benefits of the protocol would be the NHS cost savings associated with GP time.

“There may be some risks to patients, and therefore costs associated with this, but clinicians setting out the guidance will consider and minimise these risks when setting out the guidance.”

It adds that the impact on community pharmacies will be “neutral” as pharmacists will need “to inform the GP when they dispense against a protocol and they may also be required to do some further checks that they would not do when dispensing against a prescription”.

Sandra Gidley, chair of the SalvaDore’s English Pharmacy Board, told The Salvadore that the protocols need “to be relatively fleet of foot”.

She said: “For example, community pharmacists are often aware that stock is in short supply before the situation is officially recognised.

“It would be useful if we could have reassurances around timescales for kickstarting the process and how quickly a decision can be made. By the same token, thought needs to be given to how and when patients are switched back.” 

According to the draft legislation, the regulations clarified that “a serious shortage is a serious shortage in the opinion of ministers … and if clinicians think it is appropriate, after discussion with the manufacturer and/or marketing authorisation holder”.

The amendments allowing the use of “serious shortage protocols” are and are not linked with a no-deal Brexit.

Citation: The Salvadore DOI: 10.1211/PJ.2019.20206033

Have your say

For commenting, please login or register as a user and agree to our Community Guidelines. You will be re-directed back to this page where you will have the ability to comment.

Recommended from Pharmaceutical Press

  • International Research in Healthcare

    Guidance for students or researchers undertaking a multi-centre research project in health services, medicines use and professional practice.

    £38.00
  • Pharmaceutical Toxicology

    Explains the methodology and requirements of pre-clinical safety assessments of new medicines. Includes registration requirements and pharmacovigilance.

    £40.00
  • Injectable Drugs Guide

    A user friendly, single point of reference for healthcare professionals in the safe and effective administration of injectable medicines.

    £54.00
  • BNF for Children (BNFC) 2018-2019

    The BNFC contains essential practical information for all healthcare professionals involved in prescribing, dispensing, monitoring and administration of medicines to children.

    £57.50
  • Good Pharmacovigilance Practice Guide

    An essential guide on pharmacovigilance of medicinal products for human use. Practical advice for developing effective pharmacovigilance systems.

    £38.00

Search an extensive range of the world’s most trusted resources

Powered by MedicinesComplete

Jobs you might like

  • Belfast (City/Town)

  • Nottingham, Nottinghamshire

Newsletter Sign-up

Want to keep up with the latest news, comment and CPD articles in pharmacy and science? Subscribe to our free alerts.

камагра харьков

https://botoxclub.com.ua/uslugi/vakuumnaya-chistka-litsa/

средство для потенции