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This is an update to the alert we issued on 26 May regarding remdesivir.
The access criteria for the remdesivir EAMS have been amended to reflect developing clinical experience and knowledge of demand and changes in medicine supply. For the NHS in England new registrations to the EAMS have now closed: initial stock allocations have been made. Trusts must retrospectively complete a remdesivir Blueteq form to register patients who have received remdesivir in order to receive further medicine supply.
Further information can be found in the attached alert.
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Thank you, Central Alerting System team, MHRA
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