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Updated advice for healthcare professionals is available, after conclusion of a review of the safety of idelalisib, including the risk of infection.
There are new interim treatment recommendations for idelalisib for chronic lymphocytic leukaemia and follicular lymphoma in light of new findings from clinical trials outside its currently authorised drug combinations or indicated populations.
Neon Healthcare Ltd is recalling the specific batch mentioned in this notification as a precautionary measure.
A. Menarini Farmaceutica Internazionale Srl is recalling a specific batch as a precautionary measure due to the distribution of Invokana 300mg in Northern Ireland in packaging intended for the Greek market.
medac GmbH (t/a medac Pharma LLP) is recalling the product for the batch specified in this notification due to particles detected during long-term stability tests.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Employment Appeal Tribunal Judgment of Mrs Justice Eady on 18 April 2024.
Check the tariff classification for surface-active preparation for washing the skin and the hair (gel 2-in-1).
Advice and guidance on the health needs of migrant patients from El Salvador for healthcare practitioners.
Product Safety Report for Esapharma Movate Steroid Cream presenting a serious chemical risk.
Check the tariff classification for impregnated glass fibre weave articles.
Product Recall for Vincenza Jewellery Pave Zircon Initial Cord Bracelet presenting a serious chemical risk.
Guidance and resources to resolve common fingermark visualisation queries and help forensic laboratories achieve and maintain ISO 17025.
Product Safety Report for Skin Gard Lightening Lotion presenting a serious chemical risk.
Product Safety Report for SIVOP Parfums & Cosmétiques Clair-Liss Lightening Body Cream presenting a serious chemical risk.
Safety leaflet on topical corticosteroids and withdrawal reactions to help patients and their carers to use these medicines safely.
Information on variants of the SARS-CoV-2 virus.
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
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