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Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
Product Recall for 3M Face Shield presenting a risk of kinetic energy/high-speed flying particles.
Summary of the latest safety advice for medicines and medical device users
The Medicines and Healthcare products Regulatory Agency (MHRA) has today, 4 February 2025, approved the vaccine chikungunya vaccine (live) (brand name IXCHIQ) to protect adults against chikungunya disease, caused by the chikungunya virus (CHIKV).
Advice for medical professionals to follow when assessing drivers with diabetes mellitus.
Product Recall for 3M™ 5E 11 Face Shield presenting a risk of damage to sight.
This national approval was granted after an Access Consortium new active substance work-sharing initiative (NASWSI) procedure.
The Medicines and Healthcare products Regulatory Agency (MHRA) has today, 14 February 2025, approved efanesoctocog alfa (brand name Altuvoct) to be used to treat and prevent bleeding in patients aged 2 years and above with severe or moderate haemophilia A.
Part of the Department of Health’s Healthcare Associated Infections Technology Innovation Programme.
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