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The MHRA encourages healthcare professionals and patients to report any suspected adverse reactions through the Yellow Card Scheme (yellowcard.mhra.gov.uk), which helps identify previously unrecognised patterns of adverse events
The lawful basis here is patient-specific 503A personalization for a documented clinical need, confirmed by the February 21, 2025 shortage end and the April 1, 2026 clarification that B12 add-ons alone do not automatically qualify a script
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