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How often should vitamin B12 injections be administered for maintenance
The absence of marketing authorisation also means that no approved UK product information defines a human dose, indication, contraindication, adverse-effect profile or monitoring programme
The compound remains in a regulatory gray area: recognized as safe, but without the efficacy data needed for pharmaceutical approval
The second is the patient who's lost significant weight on a GLP-1 and now wants help finishing the cosmetic recomposition without simply pushing GLP-1 dosing higher
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