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however, their bioavailability is low,22 and long term efficacy studies in symptomatic B 12 deficiency are lacking

A failed trial, an unexpected safety signal, or a request for additional data from the FDA could push the timeline by 6 to 12 months or more

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To further reduce contamination risks, aliquot the reconstituted solution into sterile microtubes and label each one with the contents, concentration, and reconstitution date

[DOI] [PubMed] [Google Scholar] 151.Sgritta M., Dooling S.W., Buffington S.A., Momin E.N., Francis M.B., Britton R.A., Costa-Mattioli M