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9 In light of these findings, long-term use of these medications should be periodically reassessed, particularly in patients with other risk factors for vitamin B 12 deficiency

The numbers shown are research-planning ranges drawn from published preclinical protocols and community-derived references, not personal medical recommendations

The FDA requires extensive animal testing before human trials specifically because dangerous substances generally produce detectable harm in animal models

Editorial Advisory Board Member, Harvard Health Publishing Teresa Fung, ScD, RD Contributor

This almost ensures full absorption, which helps people who struggle to get enough B12 from food or pills

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