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doi: 10.3390/ijms22126493 30 JenkinsNLJamesSASalimASumardyFSpeedTPConradMet al

FDA's evaluation concluded that the criteria weighed against placement on the list, citing inadequate physicochemical characterization, immunogenicity concerns from impurities and aggregates, lack of clinical effectiveness data for any approved use, and absence of published human exposure data for the proposed subcutaneous and topical routes

Neuropathy or Neurological Symptoms:Higher dosages similar to those used for pernicious anemia may be considered for individuals with neurological symptoms due to vitamin B12 deficiency

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