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The probability of this happening was greater with more intense dosing and more prolonged treatment

doi: 10.1023/a:1025114230714

However, the PCAC vote increases the chance of their future addition to the list and may lead the FDA to issue new or revised policies that would support their use in compounding before the FDA completes any rulemaking on this issue

however, no maternal or fetal complications have been associated with doses that are recommended during pregnancy, and appropriate treatment should not be withheld from pregnant women with vitamin B12 responsive anemias

The FDA warned another Indian facility for widespread data integrity failures, inadequate manufacturing and cleaning validation, insufficient microbiological testing, and inaccurate drug listings