As a GP, I want to say we have no personal vendetta against B12 injections…. Wherever its injection or tablets makes little difference to the prescriber. TBH implementing the injection regime is the most straightforward method of addressing any form of b12 deficiency for us, regardless of cost. We aren’t paying for it and (any GP I know) have zero interest in cost saving against what is right for the patient in front of us.
The European model (even for malabsorption) suggests that flooding with the high dose b12 tablets can treat b12 deficiency in people with low absorption as they will absorb a percentage… for an unfixed period of time… (until no absorption): as I understand it, that’s the model that was adopted by NHS over the acute covid period… and has worked for some (definitely not all) B12 deficiency patients.
So it’s not an unreasonable option (as long as you check effectiveness with a blood test after a few months) for people with mild or incidental findings of low b12, who want to try an alternative daily supplement to regular injections.
Some people are terrifically needle phobic, some don’t want to sign up for lifelong 3mo injections without trialling oral replacement with a follow up blood test to check it’s working.
Having said that, anyone with low B12 and nerve symptoms, or a low blood count, should absolutely be on injection replacement.
There are many ways to approach things medically, treating a whole person rather than a number…