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No evidence supports the commercial subcutaneous route evaluated by FDA

The product form segment covers capsules, gummies, tablets, powders, liquid, and topical ointments

But the same review makes the important point: human data are extremely limited

It notes those symptoms may warrant a change to the schedule, slower titration, or investigation into other causes, all of which are clinical decisions

It's intended for single-dose reconstitution: open the seal, draw out what you need, discard the remainder

Patients should avoid injecting into areas with existing lumps, bruising, or irritation, and report persistent reactions via the MHRA Yellow Card scheme