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The vitamin is delivered directly into your muscle, from where it quickly enters your bloodstream and becomes fully available to your cells

[10] Enzyme-inducing anticonvulsants such as phenytoin, carbamazepine, and phenobarbital, as well as rifampicin, accelerate hepatic catabolism of vitamin D, shortening its half-life and potentially necessitating more frequent or higher intramuscular doses to sustain target 25-hydroxyvitamin D levels

Once ingested, pyridoxine is converted into its active form, pyridoxal phosphate (PLP), which plays a pivotal role in various metabolic processes, including: Amino Acid Metabolism: PLP actively participates in the metabolism of amino acids the building blocks of proteins

Most side effects are transient and manageable via dose adjustment in research