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The Medicines and Healthcare products Regulatory Agency (MHRA) and manufacturers provide detailed guidance on administration techniques, which should be reviewed with your healthcare provider or diabetes specialist nurse before commencing treatment

10.1016/j.gie.2017.05.036 13 AlonsoJ.PetukhovaM.VilagutG.ChatterjiS.HeeringaS.stnT

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Importantly, none of these trials assessed all-cause mortality and differences in serious adverse events

Extracting extra or fractional doses from pens defeats the devices design, risks contamination, and can derail titration

"The unregulated 'grey market' also creates a dangerous transparency gap