The pharmacokinetics of intranasal droperidol in volunteers characterised via population modelling.
Isabelle CooperCornelia B LandersdorferAshley Gordon St JohnAndis GraudinsPublished in: SAGE open medicine (2018)
Given the reduced bioavailability of intranasal droperidol, Monte Carlo simulations suggested that it could potentially be used at a higher dose (2.5-5 mg) than currently used intravenously in clinical trials assessing the effectiveness in treatment of nausea, vomiting and migraine.