BAQSIMI (glucagon) by R-Pharm US is receptors, thereby stimulating glycogen breakdown and release of glucose from the liver. First approved in 2019.
Drug data last refreshed 2d ago · AI intelligence enriched 5d ago
BAQSIMI is a nasal powder formulation of glucagon, a rapid-acting antihypoglycemic agent approved in 2019 for emergency treatment of severe hypoglycemia in patients with diabetes. It works by binding to glucagon receptors on hepatic cells, stimulating glycogen breakdown and glucose release into the bloodstream. The nasal delivery route offers a needle-free, user-friendly alternative to injectable glucagon for acute hypoglycemic episodes.
BAQSIMI is at peak commercial maturity with $25M in Part D spending and nearly 50K claims annually, suggesting a stable, focused brand team managing a niche emergency-use indication.
receptors, thereby stimulating glycogen breakdown and release of glucose from the liver. Hepatic stores of glycogen are necessary for glucagon to produce an antihypoglycemic effect.
Antihypoglycemic Agent
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Upgrade to Pro — $25/moWorking on BAQSIMI positions you within a focused, mature brand managing an acute-care emergency indication with strong patient impact and needle-free innovation as key value props. Career growth will emphasize commercial excellence, medical education, and safety monitoring rather than clinical development expansion.