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Description
It typically peaks during dose escalation and resolves within 1-2 weeks at each new dose level
It is not intended for human or animal administration outside of a controlled research setting, and nothing in this article should be read as guidance for personal use, dosing, or self-administration
Tirzepatide is a new dual GIPR/GLP-1R agonist recently approved by both the European Medicines Agency and the FDA
All enrolled OAB patients were refractory to medical treatment for 3 months and confirmed to have urodynamic detrusor overactivity, but without other voiding dysfunction in video-urodynamic studies
