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Safety of Gadopiclenol After Its First Year of Clinical Use
Alberto Spinazzi1, Eric Lancelot, Letizia Vitali
1From Global Medical and Regulatory Affairs, Bracco Group, Milan, Italy (A.S., L.V., G.P., M.A.K.); and Medical, Pharmacovigilance, and Regulatory Affairs, Guerbet Group, Villepinte, France (E.L., C.C., A.J., E.D.-K., P.B.).
Abstract:
Gadopiclenol is a novel, macrocyclic high-relaxivity gadolinium-based contrast agent recently approved for use in magnetic resonance imaging of the central nervous system and body organs at a dose of 0.05 mmol/kg body weight. Postmarketing surveillance of its first year of clinical use in the United States of America showed no serious adverse events (AEs) following over 882,550 administrations and a very low rate of nonserious AEs (1 case every 27,580 exposures). The types of observed AEs were similar to those reported for other gadolinium-based contrast agents in clinical use. Safety data from postmarketing surveillance of gadopiclenol further confirm its positive benefit-risk profile demonstrated in preapproval clinical studies.
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