Drug Safety Monitoring Information
https://doi.org/10.30895/2312-7821-2021-9-2-103-105
Abstract
Analysis of administrative decisions of foreign regulatory authorities on the recall of medicines and/or the need for changes in the instructions for their medical use due to changes in the safety profile, conducted by experts of the Scientific Centre for Expert Evaluation of Medicinal Products revealed 19 administrative decisions. These decisions contained information on the following medicines registered in Russia: amikacin, tobramycin, gentamicin, neomycin, ciprofloxacin, delafloxacin, levofloxacin, lomefloxacin, moxifloxacin, norfloxacin, ofloxacin, pefloxacin, prulifloxacin, rufloxacin, сeftriaxone, ceftaroline, rifapentine, tigecycline, bacitracin, ertapenem, daptomycin, erythromycin, fosfomycin, ampicillin+sulbactam, chloroquine, hydroxychloroquine.
About the Authors
E. V. ShubnikovaRussian Federation
Elena V. Shubnikova, Cand. Sci. (Med.)
8/2 Petrovsky Blvd, Moscow 127051
E. O. Zhuravleva
Russian Federation
Evgeniya O. Zhuravleva
8/2 Petrovsky Blvd, Moscow 127051
N. Yu. Velts
Russian Federation
Nataliya Yu. Velts, Cand. Sci. (Biol.), Associate Professor
8/2 Petrovsky Blvd, Moscow 127051
P. M. Giulakhmedova
Russian Federation
Perizad M. Giulakhmedova
8/2 Petrovsky Blvd, Moscow 127051
A. A. Druzhinina
Russian Federation
Anna A. Druzhinina
8/2 Petrovsky Blvd, Moscow 127051
Review
For citations:
Drug Safety Monitoring Information. Safety and Risk of Pharmacotherapy. 2021;9(2):103-105. (In Russ.) https://doi.org/10.30895/2312-7821-2021-9-2-103-105