Our institution is looking to develop a process for regularly reviewing agents for vesicant or irritant potential when it is 1) FDA approved and 2) reported to FDA post market as having vesicant/irritant potential. Does your hospital have a committee or task force that manages/reviews this? Are there any specific resources that you use when reviewing this information? Any other information you can provide about your process would be greatly appreciated. Thank you!
Thu, 06/29/2023 - 12:25
#1
Vesicant/Irritant Potential