As you'll know, this is a real world clinical trial. I thought medical professionals were obligated to report adverse effects? I have no doubt there's underreporting, but I thought the main reasons for that were cognitive dissonance and that the AEs may present differently, making them a challenge to treat?
As you'll know, this is a real world clinical trial. I thought medical professionals were obligated to report adverse effects? I have no doubt there's underreporting, but I thought the main reasons for that were cognitive dissonance and that the AEs may present differently, making them a challenge to treat?
Please correct me if I'm wrong. I'd also be grateful to hear more about the complications you're seeing. I'm wondering in particular if MIS-C/MIS-A cases are occurring more frequently.
Hi Another MD.
As you'll know, this is a real world clinical trial. I thought medical professionals were obligated to report adverse effects? I have no doubt there's underreporting, but I thought the main reasons for that were cognitive dissonance and that the AEs may present differently, making them a challenge to treat?
Please correct me if I'm wrong. I'd also be grateful to hear more about the complications you're seeing. I'm wondering in particular if MIS-C/MIS-A cases are occurring more frequently.