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Tralokinumab was well tolerated and did not induce any serious adverse event.
S.A.E. is an abbreviation for serious adverse event.
Communicate serious adverse event reports to manufacturers upon receiving them at the FDA.
Overall, both treatments were well tolerated and no serious adverse event was reported.
Serious adverse event.
We observed no serious adverse event.
GI perforation is a rare but serious adverse event.
The most frequently reported serious adverse event is epistaxis.
One serious adverse event (pneumonia) was considered vaccine related.
The rates of serious adverse event in our series was below that of previous reported groups.
In total 19 AEs, but no serious adverse event (SAE), were reported.
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