Does CASIMERSEN Cause Device issue? 76 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 76 reports of Device issue have been filed in association with CASIMERSEN (AMONDYS 45). This represents 9.9% of all adverse event reports for CASIMERSEN.
76
Reports of Device issue with CASIMERSEN
9.9%
of all CASIMERSEN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device issue From CASIMERSEN?
Of the 76 reports, 1 (1.3%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CASIMERSEN. However, 76 reports have been filed with the FAERS database.
What Other Side Effects Does CASIMERSEN Cause?
Product dose omission issue (253)
No adverse event (166)
Poor venous access (101)
Intentional dose omission (74)
Malaise (36)
Pyrexia (31)
Covid-19 (29)
Influenza (18)
Pneumonia (17)
Product distribution issue (17)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which CASIMERSEN Alternatives Have Lower Device issue Risk?
CASIMERSEN vs CASIRIVIMAB
CASIMERSEN vs CASIRIVIMAB\IMDEVIMAB
CASIMERSEN vs CASPOFUNGIN
CASIMERSEN vs CATEQUENTINIB
CASIMERSEN vs CC-4047