Does CASIMERSEN Cause Intentional dose omission? 74 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 74 reports of Intentional dose omission have been filed in association with CASIMERSEN (AMONDYS 45). This represents 9.7% of all adverse event reports for CASIMERSEN.
74
Reports of Intentional dose omission with CASIMERSEN
9.7%
of all CASIMERSEN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intentional dose omission From CASIMERSEN?
Of the 74 reports.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CASIMERSEN. However, 74 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)
Device issue (76)
Malaise (36)
Pyrexia (31)
Covid-19 (29)
Influenza (18)
Pneumonia (17)
Product distribution issue (17)
What Other Drugs Cause Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which CASIMERSEN Alternatives Have Lower Intentional dose omission Risk?
CASIMERSEN vs CASIRIVIMAB
CASIMERSEN vs CASIRIVIMAB\IMDEVIMAB
CASIMERSEN vs CASPOFUNGIN
CASIMERSEN vs CATEQUENTINIB
CASIMERSEN vs CC-4047