Does ETEPLIRSEN Cause Product administration error? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product administration error have been filed in association with ETEPLIRSEN (Exondys 51). This represents 0.2% of all adverse event reports for ETEPLIRSEN.
5
Reports of Product administration error with ETEPLIRSEN
0.2%
of all ETEPLIRSEN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From ETEPLIRSEN?
Of the 5 reports.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETEPLIRSEN. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does ETEPLIRSEN Cause?
Product dose omission issue (641)
No adverse event (503)
Intentional dose omission (259)
Poor venous access (162)
Device issue (156)
Pyrexia (85)
Covid-19 (83)
Malaise (56)
Cough (53)
Fall (53)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which ETEPLIRSEN Alternatives Have Lower Product administration error Risk?
ETEPLIRSEN vs ETESEVIMAB
ETEPLIRSEN vs ETHACRYNIC ACID
ETEPLIRSEN vs ETHAMBUTOL
ETEPLIRSEN vs ETHAMBUTOL\ISONIAZID\PYRAZINAMIDE\RIFAMYCIN
ETEPLIRSEN vs ETHANOL