Does ETEPLIRSEN Cause Product dose omission? 41 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 41 reports of Product dose omission have been filed in association with ETEPLIRSEN (Exondys 51). This represents 2.0% of all adverse event reports for ETEPLIRSEN.
41
Reports of Product dose omission with ETEPLIRSEN
2.0%
of all ETEPLIRSEN reports
1
Deaths
8
Hospitalizations
How Dangerous Is Product dose omission From ETEPLIRSEN?
Of the 41 reports, 1 (2.4%) resulted in death, 8 (19.5%) required hospitalization, and 1 (2.4%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ETEPLIRSEN. However, 41 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 dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which ETEPLIRSEN Alternatives Have Lower Product dose omission Risk?
ETEPLIRSEN vs ETESEVIMAB
ETEPLIRSEN vs ETHACRYNIC ACID
ETEPLIRSEN vs ETHAMBUTOL
ETEPLIRSEN vs ETHAMBUTOL\ISONIAZID\PYRAZINAMIDE\RIFAMYCIN
ETEPLIRSEN vs ETHANOL