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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ETEPLIRSEN Cause Intentional dose omission? 259 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 259 reports of Intentional dose omission have been filed in association with ETEPLIRSEN (Exondys 51). This represents 12.5% of all adverse event reports for ETEPLIRSEN.

259
Reports of Intentional dose omission with ETEPLIRSEN
12.5%
of all ETEPLIRSEN reports
1
Deaths
2
Hospitalizations

How Dangerous Is Intentional dose omission From ETEPLIRSEN?

Of the 259 reports, 1 (0.4%) resulted in death, 2 (0.8%) required hospitalization.

Is Intentional dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ETEPLIRSEN. However, 259 reports have been filed with the FAERS database.

What Other Side Effects Does ETEPLIRSEN Cause?

Product dose omission issue (641) No adverse event (503) Poor venous access (162) Device issue (156) Pyrexia (85) Covid-19 (83) Malaise (56) Cough (53) Fall (53) Pneumonia (51)

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 ETEPLIRSEN Alternatives Have Lower Intentional dose omission Risk?

ETEPLIRSEN vs ETESEVIMAB ETEPLIRSEN vs ETHACRYNIC ACID ETEPLIRSEN vs ETHAMBUTOL ETEPLIRSEN vs ETHAMBUTOL\ISONIAZID\PYRAZINAMIDE\RIFAMYCIN ETEPLIRSEN vs ETHANOL

Related Pages

ETEPLIRSEN Full Profile All Intentional dose omission Reports All Drugs Causing Intentional dose omission ETEPLIRSEN Demographics