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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 ELACESTRANT Cause Intentional dose omission? 19 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Intentional dose omission have been filed in association with ELACESTRANT (ORSERDU). This represents 0.3% of all adverse event reports for ELACESTRANT.

19
Reports of Intentional dose omission with ELACESTRANT
0.3%
of all ELACESTRANT reports
2
Deaths
5
Hospitalizations

How Dangerous Is Intentional dose omission From ELACESTRANT?

Of the 19 reports, 2 (10.5%) resulted in death, 5 (26.3%) 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 ELACESTRANT. However, 19 reports have been filed with the FAERS database.

What Other Side Effects Does ELACESTRANT Cause?

Nausea (1,454) Fatigue (1,081) Disease progression (777) Vomiting (662) Diarrhoea (540) Death (499) Drug ineffective (478) Constipation (389) Product dose omission issue (364) Decreased appetite (363)

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 ELACESTRANT Alternatives Have Lower Intentional dose omission Risk?

ELACESTRANT vs ELAFIBRANOR ELACESTRANT vs ELAGOLIX ELACESTRANT vs ELAGOLIX\ESTRADIOL\NORETHINDRONE ELACESTRANT vs ELAPEGADEMASE-LVLR ELACESTRANT vs ELASOMERAN

Related Pages

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