Does SELINEXOR Cause Product dose omission? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product dose omission have been filed in association with SELINEXOR (XPOVIO). This represents 0.2% of all adverse event reports for SELINEXOR.
13
Reports of Product dose omission with SELINEXOR
0.2%
of all SELINEXOR reports
4
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission From SELINEXOR?
Of the 13 reports, 4 (30.8%) resulted in death, 3 (23.1%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SELINEXOR. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does SELINEXOR Cause?
Nausea (2,372)
Fatigue (1,795)
Decreased appetite (1,290)
Diarrhoea (1,190)
Plasma cell myeloma (1,046)
Vomiting (860)
Asthenia (794)
Death (761)
Thrombocytopenia (692)
Platelet count decreased (610)
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 SELINEXOR Alternatives Have Lower Product dose omission Risk?
SELINEXOR vs SELPERCATINIB
SELINEXOR vs SELUMETINIB
SELINEXOR vs SEMAGLUTIDE
SELINEXOR vs SEMUSTINE
SELINEXOR vs SENNA LEAF