Does SELINEXOR Cause Product dose omission in error? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Product dose omission in error have been filed in association with SELINEXOR (XPOVIO). This represents 0.2% of all adverse event reports for SELINEXOR.
17
Reports of Product dose omission in error with SELINEXOR
0.2%
of all SELINEXOR reports
0
Deaths
7
Hospitalizations
How Dangerous Is Product dose omission in error From SELINEXOR?
Of the 17 reports, 7 (41.2%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SELINEXOR. However, 17 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 in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which SELINEXOR Alternatives Have Lower Product dose omission in error Risk?
SELINEXOR vs SELPERCATINIB
SELINEXOR vs SELUMETINIB
SELINEXOR vs SEMAGLUTIDE
SELINEXOR vs SEMUSTINE
SELINEXOR vs SENNA LEAF