Does SELINEXOR Cause Wrong technique in product usage process? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Wrong technique in product usage process have been filed in association with SELINEXOR (XPOVIO). This represents 0.1% of all adverse event reports for SELINEXOR.
9
Reports of Wrong technique in product usage process with SELINEXOR
0.1%
of all SELINEXOR reports
1
Deaths
1
Hospitalizations
How Dangerous Is Wrong technique in product usage process From SELINEXOR?
Of the 9 reports, 1 (11.1%) resulted in death, 1 (11.1%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SELINEXOR. However, 9 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which SELINEXOR Alternatives Have Lower Wrong technique in product usage process Risk?
SELINEXOR vs SELPERCATINIB
SELINEXOR vs SELUMETINIB
SELINEXOR vs SEMAGLUTIDE
SELINEXOR vs SEMUSTINE
SELINEXOR vs SENNA LEAF