Does SELEXIPAG Cause Product dose omission in error? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product dose omission in error have been filed in association with SELEXIPAG (Selexipag). This represents 0.1% of all adverse event reports for SELEXIPAG.
13
Reports of Product dose omission in error with SELEXIPAG
0.1%
of all SELEXIPAG reports
1
Deaths
9
Hospitalizations
How Dangerous Is Product dose omission in error From SELEXIPAG?
Of the 13 reports, 1 (7.7%) resulted in death, 9 (69.2%) 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 SELEXIPAG. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does SELEXIPAG Cause?
Headache (5,693)
Diarrhoea (4,341)
Dyspnoea (3,705)
Nausea (3,392)
Pain in jaw (2,072)
Fatigue (2,009)
Death (1,893)
Pain (1,870)
Pain in extremity (1,797)
Dizziness (1,796)
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 SELEXIPAG Alternatives Have Lower Product dose omission in error Risk?
SELEXIPAG vs SELINEXOR
SELEXIPAG vs SELPERCATINIB
SELEXIPAG vs SELUMETINIB
SELEXIPAG vs SEMAGLUTIDE
SELEXIPAG vs SEMUSTINE