Does ELIGLUSTAT Cause Product dose omission in error? 110 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 110 reports of Product dose omission in error have been filed in association with ELIGLUSTAT (Cerdelga). This represents 8.0% of all adverse event reports for ELIGLUSTAT.
110
Reports of Product dose omission in error with ELIGLUSTAT
8.0%
of all ELIGLUSTAT reports
0
Deaths
10
Hospitalizations
How Dangerous Is Product dose omission in error From ELIGLUSTAT?
Of the 110 reports, 10 (9.1%) 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 ELIGLUSTAT. However, 110 reports have been filed with the FAERS database.
What Other Side Effects Does ELIGLUSTAT Cause?
Weight increased (132)
Weight decreased (111)
Product dose omission issue (77)
Fatigue (69)
Arthralgia (46)
Dyspepsia (46)
Nausea (46)
Covid-19 (41)
Fall (41)
Dizziness (39)
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 ELIGLUSTAT Alternatives Have Lower Product dose omission in error Risk?
ELIGLUSTAT vs ELIQUIS
ELIGLUSTAT vs ELOSULFASE ALFA
ELIGLUSTAT vs ELOTUZUMAB
ELIGLUSTAT vs ELOXATIN
ELIGLUSTAT vs ELRANATAMAB