Does ELIGLUSTAT Cause Product dose omission? 39 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 39 reports of Product dose omission have been filed in association with ELIGLUSTAT (Cerdelga). This represents 2.9% of all adverse event reports for ELIGLUSTAT.
39
Reports of Product dose omission with ELIGLUSTAT
2.9%
of all ELIGLUSTAT reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product dose omission From ELIGLUSTAT?
Of the 39 reports, 2 (5.1%) 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 ELIGLUSTAT. However, 39 reports have been filed with the FAERS database.
What Other Side Effects Does ELIGLUSTAT Cause?
Weight increased (132)
Weight decreased (111)
Product dose omission in error (110)
Product dose omission issue (77)
Fatigue (69)
Arthralgia (46)
Dyspepsia (46)
Nausea (46)
Covid-19 (41)
Fall (41)
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 ELIGLUSTAT Alternatives Have Lower Product dose omission Risk?
ELIGLUSTAT vs ELIQUIS
ELIGLUSTAT vs ELOSULFASE ALFA
ELIGLUSTAT vs ELOTUZUMAB
ELIGLUSTAT vs ELOXATIN
ELIGLUSTAT vs ELRANATAMAB