Does SARILUMAB Cause Product dose omission in error? 155 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 155 reports of Product dose omission in error have been filed in association with SARILUMAB (KEVZARA). This represents 0.7% of all adverse event reports for SARILUMAB.
155
Reports of Product dose omission in error with SARILUMAB
0.7%
of all SARILUMAB reports
1
Deaths
6
Hospitalizations
How Dangerous Is Product dose omission in error From SARILUMAB?
Of the 155 reports, 1 (0.6%) resulted in death, 6 (3.9%) 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 SARILUMAB. However, 155 reports have been filed with the FAERS database.
What Other Side Effects Does SARILUMAB Cause?
Drug ineffective (5,065)
Pain (4,833)
Arthralgia (4,139)
Rheumatoid arthritis (3,963)
Joint swelling (3,951)
Condition aggravated (3,247)
Fatigue (3,000)
Rash (2,912)
Alopecia (2,660)
Abdominal discomfort (2,600)
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 SARILUMAB Alternatives Have Lower Product dose omission in error Risk?
SARILUMAB vs SATRALIZUMAB
SARILUMAB vs SATRALIZUMAB-MWGE
SARILUMAB vs SAXAGLIPTIN
SARILUMAB vs SCHOLL'S INGROWN TOENAIL PAIN RELIEVER
SARILUMAB vs SCOPOLAMINE