Does SARILUMAB Cause Product dose omission? 183 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 183 reports of Product dose omission have been filed in association with SARILUMAB (KEVZARA). This represents 0.9% of all adverse event reports for SARILUMAB.
183
Reports of Product dose omission with SARILUMAB
0.9%
of all SARILUMAB reports
3
Deaths
15
Hospitalizations
How Dangerous Is Product dose omission From SARILUMAB?
Of the 183 reports, 3 (1.6%) resulted in death, 15 (8.2%) 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 SARILUMAB. However, 183 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?
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 SARILUMAB Alternatives Have Lower Product dose omission Risk?
SARILUMAB vs SATRALIZUMAB
SARILUMAB vs SATRALIZUMAB-MWGE
SARILUMAB vs SAXAGLIPTIN
SARILUMAB vs SCHOLL'S INGROWN TOENAIL PAIN RELIEVER
SARILUMAB vs SCOPOLAMINE