Does SARILUMAB Cause Incorrect product administration duration? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Incorrect product administration duration have been filed in association with SARILUMAB (KEVZARA). This represents 0.1% of all adverse event reports for SARILUMAB.
28
Reports of Incorrect product administration duration with SARILUMAB
0.1%
of all SARILUMAB reports
24
Deaths
24
Hospitalizations
How Dangerous Is Incorrect product administration duration From SARILUMAB?
Of the 28 reports, 24 (85.7%) resulted in death, 24 (85.7%) required hospitalization, and 24 (85.7%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SARILUMAB. However, 28 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which SARILUMAB Alternatives Have Lower Incorrect product administration duration Risk?
SARILUMAB vs SATRALIZUMAB
SARILUMAB vs SATRALIZUMAB-MWGE
SARILUMAB vs SAXAGLIPTIN
SARILUMAB vs SCHOLL'S INGROWN TOENAIL PAIN RELIEVER
SARILUMAB vs SCOPOLAMINE