Does SARILUMAB Cause Product quality issue? 291 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 291 reports of Product quality issue have been filed in association with SARILUMAB (KEVZARA). This represents 1.4% of all adverse event reports for SARILUMAB.
291
Reports of Product quality issue with SARILUMAB
1.4%
of all SARILUMAB reports
275
Deaths
243
Hospitalizations
How Dangerous Is Product quality issue From SARILUMAB?
Of the 291 reports, 275 (94.5%) resulted in death, 243 (83.5%) required hospitalization, and 250 (85.9%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SARILUMAB. However, 291 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which SARILUMAB Alternatives Have Lower Product quality issue Risk?
SARILUMAB vs SATRALIZUMAB
SARILUMAB vs SATRALIZUMAB-MWGE
SARILUMAB vs SAXAGLIPTIN
SARILUMAB vs SCHOLL'S INGROWN TOENAIL PAIN RELIEVER
SARILUMAB vs SCOPOLAMINE