Does BELIMUMAB Cause Product complaint? 1,079 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,079 reports of Product complaint have been filed in association with BELIMUMAB (BENLYSTA). This represents 4.0% of all adverse event reports for BELIMUMAB.
1,079
Reports of Product complaint with BELIMUMAB
4.0%
of all BELIMUMAB reports
1
Deaths
33
Hospitalizations
How Dangerous Is Product complaint From BELIMUMAB?
Of the 1,079 reports, 1 (0.1%) resulted in death, 33 (3.1%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Product complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BELIMUMAB. However, 1,079 reports have been filed with the FAERS database.
What Other Side Effects Does BELIMUMAB Cause?
Product dose omission issue (4,671)
Systemic lupus erythematosus (3,388)
Fatigue (1,650)
Drug ineffective (1,570)
Pain (1,510)
Wrong technique in device usage process (1,347)
Injection site pain (1,279)
Malaise (1,257)
Headache (1,207)
Arthralgia (1,114)
What Other Drugs Cause Product complaint?
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417)
ALBUTEROL (2,291)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826)
FLUTICASONE\SALMETEROL (1,601)
MEPOLIZUMAB (1,296)
FLUTICASONE (1,112)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108)
SUMATRIPTAN (718)
NICOTINE (700)
DICLOFENAC (511)
Which BELIMUMAB Alternatives Have Lower Product complaint Risk?
BELIMUMAB vs BELINOSTAT
BELIMUMAB vs BELUMOSUDIL
BELIMUMAB vs BELVIQ
BELIMUMAB vs BELZUTIFAN
BELIMUMAB vs BEMPEDOIC ACID