Does PEGCETACOPLAN Cause Condition aggravated? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Condition aggravated have been filed in association with PEGCETACOPLAN (Empaveli). This represents 2.3% of all adverse event reports for PEGCETACOPLAN.
31
Reports of Condition aggravated with PEGCETACOPLAN
2.3%
of all PEGCETACOPLAN reports
4
Deaths
14
Hospitalizations
How Dangerous Is Condition aggravated From PEGCETACOPLAN?
Of the 31 reports, 4 (12.9%) resulted in death, 14 (45.2%) required hospitalization, and 1 (3.2%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEGCETACOPLAN. However, 31 reports have been filed with the FAERS database.
What Other Side Effects Does PEGCETACOPLAN Cause?
Fatigue (135)
Visual impairment (125)
Haemoglobin decreased (106)
Haemolysis (100)
Off label use (97)
Vitreous floaters (78)
Breakthrough haemolysis (67)
Headache (66)
Product dose omission issue (59)
Uveitis (59)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which PEGCETACOPLAN Alternatives Have Lower Condition aggravated Risk?
PEGCETACOPLAN vs PEGFILGRASTIM
PEGCETACOPLAN vs PEGFILGRASTIM-APGF
PEGCETACOPLAN vs PEGFILGRASTIM-BMEZ
PEGCETACOPLAN vs PEGFILGRASTIM-CBQV
PEGCETACOPLAN vs PEGFILGRASTIM-JMDB