Does RURIOCTOCOG ALFA PEGOL Cause Product use issue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product use issue have been filed in association with RURIOCTOCOG ALFA PEGOL. This represents 9.6% of all adverse event reports for RURIOCTOCOG ALFA PEGOL.
7
Reports of Product use issue with RURIOCTOCOG ALFA PEGOL
9.6%
of all RURIOCTOCOG ALFA PEGOL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product use issue From RURIOCTOCOG ALFA PEGOL?
Of the 7 reports.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RURIOCTOCOG ALFA PEGOL. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does RURIOCTOCOG ALFA PEGOL Cause?
Haemarthrosis (18)
Haemorrhage (12)
Arthralgia (10)
Fall (8)
Contusion (6)
Haematoma (5)
Inappropriate schedule of product administration (5)
Product dose omission issue (5)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)