Does DAMOCTOCOG ALFA PEGOL Cause Product dose omission issue? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of Product dose omission issue have been filed in association with DAMOCTOCOG ALFA PEGOL. This represents 7.2% of all adverse event reports for DAMOCTOCOG ALFA PEGOL.
55
Reports of Product dose omission issue with DAMOCTOCOG ALFA PEGOL
7.2%
of all DAMOCTOCOG ALFA PEGOL reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product dose omission issue From DAMOCTOCOG ALFA PEGOL?
Of the 55 reports, 2 (3.6%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DAMOCTOCOG ALFA PEGOL. However, 55 reports have been filed with the FAERS database.
What Other Side Effects Does DAMOCTOCOG ALFA PEGOL Cause?
Haemarthrosis (299)
Haemorrhage (218)
Arthralgia (44)
Limb injury (39)
Joint injury (38)
Muscle haemorrhage (36)
Traumatic haemorrhage (29)
Fall (24)
Contusion (21)
Joint swelling (19)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which DAMOCTOCOG ALFA PEGOL Alternatives Have Lower Product dose omission issue Risk?
DAMOCTOCOG ALFA PEGOL vs DANAPAROID
DAMOCTOCOG ALFA PEGOL vs DANAZOL
DAMOCTOCOG ALFA PEGOL vs DANICOPAN
DAMOCTOCOG ALFA PEGOL vs DANTROLENE
DAMOCTOCOG ALFA PEGOL vs DAPAGLIFLOZIN