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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

DAMOCTOCOG ALFA PEGOL for Factor viii deficiency: Side Effects & Safety Data

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There are 310 adverse event reports in the FDA FAERS database where DAMOCTOCOG ALFA PEGOL was used for Factor viii deficiency.

Most Reported Side Effects for DAMOCTOCOG ALFA PEGOL

Side Effect Reports % Deaths Hosp.
Haemarthrosis 299 39.2% 0 11
Haemorrhage 218 28.6% 0 10
Product dose omission issue 55 7.2% 0 2
Arthralgia 44 5.8% 0 1
Limb injury 39 5.1% 0 1
Joint injury 38 5.0% 0 3
Muscle haemorrhage 36 4.7% 0 3
Traumatic haemorrhage 29 3.8% 0 1
Fall 24 3.2% 0 2
Contusion 21 2.8% 0 1
Joint swelling 19 2.5% 0 1
Weight increased 17 2.2% 0 3
Pain 14 1.8% 0 3
Spontaneous haemorrhage 14 1.8% 0 0
Weight decreased 14 1.8% 0 2

Other Indications for DAMOCTOCOG ALFA PEGOL

Prophylaxis (65) Haemorrhage (45) Haemophilia (14) Haemorrhage prophylaxis (14) Intermenstrual bleeding (6) Haemarthrosis (5)

Other Drugs Used for Factor viii deficiency

EMICIZUMAB-KXWH (6,532) ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (4,268) EFMOROCTOCOG ALFA (832) --BLOOD-COAGULATION FACTOR VIII FUSION PROTEIN WITH IMMUNOGLOBULIN G1 , ,-BIS WITH IMMUNOGLOBULIN G1 (722) ANTIHEMOPHILIC FACTOR, PEGYLATED HUMAN SEQUENCE RECOMBINANT (352) ANTI-INHIBITOR COAGULANT COMPLEX (317) EMICIZUMAB (315) EFANESOCTOCOG ALFA (292) ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT RESIDUES 743-1636 DELETED (180) ANTIHEMOPHILIC FACTOR HUMAN (161)

Related Pages

DAMOCTOCOG ALFA PEGOL Full Profile All Factor viii deficiency Drugs DAMOCTOCOG ALFA PEGOL Demographics DAMOCTOCOG ALFA PEGOL Timeline