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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.

EFANESOCTOCOG ALFA for Factor viii deficiency: Side Effects & Safety Data

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There are 292 adverse event reports in the FDA FAERS database where EFANESOCTOCOG ALFA was used for Factor viii deficiency.

Most Reported Side Effects for EFANESOCTOCOG ALFA

Side Effect Reports % Deaths Hosp.
Haemorrhage 201 32.3% 0 20
Traumatic haemorrhage 55 8.8% 0 4
Arthralgia 45 7.2% 0 5
Fall 35 5.6% 0 3
Haemarthrosis 29 4.7% 0 7
Joint injury 29 4.7% 0 0
Limb injury 29 4.7% 0 4
Inappropriate schedule of product administration 24 3.9% 0 3
Contusion 23 3.7% 0 3
Epistaxis 23 3.7% 0 1
Dizziness 20 3.2% 0 2
Dyspnoea 19 3.1% 0 3
Headache 18 2.9% 0 4
Joint swelling 17 2.7% 0 2
Head injury 16 2.6% 0 0

Other Indications for EFANESOCTOCOG ALFA

Haemorrhage prophylaxis (42) Haemorrhage (33) Prophylaxis (19) Haemophilia (14) Product used for unknown indication (10)

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) DAMOCTOCOG ALFA PEGOL (310) ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT RESIDUES 743-1636 DELETED (180) ANTIHEMOPHILIC FACTOR HUMAN (161)

Related Pages

EFANESOCTOCOG ALFA Full Profile All Factor viii deficiency Drugs EFANESOCTOCOG ALFA Demographics EFANESOCTOCOG ALFA Timeline