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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.

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

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There are 832 adverse event reports in the FDA FAERS database where EFMOROCTOCOG ALFA was used for Factor viii deficiency.

Most Reported Side Effects for EFMOROCTOCOG ALFA

Side Effect Reports % Deaths Hosp.
Haemorrhage 836 45.6% 1 100
Traumatic haemorrhage 139 7.6% 0 28
Arthralgia 137 7.5% 1 23
Limb injury 120 6.6% 0 13
Fall 114 6.2% 1 26
Haemarthrosis 114 6.2% 0 11
Spontaneous haemorrhage 99 5.4% 0 13
Joint injury 97 5.3% 0 15
Contusion 73 4.0% 0 5
Head injury 67 3.7% 0 15
Pain 61 3.3% 0 15
Epistaxis 53 2.9% 0 6
Off label use 52 2.8% 0 4
Pain in extremity 49 2.7% 0 11
Weight increased 48 2.6% 0 16

Other Indications for EFMOROCTOCOG ALFA

Haemorrhage (219) Prophylaxis (61) Immune tolerance induction (46) Product used for unknown indication (46) Haemophilia (34) Haemorrhage prophylaxis (22) Haemarthrosis (10)

Other Drugs Used for Factor viii deficiency

EMICIZUMAB-KXWH (6,532) ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (4,268) --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) EFANESOCTOCOG ALFA (292) ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT RESIDUES 743-1636 DELETED (180) ANTIHEMOPHILIC FACTOR HUMAN (161)

Related Pages

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