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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.

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

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There are 17 adverse event reports in the FDA FAERS database where EFTRENONACOG ALFA was used for Factor viii deficiency.

Most Reported Side Effects for EFTRENONACOG ALFA

Side Effect Reports % Deaths Hosp.
Haemorrhage 802 37.5% 0 82
Haemarthrosis 196 9.2% 0 31
Fall 151 7.1% 0 36
Contusion 108 5.1% 0 15
Arthralgia 104 4.9% 0 13
Traumatic haemorrhage 93 4.4% 0 14
Limb injury 83 3.9% 0 8
Head injury 76 3.6% 0 24
Epistaxis 73 3.4% 0 11
Spontaneous haemorrhage 71 3.3% 0 6
Joint injury 63 3.0% 0 5
Joint swelling 62 2.9% 0 11
Pain 61 2.9% 0 13
Muscle haemorrhage 46 2.2% 0 3
Injury 45 2.1% 0 8

Other Indications for EFTRENONACOG ALFA

Factor ix deficiency (1,133) Haemophilia (148) Haemorrhage (109) Product used for unknown indication (93) Prophylaxis (77) Haemorrhage prophylaxis (34) Immune tolerance induction (16) Haemarthrosis (6)

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) EFANESOCTOCOG ALFA (292) ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT RESIDUES 743-1636 DELETED (180)

Related Pages

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