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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.

DESMOPRESSIN for Factor viii deficiency: Side Effects & Safety Data

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There are 69 adverse event reports in the FDA FAERS database where DESMOPRESSIN was used for Factor viii deficiency.

Most Reported Side Effects for DESMOPRESSIN

Side Effect Reports % Deaths Hosp.
Hyponatraemia 686 17.6% 23 524
Drug ineffective 456 11.7% 17 83
Headache 238 6.1% 1 56
Off label use 224 5.7% 12 99
Product use in unapproved indication 164 4.2% 18 55
Nasal discomfort 163 4.2% 0 0
Product storage error 162 4.2% 0 4
Nausea 131 3.4% 1 55
Blood sodium decreased 125 3.2% 0 58
Seizure 125 3.2% 1 93
Fatigue 119 3.1% 1 38
Recalled product administered 119 3.1% 1 32
Dizziness 115 3.0% 1 34
Vomiting 115 3.0% 1 66
Epistaxis 96 2.5% 1 6

Other Indications for DESMOPRESSIN

Product used for unknown indication (973) Diabetes insipidus (904) Nocturia (386) Von willebrand's disease (288) Enuresis (157) Polyuria (56) Hypopituitarism (53) Urinary incontinence (53) Pollakiuria (44) Haemorrhage (35)

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

DESMOPRESSIN Full Profile All Factor viii deficiency Drugs DESMOPRESSIN Demographics DESMOPRESSIN Timeline