Zulresso

GPTKB entity

Statements (58)
Predicate Object
gptkbp:instance_of gptkb:drug
gptkbp:bfsLayer 5
gptkbp:bfsParent gptkb:Sage_Therapeutics
gptkbp:activities GABA receptor modulation
gptkbp:brand brexanolone
gptkbp:clinical_trial Phase 3
short-term treatment
published in medical journals
Study 201
Study 202
Study 203
gptkbp:contraindication hypersensitivity to brexanolone
gptkbp:dissolved water-soluble
gptkbp:dosage_form gptkb:software_framework
gptkbp:duration 60 hours
continuous infusion
gptkbp:education important for understanding treatment
gptkbp:effective_date March 19, 2019
gptkbp:feedback generally positive
gptkbp:frequency once per treatment cycle
gptkbp:healthcare first drug specifically for postpartum depression
https://www.w3.org/2000/01/rdf-schema#label Zulresso
gptkbp:ingredients brexanolone
gptkbp:interacts_with CNS depressants
gptkbp:is_monitored_by required during infusion
gptkbp:is_used_for postpartum depression
gptkbp:manager intravenous
gptkbp:manufacturer gptkb:Sage_Therapeutics
gptkbp:market gptkb:stock_market_index
gptkbp:marketing_strategy ongoing
gptkbp:packaging single-use vial
gptkbp:population women with postpartum depression
gptkbp:price approximately $34,000 for treatment
gptkbp:provides_information_on considered for severe cases
hospital or healthcare facility
included in postpartum depression management
gptkbp:receives_funding_from supported by NIH
gptkbp:requires available online
gptkbp:research ongoing efficacy studies
gptkbp:safety_features monitor for excessive sedation
gptkbp:scholarships available through manufacturer
gptkbp:side_effect anxiety
dizziness
headache
nausea
vomiting
insomnia
sedation
infusion site reactions
gptkbp:social_structure C21 H30 O5 S
gptkbp:storage refrigerated
gptkbp:student_enrollment adults only
gptkbp:supports granted by FDA
gptkbp:training recommended for administration
gptkbp:treatment shown in clinical trials
enhances GAB Aergic transmission
reduction in depression symptoms
gptkbp:type_of_insurance varies by plan