Properties (58)
Predicate | Object |
---|---|
gptkbp:instanceOf |
medication
|
gptkbp:activeDuring |
C1 esterase inhibitor
|
gptkbp:administrativeDivision |
every 3 to 4 days
|
gptkbp:availability |
prescription only
|
gptkbp:clinicalTrials |
improved quality of life
Phase III ongoing studies preventive treatment recommended for HAE patients reduced frequency of attacks shown in clinical trials |
gptkbp:community_service |
available
|
gptkbp:contraindication |
thromboembolic events
anaphylaxis hypersensitivity_to_C1_esterase_inhibitor |
gptkbp:customerFeedback |
generally positive
|
gptkbp:date |
2008-10-07
|
gptkbp:dosageForm |
solution
1 mL/min |
gptkbp:drugInterdiction |
none reported
injectable solution half-life of 3-4 days increases C1 inhibitor levels |
gptkbp:formulation |
human plasma-derived
|
gptkbp:hasCapacity |
available through manufacturer
|
gptkbp:hasCompetitors |
other HAE treatments
|
gptkbp:hasPopulation |
adults and children
|
gptkbp:healthcare |
important for adherence
|
https://www.w3.org/2000/01/rdf-schema#label |
Cinryze
|
gptkbp:is_monitored_by |
C1 inhibitor levels
|
gptkbp:isSubjectTo |
10 mL
|
gptkbp:label |
risk of hypersensitivity reactions
risk of thromboembolic events |
gptkbp:mandates |
gptkb:hereditary_angioedema
|
gptkbp:manufacturer |
ViroPharma
|
gptkbp:marketedAs |
gptkb:Canada
gptkb:European_Union gptkb:United_States |
gptkbp:marketSegment |
ongoing
|
gptkbp:offers |
varies by region
|
gptkbp:packaging |
single-use vial
|
gptkbp:receives_funding_from |
available in many insurance plans
|
gptkbp:regulatoryCompliance |
FDA_approved
EMA_approved Health_Canada_approved |
gptkbp:research |
various sources
|
gptkbp:researchFocus |
improving efficacy
reducing side effects |
gptkbp:route |
intravenous
|
gptkbp:safetyFeatures |
required
|
gptkbp:sideEffect |
headache
nausea abdominal pain diarrhea |
gptkbp:storage |
refrigerated
|
gptkbp:supplyChain |
managed by manufacturer
|
gptkbp:training |
required for patients
|
gptkbp:usedFor |
prevention of hereditary angioedema attacks
|