Statements (64)
Predicate | Object |
---|---|
gptkbp:instance_of |
gptkb:physicist
|
gptkbp:appointed_by |
intravenous infusion
|
gptkbp:approves |
gptkb:FDA
gptkb:EMA |
gptkbp:clinical_trial |
gptkb:granulomatosis_with_polyangiitis
gptkb:microscopic_polyangiitis gptkb:healthcare_organization gptkb:rheumatoid_arthritis ongoing autoimmune diseases |
gptkbp:contains |
monoclonal antibodies
|
gptkbp:contraindication |
active infections
severe hypersensitivity history of progressive multifocal leukoencephalopathy |
gptkbp:developed_by |
gptkb:Rituximab
|
gptkbp:dosage_form |
varies by indication
|
gptkbp:education |
follow-up appointments
recognizing side effects importance of adherence |
gptkbp:formulation |
gptkb:item
|
gptkbp:frequency |
every few weeks
|
https://www.w3.org/2000/01/rdf-schema#label |
Rituximab biosimilars
|
gptkbp:interacts_with |
immunosuppressants
live vaccines other biologics |
gptkbp:invention |
off-patent
|
gptkbp:is_compared_to |
original Rituximab
|
gptkbp:is_compatible_with |
original Rituximab
|
gptkbp:is_monitored_by |
blood tests
vital signs |
gptkbp:manager |
IV
|
gptkbp:manufacturer |
various pharmaceutical companies
|
gptkbp:marketed_as |
multiple countries
various brand names |
gptkbp:pharmacokinetics |
adverse event reporting
C D20 targeting variable half-life |
gptkbp:population |
adults
pediatric patients |
gptkbp:provides_information_on |
ASCO guidelines
NCCN guidelines |
gptkbp:regulatory_compliance |
approved
|
gptkbp:research_areas |
oncology
rheumatology |
gptkbp:research_focus |
efficacy studies
safety studies cost-effectiveness studies |
gptkbp:sales |
growing
|
gptkbp:serves |
gptkb:healthcare_organization
gptkb:non-Hodgkin_lymphoma |
gptkbp:side_effect |
fatigue
headache nausea diarrhea rash cardiovascular events infections infusion reactions hypersensitivity reactions tumor lysis syndrome |
gptkbp:supply_chain |
cold chain management
|
gptkbp:used_in |
oncology
|
gptkbp:bfsParent |
gptkb:Rituximab
|
gptkbp:bfsLayer |
5
|