Eligard 30 mg

GPTKB entity

Statements (59)
Predicate Object
gptkbp:instance_of gptkb:pharmaceuticals
gptkbp:atccode L02 AE01
gptkbp:availability prescription only
gptkbp:brand gptkb:Eligard
gptkbp:class gonadotropin-releasing hormone agonists
gptkbp:clinical_trial Phase III
gptkbp:clinical_use hormone therapy
gptkbp:contraindication hypersensitivity to leuprolide
gptkbp:counseling_services report any severe side effects
gptkbp:dosage_form 30 mg
gptkbp:drug_interactions may increase blood sugar levels
gptkbp:duration as directed by physician
gptkbp:effective_date gptkb:2000
FDA approved
gptkbp:excretion urine
gptkbp:form injection
https://www.w3.org/2000/01/rdf-schema#label Eligard 30 mg
gptkbp:incompatibilities do not mix with other medications
gptkbp:indication advanced prostate cancer
gptkbp:ingredients gptkb:leuprolide_acetate
gptkbp:interacts_with anticoagulants
CYP3 A4 inhibitors
gptkbp:is_monitored_by testosterone levels
gptkbp:lifespan 3 hours
gptkbp:manufacturer gptkb:Taro_Pharmaceuticals
gptkbp:marketed_as gptkb:Eligard
gptkbp:mechanism_of_action Gn RH agonist
gptkbp:packaging single-use vial
gptkbp:patient_education inform about potential side effects
gptkbp:patient_population adult men
gptkbp:pharmacokinetics subcutaneous absorption
decreases testosterone production
gptkbp:previous_name gptkb:leuprolide_acetate
gptkbp:price varies by pharmacy
gptkbp:provides_guidance_on follow oncologist recommendations
gptkbp:recommissioned requires reconstitution before use
gptkbp:requires gptkb:true
gptkbp:route_of_administration subcutaneous
gptkbp:safety not for use in children
not for use in women
gptkbp:service_frequency every 3 months
gptkbp:shelf_life 24 months
gptkbp:side_effect gptkb:anemia
fatigue
headache
nausea
insomnia
weight gain
osteoporosis
mood changes
hot flashes
decreased libido
gptkbp:storage store in refrigerator
gptkbp:structure C59 H84 N16 O12
gptkbp:therapeutic_category oncology
gptkbp:used_for gptkb:Oncology
gptkbp:website abdomen
gptkbp:bfsParent gptkb:Eligard
gptkbp:bfsLayer 6