anthrax vaccine adsorbed (AVA)

GPTKB entity

Statements (50)
Predicate Object
gptkbp:instance_of gptkb:vaccine
gptkbp:administered_by injection
gptkbp:administration_schedule 0, 7, and 21 or 28 days
gptkbp:antigen protective antigen
gptkbp:approves gptkb:1970
gptkb:U._S._Food_and_Drug_Administration
gptkbp:associated_with gptkb:Bacillus_anthracis
gptkbp:booster_required every 1 to 3 years
gptkbp:clinical_trial conducted for safety and efficacy
high-risk occupations
gptkbp:contraindication severe allergic reactions
gptkbp:developed_by gptkb:U._S._Army_Medical_Research_Institute_of_Infectious_Diseases
gptkbp:dosage_form 3 doses
gptkbp:duration_of_immunity approximately 2 years
https://www.w3.org/2000/01/rdf-schema#label anthrax vaccine adsorbed (AVA)
gptkbp:is_recommended_for gptkb:military_personnel
laboratory workers
gptkbp:is_vulnerable_to varies by provider
intramuscular
subunit vaccine
supported by government and private sectors
high in healthy adults
based on clinical trials
available through select healthcare providers
based on research from the 1950s
continues for improved formulations
developed in response to anthrax outbreaks
limited to specific populations
lower in immunocompromised individuals
significant in preventing anthrax outbreaks
gptkbp:manufacturer gptkb:Emergent_Bio_Solutions
gptkbp:notable_for bioterrorism preparedness
gptkbp:post_exposure_prophylaxis not recommended
gptkbp:safety_measures ongoing post-marketing surveillance
gptkbp:serological_response measured by antibody levels
gptkbp:side_effect fatigue
headache
muscle pain
nausea
fever
local reactions
systemic reactions
gptkbp:storage refrigerated
gptkbp:targets gptkb:disease
gptkbp:type inactivated vaccine
gptkbp:used_for prevention of anthrax
gptkbp:vaccine_labeling includes contraindications and warnings
gptkbp:vaccine_regulation regulated by the FDA
gptkbp:bfsParent gptkb:inhalation_anthrax
gptkbp:bfsLayer 5