Inactivated vaccine: 0.25-0.5 mL IM / Live-attenuated vaccine: 0.1 mL each nostril
Influenza vaccine dosing for children 6 months through 8 years
Who have only received 1 lifetime dose, require 2 doses > 4 weeks apart
Influenza vaccine timing
Vaccinate annually, ideally during September/October (may vaccinate throughout season)
Influenza vaccine efficacy
Median 47% (dependent on age, co-morbidities, and match) – vaccination reduces symptomatic illness, medical visits, hospitalization, and death. Note: immunitydelayed ~ 2 weeks after vaccination
Influenza vaccine contraindications
IIV4 and LAIV4: h/o anaphylaxis to the influenza vaccine (ccIIV and RIV may be used with caution if previous reaction was to IIV or LAIV). Eggallergy no longer considered a contraindication.
LAIV4 only: Pregnancy, immunocompromise, children aged 2-4 y w/ asthma, children/adolescents treated w/ aspirin/salicylates – risk of Reye syndrome, treatment w/ influenza antivirals w/in past 48 h (see CDC* for other C/Is)
Influenza vaccine common ADRs
IIV4/ccIIV4/RIV4/HD-IIV4/aIIV4: Transient injection site reactions predominate (e.g., pain lasting 1-2 d up to 65%)
Cell-cultured and recombinant influenza vaccines no longer contain eggprotein because they are not produced by growing flu viruses in eggs, unlike other IIV4 vaccines.
Pfizer and Moderna: h/o anaphylaxis or an immediate allergic reaction (e.g., hives, swelling, wheezing), even if not severe, to any ingredient in an mRNA COVID-19 vaccine – includes PEG (Novavax vaccines does not contain PEG)
COVID-19 vaccine common ADRs
Local injection site reactions up to 90% (pain, erythema, swelling), fatigue up to 60-80%, fever up to 20-25%, chills up to 40-50%, headache up to 60-75%, myalgia up to 45-60%, arthralgia up to 20-50%, axillary lymphadenopathy (swelling and tenderness) up to 30% (data only with SPIKEVAX)
COVID-19 vaccine rare but serious ADRs
Myocarditis and pericarditis: Chest pain, shortness of breath, feelings of a rapid/fluttering/pounding heart – rare, most common among adolescents and young adult males
Vaxneuvance™, Prevnar-20®, Pneumovax-23®: Suspension for injection (0.5 mL dose), single-dose prefilled syringe
Pneumococcal vaccine types
Conjugate vaccine (PCV) – Conjugated to a diphtheria toxoid protein and contains aluminum as an adjuvant
Polysaccharide vaccine (PPSV)
Pneumococcal vaccine recommended age
PCV13, PCV15, PCV20: Age > 6 weeks (note: PCV13 no longer recommended, to be discontinued)
PPSV23: Age > 2 years
Pneumococcal vaccine storage
Refrigerate (2 to 8°C)
Pneumococcal vaccine dosing/route
PCV15/20: 0.5 mL IM – Refer to CDC/ACIP recommendations, with attention to high-risk conditions/dose spacing
PPSV23: 0.5 mL IM or SC – Refer to CDC/ACIP recommendations, with attention to high-risk conditions/dose spacing
Pneumococcal vaccine efficacy
Pediatric: Since approval of PCV, invasive disease in children caused by serotypes in PCV7 and PCV13 declined 99% and 90%, respectively / Adult: PCV13 – 46% efficacy against vaccine-type pneumonia and 75% efficacy against invasive pneumococcal disease (note: immunogenicity of PCV20 comparable to PCV13)
Febrile seizures in young children if given on the same day as IIV.
Pneumococcal vaccine special considerations
Patients with functional or anatomic asplenia are at very high risk (up to 50X risk) for invasive pneumococcal disease and therefore require vaccination; Patients with a high-risk medical condition may receive either PCV20 or PCV15 followed by PPSV23 – when both PCV and PPSV are indicated, always administer PCV first.