Arexvy Dosage and Administration
Arexvy is administered as a single 0.5 mL intramuscular injection, and only one lifetime dose is currently recommended—adults who have already received any RSV vaccine should not receive another dose. 1, 2
Dosing Schedule
- Single lifetime dose: Administer one 0.5 mL intramuscular injection 1, 2
- No booster doses: Adults previously vaccinated with any RSV vaccine (Arexvy, Abrysvo, or mResvia) should not receive additional doses 1, 2
- Duration of protection: Current evidence demonstrates protection lasting through at least two consecutive RSV seasons 2
Optimal Timing for Administration
- Preferred timing: Administer between September and November (late summer to early fall), just before RSV season begins to maximize protection during peak transmission months 2, 3
- Flexible administration: Eligible adults who have not been previously vaccinated may receive the vaccine at any time of year 2
Who Should Receive Arexvy
Adults ≥75 Years
- Universal recommendation: All adults aged ≥75 years should receive RSV vaccination, regardless of comorbidities or health status 1, 2
Adults 60-74 Years with Risk Factors
- Chronic obstructive pulmonary disease (COPD), asthma, or other chronic respiratory conditions 2, 3
- Chronic heart failure, coronary artery disease, or congenital heart disease (excluding isolated hypertension) 3
- Chronic kidney disease, especially end-stage renal disease or hemodialysis dependence 2, 3
- Diabetes with complications (chronic kidney disease, neuropathy, retinopathy, or other end-organ damage) 3
- Chronic liver disease 2, 3
- Neurologic/neuromuscular conditions causing impaired airway clearance or respiratory muscle weakness 2, 3
- Severe obesity (BMI ≥40 kg/m²) 2, 3
- Moderate or severe immunocompromise (solid organ transplant, hematopoietic stem cell transplant, malignancies, immunosuppressive medications, asplenia) 2, 4
- Nursing home or long-term care facility residents 1, 2
Adults 50-59 Years with Risk Factors
- Arexvy is the only RSV vaccine approved for adults aged 50-59 years with risk factors for severe RSV disease 2, 3
- Same risk factor criteria apply as for the 60-74 year age group 2, 3
Administration Technique
- Route: Intramuscular injection 1
- Volume: 0.5 mL per dose 1
- Co-administration: Can be given simultaneously with seasonal influenza vaccine at different injection sites 2, 3
Critical Implementation Points
- Patient attestation is sufficient: Vaccination should not be denied due to lack of formal medical documentation—patient self-report of risk factors is adequate evidence 2, 3
- Qualified vaccinators: Pharmacists, nurse practitioners, and other providers (based on state law) may determine eligibility based on clinical assessment 1
- Do not delay for documentation: Adults ≥75 years should not have vaccination delayed while waiting for documentation, as age alone is sufficient indication 2
Priority if Supply is Limited
If vaccine availability is constrained, prioritize in this order: 2, 4
- Adults aged ≥75 years
- Adults aged 60-74 years with multiple comorbidities
- Residents of long-term care facilities
- Adults aged 50-59 years with multiple comorbidities
Common Pitfalls to Avoid
- Do not revaccinate: The single-dose recommendation applies even if the patient received a different RSV vaccine brand previously 1, 2
- Do not withhold based on isolated hypertension: Hypertension alone without other cardiovascular disease does not qualify as a risk factor 3
- Do not require extensive documentation: Patient attestation alone is sufficient—do not create barriers by demanding medical records 2, 3
- Previous RSV infection does not contraindicate vaccination: Natural infection does not confer long-lasting immunity, and vaccination is still indicated 2