| Drug | Class | Adult | Paediatric | Notes |
|---|---|---|---|---|
| Nirsevimab[1] | Long-acting anti-RSV F protein monoclonal antibody | Not applicable — paediatric prophylaxis | Infants <5 kg: 50 mg IM single dose; ≥5 kg: 100 mg IM single dose at start of RSV season; second-season at-risk: 200 mg IM | Replaces palivizumab in most settings; provides 5-month protection from one dose; reduces RSV bronchiolitis hospitalisation by ~80% |
| Palivizumab[1] | Anti-RSV F protein monoclonal antibody | Not applicable — paediatric prophylaxis | 15 mg/kg IM monthly throughout RSV season (max 5 doses) | Reserved for ex-prematurity, congenital heart disease, chronic lung disease where nirsevimab not available; replaced by nirsevimab in most national programmes from 2024 |
| Nebulised hypertonic 3% saline (selected inpatients)[1] | Mucolytic / hyperosmolar | Not applicable — paediatric prophylaxis | 4 mL nebulised every 2–4 h for first 24 h then less frequent | Inpatients with anticipated stay >24 h; not for outpatient use; pre-treat with bronchodilator if reactive airways concern |
Diagnosis and supportive care for acute viral bronchiolitis in infants <2 years; nirsevimab and palivizumab prophylaxis pathways.