Clesrovimab (ENFLONSIA clesrovimab 105 mg in 0.7 mL solution for injection prefilled syringe)
What to know about Clesrovimab — also sold as ENFLONSIA clesrovimab 105 mg in 0.7 mL solution for injection prefilled syringe: uses, side effects, interactions, and safety considerations for people taking it or caring for someone who is.
Clesrovimab (brand names: ENFLONSIA clesrovimab 105 mg in 0.7 mL solution for injection prefilled syringe) is classified as Low risk (1 risk points) by AllMeds. It is a S4 medication under the TGA in Australia. Monoclonal antibody for RSV prevention with minimal workplace safety impact.
Key Takeaways
- TGA Schedule: S4 in Australia
- Risk level: Low (1 points)
Scheduling and Classification
| Jurisdiction | Classification | Status |
|---|---|---|
| Australia (TGA) | S4 | Not PBS listed |
Risk Profile
Monoclonal antibody for RSV prevention with minimal workplace safety impact.
How Clesrovimab is regulated
Clesrovimab is overseen by medicines regulators in each country. The rules below explain how it's scheduled, what oversight applies, and what to discuss with your doctor or pharmacist before starting, changing, or stopping this medication.
Australia TGA / PBS / State Schemes
Classified as S4 under the Therapeutic Goods Administration (TGA).
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Important: This page is general health information, not personal medical advice. If you have questions about your medication — including starting it, stopping it, changing the dose, or combining it with something else — speak with your doctor or pharmacist. For an emergency or suspected overdose, call your local emergency number or poison information service immediately. Information is drawn from regulator and clinical guideline sources (TGA, FDA, MHRA, NICE, PBS, CDC); see our methodology for details.