Summary & Overview
HCPCS Q0247: Injection, sotrovimab, 500 mg
HCPCS Level II code Q0247 denotes the administration of sotrovimab, 500 mg, an intravenous monoclonal antibody therapy. This code is used to bill for the drug product and its administration when sotrovimab is provided for eligible patients. Nationally, monoclonal antibody infusions represent a significant component of outpatient specialty therapeutics and billing for these agents has implications for payer coverage policies, site-of-care considerations, and provider reimbursement workflows.
Key payers covered in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of clinical and billing context for Q0247, common service settings where sotrovimab is administered, and the types of benchmarks and policy topics typically associated with high-cost outpatient infusions. The publication outlines typical coding use, payer coverage patterns, and relevant administrative considerations such as site-of-service designation and service line placement.
This summary also identifies where data is available or absent and highlights areas readers can expect to explore further: reimbursement benchmarks, prior authorization practice, and payer-specific coding guidance. Data not available in the input will be clearly noted in the detailed sections.
Billing Code Overview
HCPCS Level II code Q0247 represents Injection, sotrovimab, 500 mg. This code denotes administration of the monoclonal antibody sotrovimab in a 500 mg dose vial for intravenous infusion.
Service Type: Intravenous monoclonal antibody infusion
Typical Site of Service: Outpatient infusion center, physician office, or hospital outpatient department
Clinical & Coding Specifications
Clinical Context
A typical patient is an adult with laboratory-confirmed SARS-CoV-2 infection who is at high risk for progression to severe COVID-19 (for example, age ≥65, immunocompromised state, or chronic medical conditions such as diabetes or chronic kidney disease). The patient presents to an infusion center, emergency department observation unit, or outpatient clinic within the early symptomatic window (generally within 5–7 days of symptom onset) and is evaluated by a treating clinician. After eligibility assessment, informed consent, and screening for contraindications (allergy to monoclonal antibodies, current severe oxygen requirement for COVID-19), a single 500 mg dose of sotrovimab is prepared and administered as an intravenous infusion. Vital signs and infusion reaction precautions are documented; the patient is monitored during and for at least 1 hour after infusion for hypersensitivity or infusion-related reactions. Documentation includes indication, date/time of infusion, lot number, dose 500 mg, site of administration, and any immediate adverse events. Typical sites of service are hospital outpatient infusion centers, ambulatory infusion clinics, emergency departments, and skilled nursing facility medical suites capable of intravenous administration and monitoring.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
23 | Unusual procedural service | When general anesthesia is administered for the infusion in an unusual circumstance |