Summary & Overview
HCPCS J7169: Andexxa (Coagulation Factor Xa Recombinant) 10 mg Injection
HCPCS Level II code J7169 designates a 10 mg injection of recombinant, inactivated coagulation factor Xa (andexxa), a specialized reversal agent used in acute management of life-threatening bleeding associated with factor Xa inhibitors. The code is clinically significant nationwide due to its role in emergent care and its high-cost, single-use therapeutic profile that affects hospital formularies, utilization management, and payer coverage policies.
Key payers analyzed include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find an overview of clinical context for andexxa use, typical sites of service where the agent is administered, and the payer landscape relevant to coverage and billing for high-cost reversal agents. The publication summarizes benchmark considerations, coding and billing implications for inpatient and emergency use, and recent policy developments affecting access and prior authorization practices.
This analysis helps clinicians, coders, and policy stakeholders understand where J7169 fits into acute care workflows, how major payers approach coverage, and what operational and documentation elements commonly affect reimbursement and utilization.
Billing Code Overview
HCPCS Level II code J7169 represents an injection of recombinant, inactivated coagulation factor Xa (andexxa) at 10 mg. This product is indicated for the reversal of anticoagulant effects of certain factor Xa inhibitors in acute, life-threatening bleeding situations and other clinical scenarios where rapid factor Xa activity neutralization is required.
Service Type: Therapeutic injection / reversal agent administration
Typical Site of Service: Hospital inpatient and emergency department settings, including intensive care units and perioperative care where urgent reversal of factor Xa inhibitors is needed.
Data not available in the input.
Clinical & Coding Specifications
Clinical Context
A typical patient is an adult hospitalized for life-threatening bleeding or requiring urgent reversal of factor Xa inhibitor anticoagulation prior to an emergent procedure. The patient may be receiving apixaban, rivaroxaban, or edoxaban and presents with intracranial hemorrhage, major gastrointestinal bleeding, or needs immediate surgical hemostasis. After initial assessment in the emergency department or inpatient ward, the team documents the anticoagulant and last dose time, assesses renal function, obtains baseline coagulation studies, and consults hematology or anesthesia as indicated. The pharmacy prepares J7169 (andexanet alfa) in 10 mg increments; dosing is weight‑ and agent‑based and delivered as an intravenous bolus followed by infusion per product guidelines. The medication is administered in the ED, OR, or ICU with continuous monitoring for thrombotic events and hemostasis. Documentation includes indication, anticoagulant type and dose, time since last dose, dosing regimen of andexanet, lot numbers, expired/unadministered drug discarded (if applicable), and informed consent when feasible.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
JW | Drug discarded/unused portion | Use when part of the single‑use vial is discarded and documentation supports discarded amount. |