THE EUFLEXXA Solution Center

Assists with benefits investigations and reimbursement



Our dedicated team of highly trained reimbursement professionals is able to perform benefits investigations and
provide you with reimbursement information for EUFLEXXA.
Submissions can be made online or via phone or fax, and all inquiries are handled within 24 hours.*†
Live customer service is available Monday through Friday from 8:30 AM to 6 PM or by visiting euflexxaonline.com.

AS OF SUMMER 2018. MORE THAN 450,000 COMPLETED CASES; 97% WITHIN 24 HOURS. >8 YEARS ASSISTING CUSTOMERS. YTD RATE FOR DENIALS ON MEDICAL BENEFITS IS .039%.

*The EUFLEXXA Solution Center will respond to each fax submission within 24 hours, notifying you of a patient’s coverage via the Benefits Investigation Report.
The EUFLEXXA Solution Center does not file claims or appeal claims and cannot guarantee that you will be successful in obtaining reimbursement. Third-party payment for medical products and services is affected by numerous factors, none of which can be anticipated or resolved by the Solution Center.

Please See Important Safety Information and Full Prescribing Information.

INDICATION

EUFLEXXA® [1% sodium hyaluronate] is indicated for the treatment of pain in osteoarthritis [DA] of the knee in patients who have failed to respond adequately to conservative nonpharmacologic therapy and simple analgesics [eg, acetaminophen].

IMPORTANT SAFETY INFORMATION

EUFLEXXA is contraindicated in patients who have a known hypersensitivity to hyaluronate preparations or who have knee joint infections, infections, or skin disease in the area of the injection site.

EUFLEXXA should not be administered through a needle previously used with medical solutions containing benzalkonium chloride. Do not use skin disinfectants for skin preparation that contain quaternary ammonium salts.

Do not inject intravascularly due to potential for systemic adverse events.

The safety and effectiveness of injection in conjunction with other intra-articular injectables, or into joints other than the knee have not been studied. Remove any joint effusion prior to injecting. Transient pain or swelling of the injected joint may occur after intra-articular injection with EUFLEXXA.

The most common adverse events related to EUFLEXXA injections reported in 12- and 26-week clinical studies were arthralgia, back pain, pain in extremity, musculoskeletal pain, and joint swelling. In an open-label extension of the 26-week clinical study with repeat series of injections, the most common adverse events related to EUFLEXXA at Week 52 were arthralgia and joint swelling.

Please see Full Prescribing Information.

Please see Full Prescribing Information.