Order Your EUFLEXXA (1% Sodium Hyaluronate) Today
Besse Medical offers EUFLEXXA (1% Sodium Hyaluronate). EUFLEXXA is a treatment to help relieve knee pain due to osteoarthritis in patients who have not responded adequately to nonpharmacologic therapy or simple analgesics. EUFLEXXA has been used by thousands of people to help manage their OA knee pain and to help them stay active. Besse offers extended terms, credit card privileges and volume discounts on EUFLEXXA.
Why should you consider EUFLEXXA?
EUFLEXXA was shown to have 81% overall patient satisfaction in its pivotal clinical trial.
Significant and sustained relief of OA knee pain at 6 months proven in the FLEXX trial.
ZERO joint effusions over 1 year and proven safe with repeated injection cycles up to 1 year.*
| ORDER - To place an order click on the item link below (must be logged in to place order) or Call 1-888-838-7687
||EUFLEXXA® 1% Prefilled Syringes 3/carton
NDC 55566-4100-01 Ferring Pharmaceuticals Inc.
* VOLUME PRICE BREAKS MAY BE AVAILABLE *
HCPCS CODE: J7323
120 DAY TERMS
Simplifying reimbursement for your practice.
fax: 1.866.EUFLEX2 (1.866.383.5392)
phone: 1.866.EUFLEX1 (1.866.383.5391) Weekdays 8:30AM - 6:00PM (EST)
Important Links & Resources
EUFLEXXA (1% sodium hyaluronate) is indicated for the treatment of pain in osteoarthritis (OA) of the knee in patients who have failed to respond adequately to conservative nonpharmacologic therapy and simple analgesics (e.g., 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.
EUFLEXXA® is a registered trademark of Ferring B.V.
All other trademarks are property of their respective owner.
*In the 12-week trial, there was 1 joint effusion reported in the EUFLEXXA group (n=160) vs 13 joint effusions in the Synvisc® group (n=161).