HAppy knees, HAppy you!

To achieve the best outcomes and high satisfaction with your own patients—and reduce the time spent on follow-up:

  1. Schedule all 3 injections at one time.
  2. Encourage patients to take advantage of the Happy Knees Patient Program—enrollment is just one click away at www.euflexxa.com.
    1. Download the document below.
    2. Provide to your patient as soon as you decide that EUFLEXXA
      is the right choice for them.
  3. Once enrolled, a patient will receive a reminder text before every appointment and tips for keeping their knees healthy and happy.

Please See Important Safety Information and Full Prescribing Information.


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].


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.