Sanofi Patient Connection
Our goal is to ensure that patients have hassle-free access to Synvisc-One® (hylan G-F 20) and SYNVISC® (hylan G-F 20).
Contact a reimbursement specialist
Sanofi Patient Connection is a comprehensive program designed to assist patient and healthcare professionals with a wide variety of services, such as:
- Insurance Verification (IV)
- Prior authorization (PA) assistance
- Billing and coding support
- Claims management and appeals assistance
- Patient assistance program
- Resource connection
- Specialty Pharmacy Provider (SPP) triage
Provider Portal (www.visitspconline.com)
- Provides online access to Sanofi Patient Connection
- Electronically submit IV and PA requests
- Manage patients, providers, and multiple office locations through one user profile
- Generates custom activity reports
Order Synvisc-One
and SYNVISC
Learn about the
different ordering
options available
for your patients.
Indication
SYNVISC® (hylan G-F 20) and Synvisc-One® (hylan G-F 20) are 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
SYNVISC and Synvisc-One are contraindicated in patients with known hypersensitivity to hyaluronan products or
patients with infections in or around the target knee.
Do not concomitantly use disinfectants containing quaternary ammonium salts for skin preparation because hyaluronan can precipitate in their presence.
Do not inject SYNVISC or Synvisc-One extraarticularly, into the synovial tissues, into the fat pad or joint capsule, or intravascularly.
The safety and efficacy of Synvisc-One in locations other than the knee, or for conditions other than osteoarthritis, or in combination with other intra-articular injectables, or in severely
inflamed knee joints have not been established. Use caution when injecting SYNVISC or Synvisc-One in patients allergic to avian proteins,
feathers, or egg products; who have evidence of lymphatic or venous stasis in the leg to be treated; or who have severe inflammation in the knee to be treated.
Remove any synovial fluid or effusion before injecting SYNVISC or Synvisc-One. Strict adherence to aseptic technique must be followed to avoid joint infection.
The safety and effectiveness of SYNVISC and Synvisc-One have not been established in children (≤21years old) or in pregnant or lactating women.
Patients should be advised to avoid strenuous or prolonged weight-bearing activities for approximately 48 hours after treatment.
For SYNVISC
In clinical trials, the most commonly reported adverse events were transient pain, swelling, and or joint effusion in the injected knee.
The following reported adverse events are among those that may occur in association with intra-articular injections, including Synvisc:
arthralgia, joint stiffness, joint effusion, joint swelling, joint warmth, injection site pain, arthritis, arthropathy, and gait disturbance.
Full Prescribing Information for SYNVISC (PDF)
For Synvisc-One
The most commonly reported adverse events were arthralgia, arthritis, arthropathy, injection site pain, and joint effusion.
The following reported adverse events are among those that may occur in association with intra-articular injections, including Synvisc-One:
arthralgia, joint stiffness, joint effusion, joint swelling, joint warmth, injection site pain, arthritis, arthropathy, and gait disturbance.
Full Prescribing Information for Synvisc-One (PDF)
