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Shared Solutions®
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Copaxone® is the #1 prescribed brand for relapsing MS in the US 1*

Helping patients stay committed to their COPAXONE® therapy

Teva’s Shared Solutions® offers a full range of support services to help your patients stay the course and reach their COPAXONE® treatment goals

Teva-trained nurses

Reliable partners for your patients and your practice

Teva-trained nurses provide your patients with services to help them stay on track, including

Small Change, Big Difference

Teva-trained nurses can help encourage your patients to stay on therapy.

See Services Offered

Personalized communication from Teva’s Shared Solutions® helps to offer patients the support they need throughout their therapy experience

Teva’s Shared Solutions® gives personal attention to COPAXONE® patients — patients receive ongoing contact from the team at Shared Solutions® via email, mail, and phone, so you can be confident that they have support every step of the way.

Teva’s Shared Solutions® PLUS

Teva’s Shared Solutions® PLUS — Compliance and adherence support for the critical first 90 days on COPAXONE®

Teva understands that some patients may be at a higher risk of discontinuing therapy. That's why Teva’s Shared Solutions® PLUS provides extra high-touch support so that you can be reassured that these patients are feeling cared for.

Who can benefit most from Teva’s Shared Solutions® PLUS?

Characteristics that may present barriers to compliance/adherence include

COPAXONE iTracker® 2.0

COPAXON® iTracker 2.0

A mobile tool to help patients track their injections

Teva’s Shared Solutions® presents the COPAXONE iTracker® 2.0 — an app that lets patients manage their injection routines using their Apple® or AndroidTM mobile devices. After analyzing patient feedback, several improvements have been incorporated into this new app.

The COPAXONE iTracker® 2.0 was designed with a user-friendly interface and includes features and resources that allow patients to:

  • Easily keep track of injection dates and sites
  • Customize their injection settings (device, method, site, dosage, and schedule).
  • Set personalized medication reminders
  • Record injections, notes, and photos within a journal.
  • Review past and future injections on a calendar.
  • Export and share their injection reports by email.
  • Connect directly to Teva's Shared Solutions® by phone for therapy support.
  • Get helpful tips about injection best practices.

Ask your patients to download COPAXONE iTracker® 2.0 from the App Store® or Google PlayTM.

App Store icon Google play icon

The autoject ®2 for glass syringe helps patients to manage their COPAXONE® injections

  • Patients do not have to see the needle while injecting
  • COPAXONE® therapy is delivered at the touch of a button
  • The autoject®2 for glass syringe can be used with both 20 mg/mL and 40 mg/mL formulations

autoject® 2 for glass syringe
Not actual size.

The autoject®2 for glass syringe is available through Teva’s Shared Solutions® for free with a physician's prescription.

  • Free replacements with prescription
  • Designed for 1,000 injections or 3 years of use, whichever comes first1

Look for the blue plunger

Teva's 3-times-a-week COPAXONE® 40 mg can be identified by the blue plunger.

COPAXONE® 40 mg can be identified by the blue plunger
Not actual size.

Teva’s Shared Solutions® is committed to helping your patients find financial solutions to start and stay on their COPAXONE® treatment
Explore financial solutions
In-home initial injection trainings help support patients' injection experience
Learn more
Explore milestones in the development of COPAXONE® as an enduring option in relapsing MS care.
VIEW OUR TIMELINE

Reference

  1. COPAXONE® (glatiramer acetate injection) Current Prescribing Information. Teva Neuroscience, Inc.

Injections for 3-times-a-week COPAXONE® 40 mg must be at least 48 hours apart.

IMPORTANT SAFETY INFORMATION

COPAXONE® is contraindicated in patients with known hypersensitivity to glatiramer acetate or mannitol.
Approximately 16% of patients exposed to COPAXONE® 20 mg per mL compared to 4% of those on placebo, and approximately 2% of

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