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Iʼm an OmniSource Case Manager (OCM) and Iʼm here to help get you enrolled in OmniSource, to welcome you to the program, and to support along the way.
To get started, Iʼll work closely with your doctor throughout the onboarding process – helping with Benefits Investigation (BI) and Prior Authorization (PA) forms and any potential appeals.
Once youʼre enrolled, Iʼll work with you to explain all of the OmniSource services available to you and your family, and help you determine which options are best for you.
Itʼs my job to help you make the most of your treatment journey, so if you have any questions along the way, you know who to ask!
I’m an OmniSource Nurse Trainer and it’s my role to help you get as comfortable as possible with administering your treatment at home.
I know that getting used to an injection routine can be challenging. That’s why I’m here to help you and your family to learn how to inject safely, at a pace that works for you.
There are three ways that we can work together. I offer injection training in person at your home, over the telephone or by video chat – however you are most comfortable.
If at any point, you would like a refresher or some additional training, call your OCM and they will be able to help coordinate a Nurse Trainer for you.
Here’s a look at what to expect, step by step, along the growth journey.
Our OmniSource Nurse Trainers and injection training resources can help.
Personalized support, each step of the way. Click here to enroll.
Omnitrope is a prescription medicine that contains human growth hormone and is used to treat:
Who should not take Omnitrope®?
Omnitrope should not be used by children or adults that have:
What should patients tell their healthcare provider before taking Omnitrope?
Patients should tell their healthcare provider about all of their medical conditions, including if they:
What are the most common side effects of Omnitrope?
Other possible side effects of Omnitrope are:
Please see full Prescribing Information for Omnitrope
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088. To report SUSPECTED ADVERSE REACTIONS, contact Sandoz Inc. at 1-800-525-8747 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch