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FlexPro®

Life is filled with special moments, including the ones you plan and the ones that surprise you. Novo Nordisk wants to help patients get the most out of every single moment.

Easy to learn to use

The FlexPro® pen comes in 3 different "strengths", the 5, 10 and 15 mg. Your doctor will decide which strength is right for you based on the dose you need. After your doctor tells you how much you will need, the pen makes it easy to select the appropriate dose. You just turn the dial to the correct amount. You can adjust the dose, up or down, with a simple twist. And it's designed so you can feel and hear the difference depending on which way you are dialing. To reduce hassle even more, FlexPro® pens require no mixing, loading or changing of cartridges or batteries.

We also want to help you feel more comfortable about injections. That's why all Norditropin® pens use NovoFine® needles. They're very small and thin,to help lessen the discomfort of daily injections. The needles come with different options to help meet your needs. This includes one with a protective outer shield that hides the needle before, during and after the injection and locks into place to help reduce needlestick injuries.

FlexPro®

Ready to go with you

While most other growth hormones have to be kept refrigerated at all times, the FlexPro® 5- and 10-mg pens can be left at room temperature for up to 3 weeks after first use.* This allows for greater flexibility with overnight visits, vacations—even last-minute trips.

In fact FlexPro® is so easy, in a recent study of child and teenage patients, 100% said FlexPro® was easy to learn to use and 97% said it was easy to use.

*All Norditropin® products must be refrigerated prior to first use. Do not freeze. After initial use, FlexPro® 5 mg/1.5 mL and 10 mg/1.5 mL delivery pens can either be stored outside of the refrigerator (at up to 77°F) for use within 3 weeks, or in the refrigerator (between 36°F and 46°F) for use within 4 weeks. The FlexPro® 15 mg/1.5 mL and NordiFlex® 30 mg/3 mL delivery pens must always be refrigerated (between 36°F and 46°F)—both prior to and after the initial injection—for use within 4 weeks.

click here to learn more about using the Norditropin® pen

click here to learn how to personalize your Norditropin® pen

FlexPro®

Safety and Efficacy

The safety profile of Norditropin® has been established in multiple clinical studies conducted worldwide.

Important Safety Information Jump Link

Indications and Usage

Norditropin® (somatropin [rDNA origin] injection) is used to treat: children who have growth failure because of low or no growth hormone; children who are short (in stature) and who have Noonan syndrome or Turner syndrome; children who are short (in stature) because they were born small (small for gestational age-SGA) and have not caught-up in growth by age 2 to 4 years; and adults who do not make enough growth hormone.

Important Safety Information

Do not use Norditropin® if: you have a critical illness caused by certain types of heart or stomach surgery, trauma or breathing (respiratory) problems; you are a child with Prader-Willi syndrome who is severely obese or has breathing problems including sleep apnea; you have cancer or other tumors; your healthcare provider tells you that you have certain types of eye problems caused by diabetes; you are a child with closed bone growth plates (epiphyses) or you are allergic to any of the ingredients in the medicine.

Before you take Norditropin®, tell your healthcare provider if you: have diabetes; had cancer or any tumor; have any other medical condition; are pregnant or plan to become pregnant; are breast-feeding or plan to breast-feed.

Norditropin® can cause serious side effects, including: high risk of death in people who have critical illnesses because of heart or stomach surgery, trauma or serious breathing (respiratory) problems; high risk of death in children with Prader-Willi syndrome who are severely obese or have breathing problems including sleep apnea; return of tumor or cancerous growths; high blood sugar (hyperglycemia); increase in pressure in the skull (intracranial hypertension); swollen hands and feet due to fluid retention; decrease in thyroid hormone levels; hip and knee pain or a limp in children (slipped capital femoral epiphysis); worsening of pre-existing curvature of the spine (scoliosis); middle ear infection, hearing problems or ear problems in patients with Turner syndrome.

Patients with Noonan syndrome and Turner syndrome should be closely monitored by their doctors as they are more likely to have congenital heart disease.

The most common side effects of Norditropin® include: headaches, muscle pain, joint stiffness, high blood sugar (hyperglycemia), sugar in your urine (glucosuria), swollen hands and feet due to fluid retention, and redness and itching in the area you inject. If you have headaches, eye problems, nausea or vomiting (these may be symptoms of raised pressure in the brain), contact your healthcare provider right away.

Norditropin® may affect how other medicines work, and other medicines may affect how Norditropin® works so be sure to tell your healthcare provider about all the medicines you take including prescription and non-prescription medicines, vitamins, and herbal supplements.

Especially tell your healthcare provider if you take: glucocorticoid medication, thyroid hormone, insulin or other medicine for diabetes, medicines that are metabolized by the liver (e.g., corticosteroids, sex steroids, anticonvulsants, cyclosporine), or oral estrogen replacement medicine.

For more information, please click here for complete Norditropin® Prescribing Information.

Norditropin® is a prescription medication.

Novo Nordisk provides patient assistance for those who qualify. Please call 1-866-310-7549 to learn more about Novo Nordisk assistance programs.

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