Patient info

Norditropin Flexpro 15 mg / 1.5 ml solution for injection in Pre-filled pen – patient leaflet, side effects, dosage

Updated:
Key facts
Status:
Prescription only (POM) Controlled drug (Schedule 4)
Medicine strength:
15 mg / 1.5 ml (10 mg/ml)
Contains active substance:
ATC code:

Patient leaflet - Norditropin Flexpro 15 mg / 1.5 ml solution for injection in Pre-filled pen

1. What Norditropin® FlexPro® is and what it is used for

Norditropin® FlexPro® contains a biosynthetic human growth hormone called somatropin which is identical to the growth hormone produced naturally in the body. Children need growth hormone to help them grow, but adults also need it for their general health.

Norditropin® FlexPro® is used to treat growth failure in children

•

If they have no or very low production of growth hormone (growth hormone deficiency)

•

If they have Turner syndrome (a genetic

problem which may affect growth)

•

If they have reduced kidney function

•

If they are short and were born small for gestational age (SGA)

•

If they have Noonan syndrome (a genetic problem which may affect growth).

Norditropin® FlexPro® is used as a growth hormone replacement in adults

In adults Norditropin® FlexPro® is used to replace growth hormone if their growth hormone production has been decreased since childhood or has been lost in adulthood because of a tumour, treatment of a tumour, or a disease that affects the gland which produces growth hormone. If you have been treated for growth hormone deficiency during childhood, you will be retested after completion of growth. If growth hormone deficiency is confirmed, you should continue treatment.

1

Package leaflet: Information for the user

Norditropin® FlexPro® 15 mg/1.5 ml solution for injection in pre-filled pen

somatropin

VV-LAB-141935 1.0

.

2. What you need to know before you use Norditropin® FlexPro®

Do not use Norditropin® FlexPro®

•

If you are

allergic to somatropin, to phenol, or to any of the other ingredients of this medicine (listed in section 6)

•

If you have had a

kidney transplant

•

If you have an

active tumour (cancer). Tumours must be inactive and you must have finished your antitumour treatment before you start your treatment with Norditropin® FlexPro®

•

If you have an

acute critical illness, e.g. open heart surgery, abdominal surgery, multiple accidental trauma or acute respiratory failure

•

If you have stopped growing (closed epiphyses)

and you do not have growth hormone deficiency.

Warnings and precautions

Talk to your doctor or pharmacist before using Norditropin® FlexPro®

•

If you have

diabetes

•

If you have ever had a

cancer or another kind of tumour

•

If you have recurrent

headaches, eyesight problems, nausea or if vomiting occurs

•

If you have abnormal

thyroid function

•

An increase in sideways curvature of the spine

(scoliosis) may progress in any child during rapid growth. During treatment with Norditropin® FlexPro®, your doctor will check you (or your child) for signs of scoliosis

•

If you walk with a limp or if you start to limp

during your growth hormone treatment, you should inform your doctor

•

If you are

over 60 years of age, or have received somatropin treatment as an adult for more than 5 years, as experience is limited

•

If you suffer from

kidney disease, as your kidney function should be monitored by your physician

•

If you have a

replacement therapy with glucocorticoids, you should consult your doctor regularly, as you may need adjustment of your glucocorticoid dose

•

Norditropin® FlexPro® may cause an inflammation of the pancreas, which causes severe pain in the abdomen and back. Contact your doctor if you or your child develops stomach ache after taking Norditropin® FlexPro®.

Other medicines and Norditropin® FlexPro®

Tell your doctor or pharmacist if you are using, have recently used or might use any other medicines.

In particular, inform your doctor if you are taking or have recently taken any of the following medicines. Your doctor may need to adjust the dose of Norditropin® FlexPro® or of the other medicines:

•

Glucocorticoids – your adult height may be affected if you use Norditropin® FlexPro® and glucocorticoids at the same time

•

Ciclosporin (immunosuppressive) – as your dose may need to be adjusted

•

Insulin – as your dose may need to be adjusted

•

Thyroid hormone – as your dose may need to be adjusted

•

Gonadotropin (gonad stimulating hormone) – as your dose may need to be adjusted

•

Anticonvulsants – as your dose may need to be adjusted

•

Oestrogen taken orally or other sex hormones.

Pregnancy and breast-feeding

Somatropin containing products are not recommended in women of childbearing potential not using contraception.

•

Pregnancy - stop the treatment and tell your doctor if you become pregnant while you are using Norditropin® FlexPro®

•

Breast-feeding - do not use Norditropin® FlexPro® while you are breast-feeding because somatropin might pass into your milk.

Driving and using machines

Norditropin® FlexPro® does not affect the use of any machines or the ability to drive safely.

2

Norditropin® contains sodium

Norditropin® contains less than 1 mmol sodium (23 mg) per 1.5 ml, that is to say essentially `sodium-free’.

3. How to use Norditropin® FlexPro®

Always use this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.

The dose for children depends on their body weight and body surface area. Later in life, the dose depends on your height, weight, gender and growth hormone sensitivity and will be adjusted until you are on the right dose.

•

Children with low production or lack of

growth hormone:

The usual dose is 0.025 to 0.035 mg per kg

body weight per day or 0.7 to 1.0 mg per m2 body surface area per day

•

Children with Turner syndrome:

The usual dose is 0.045 to 0.067 mg per kg

body weight per day or 1.3 to 2.0 mg per m2 body surface area per day

•

Children with kidney disease:

The usual dose is 0.050 mg per kg body

weight per day or 1.4 mg per m² body surface area per day

•

Children born small for gestational age (SGA):

The usual dose is 0.035 mg per kg body

weight per day or 1.0 mg per m2 body surface area per day until final height is reached. (In clinical trials of short children born SGA doses of 0.033 and 0.067 mg per kg body weight per day have typically been used)

•

Children with Noonan syndrome:

The usual dose is 0.066 mg per kg body

weight per day, however your doctor may decide that 0.033 mg per kg body weight per day is sufficient

•

Adults with low production or lack of growth hormone:

If your growth hormone deficiency continues after completion of growth, treatment should be continued. The usual starting dose is 0.2 to 0.5 mg per day. The dose will be adjusted until you are on the right dose. If your growth hormone deficiency starts during adult life, the usual starting dose is 0.1 to 0.3 mg per day. Your doctor will increase this dose each month until you are getting the dose you need. The usual maximum dose is 1.0 mg per day.

When to use Norditropin® FlexPro®

Inject your daily dose into the skin every evening just before bedtime.

How to use Norditropin® FlexPro®

Norditropin® FlexPro® growth hormone solution comes in a multidose disposable 1.5 ml pre-filled pen.

Full instructions on how to use Norditropin® FlexPro® are given overleaf. The instructional key points are as follows:

•

Check the solution before use by turning the pen upside down once or twice. Do not use the pen if the solution is cloudy or discoloured (see page 8, step A)

•

Norditropin® FlexPro® is designed to be used with NovoFine® or NovoTwist® disposable needles up to a length of 8 mm

•

Always use a new needle for each injection

•

Vary the area you inject so you do not harm your skin

•

To make sure you get the proper dose and do not inject air, check the growth hormone flow before the first injection from a new Norditropin® FlexPro® pen. Do not use the pen if a drop of growth hormone solution does not appear at the needle tip (see pages 10 to 11, steps E to G)

•

Do not share your Norditropin® FlexPro® pen with anyone else.

3

How long you will need treatment for

•

Children with growth failure because of Turner

syndrome, kidney disease, SGA or Noonan syndrome: Your doctor will recommend you continue treatment until you stop growing

•

Children or adolescents who lack growth

hormone: Your doctor will recommend you continue treatment into adulthood

Do not stop using Norditropin® FlexPro® without discussing it with your doctor first.

If you use more Norditropin® FlexPro® than you should

Tell your doctor if you inject too much somatropin. Long-term overdosing can cause abnormal growth and coarsening of facial features.

If you forget to use Norditropin® FlexPro®

Take the next dose as usual, at the normal time. Do not take a double dose to make up for a forgotten dose.

If you stop using Norditropin® FlexPro®

Do not stop using Norditropin® FlexPro® without discussing it with your doctor first.

If you have any further questions on the use of this medicine, ask your doctor or pharmacist.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Effects seen in children and adults (unknown frequency)

•

Rash; wheezing; swollen eyelids, face or lips; complete collapse. Any of these may be signs of an allergic reaction

•

Headache, eyesight problems, feeling sick (nausea) and being sick (vomiting). These may be signs of raised pressure in the brain

•

Serum thyroxin levels may decrease

•

Hyperglycaemia (elevated levels of blood glucose).

If you get any of these effects, see a doctor as soon as possible. Stop using Norditropin® FlexPro® until your doctor says you can continue treatment.

Formation of antibodies directed against somatropin has rarely been observed during Norditropin® therapy.

Increased levels of liver enzymes have been reported.

Cases of leukaemia and relapse of brain tumours have also been reported in patients treated with somatropin (the active ingredient in Norditropin® FlexPro®), although there is no evidence that somatropin was responsible for this.

If you think you are suffering from any of these diseases, talk to your doctor.

Additional side effects in children

Uncommon (may affect up to 1 in 100 children)

•

Headache

•

Redness, itching and pain in the area of injection

•

Breast enlargement (gynaecomastia).

Rare (may affect up to 1 in 1,000 children)

•

Rash

•

Muscle and joint pain

•

Swollen hands and feet due to fluid retention.

In rare cases, children using Norditropin® FlexPro® have experienced hip and knee pains or have started limping. These symptoms may be a

consequence of the end of the bone having slipped from the cartilage (slipped capital femoral epiphysis) or a disease affecting the top of the thigh bone (osteonecrosis of femoral head including Legg-Calvé disease). Talk to your doctor about persistent pain.

In children with Turner syndrome, a few cases of increased growth of hands and feet compared to height have been observed in clinical trials.

4

A clinical trial in children with Turner syndrome has shown that high doses of Norditropin® can possibly increase the risk of getting ear infections.

If any of these side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist, as the dose may need to be reduced.

Additional side effects in adults

Very common (may affect more than 1 in 10 adults)

•

Swollen hands and feet due to fluid retention.

Common (may affect up to 1 in 10 adults)

•

Headache

•

Feeling of

skin crawling (formication) and numbness or pain mainly in fingers

•

Joint pain and stiffness; muscle pain.

Uncommon (may affect up to 1 in 100 adults)

•

Type 2 diabetes

•

Carpal tunnel syndrome; tingling and pain in fingers and hands

•

Itching (can be intense) and pain in the area of injection

•

Muscle stiffness

•

Breast enlargement

(gynaecomastia).

Reporting of side effects

If you get any side effect, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet.

You can also report side effects directly via the Yellow Card Scheme Website: https://yellowcard. mhra.gov.uk/ or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects you can help provide more information on the safety of this medicine.

5. How to store Norditropin® FlexPro®

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiry date which is stated on the package after EXP/. The expiry date refers to the last day of that month.

Store unused Norditropin® FlexPro® pens in a refrigerator (2°C – 8°C) in the outer carton, in order to protect them from light. Do not freeze or expose to heat. Do not store close to any cooling elements.

While using Norditropin® FlexPro® 15 mg/1.5 ml you can either:

•

Keep it for up to 4 weeks in a refrigerator

(2°C – 8°C), or

•

Keep it for up to 3 weeks at room temperature

(below 25°C).

Do not continue to use Norditropin® FlexPro® pens if they have been frozen or exposed to excessive temperatures.

Do not use Norditropin® FlexPro® pens where the growth hormone solution is cloudy or discoloured.

Always store Norditropin® FlexPro® without a needle attached.

Always keep the pen cap fully closed on the Norditropin® FlexPro® pen when you are not using it.

Always use a new needle for each injection.

Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

6. Contents of the pack and other information

What Norditropin® FlexPro® contains

•

The active substance is somatropin

•

The other excipients are mannitol, histidine, poloxamer 188, phenol, water for injection, hydrochloric acid and sodium hydroxide.

5

What Norditropin® FlexPro® looks like and contents of the pack

Norditropin® FlexPro® is a clear and colourless solution for injection in a multidose disposable 1.5 ml pre-filled pen.

1 ml of solution contains 10 mg somatropin.

1 mg of somatropin corresponds to 3 IU of somatropin.

Norditropin® FlexPro® is available in three strengths:

5 mg/1.5 ml, 10 mg/1.5 ml and 15 mg/1.5 ml (equivalent to 3.3 mg/ml, 6.7 mg/ml and 10 mg/ml, respectively) in pack sizes of 1 or 5 pre-filled pens. Not all pack sizes may be marketed.

Marketing Authorisation Holder and Manufacturer

Marketing Authorisation Holder

Novo Nordisk Limited

3 City Place

Beehive Ring Road

Gatwick

West Sussex

RH6 0PA

Manufacturer

Novo Nordisk A/S

Novo Allé

DK-2880 Bagsværd

Denmark

This leaflet was last revised in 06/2026

Other sources of information

Detailed information on this medicine is available on the website of: MHRA

6

Instructions on how to use Norditropin® FlexPro®

Please read these instructions carefully before using your Norditropin® FlexPro® pen.

Start by checking the name, strength and coloured label of your Norditropin® FlexPro® pen to make sure that it contains the growth hormone strength you need.

Read on to learn about:

Preparing your Norditropin® FlexPro® pen

Checking the growth hormone flow with each new pen

Selecting your dose

Injecting your dose

Caring for your Norditropin® FlexPro® pen

Important information

Your Norditropin® FlexPro® pen is a pre-filled growth hormone pen. Norditropin® FlexPro® contains 15 mg human growth hormone solution and delivers doses from 0.1 mg to 8.0 mg, in increments of 0.1 mg. Norditropin® FlexPro® is designed to be used with NovoFine® or NovoTwist® disposable needles up to a length of 8 mm.

7

Norditropin® FlexPro®

Needle (example)

Pen cap

Growth hormone scale

Display

Pointer

Dose selector

Dose button

Outer needle cap

Inner needle cap

Needle

Paper tab

Preparing your Norditropin® FlexPro® pen

Check the name, strength and coloured label of your Norditropin® FlexPro® pen to make sure that it contains the growth hormone strength you need.

8

Pull off the pen cap.

Check that the growth hormone solution in the pen is clear and colourless by tipping it upside down once or twice. If the solution looks unclear or cloudy, do not use the pen.

Take a new disposable needle. Tear the paper tab off and screw the needle straight onto the pen. Make sure the needle is on tight.

Always use a new needle for each injection. This reduces the risk of contamination, infection, leakage of growth hormone, blocked needles and inaccurate dosing.

Never bend or damage the needle.

A

B

A

B

9

C

C

Pull off the outer needle cap and save it.

After injection, you will need it to correctly remove the needle from the pen.

D

D

Pull off the inner needle cap and throw it away.

If you try to put it back on, you may accidentally stick yourself with the needle.

A drop of growth hormone may appear at the needle tip. This is normal.

Checking the growth hormone flow with each new pen

Make sure that you receive your full dose by checking the growth hormone flow before you select and inject your first dose with each new pen.

10

Turn the dose selector to select the minimum dose, 0.1 mg.

Hold the pen with the needle pointing up.

Tap the top of the pen a few times to let any air bubbles rise to the top.

E

F

E

0.1 mg selected

F

11

G

G

Press the dose button until the figure 0 in the display lines up with the pointer and a drop of growth hormone appears at the needle tip.

If no drop appears, repeat steps E to G up to 6 times. If no drop appears after these new attempts, change the needle and repeat steps E to G once more.

Do not use the pen if a drop of growth hormone still does not appear.

Always make sure that a drop appears at the needle tip before you inject your first dose with each new pen.

12

Selecting your dose

Use the dose selector on your Norditropin® FlexPro® pen to select up to 8.0 mg per dose.

H

H

Select or adjust the dose you need by turning the dose selector forwards or backwards until the right number of mg lines up with the pointer.

When the pen contains less than 8.0 mg, the dose selector stops at the number of mg left.

How much growth hormone is left?

You can use the growth hormone scale to see approximately how much growth hormone is left in the pen.

You can use the dose selector to see exactly how much growth hormone is left – if the pen contains less than 8.0 mg:

Turn the dose selector until it stops. The figure that lines up with the pointer shows how many mg are left.

If you need more growth hormone than you have left in your pen, you can use a new pen or split your dose between your current pen and a new pen.

Never use the pen clicks to count the number of mg you select. Only the display and pointer will indicate the exact number of mg.

Never use the growth hormone scale to measure how much growth hormone to inject. Only the display and pointer will indicate the exact number of mg.

1.2 mg selected

5.9 mg selected

The dose selector clicks differently when turned forwards, backwards or past the number of mg left.

13

I

J

Insert the needle into your skin as your doctor or nurse has shown you. Press the dose button to inject until the figure 0 in the display lines up with the pointer.

As you do this, you may hear or feel a click.

Leave the needle under the skin for at least 6 seconds to make sure that you get your full dose.

You can let go of the dose button while you wait.

Remove the needle from the skin.

After that, you may see a drop of growth hormone at the needle tip. This is normal and has no effect on the dose you just received.

Never use the pen clicks to count the number of mg you inject. Only the display and pointer will indicate the exact number of mg.

Never touch the display when you inject, as this can block the injection.

Injecting your dose

Make sure that you receive your full dose by using the right injection technique.

J

I

6 seconds

14

K

K

Put the outer needle cap back on carefully without touching the needle. Unscrew the needle and throw it away carefully as instructed by your doctor or nurse.

Put the pen cap back on after every use.

When the pen is empty, throw it away without a needle on as advised by your doctor or nurse and local authorities.

Never put the inner needle cap back on once you have removed it from the needle. You may accidentally stick yourself with the needle.

Always store the pen without a needle attached. This reduces the risk of contamination, infection, leakage of growth hormone, blocked needles and inaccurate dosing.

15

Caring for your Norditropin® FlexPro® pen

Important information

Treat your Norditropin® FlexPro® pen with care:

•

Do not drop your pen or knock it against hard surfaces. If you do drop it or suspect that something is wrong with it, always screw on a new disposable needle and check the growth hormone flow before you inject.

•

Do not try to refill your pen – it is pre-filled.

•

Do not try to repair your pen or pull it apart.

•

Do not expose your pen to dust, dirt, liquid or direct light.

•

Do not try to wash, soak or lubricate your pen. If necessary, clean it with a mild detergent on

a moistened cloth.

•

Do not freeze your pen or store it close to any cooling element, e.g. in a refrigerator.

•

See section 5 “How to store Norditropin® FlexPro®” for information about how to store your pen.

•

Always keep your pen and needles out of reach of others, especially children.

•

Never share your pen or your needles with other people. It might lead to cross-infection.

•

Caregivers must

be very careful when handling used needles – to reduce the risk of needle injury and cross-infection.

Important information

Pay special attention to these notes as they are important for safe use of the pen.

Additional information

8-2052-01-001-4

Norditropin® FlexPro®

15 mg/1.5 ml somatropin

Norditropin® and FlexPro® are trademarks owned by Novo Nordisk Health Care AG, Switzerland

NovoFine® and NovoTwist® are trademarks owned by Novo Nordisk A/S, Denmark

© 2026 Novo Nordisk A/S

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 03132/0155

Last revision stated in the text: June 2026 · MHRA data as of 13 October 2026

Found a mistake? Tell us on the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Facts about Norditropin Flexpro 15 mg / 1.5 ml solution for injection in Pre-filled pen

Prescription needed? Yes, prescription-only medicine (POM)
Controlled drug
Yes, Schedule 4 of the Misuse of Drugs Regulations?
  • Controlled drugs are medicines that UK law controls more strictly because they can be misused or cause dependence. The Misuse of Drugs Regulations 2001 divide them into 5 schedules: schedule 1 has the strictest rules, schedule 5 the lightest.
  • Schedule 4 has lighter rules. Its part II covers anabolic steroids and hormones such as growth hormone.
  • A prescription is valid for 28 days and usually covers up to 30 days of treatment.
  • Travelling abroad: you can usually carry up to 3 months' supply. Take your prescription or a letter from your doctor to show it is yours, and check the rules of the country you are going to (GOV.UK).
  • Never give it to anyone else.
Active substance Somatropin
Strength 15 mg / 1.5 ml (10 mg/ml)
Pharmaceutical form Solution for injection
Clear, colourless solution
How is it taken Subcutaneous
Excipients Mannitol, Histidine, Poloxamer 188, Phenol, Water for injection, Hydrochloric acid for pH adjustment, Sodium hydroxide for pH adjustment
Pack sizes 1 pre-filled disposable injection
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 2 years.
After first opening: Store for a maximum of 4 weeks in a refrigerator (2°C – 8°C).
Alternatively, the medicinal product may be stored for a maximum of 3 weeks below 25°C.
Storage Store in a refrigerator (2°C – 8°C) in the outer carton, in order to protect it from light. Do not freeze. Do not store close to any cooling elements.
For storage conditions after first opening of the medicinal product, see section 6.3.
Do not freeze.
When in use, always replace the pen cap on the Norditropin FlexPro pre-filled pen after each injection. Always use a new needle for each injection.
The needle must not be screwed onto the pre-filled pen when it is not in use.
Drug group (ATC) Somatropin and somatropin agonists. ATC: H01AC01
  1. H Systemic hormonal preparations, excl. sex hormones and insulins
    1. H01 Pituitary and hypothalamic hormones and analogues
      1. H01A Anterior pituitary lobe hormones and analogues
        1. H01AC Somatropin and somatropin agonists
          1. H01AC01 somatropin
Marketing authorisation PL 03132/0155 (first authorised 15 January 2010)
Marketing authorisation holder Novo Nordisk Limited
Codes GTIN 5712249112585 · BNF 06050100

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.2.0 of 19 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.