This page is for general information. Consult a doctor for personal advice. Call emergency services if symptoms are severe.

How to use SOGROYA 15 MG/1.5 ML INJECTABLE SOLUTION IN PRE-FILLED PEN

Introduction

Package Leaflet: Information for the User

Sogroya 15mg/1.5ml solution for injection in a pre-filled pen

somapacitan

This medicine is subject to additional monitoring, which will allow for quick identification of new safety information. You can help by reporting any side effects you may get. The last section of this leaflet includes information on how to report side effects.

Read all of this leaflet carefully before you start using this medicine, because it contains important information for you.

Keep this leaflet, you may need to read it again.
If you have any further questions, ask your doctor, pharmacist, or nurse.
This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
If you get any side effects, talk to your doctor, pharmacist, or nurse. This includes any possible side effects not listed in this leaflet. See section 4.

Contents of the pack

What is Sogroya and what is it used for
What you need to know before you use Sogroya
How to use Sogroya
Possible side effects
Storage of Sogroya
Contents of the pack and other information

1. What is Sogroya and what is it used for

Sogroya contains the active substance somapacitan: a long-acting version of the natural growth hormone produced by the body with an amino acid substitution. Growth hormone regulates fat, muscle, and bone composition in adults.

The active substance in Sogroya is produced using "recombinant DNA technology" from cells that have received a gene (DNA) that makes them produce growth hormone. In Sogroya, a small side chain has been added to the growth hormone that binds Sogroya to the protein (albumin) naturally present in the blood to slow down its elimination from the body, allowing the medicine to be administered less frequently.

Sogroya is used to treat growth retardation in children from 3 years of age and adolescents if they have a very low or no production of growth hormone (growth hormone deficiency) and adults with growth hormone deficiency.

Your doctor will assess, based on your response to Sogroya, whether you should continue treatment with Sogroya one year after starting this medicine.

2. What you need to know before you use Sogroya

Do not use Sogroya

if you or a child in your care is allergic to somapacitan or any of the other ingredients of this medicine (listed in section 6).
if you or a child in your care has a benign or malignant tumor in development. You must have completed anti-tumor treatment before starting treatment with Sogroya. If the tumor grows, you must stop receiving Sogroya.

if you or a child in your care has recently undergone open-heart or abdominal surgery or has suffered multiple accidental trauma or has severe respiratory problems or similar conditions.
in children and adolescents who have stopped growing due to the closure of their growth plates (closed epiphyses), which means that your doctor has indicated to you or the child in your care that their bones have stopped growing.

In case of doubt, consult your doctor, pharmacist, or nurse.

Warnings and precautions

Consult your doctor, pharmacist, or nurse before using Sogroya if:

you or a child in your care has ever had any type of tumor
you or a child in your care has a high blood sugar level (hyperglycemia), as you may need to regularly check your blood sugar level and adjust the dose of your diabetes medicine
you or a child in your care is receiving corticosteroid replacement therapy because your body does not produce enough (adrenal insufficiency). Talk to your doctor, as you may need regular adjustments
you or a child in your care experiences severe headache, vision problems, nausea, or vomiting, as these may be symptoms of increased pressure in the brain (benign intracranial hypertension), and you may need to interrupt treatment
you or a child in your care has thyroid problems, you should periodically check your thyroid hormones and may need to adjust the dose of thyroid hormones
you are a woman taking oral contraceptives or hormone replacement therapy with estrogens, you may need a higher dose of Sogroya. If you stop taking oral estrogens, you may need a lower dose of somapacitan. Your doctor may recommend that you change the way you take estrogens (e.g., transdermal, vaginal) or use another contraceptive method
you or a child in your care is seriously ill (e.g., complications from open-heart surgery, abdominal surgery, accidental trauma, acute respiratory failure, or similar diseases). If you have undergone or are going to undergo major surgery, or are going to be hospitalized for any of the above reasons, inform your doctor and remind other doctors who may treat you that you are being treated with growth hormone
you or a child in your care suffers from severe stomach pain during treatment with Sogroya, as this could be a symptom of pancreatitis observed in treatments with other growth hormone medicines
you or a child in your care suffers from persistent hip or knee pain when walking, or if you or a child in your care starts to limp during growth hormone treatment. These could be symptoms of a disease that affects the femur where it inserts into the hip (slipped capital femoral epiphysis) and occurs more frequently in children with rapid growth and children with endocrine disorders, including growth hormone deficiency. Inform your doctor if you experience persistent pain in any joint.

Changes in the skin at the injection site

The injection site of Sogroya should be rotated to prevent changes in the fatty tissue under the skin, such as thickening of the skin, shrinkage of the skin, or lumps under the skin. Change the injection site on your body every week.

Antibodies

It is not expected that you will develop antibodies against somapacitan. However, in very rare cases, the child may develop antibodies. If your treatment with Sogroya does not work, your doctor will need to check if you have developed antibodies to somapacitan.

Other medicines and Sogroya

Tell your doctor or pharmacist if you or a child in your care is using, has recently used, or might use any other medicines.

In particular, tell your doctor if you or a child in your care is taking or has recently taken any of the following medicines.

The reason is that your doctor may need to adjust the doses of your medicines:

Corticosteroids such as hydrocortisone, dexamethasone, and prednisolone
Estrogens as part of oral contraception or hormone replacement therapy with estrogens
Male sex hormones (androgens) such as testosterone

Gonadotropins (gonad-stimulating hormones, such as luteinizing hormone and follicle-stimulating hormone), which stimulate the production of sex hormones
Insulin or other diabetes medicines
Thyroid hormone medicines such as levothyroxine
Medicines for treating epilepsy or seizures (epileptic fits) such as carbamazepine
Cyclosporins (immunosuppressant), a medicine that suppresses the immune system's response.

Pregnancy

If you can become pregnant, you must not use Sogroya unless you are using a reliable method of contraception. This is because it is not known whether it could harm the fetus. If you become pregnant during treatment with Sogroya, inform your doctor immediately. If you wish to become pregnant, talk to your doctor, as you may need to stop using the medicine.

Breast-feeding

It is not known whether Sogroya is excreted in breast milk. Inform your doctor if you are breast-feeding or plan to breast-feed. Your doctor will help you decide whether to stop breast-feeding or stop using Sogroya, considering the benefit of breast-feeding to the baby and the benefit of Sogroya to the mother.

Driving and using machines

Sogroya does not affect the ability to drive and use machines.

Sodium content

This medicine contains less than 1 mmol of sodium (23 mg) per dose; this is essentially "sodium-free".

3. How to use Sogroya

Follow the instructions for administration of this medicine exactly as indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.

Sogroya is injected under the skin (subcutaneous injection) with a pre-filled pen. You can administer the injection yourself. Your doctor or nurse will show you how to inject Sogroya when you or a child in your care starts treatment.

When to use Sogroya

You or a child in your care should use Sogroya once a week, on the same day of the week if possible.
The injection can be administered at any time of day.

If you or a child in your care changes from another weekly growth hormone treatment to Sogroya, it is recommended to continue injecting on the same day of the week.

If you or a child in your care changes from daily growth hormone treatment to Sogroya, choose the preferred day for weekly administration and inject the last dose of daily treatment the day before (or at least 8 hours before) the first dose of Sogroya.

Any change from another type or brand of growth hormone should be made by your doctor.

If it is not possible for you or a child in your care to inject Sogroya on the usual day of the week, you can administer Sogroya up to 2 days before or 3 days after the scheduled day. The next week, you can inject the next dose as usual.

If necessary, you can change the day of the weekly Sogroya injection, as long as at least 4 days have passed since the last injection. Once the new administration day is selected, you should continue injecting the dose on the same day every week.

For how long you will need treatment

You may need Sogroya as long as your body does not produce enough growth hormone

If you or a child in your care is using Sogroya for growth retardation, you will continue using Sogroya until you stop growing
If you or a child in your care still has a growth hormone deficiency after stopping growth, you may need to continue treatment with Sogroya until adulthood

Do not stop your treatment with Sogroya without talking to your doctor first.

How much to use

Children and adolescents

The dose for children and adolescents depends on body weight.

The recommended dose of Sogroya is 0.16 mg per kg of body weight administered once a week.

Adults

The usual initial dose is 1.5 mg once a week if you are receiving growth hormone treatment for the first time. The usual initial dose is 2 mg once a week if you have previously received daily growth hormone treatment (somatropin).

If you are a woman taking oral estrogens (contraceptives or hormone replacement therapy), you may need a higher dose of somapacitan. If you are over 60 years old, you may need a lower dose. See Table 1 below.

Your doctor may gradually increase or decrease the dose until you find the right dose according to your individual needs and the side effects experienced.

Do not use more than 8 mg once a week.
Do not change the dose unless your doctor tells you to.

Table 1 Recommended dose

Adult population with growth hormone deficiency	Recommended initial dose
Has not previously received daily growth hormone treatment
Is ≥18 and <60 years old Is a woman on oral estrogen treatment regardless of age Is 60 years old or older	1.5 mg/week 2 mg/week 1 mg/week
Has previously received daily growth hormone treatment
Is ≥18 and <60 years old Is a woman on oral estrogen treatment regardless of age Is 60 years old or older	2 mg/week 4 mg/week 1.5 mg/week

After reaching the correct dose, your doctor will assess your treatment every 6 to 12 months. You may need to review your body mass index and have blood samples taken.

How to use Sogroya

Your doctor or nurse will show you how to inject Sogroya under the skin.

The best places to inject are:

the front of the thigh
the front of the waist (abdomen)
the buttocks
the upper arms.

Change the injection site on your body every week.

Detailed instructions on how to inject Sogroya, instructions for use, are included at the end of this leaflet.

If you use more Sogroya than you should

If you or a child in your care accidentally uses more Sogroya than you should, consult your doctor, as you may need to check your blood sugar levels.

If you forget to use Sogroya

If you or a child in your care forgets to inject a dose:

and it has been 3 days or less since you should have used Sogroya, administer it as soon as you remember. Then, inject the next dose on the usual injection day
and it has been more than 3 days since you should have used Sogroya, skip the missed dose. Then, inject the next dose as usual, on the next scheduled day.

Do not inject an extra dose or increase the dose to make up for the missed dose.

If you stop treatment with Sogroya

Do not stop your treatment with Sogroya without consulting your doctor.

If you have any other questions about the use of this medicine, ask your doctor, pharmacist, or nurse.

4. Possible side effects

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

Side effects observed in children and adolescents

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

Headache.

Common (may affect up to 1 in 10 people)

Swelling in hands and feet due to fluid accumulation under the skin (peripheral edema)
The adrenal glands do not produce enough steroid hormones (adrenal insufficiency)
Decreased thyroid hormone (hypothyroidism)
Redness and pain at the injection site (injection site reactions)
Joint pain (arthralgia)
Pain in arms or legs (pain in the limbs)
High blood sugar level (hyperglycemia)
Feeling very tired (fatigue).

Side effects observed in adults

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

Headache.

Common (may affect up to 1 in 10 people)

The adrenal glands do not produce enough steroid hormones (adrenal insufficiency)
Decreased thyroid hormone (hypothyroidism)
High blood sugar level (hyperglycemia)
Feeling of "tingling", especially in the fingers (paresthesia)
Rash
Hives
Joint pain (arthralgia), muscle pain (myalgia), muscle stiffness
Swelling in hands and feet due to fluid accumulation under the skin (peripheral edema)
Feeling very tired or weak (fatigue or asthenia)
Redness and pain at the injection site (injection site reactions).

Uncommon (may affect up to 1 in 100 people)

Thickening of the skin at the injection site (lipoatrophy)
Feeling of numbness and tingling in the hands (carpal tunnel syndrome)
Itching (pruritus)
Joint stiffness.

Reporting of side effects

If you experience any side effects, talk to your doctor, pharmacist, or nurse, even if it is possible that they are not listed in this leaflet. You can also report side effects directly through the national reporting system listed in Appendix V. By reporting side effects, you can help provide more information on the safety of this medicine.

5. Storage of Sogroya

Keep this medicine out of sight and reach of children.

Do not use this medicine after the expiry date which is stated on the label and on the carton of the pen after “EXP”. The expiry date is the last day of the month indicated.

Store in a refrigerator (between 2 °C and 8 °C). Do not freeze. Keep away from the cooling element of the refrigerator.

After first use

Use within 6 weeks after first use. Store in a refrigerator (between 2 °C and 8 °C).

Before and after first use

If you cannot refrigerate it (for example, during travel), Sogroya can be temporarily stored at temperatures below 30 °C for a maximum total of 72 hours (3 days). Return Sogroya to the refrigerator after storing it at this temperature. If you have stored it out of the refrigerator and then put it back in the refrigerator, the total time out of refrigeration must not exceed 3 days; keep track of this carefully. Discard the Sogroya pen if it has been stored at 30 °C for more than 72 hours or above 30 °C for any period of time.

Record the time out of refrigerator:_____________

Keep Sogroya in the outer packaging with the pen cap on to protect it from light.

Always remove the needle after each injection and store the pen without the needle attached.

Do not use this medicine if you notice that the solution is not transparent or slightly opalescent, colorless to slightly yellow, and is not free of visible particles.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of the packaging and medicines that are no longer needed. This will help protect the environment.

6. Container Contents and Additional Information

Composition of Sogroya

The active substance is somapacitan. One ml of solution contains 10 mg of somapacitan. Each pre-filled pen contains 15 mg of somapacitan in 1.5 ml of solution.
The other ingredients are: histidine, mannitol, poloxamer 188, phenol, water for injections, hydrochloric acid (for pH adjustment), sodium hydroxide (for pH adjustment). Also, refer to section 2 "What you need to know before you start using Sogroya" for more information on sodium.

Appearance and Container Contents of the Product

Sogroya is an injectable liquid in a pre-filled pen with a transparent or slightly opalescent appearance, colorless or slightly yellow, and free of visible particles.

Sogroya 15 mg/1.5 ml solution for injection in a pre-filled pen with a ruby red push button is available in the following pack sizes: one pack containing 1 pre-filled pen or a multipack containing 5 packs, each with 1 pre-filled pen.

Not all pack sizes may be marketed.

Marketing Authorisation Holder and Manufacturer

Novo Nordisk A/S

Novo Allé

DK-2880 Bagsværd

Denmark

Date of Last Revision of this Leaflet:06/2025

Other Sources of Information

Detailed information on this medicinal product is available on the European Medicines Agency web site: http://www.ema.europa.eu.

Instructions for Use Overview of the Sogroya 15mg/1.5ml Pen Needle (Example)
How to Use the Sogroya Pen Follow 5 Steps During Sogroya Injection: Step 1. Preparation of the Sogroya Pen..........................................................................................89 Step 2. Checking the Flow with Each New Pen.....................................................................90 Step 3. Dose Selection..............................................................................................................91 Step 4. Injection of the Dose........................................................................................................92 Step 5. After Injection........................................................................................................93 *For More Information on the Pen, See Sections:Check How Much Sogroya is Left, How to Care for the Pen, Important Information.* Read the leaflet and these instructions carefully before using the pre-filled Sogroya pen. Pay special attention to these notes because they are important for the safe use of the pen. Additional Information Sogroya contains 15 mg of somapacitan and can be used to inject doses from 0.10 mg to 8 mg in 0.1 mg increments. Sogroya can only be used under the skin (subcutaneously). Needles are not included and must be obtained separately. The pre-filled Sogroya pen is designed to be used with disposable needles of 4 mm to 8 mm in length and 30 G to 32 G in thickness. Do Notshare the Sogroya pen or needles with another person. You may infect them or get an infection. Do Not Use**the pen without proper training from your doctor or nurse. Make sure you feel confident to inject yourself with the pen before starting treatment. If you are blind or have low vision and cannot read the dose counter on the pen, do not use this pen without help. Ask for help from a person without vision problems and trained in the use of the pen.
Step 1. Preparation of the Sogroya Pen
Wash your hands with water and soap. Check the Name, Concentration, and Colorof your pen label to ensure it contains Sogroya and the correct concentration. Remove the pen cap. Turn the pen upside down one or two times to check that the contents of the Sogroya pen are transparent or slightly opalescent or colorless to slightly yellow. See Figure A. If Sogroya Contains Visible Particles, do not use the pen. Make Sure You Are Using the Correct Pen. Especially if you use more than one type of injectable medication. Using the wrong medication can be harmful to your health.
When you are ready to inject, take a new disposable needle. First, remove the paper tab. Second, place the needle straight onto the pen. Turn the needle clockwise until it is well secured. See Figure B.
Remove the outer needle cap and set it aside for later. You will need it after the injection to safely remove the needle from the Sogroya pen. See Figure C. The needle is protected by two caps. You must remove both caps. If you forget to remove any, no medication will be injected. See Figures C and D.
Remove the inner needle cap and discard it. If you try to put it back, you may accidentally prick yourself with the needle. See Figure D. A drop of Sogroya may appear at the tip of the needle. This is normal, but you must still check the flow with each new pen. See Step 2.
Always Use a New Needle for Each Injection.This reduces the risk of contamination, infection, loss of Sogroya, and needle blockage, which can lead to inaccurate dosing. Never use a bent or damaged needle.
Step 2. Checking the Flow with Each New Pen
If Your Pen is Already in Use, go to Step 3. Before Using a New Pen, check the flow to ensure that Sogroya can pass through the pen and needle. Turn the dose selector clockwise until it stops at the mark to select 0.10 mg. You may hear a slight click. See Figure E.
One Mark Equals 0.10 mgon the dose counter. See Figure F.
Hold the pen with the needle pointing upwards. Press and hold the push button until the dose counter returns to “0”. The “0” must be aligned with the dose marker. See Figure G.
Check that a drop of Sogroya appears at the tip of the needle. See Figure H. If Sogroya Does Not Appear, repeat Step 2 a maximum of 6 times. If no drop of Sogroya still appears, change the needle once as described in Step 5 and repeat Steps 1 and 2 again.
If Sogroya does not appear when checking the flow, the needle may be blocked or damaged. Do not use the pen if Sogroya still does not appear after changing the needle. The pen may be defective.
Step 3. Dose Selection
To start, check that the dose counter is at “0”. Turn the dose selector clockwise to select the dose you need. See Figure I. Once you have selected the dose, proceed to Step 4. If There is Not Enough Sogroya Leftto select a full dose, refer to Check How Much Sogroya is Left.
The dose counter shows the dose in mg. See Figures J and K. Always use the dose marker to select the exact dose. Do Not Count the Pen Clicks. Do Not Use the Pen Scale(see Overview of the Sogroya Pen) to measure the amount of growth hormone to be injected. Only the dose marker will indicate the exact number of mg.
If you select an incorrect dose, you can turn the dose selector clockwise or counterclockwise to correct the dose. See Figure L. The pen clicks sound and feel different when turning the dose selector clockwise or counterclockwise or if you accidentally pass the remaining mg.
Step 4. Injection of the Dose
Insert the needle under the skin as your doctor or nurse has taught you. See Figure M. Make sure you can see the dose counter. Do Not Cover it with Your Fingers. This could block the injection. Remember to Change the Injection Site Each Week.
Keep the push button fully pressed until the dose counter shows “0” (See Figure N). The “0” must be aligned with the dose marker. You may hear or feel a “click”. Continue to Press the Push Button with the Needle in the Skin.
Keep the Push Button Pressed with the Needle Under the Skin and Slowly Count to 6to ensure you administer the full dose (see Figure O).
If the “0” does not appear on the dose counter after continuously pressing the push button, the needle or pen may be blocked or damaged and you may not have received any Sogroya, even though the dose counter has moved from the original dose you set. Remove the needle as described in Step 5 and repeat Steps 1 to 4.
Carefully remove the needle from the skin. See Figure P. If blood appears at the injection site, press lightly. Do not rub the area. A drop of Sogroya may appear at the tip of the needle after injection. This is normal and does not affect the dose.
Step 5. After Injection
Insert the needle tip into its outer cap, placed on a flat surface, without touching the needle or outer cap. See Figure Q.
When the needle is covered, carefully and fully press the outer cap. See Figure R.
Unscrew the needle and carefully dispose of it as your doctor, nurse, pharmacist, or local authorities have instructed. Always Dispose of the Needle After Each Injection. When the pen is empty, remove and dispose of the needle as described above and discard the pen separately, following the instructions of your doctor, nurse, pharmacist, or local authorities. The pen cap and empty packaging can be thrown away in the trash.
Put the pen cap back on after each use to protect Sogroya from direct light. See Figure T. For storage of the pen, refer to Storage of Sogroyain this leaflet.
Do Not Attempt to Put the Inner Needle Cap Back On. You could prick yourself with the needle. Always remove the needle from the pen immediately after each injection. This reduces the risk of contamination, infection, loss of Sogroya, and needle blockage, which can lead to inaccurate dosing.
Check How Much Sogroya is Left
The pen scale shows the approximate amount of Sogroya left in the pen. See Figure U.
To find out how much Sogroya is left, use the dose counter: Turn the dose selector clockwise until it stops. You can select a maximum dose of 8 mg. If it shows “8”, there are at least 8 mg left in the pen. If the dose counter stops at “4.8”, there are only 4.8 mg left in the pen. See Figure V.
What if I Need a Dose Larger than What is Left in the Pen?	It is not possible to select a dose larger than the amount of mg left in the pen. If you need more Sogroya than what is left in the pen, you can use a new pen or divide the dose between the pen in use and the new one. You can only divide the dose if your doctor or nurse has recommended it and you have received the relevant training. Use a calculator to plan the doses following your doctor's or nurse's instructions. Be Very Careful to Calculate Correctly, as This Can Cause a Medication Error. In case of doubt about how to divide the dose into two pens, select and inject the dose you need with a new pen.
How to Care for the Pen
How Should I Care for the Pen?	Be careful not to drop the pen or hit it against hard surfaces. Do not expose the pen to dust, dirt, liquids, or direct light. Do not attempt to refill the pen; it is pre-filled and should be discarded when empty.
What if the Pen is Dropped?	If the pen is dropped or you think it is not working correctly, insert a new disposable needle and check the flow before injection, see Steps 1 and 2. If the pen has been dropped, check the cartridge; if it is cracked, do not use the pen.
How Do I Clean the Pen?	Do not wash, soak, or lubricate the pen. It can be cleaned with a mild detergent and a damp cloth.
Important Information People caring for patients should be very careful when handling needles to reduce the risk of needlestick injury and cross-infection. Always keep the pen and needles out of reach of others, especially children. Do Not Use the Penif it is damaged. Do not attempt to repair the pen or disassemble it. For storage of the pen, refer to Storage of Sogroyain this leaflet.