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LYXUMIA 10 MICROGRAMS INJECTABLE SOLUTION

LYXUMIA 10 MICROGRAMS INJECTABLE SOLUTION

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

How to use LYXUMIA 10 MICROGRAMS INJECTABLE SOLUTION

Introduction

Package Leaflet: Information for the User

Lyxumia 10micrograms solution for injection

Lyxumia 20micrograms solution for injection

Lixisenatide

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 symptoms are the same as yours.
    • If you experience 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:

  1. What is Lyxumia and what is it used for
  2. What you need to know before you use Lyxumia
  3. How to use Lyxumia
  4. Possible side effects
  5. Storage of Lyxumia
  6. Contents of the pack and other information

1. What is Lyxumia and what is it used for

Lyxumia contains the active substance lixisenatide.

It is an injectable medicine used to help your body control your blood sugar levels when they are too high. It is prescribed for adult patients with type 2 diabetes.

Lyxumia is used together with other diabetes medicines when your blood sugar levels are not adequately controlled, such as:

  • oral anti-diabetics (such as metformin, pioglitazone, sulfonylureas) and/or,
  • a basal insulin, a type of insulin that acts throughout the day.

2. What you need to know before you use Lyxumia

Do not use Lyxumia if

  • you are allergic to lixisenatide or any of the other ingredients of this medicine (listed in section 6).

Warnings and precautions

Talk to your doctor, pharmacist, or nurse before using Lyxumia if:

  • you have type 1 diabetes or "diabetic ketoacidosis" (a complication of diabetes that occurs when your body cannot break down glucose because there is not enough insulin), as this medicine is not suitable for you.
  • you have or have ever had pancreatitis (inflammation of the pancreas),
  • you have a severe intestinal or gastric problem, such as a disease of the stomach muscles called "gastroparesis" that leads to delayed gastric emptying,
  • you have severe kidney disease or are on dialysis, as the use of this medicine is not recommended,
  • you are also taking a sulfonylurea or a basal insulin. This is because you may experience low blood sugar (hypoglycemia). Your doctor may want to monitor your blood sugar levels and then decide to reduce your dose of basal insulin or sulfonylurea. Lyxumia should not be used with the combination of both, a basal insulin and a sulfonylurea.
  • you are taking other medicines, as there are other medicines such as antibiotics or enteric-coated tablets or capsules that should not stay in the stomach for too long (see section "Using Lyxumia with other medicines").
  • you experience fluid loss/dehydration; for example, in case of vomiting, nausea, and diarrhea. It is essential that you drink plenty of fluids to avoid dehydration, especially when starting treatment with Lyxumia.
  • you have heart problems that can cause you difficulty breathing or swelling in the ankles, as there is limited experience in this population.

Children and adolescents

There is no experience with Lyxumia in children and adolescents under 18 years, and therefore, the use of Lyxumia is not recommended in this age group.

Using Lyxumia with other medicines

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

The effect of some medicines you take may be affected by Lyxumia. It may be necessary for some medicines, such as antibiotics or enteric-coated tablets or capsules that should not stay in your stomach for too long, to be taken at least one hour before or 4 hours after the injection of Lyxumia.

Pregnancy and breastfeeding

Lyxumia should not be used during pregnancy. It is not known if Lyxumia could harm the fetus.

Lyxumia should not be used during breastfeeding. It is not known if Lyxumia passes into breast milk.

If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before using this medicine.

Driving and using machines

If you use Lyxumia with a sulfonylurea or a basal insulin, you may experience low blood sugar (hypoglycemia). This could make it difficult to concentrate and you may feel dizzy or drowsy. If this happens, do not drive or use tools or machines.

Important information about some of the ingredients of Lyxumia

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

This medicine contains metacresol, which may cause allergic reactions.

3. How to use Lyxumia

Follow exactly the administration instructions of this medicine given by your doctor, pharmacist, or nurse. If you are unsure, ask your doctor, pharmacist, or nurse again.

How much to inject

  • The starting dose is 10 micrograms once a day for the first 14 days (injected using the greenpen).
  • After that, the dose will be 20 micrograms once a day (using the purplepen).

When to inject

Inject Lyxumia within the hour before any meal of the day. It is preferable to inject Lyxumia before the same meal every day, once you have chosen the most suitable meal for your injection.

Where to inject

Inject Lyxumia into the skin (subcutaneously) of your stomach (abdomen), the top of your leg (thigh), or the top of your arm.

Learning to use the pre-filled pens

Before using the pen for the first time, your doctor or nurse will teach you how to inject Lyxumia.

  • Always read the "Instructions for Use" that come with the box.
  • Always use the pen as indicated in the "Instructions for Use".

Other important information about using the pre-filled pens

You can find more information about using the pens in the "Instructions for Use". The key points are:

  • Always use a new needle for each injection. The needle should be discarded after each use in an appropriate container for sharp objects, following local recommendations. Talk to your doctor, nurse, or pharmacist about how to dispose of the needles.
  • Only use needles compatible with the Lyxumia pen (see "Instructions for Use").
  • You must activate the Lyxumia pen before using it for the first time.This is to ensure that it works correctly and that the dose of the first injection is correct.
  • If you think the Lyxumia pen may be damaged, do not use it. Get a new one. Do not try to repair the pen.

If you use more Lyxumia than you should

If you use more Lyxumia than you should, call your doctor immediately. Too much Lyxumia may make you feel nauseous or vomit.

If you forget to use Lyxumia

If you forget a dose of Lyxumia, you can inject it within the hour before your next meal. Do not inject two doses at the same time to make up for a forgotten dose.

If you stop using Lyxumia

Do not stop using Lyxumia without talking to your doctor first. If you stop using Lyxumia, your blood sugar levels may increase.

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

4. Possible side effects

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

Rarely, some serious allergic reactions (such as anaphylaxis) have been reported in patients taking Lyxumia. You should seek immediate medical attention if you experience symptoms such as swelling of the face, tongue, or throat that make it difficult to breathe.

Stop using Lyxumia and contact your doctor immediately if you notice any of the following serious side effects:

  • Severe and persistent abdominal pain (in the stomach area) that may radiate to your back, as well as nausea and vomiting, as these may be signs of pancreatitis.

The most frequently reported side effects with Lyxumia that may affect more than 1 in 10 users (frequency: very common) were nausea (feeling sick) and vomiting. These side effects were mostly mild and usually disappeared over time.

Other side effects

Very common: may affect more than 1 in 10 people

  • Diarrhea
  • Headache
  • Low blood sugar (hypoglycemia) especially when Lyxumia is used with insulin or a sulfonylurea.

The warning signs of low blood sugar may include: cold sweats, cool pale skin, headache, drowsiness, weakness, dizziness, confusion or irritability, feeling hungry, rapid heartbeat, and nervousness. Your doctor will tell you what to do if you experience low blood sugar.

This is more likely to happen if you are taking a sulfonylurea or a basal insulin at the same time. Your doctor may reduce the dose of these medicines before you start using Lyxumia.

Common: may affect up to 1 in 10 people

  • Influenza (flu)
  • Upper respiratory tract infection (cold)
  • Dizziness
  • Indigestion (dyspepsia)
  • Back pain
  • Cystitis
  • Viral infection
  • Low blood sugar (when Lyxumia is taken with metformin)
  • Drowsiness. Reactions at the injection site (such as itching).

Uncommon: may affect up to 1 in 100 people

    • Hives
  • Gallstones
    • Inflammation of the gallbladder.

Rare: may affect up to 1 in 1,000 people

  • Delayed emptying of the stomach.

If you experience any side effects, talk to your doctor, pharmacist, or nurse, even if it is possible side effects not listed in this leaflet.

Reporting of side effects

If you experience any side effects, talk to your doctor, pharmacist, or nurse, even if it is possible side effects 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 Lyxumia

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 label and carton after EXP. The expiry date refers to the last day of the month shown.

Before first use

Store in a refrigerator (2°C to 8°C). Do not freeze. Keep away from the freezer compartment.

During use of the pen

The pen can be used for 14 days when stored below 30°C. Do not freeze. Do not store with a needle attached. When not using the pen, keep the cap on the pen to protect it from light.

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

6. Container Contents and Additional Information

Composition of Lyxumia

  • The active substance is lixisenatide.
  • Lyxumia 10 micrograms solution for injection: Each dose contains 10 micrograms of lixisenatide (50 micrograms per ml).
  • Lyxumia 20 micrograms solution for injection: Each dose contains 20 micrograms of lixisenatide (100 micrograms per ml)
  • The other ingredients are glycerol 85%, sodium acetate trihydrate, methionine, metacresol, hydrochloric acid (for pH adjustment), and sodium hydroxide solution (for pH adjustment) and water for injections.

Appearance of Lyxumia and Container Contents

Lyxumia is a clear and colorless injectable solution, contained in a glass cartridge inserted into a pre-filled pen.

Each green pen of Lyxumia 10 micrograms solution for injection contains 3 ml of solution that contains 14 doses of 10 micrograms. Pack with 1 pre-filled pen.

Each purple pen of Lyxumia 20 micrograms solution for injection contains 3 ml of solution that contains 14 doses of 20 micrograms. Packs with 1, 2, or 6 pre-filled pens. Only some pack sizes may be available in your country.

A starter pack is also available for use during the first 28 days of treatment, which contains a green pen of Lyxumia 10 micrograms solution for injection and a purple pen of Lyxumia 20 micrograms solution for injection.

Marketing Authorization Holder

sanofi-aventis groupe

54, rue La Boétie

F – 75008 Paris

France

Manufacturer

Sanofi-Aventis Deutschland GmbH

Industriepark Höchst - 65926 Frankfurt am Main

Germany

You can request more information about this medicinal product by contacting the local representative of the marketing authorization holder:

Belgium/Belgique/Belgien

Sanofi Belgium

Tel: +32 (0)2 710 54 00

Luxembourg/Luxemburg

Sanofi Belgium

Tel: +32 (0)2 710 54 00 (Belgique/Belgien)

Bulgaria

sanofi-aventis Bulgaria EOOD

Tel: +359 (0)2 970 53 00

Hungary

SANOFI-AVENTIS Zrt.

Tel: +36 1 505 0050

Czech Republic

sanofi-aventis, s.r.o.

Tel: +420 233 086 111

Malta

Sanofi Malta Ltd.

Tel: +356 21493022

Denmark

sanofi-aventis Denmark A/S

Tel: +45 45 16 70 00

Netherlands

sanofi-aventis Netherlands B.V.

Tel: +31 (0)182 557 755

Germany

Sanofi-Aventis Deutschland GmbH

Tel: +49 (0)180 2 222010

Norway

sanofi-aventis Norge AS

Tel: +47 67 10 71 00

Estonia

sanofi-aventis Estonia OÜ

Tel: +372 627 34 88

Austria

sanofi-aventis GmbH

Tel: +43 1 80 185 – 0

Greece

sanofi-aventis AEBE

Tel: +30 210 900 16 00

Poland

Sanofi-aventis Sp. z o.o.

Tel: +48 22 280 00 00

Spain

sanofi-aventis, S.A.

Tel: +34 93 485 94 00

Portugal

sanofi - Produtos Farmacêuticos, Lda.

Tel: +351 21 35 89 400

France

sanofi-aventis France

Tel: 0 800 222 555

Call from abroad: +33 1 57 63 23 23

Croatia

sanofi-aventis Croatia d.o.o.

Tel: +385 1 600 34 00

Romania

Sanofi Romania SRL

Tel: +40 (0) 21 317 31 36

Ireland

sanofi-aventis Ireland Ltd. T/A

Tel: +353 (0) 1 403 56 00

Slovenia

sanofi-aventis d.o.o.

Tel: +386 1 560 48 00

Iceland

Vistor hf.

Tel: +354 535 7000

Slovakia

sanofi-aventis Pharma Slovakia s.r.o.

Tel: +421 2 33 100 100

Italy

Sanofi S.p.A.

Tel: 800 13 12 12 (technical questions)

800 536 389 (other questions)

Finland

Sanofi Oy

Tel: +358 (0) 201 200 300

Cyprus

sanofi-aventis Cyprus Ltd.

Tel: +357 22 871600

Sweden

Sanofi AB

Tel: +46 (0)8 634 50 00

Latvia

sanofi-aventis Latvia SIA

Tel: +371 67 33 24 51

United Kingdom

Sanofi

Tel: +44 (0) 845 372 7101

Lithuania

UAB « SANOFI-AVENTIS LIETUVA »

Tel: +370 5 2755224

Date of Last Revision of this Leaflet:

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

Lyxumia 10 micrograms solution for injection

lixisenatide

INSTRUCTIONS FOR USE

A pre-filled pen contains 14 doses, and each dose contains 10micrograms in 0.2ml.

Section 1 – IMPORTANT INFORMATION

Read these instructions carefully before using your Lyxumia pen.

Keep this leaflet for future reference.

Information about the Lyxumia pen

Lyxumia is a pre-filled pen for injection

  • Inject only one dose each day.
  • Each Lyxumia pen contains 14 pre-selected doses. You do not need to measure each dose.
  • Talk to your doctor, pharmacist, or nurse about the correct way to perform the injection before using Lyxumia.
  • If you cannot strictly follow the instructions by yourself or are not able to handle the pen (for example, if you have vision problems), use it only if you have help from another person.

About your Lyxumia pen

Activation window with bold text and white uppercase letters on a light gray backgroundInjection button with black text on a white background indicating the area of medication administrationRubber seal on a white background with large, legible black text

Lyxumia 10 green and white pen with numbers and arrows indicating parts of the device

Stylized arrow window with a pointed tip and decorative feathers in black on a white backgroundPain scale with faces varying from happy to crying, indicating increasing intensityStylized arrow window in black and white with the tip pointing to the right

Lyxumia deposit with bold text and uppercase letters on a white backgroundPain scale with bold text indicating intensity levels and intermediate points representedWhite protective cap on the tip of a transparent hypodermic needle

Transparent protective cap on the tip of a medication injector pen with explanatory textWindow with a stylized arrow pointing down with text that saysMedication cartridge with black text on a white background

Pre-filled syringe with Lyxumia showing numbered dose units and the name of the medication in green and orange

Black plunger advancing along a dose scale with visible numbers indicating remaining doses

  • This pen is for individual use only. Do not share it with anyone else.
  • Always check the label to ensure you are using the correct Lyxumia pen. Also, check that it has not passed its expiration date. Using the wrong medication can be harmful to your health.
  • Do not attempt to withdraw liquid from the cartridge with a syringe.

About your needle(supplied separately)

Components of a medication delivery device showing the plunger, cylinder, needle, and protective connector

Transparent protective cap covering the metal tip of a silver hypodermic needleProtective seal with black text on a white background indicating product safetyTransparent protective cap covering the metal tip of a hypodermic needle with superimposed text

  • Use only needles approved for use with Lyxumia. Use disposable pen needles of 29 to 32 gauge with the Lyxumia pen. Ask your doctor, pharmacist, or nurse what gauge and length of needle are most suitable for you.
  • If someone else is giving you the injection, they must be careful to avoid needle accidents, as they could transmit an infection.
  • Always use a new needle for each injection. This helps prevent contamination of Lyxumia or possible blockage of the needle.

Section 2 – FIRST STEPS

  • Activatethe pen on the same day as your first injection

First, activate your new pen

  • Before injecting a dose:before injection, you must eliminate excess liquid from the new pen. This is done only once and is called the "activation" process. The following steps, from 1 to 5, show how to do it.
  • Activation is performed to ensure that the pen works correctly and that the dose of the first injection is correct.
  • Do not repeatthe activation process, as you will then not get the 14 doses from your Lyxumia pen.

The following images show how the activation window of the injection button of the pen changes after activation.

New pen

(orange window)

Auto-injector device with a red button visible on the top and a white body with green stripes

Pen ready for injections

(white window)

White and green applicator device with an oval push button and horizontal grooves

The pen is activated and ready for injections. The window remains white after activation.

How to activate your new Lyxumia pen

Step 1 Remove the cap and check the pen

Light green Lyxumia 10 pen with a numerical scale and blue arrows indicating parts of the device

Auto-injector window with an orange color indicator visible and text indicating verification of the color Check the liquid. It should be transparent, colorless, and without visible particles. If it is not, do not use this pen. Contact your doctor, pharmacist, or nurse.

Step 2 Place a needle and remove the caps

Pre-filled syringe with a transparent plunger and a blue ring showing the direction of rotation to prepare the injection

Always use a new needlefor activation.

Remove the protective seal from the outer cap of the needle.

Align the needle with the pen. Keep it straight while screwing it on.

Needle protector removed from the needle of the injector pen with blue arrows indicating the direction of extraction

Be careful not to prick yourself when the needle is exposed.

Remove the inner and outer caps of the needle. Keep the outer cap, as you will need it to dispose of the needle later.

Step 3 Pull the injection button out

Green and white auto-injector device with a blue ring highlighting the dose window and a blue directional arrow

Pull the injection button firmly until it stops.

Pre-filled syringe with a green plunger and a black button inside a blue circle

Now the arrow will be pointing towards the needle.

Step 4 Press and hold the injection button to eliminate excess liquid

Hand holding a white and green auto-injector with an exposed needle over a white empty container

Direct the needle towards a suitable container (such as a glass or a paper towel) to collect the liquid and dispose of it.

Press the injection button all the way.You may hear or feel a "click".

Hold the injection button down and count slowly to 5to extract the last drops

TextCurved blue text that saysHand holding a green and white auto-injector with a drop coming out of the needle over a small container and a blue circle with the number 5

If no liquid comes out, consult the "Questions and Answers" section.

Check that the activation window is now white.

Step 5 The pen is now activated.

Do not activate it again.

It is not necessaryto replace the needle between pen activation and the first injection.

To inject the first dose, go directly to Section 3, step C.

Turn over

Section 3 - DAILY USE OF THE PEN

Go to this section only when the activation window iswhite.

Injectonly one dose each day.

White and green applicator device with an oval push button and horizontal grooves

Step A. Remove the cap and check the pen

Green and white injectable pen with a dose indicator showing 10 units, a blue arrow pointing to the adjustment mechanism, and a magnifying glass over the dose window

Check the liquid. It should be transparent, colorless, and without visible particles. If it is not, do not use this pen. If you notice air bubbles, consult the "Questions and Answers" section.

Check the number of doses of the pen. It is shown by the position of the black plunger on the dose scale.

Check that the activation window is white. If it is orange, go to Section 2. Check the pen label to ensure you are using the correct medication.

Step B. Place a new needle and remove the caps

Pre-filled syringe with a transparent plunger and a blue ring showing the direction of rotation to prepare the injection

Always use a new needlefor each injection.

Remove the protective seal from the outer cap of the needle.

Align the needle with the pen. Keep it straight while screwing it on.

Text in bold that says

Needle protector removed from the needle of the injector pen with blue arrows indicating the direction of extraction

Be careful not to prick yourself when the needle is exposed.

Remove the inner and outer caps of the needle. Keep the outer cap, as you will need it to dispose of the needle later.

Step C. Pull the injection button out

Green and white auto-injector device with a circular blue window showing the dose indicator and a blue directional arrow

Pull the injection button firmly until it stops.

Applicator device with a green and white button highlighted with a blue circle and a directional arrow indicating the direction of pressure

Now the arrow will be pointing towards the needle.

Step D. Press and hold the injection button to inject the dose

Transparent pre-filled syringe with yellow liquid and a gray needle connected, ready for injection

Hand holding an auto-injector with a needle inserted into the abdomen, a blue arrow indicating the point of injectionHand holding an injection device pressing against the skin of the abdomen with the needle inserted

Hand holding a cream applicator with green and white parts next to a blue circle with the number 5 inside

seconds

Grasp a skin fold and insert the needle into it (see the "Injection Sites" section to know where to inject).

Press the injection button all the way.You may hear or feel a "click".

Holdthe injection button down and count slowly to 5to get the full dose.

Then the dose will have been administered. Remove the needle from the skin.

Step E. Remove and dispose of the needle after each injection

Needle inserted into a transparent device with a blue arrow indicating the direction of injection and a numerical scale on the plunger

Place the outer cap of the needle on a flat surface. Guide the needle into the outer cap.

Replace the outer cap of the needle.

Hand holding a white auto-injector with blue arrows indicating rotation to activate the graduated device

Squeeze the outer cap to grasp the needle and use it to unscrew it from the pen.

Green pen with a visible numerical scale and a blue arrow indicating the direction of dose adjustment

Ask your pharmacist how to dispose of the needle that you will not use again.

Replace the cap on the pen

Step F. Repeat all the steps of Section 3 for each injection.

Dispose of the pen 14 days after activation. Do this even if there is still some medication left in the pen.

Activation and Disposal Table

Write the date you activated your pen in this table

and the date on which it must be discarded, 14 days later.

Pen

Activation date

Disposal date

1

Storage

General information

  • Keep Lyxumia pens in a safe place, out of sight and reach of children.
  • Protect the Lyxumia pen from dust and dirt.
  • Replace the pen cap after each use to protect it from light.
  • Do not use Lyxumia after the expiration date shown on the label and carton. The expiration date is the last day of the indicated month.

Before activating the pen:

  • Store unused Lyxumia pens in the refrigerator (2°C to 8°C).
  • Do not freeze Lyxumia pens and do not use Lyxumia if it has been frozen.
  • Allow the pen to reach room temperature before using it.

After activating the pen:

  • Once activated, keep the Lyxumia pen below 30°C. Do not freeze Lyxumia once it has been activated.
  • Do not store the Lyxumia pen with the needle attached, as this may cause contamination and possible air entry, which could affect the accuracy of the doses.
  • Once the Lyxumia pen has been activated, it can be used for 14 days. Discard the used Lyxumia pen after 14 days. Do this even if there is still some medication left in the pen.

Disposal

  • Put the Lyxumia pen cap back on before disposing of it.
  • Discard the Lyxumia pen as your pharmacist has told you to dispose of medicines that are no longer needed.

Maintenance

  • Handle the Lyxumia pen with care.
  • The outside of the Lyxumia pen can be cleaned with a damp cloth.
  • Do not get the Lyxumia pen wet, wash it, or put liquid on it (lubricate it), as this may damage it.
  • If you think the Lyxumia pen may have been damaged, do not use it. Do not attempt to repair the pen.

Injection sites

Text indicating “Front part” in thick black letters on a white background

Body diagram showing recommended injection areas in blue, including arms, thighs, and abdomen

The Lyxumia pen is for injection under the skin, and injections can be given in any of the areas shown in blue in the previous image. These are the thigh, abdominal area, or arm. Consult your doctor, pharmacist, or nurse about the correct injection technique.

Questions and answers

What happens if I forget to activate the Lyxumia pen or inject before activation?

If you accidentally inject before activating the pen, do not correct this by administering a second injection. Contact your doctor, pharmacist, or nurse if a blood sugar check is necessary.

What if there are air bubbles in the reservoir?

It is normal to have small air bubbles in the reservoir; they are not harmful to you. Your dose will be correct, and you can continue following the instructions. Contact your doctor, pharmacist, or nurse if you need help.

Why doesn't liquid come out during activation?

The needle may be blocked, or it may not have been screwed on properly. Remove the needle from the pen, attach a new one, and repeat steps 4 and 5. If the liquid still does not come out, the Lyxumia pen may be damaged. Do not use this Lyxumia pen. Ask your doctor, pharmacist, or nurse for advice.

What if it's hard to push the injection button all the way?

The needle may be blocked, or it may not have been screwed on properly. Remove the needle from the skin and from the pen. Insert a new needle and repeat steps D and E. If it's still hard to press the injection button, the Lyxumia pen may be damaged. Do not use this Lyxumia pen. Ask your doctor, pharmacist, or nurse for advice.

If you have any questions about Lyxumia or diabetes, consult your doctor, pharmacist, or nurse, or contact the local representative of the Marketing Authorization Holder listed in this "package leaflet: information for the user" (which is included separately in the box).

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