MOUNJARO 10 mg/dose KwikPen prefilled pen injector solution

2. What you need to know before you use Mounjaro KwikPen

Do not use Mounjaro KwikPen

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

Warnings and precautions

Talk to your doctor, nurse, or pharmacist before starting Mounjaro if:

• you have severe problems with food digestion or food stays in your stomach longer than usual (including severe gastroparesis).
• you have ever had pancreatitis (inflammation of the pancreas, which can cause severe stomach and back pain that does not go away).
• you have any eye problems (diabetic retinopathy or macular edema).
• you are taking a sulfonylurea (another diabetes medicine) or insulin for diabetes, as low blood sugar (hypoglycemia) may occur. Your doctor may need to adjust the dose of these medicines to reduce this risk.

When starting treatment with Mounjaro, you may experience fluid loss/dehydration, such as vomiting, nausea, and/or diarrhea, which can cause a decrease in kidney function. To avoid dehydration, it is essential to drink plenty of fluids. Contact your doctor if you have any questions or concerns.

If you know you are going to have surgery, inform your doctor that you are taking Mounjaro.

Children and adolescents

This medicine must not be used in children and adolescents under 18 years of age because it has not been studied in this age group.

Other medicines and Mounjaro

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

Pregnancy

If you are pregnant, think you may be pregnant, or are planning to have a baby, ask your doctor for advice before taking this medicine. This medicine must not be used during pregnancy as its effects on the fetus are unknown. Therefore, it is recommended to use contraceptive methods while using this medicine.

Breast-feeding

It is not known whether tirzepatida passes into breast milk. A risk to newborns/babies cannot be ruled out. If you are breast-feeding or plan to breast-feed, ask your doctor for advice before taking this medicine. You and your doctor will decide whether you should stop breast-feeding or stop using Mounjaro.

Driving and using machines

This medicine is unlikely to affect your ability to drive or use machines. However, if you use Mounjaro with a sulfonylurea or insulin, low blood sugar (hypoglycemia) may occur, which can reduce your ability to concentrate. Avoid driving or using machines if you have any signs of low blood sugar, such as headache, drowsiness, weakness, dizziness, feeling hungry, confusion, irritability, rapid heartbeat, and sweating (see section 4). See section 2, "Warnings and precautions" for information on the increased risk of low blood sugar. Consult your doctor for more information.

Mounjaro KwikPen contains sodium

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

Mounjaro KwikPen contains benzyl alcohol

This medicine contains 5.4 mg of benzyl alcohol in each 0.6 ml dose. Benzyl alcohol may cause allergic reactions.

Consult your doctor, nurse, or pharmacist if you are pregnant, breast-feeding, or have liver or kidney disease. This is because large amounts of benzyl alcohol can accumulate in the body and cause side effects (known as "metabolic acidosis").

3. How to use Mounjaro KwikPen

Follow the instructions for administration of this medicine exactly as told by your doctor or pharmacist. If you are unsure, consult your doctor or pharmacist again.

A small amount of medicine may remain in the pen after you have correctly administered all doses. Do not attempt to use leftover medicine. After administering four doses, the pen must be disposed of properly.

How much to use

• The initial dose is 2.5 mg once a week for four weeks. After four weeks, your doctor will increase your dose to 5 mg once a week.

• Your doctor may increase your dose in increments of 2.5 mg up to 7.5 mg, 10 mg, 12.5 mg, or 15 mg once a week if needed. In each case, your doctor will tell you to stay on a specific dose for at least 4 weeks before moving to a higher dose.

Do not change your dose unless your doctor tells you to.

When to use Mounjaro

You can use your pen at any time of day, with or without food. If possible, you should use it on the same day each week. To help you remember when to use Mounjaro, you can write it down on a calendar if you wish.

If necessary, you can change the day of your weekly Mounjaro injection, provided at least 3 days have passed since your last injection. After selecting a new dosing day, continue with once-weekly administration on that new day.

How to inject Mounjaro KwikPen

Mounjaro is injected under the skin (subcutaneous injection) in the abdominal area at a minimum distance of 5 cm from the navel or in the upper thigh or upper arm. You may need help from another person if you want to inject into the upper arm.

If you want, you can inject into the same area of your body each week. However, make sure to choose different injection sites within the same area. If you also inject insulin, choose a different injection site for that injection.

Before using Mounjaro KwikPen, carefully read the "Instructions for use" of the pen.

Monitoring blood sugar levels

If you are using Mounjaro with a sulfonylurea or insulin, it is essential to monitor your blood sugar levels as instructed by your doctor, nurse, or pharmacist (see section 2, "Warnings and precautions").

If you use more Mounjaro than you should

If you use more Mounjaro than you should, consult your doctor immediately. Too much medicine can cause your blood sugar levels to drop too low (hypoglycemia) and may also cause nausea or vomiting.

If you forget to use Mounjaro

If you forget to inject a dose and,

• it has been 4days or lesssince you should have used Mounjaro, use it as soon as you remember. Then, inject your next dose as usual on your scheduled day.
• it has been more than 4dayssince you should have used Mounjaro, skip the missed dose. Then, inject your next dose as usual on your scheduled day.

Do not inject a double dose to make up for a missed dose. The minimum time between two doses must be at least 3 days.

If you stop using Mounjaro

Do not stop using Mounjaro without consulting your doctor. If you stop using Mounjaro and have type 2 diabetes, your blood sugar levels may increase.

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

4. Possible side effects

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

Serious side effects

Uncommon(may affect up to 1 in 100 people)

• Pancreatitis (inflammation of the pancreas) that could cause severe stomach and back pain that does not go away. See your doctor immediately if you experience these symptoms.

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

• Severe allergic reactions (e.g., anaphylactic reaction, angioedema). You should get medical help immediately and inform your doctor if you experience symptoms such as breathing problems, rapid swelling of the lips, tongue, and/or throat with difficulty swallowing, and rapid heartbeat.

Other side effects

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

• Nausea
• Diarrhea
• Stomach pain (abdominal pain) reported in patients treated for weight management
• Vomiting reported in patients treated for weight management
• Constipation reported in patients treated for weight management

These side effects are usually not serious. Nausea, diarrhea, and vomiting are more common when starting tirzepatida but decrease over time in most patients.

• Low blood sugar (hypoglycemia) is very common when tirzepatida is used with a sulfonylurea and/or insulin. If you are taking a sulfonylurea or insulin for type 2 diabetes, you may need to have your dose reduced while using tirzepatida (see section 2, "Warnings and precautions"). Symptoms of low blood sugar can include headache, drowsiness, weakness, dizziness, feeling hungry, confusion, irritability, rapid heartbeat, and sweating. Your doctor should tell you how to treat low blood sugar levels.

Common(may affect up to 1 in 10 people)

• Low blood sugar (hypoglycemia) when tirzepatida is used for type 2 diabetes with metformin and a sodium-glucose cotransporter 2 (SGLT2) inhibitor (another diabetes medicine)
• Allergic reaction (hypersensitivity) (e.g., rash, itching, and eczema)
• Dizziness reported in patients treated for weight management
• Low blood pressure reported in patients treated for weight management

• Decreased appetite reported in patients treated for type 2 diabetes
• Stomach pain (abdominal pain) reported in patients treated for type 2 diabetes
• Vomiting reported in patients treated for type 2 diabetes – usually decreases over time
• Indigestion (dyspepsia)
• Constipation reported in patients treated for type 2 diabetes
• Bloating
• Belching
• Gas (flatulence)
• Acid reflux or heartburn (also called gastroesophageal reflux disease – GERD) – a disease caused by stomach acid flowing back up into the tube that connects the stomach to the mouth

• Hair loss reported in patients treated for weight management
• Fatigue
• Injection site reactions (e.g., itching or redness)
• Rapid heartbeat

• Increased levels of pancreatic enzymes (such as lipase and amylase) in the blood.
• Increased levels of calcitonin in the blood in patients treated for weight management.

Uncommon(may affect up to 1 in 100 people)

• Low blood sugar (hypoglycemia) when tirzepatida is used with metformin for type 2 diabetes
• Gallstones
• Gallbladder inflammation
• Weight loss reported in patients treated for type 2 diabetes
• Pain at the injection site
• Increased levels of calcitonin in the blood in patients treated for type 2 diabetes or for OSA with obesity
• Altered sense of taste
• Changes in skin sensitivity
• Delayed stomach emptying

Reporting of side effects

If you experience any side effects, talk to your doctor, pharmacist, or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Spanish Medicines Monitoring System for Human Use: www.notificaRAM.es. By reporting side effects, you can help provide more information on the safety of this medicine.

5. Storing Mounjaro KwikPen

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 of the pen and on the carton after EXP. The expiry date is the last day of the month shown.

Store in a refrigerator (2°C to 8°C). Do not freeze. If the pen has been frozen, DO NOT USE IT.

Mounjaro KwikPen can be stored without refrigeration below 30°C for a maximum of 30 days after first use, and then the pen must be discarded.

Do not use this medicine if you notice that the pen is damaged or the medicine is cloudy, has color, or contains particles.

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 Mounjaro KwikPen

The active ingredient is tirzepatide.

Mounjaro 2.5mg/doseKwikPen:Each dose contains 2.5 mg of tirzepatide in 0.6 ml of solution. Each pre-filled multi-dose pen contains 10 mg of tirzepatide in 2.4 ml (4.17 mg/ml). Each pen delivers 4 doses of 2.5 mg.

Mounjaro 5mg/doseKwikPen:Each dose contains 5 mg of tirzepatide in 0.6 ml of solution. Each pre-filled multi-dose pen contains 20 mg of tirzepatide in 2.4 ml (8.33 mg/ml). Each pen delivers 4 doses of 5 mg.

Mounjaro 7.5mg/doseKwikPen:Each dose contains 7.5 mg of tirzepatide in 0.6 ml of solution. Each pre-filled multi-dose pen contains 30 mg of tirzepatide in 2.4 ml (12.5 mg/ml). Each pen delivers 4 doses of 7.5 mg.

Mounjaro 10mg/doseKwikPen:Each dose contains 10 mg of tirzepatide in 0.6 ml of solution. Each pre-filled multi-dose pen contains 40 mg of tirzepatide in 2.4 ml (16.7 mg/ml). Each pen delivers 4 doses of 10 mg.

Mounjaro 12.5mg/doseKwikPen:Each dose contains 12.5 mg of tirzepatide in 0.6 ml of solution. Each pre-filled multi-dose pen contains 50 mg of tirzepatide in 2.4 ml (20.8 mg/ml). Each pen delivers 4 doses of 12.5 mg.

Mounjaro 15mg/doseKwikPen:Each dose contains 15 mg of tirzepatide in 0.6 ml of solution. Each pre-filled multi-dose pen contains 60 mg of tirzepatide in 2.4 ml (25 mg/ml). Each pen delivers 4 doses of 15 mg.

The other components are disodium hydrogen phosphate heptahydrate (E339), benzyl alcohol (E1519) (see section 2 "Mounjaro KwikPen contains benzyl alcohol" for more information), glycerol, phenol, sodium chloride, and sodium hydroxide (see section 2 "Mounjaro contains sodium" for more information); concentrated hydrochloric acid and water for injectable preparations.

Appearance and Container Contents

Mounjaro is a clear, colorless to slightly yellowish injectable solution in a pre-filled pen (KwikPen).

Each KwikPen contains 2.4 ml of injectable solution (4 doses of 0.6 ml) and excess for purging.

Needles are not included.

Container sizes of 1 and 3 KwikPens.

Only some container sizes may be marketed.

Marketing Authorization Holder

Eli Lilly Nederland B.V., Papendorpseweg 83, 3528 BJ Utrecht, Netherlands.

Manufacturer

Eli Lilly Italia S.p.A., Via Gramsci 731/733, 50019, Sesto Fiorentino, Florence (FI), Italy

Lilly S.A., Avda. de la Industria, 30, 28108 Alcobendas, Madrid, Spain

Lilly France, 2, rue du Colonel Lilly, 67640 Fegersheim, France

Millmount Healthcare Limited, Block 7 City North Business Campus, Stamullen, K32 YD60, Ireland

Millmount Healthcare Limited, IDA Science And Technology Park, Mullagharlin, Dundalk, Co. Louth, A91 DET0, Ireland

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

Date of Last Revision of this Prospectus:

Other Sources of Information

Detailed information on this medicine is available on the European Medicines Agency website: http://www.ema.europa.eu, and on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es/).

Important Information You Should Know Before Injecting Mounjaro KwikPen.

Read these instructions for use and the leaflet before starting to inject Mounjaro KwikPen and each time you get a new pen. There may be new information. This information does not replace the conversation with your doctor, nurse, or pharmacist about your medical condition or treatment.

Mounjaro KwikPen is a pre-filled multi-dose pen. The pen contains 4 fixed doses, one dose administered weekly.Inject one single injection weekly, under the skin (subcutaneously).

After 4 doses, discard (throw away) the pen, including any unused medicine. The pen will prevent you from dialing a full dose after 4 weekly doses have been administered. Do notinject leftover medicine. Do not transfer medicine from the pen to a syringe.

Do notshare your Mounjaro KwikPen with other people, even if you have changed the needle on the pen. You may give other people a serious infection or get a serious infection from them.

Blind or visually impaired people should not use the pen without the help of a trained person to use it.

Parts Guide

Parts of Mounjaro KwikPen

Materials Needed to Inject

• Mounjaro KwikPen
• Needle compatible with KwikPen (If you do not know which needle to use for the pen, talk to your healthcare professional)
• Cotton swab, gauze, or cotton ball
• Container for disposing of sharp objects or household container

Preparation to Inject Mounjaro KwikPen

Injecting Mounjaro KwikPen

After Your Mounjaro KwikPen Injection

Storing your Mounjaro KwikPen

Unused pens:

? Store unused pensin the refrigeratorbetween 2°C and 8°C.

• Unused pens can be used until the expiration date printed on the label if the pen has been stored in the refrigerator.
• Donot freeze the pen. Discard (throw away) the pen if it has been frozen.

Used pens:

• You can store your used penat room temperaturebelow 30°C after injection.
• Keep the pen and needles out of sight and reach of children.
• Discard the pen 30 days after its first use, even if it still contains medication.
• Discard the pen after receiving 4 weekly doses. If you try to inject the remaining medication, the dose may be incomplete, even if there is still medication in the pen.

Excess medication:

• After finishing the fourth injection, you will see some excess medication, which is normal. This excess medication ensures the proper functioning of the pen.

• Discard the pen.
• Even if there is still medication in the pen, donot attempt to inject the excess medication. If you try to inject the excess medication, you may receive an incomplete dose.

Disposal of Mounjaro KwikPen and pen needles

• Place used pen needles in a puncture-resistant container or a hard plastic container with a tight-fitting lid.
• Donot throw (discard) used pen needles loose in household trash.
• Discard the used pen by following the instructions of your healthcare professional.
• Ask your healthcare professional about options for properly disposing of the puncture-resistant container.
• Do not recycle your used puncture-resistant container.

Frequently asked questions

• If you cannot remove the pen cap, gently turn it back and forth and then pull the cap off.
• If you cannot turn the dosing button until it appears in the dosing window:
• • discard the pen, including any unused medication. There may not be enough medication in the pen to administer a full dose. Donot attempt to inject the excess medication.
• If you have trouble pressing the dosing button:
• • pressing the dosing button more slowly will make it easier to inject.
  • your needle may be clogged. Put on a new needle and prime the pen.
  • there may be dust, food, or liquid inside the pen. Discard the pen and purchase a new one.
• If you have any questions or additional problems with Mounjaro KwikPen, contact Lilly or your doctor, nurse, or pharmacist.

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