Mounjaro
2.5 Mg
5 Mg
7.5 Mg
10 Mg
12.5 Mg
15 Mg
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, nurse or pharmacist.
– 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, nurse or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4
What is in this leaflet
1. What Mounjaro is and what it is used for
Mounjaro contains an active substance called tirzepatide and is used to treat adults with type 2 diabetes mellitus. Mounjaro reduces the level of sugar in the body only when the levels of sugar are
high.
Mounjaro is also used to treat adults with obesity or overweight (with BMI of at least 27 kg/m2).
Mounjaro influences appetite regulation, which may help you eat less food and reduce your body weight.
In type 2 diabetes, Mounjaro is used:
– on its own when you can’t take metformin (another diabetes medicine).
– with other medicines for diabetes when they are not enough to control your blood sugar levels. These other medicines may be medicines taken by mouth and/or insulin given by injection.
Mounjaro is also used together with diet and exercise for weight loss and to help keep the weight under control in adults, who have:
– a BMI of 30 kg/m² or greater (obesity) or
– a BMI of at least 27 kg/m² but less than 30 kg/m² (overweight) and weight-related health problems (such as prediabetes, type 2 diabetes, high blood pressure, abnormal levels of fats in the blood, breathing problems during sleep called ‘obstructive sleep apnoea’ or a history of heart attack, stroke or blood vessel problems)
BMI (Body Mass Index) is a measure of your weight in relation to your height.
It is important to continue to follow the advice on diet and exercise given to you by your doctor, nurse
or pharmacist
2. What you need to know before you use Mounjaro
Do not use Mounjaro
– if you are allergic to tirzepatide or any of the other ingredients of this medicine (listed in section 6).
Warnings and precautions
Talk to your doctor, nurse or pharmacist before using Mounjaro if:
– you have severe problems with food digestion or food remaining in your stomach for longer than normal (including severe gastroparesis).
– you have ever had pancreatitis (inflammation of the pancreas which may cause severe pain in the stomach and back which does not go away).
– you have a problem with your eyes (diabetic retinopathy or macular oedema).
– you are using a sulphonylurea (another diabetes medicine) or insulin for your diabetes, as low blood sugar (hypoglycaemia) can occur. Your doctor may need to change your dose of these other medicines to reduce this risk.
When starting treatment with Mounjaro, in some cases you may experience loss of fluids/dehydration, e.g. due to vomiting, nausea and/or diarrhoea, which may lead to a decrease in kidney function. It is important to avoid dehydration by drinking plenty of fluids. Contact your doctor if you have any questions or concerns.
If you know that you are due to have surgery where you will be under anaesthesia (sleeping), please tell your doctor that you are taking Mounjaro.
Children and adolescents
This medicine should not be given to 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 using this medicine. This medicine should not be used during pregnancy as the effects of this medicine on an unborn child are not known. Therefore, it is recommended to use contraception while using this medicine.
Breast-feeding
It is unknown whether tirzepatide passes into breast milk. A risk to newborns/infants cannot be ruled out. If you are breast-feeding or are planning to breast-feed, talk to your doctor before using this medicine. You and your doctor should decide if you should stop breast-feeding or delay using Mounjaro.
Driving and using machines
It is unlikely that this medicine will affect your ability to drive and use machines. However, if you use Mounjaro in combination with a sulphonylurea or insulin, low blood sugar (hypoglycaemia) may
occur which may reduce your ability to concentrate. Avoid driving or using machines if you get any signs of low blood sugar, e.g. headache, drowsiness, weakness, dizziness, feeling hungry, confusion, irritability, fast heartbeat and sweating (see section 4). See section 2, ‘Warnings and precautions’ for information on increased risk of low blood sugar. Talk to your doctor for further information.
Mounjaro contains sodium
This medicine contains less than 1 mmol sodium (23 mg) per dose, that is to say essentially ‘sodium-free’
3. How to use Mounjaro
Always use this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure how to use this medicine.
How much to use
• The starting 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 by 2.5 mg increments to 7.5 mg, 10 mg, 12.5 mg or 15 mg once a week if you need it. In each case your doctor will tell you to stay on a particular dose for at least 4 weeks before going to a higher dose.Do not change your dose unless your doctor has told you to.
Each pen contains one dose of Mounjaro either 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, or 15 mg.
Choosing when to use Mounjaro
You can use your pen at any time of the day, with or without meals. You should use it on the same day each week if you can. To help you remember, when to use Mounjaro, you may wish to tick the day of
the week when you inject your first dose on the box that your pen comes in, or mark it on a calendar.
If necessary, you can change the day of your weekly Mounjaro injection, as long as it has been at least 3 days since your last injection. After selecting a new dosing day, continue with once-a-week dosing on that new day.
How to inject Mounjaro
Mounjaro is injected under the skin (subcutaneous injection) of your stomach area (abdomen) at least 5 cm from the belly button or upper leg (thigh) or upper arm. You may need help from someone else if you want to inject in your upper arm.
If you want to do so, you can use the same area of your body each week. But be sure to choose a different injection site within that area. If you also inject insulin choose a different injection site for
that injection. Read the “Instructions for Use” for the pen carefully before using Mounjaro.
Testing blood glucose levels
If you are using Mounjaro with a sulphonylurea or insulin, it is important that you test your blood glucose 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 talk to your doctor immediately. Too much of this medicine may cause low blood sugar (hypoglycaemia) and can make you feel sick or be sick.
If you forget to use Mounjaro
If you forget to inject a dose and,
• it has been 4 days or less since you should have used Mounjaro, use it as soon as you remember. Then inject your next dose as usual on your scheduled day.
• If it has been more than 4 days since you should have used Mounjaro, skip the missed dose. Then inject your next dose as usual on your scheduled day. Do not use a double dose to make up for a forgotten dose. The minimum time between two doses must be at least 3 days.
If you stop using Mounjaro
Do not stop using Mounjaro without talking with your doctor. If you stop using Mounjaro, and you have type 2 diabetes, your blood sugar levels can increase. If you have any further questions on the use of this medicine, ask your doctor, nurse or pharmacist
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)
– Inflamed pancreas (acute pancreatitis) which could cause severe pain in the stomach and back which does not go away. You should see a doctor immediately if you experience such symptoms.
Rare (may affect up to 1 in 1 000 people)
– Severe allergic reactions (e.g. anaphylactic reaction, angioedema). You should get immediate medical help 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 a fast heartbeat.
Other side effects
Very common (may affect more than 1 in 10 people)
– Feeling sick (nausea)
– Diarrhoea
– Stomach (abdominal) pain reported in patients treated for weight management
– Being sick (vomiting) reported in patients treated for weight management
– Constipation reported in patients treated for weight management
These side effects are usually not severe. Nausea, diarrhoea, and vomiting are most common when first starting tirzepatide but decrease over time in most patients.
– Low blood sugar (hypoglycaemia) is very common when tirzepatide is used with medicines that contain a sulphonylurea and/or insulin. If you are using a sulphonylurea or insulin for type 2 diabetes, the dose may need to be lowered while you use tirzepatide (see section 2, ‘Warnings and precautions’). Symptoms of low blood sugar may include headache, drowsiness, weakness, dizziness, feeling hungry, confusion, irritability, fast heartbeat and sweating. Your doctor
should tell you how to treat low blood sugar.
Common (may affect up to 1 in 10 people)
– Low blood sugar (hypoglycaemia) when tirzepatide is used for type 2 diabetes with both metformin and a sodium-glucose co-transporter 2 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
– Feeling less hungry (decreased appetite) reported in patients treated for type 2 diabetes
– Stomach (abdominal) pain reported in patients treated for type 2 diabetes
– Being sick (vomiting) reported in patients treated for type 2 diabetes – this usually decreases over time
– Indigestion (dyspepsia)
Constipation reported in patients treated for type 2 diabetes
– Bloating of the stomach
– Burping (eructation)
– Gas (flatulence)
– Reflux or heartburn (also called gastroesophageal reflux disease – GERD) -–a disease caused by
stomach acid coming up into the tube from your stomach to your mouth
– Hair loss reported in patients treated for weight management
– Feeling tired (fatigue)
– Injection site reactions (e.g. itching or redness)
– Fast pulse
– Increased levels of pancreatic enzymes (such as lipase and amylase) in blood
– Increased calcitonin levels in blood in patients treated for weight management.
Uncommon (may affect up to 1 in 100 people)
– Low blood sugar (hypoglycaemia) when tirzepatide is used with metformin for type 2 diabetes.
– Gallstones
– Inflammation of the gallbladder
– Weight loss reported in patients treated for type 2 diabetes
– Injection site pain
– Increased calcitonin levels in blood in patients treated for type 2 diabetes
– Changed sense of taste
Reporting of side effects
If you get any side effects, talk to your doctor, nurse or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via 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. How to store Mounjaro
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 pen label and on the carton after EXP. The expiry date refers to the last day of that month.
Store in a refrigerator (2 °C – 8 °C). Do not freeze. If the pen has been frozen, DO NOT USE.
Store in the original packaging in order to protect from light.
Mounjaro can be stored unrefrigerated below 30 ºC for up to 21 cumulative days 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, discoloured or has particles in it.
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 Mounjaro contains
The active substance is tirzepatide.
– Mounjaro 2.5 mg: Each pre-filled pen contains 2.5 mg of tirzepatide in 0.5 ml solution (5 mg/ml).
– Mounjaro 5 mg: Each pre-filled pen contains 5 mg of tirzepatide in 0.5 ml solution (10 mg/ml).
– Mounjaro 7.5 mg: Each pre-filled pen contains 7.5 mg of tirzepatide in 0.5 ml solution (15 mg/ml).
– Mounjaro 10 mg: Each pre-filled pen contains 10 mg of tirzepatide in 0.5 ml solution (20 mg/ml).
– Mounjaro 12.5 mg: Each pre-filled pen contains 12.5 mg of tirzepatide in 0.5 ml solution (25 mg/ml).
– Mounjaro 15 mg: Each pre-filled pen contains 15 mg of tirzepatide in 0.5 ml solution (30 mg/ml).
The other ingredients are disodium hydrogen phosphate heptahydrate (E339), sodium chloride, sodium hydroxide (see section 2 under ‘Mounjaro contains sodium’ for further information); concentrated hydrochloric acid and water for injections.
What Mounjaro looks like and contents of the pack
Mounjaro is a clear, colourless to slightly yellow, solution for injection in a pre-filled pen.
The pre-filled pen has a hidden needle which will automatically insert into the skin when the injection button is pressed. The pre-filled pen will retract the needle when the injection is completed.
Each pre-filled pen contains 0.5 ml solution.
The pre-filled pen is for single use only.
Pack sizes of 2 pre-filled pens, 4 pre-filled pens or multipack of 12 (3 packs of 4) pre-filled pens. Not all pack sizes may be available in your country
Marketing Authorisation Holder
Eli Lilly Nederland B.V., Papendorpseweg 83, 3528 BJ Utrecht, The Netherlands.
Manufacturer
Eli Lilly Italia S.p.A.,Via Gramsci 731/733, 50019, Sesto Fiorentino, Firenze (FI), Italy Lilly France, 2, rue du Colonel Lilly, 67640 Fegersheim, France
For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder:
Belgique/België/Belgien
Eli Lilly Benelux S.A./N.V. Tél/Tel: + 32-(0)2 548 84 84
Lietuva
Eli Lilly Lietuva
Tel. +370 (5) 2649600
България
ТП “Ели Лили Недерланд” Б.В. – България тел. + 359 2 491 41 40
Luxembourg/Luxemburg Eli Lilly Benelux S.A./N.V. Tél/Tel: + 32-(0)2 548 84 84
Česká republika
ELI LILLY ČR, s.r.o.
Tel: + 420 234 664 111
Magyarország
Lilly Hungária Kft. Tel: + 36 1 328 5100
Danmark
Eli Lilly Danmark A/S Tlf: +45 45 26 60 00
Malta
Charles de Giorgio Ltd. Tel: + 356 25600 500
Deutschland
Lilly Deutschland GmbH Tel. + 49-(0) 6172 273 2222
Nederland
Eli Lilly Nederland B.V. Tel: + 31-(0) 30 60 25 800
Eesti
Eli Lilly Nederland B.V. Tel: +372 6 817 280
Norge
Eli Lilly Norge A.S. Tlf: + 47 22 88 18 00
Ελλάδα
ΦΑΡΜΑΣΕΡΒ-ΛΙΛΛΥ Α.Ε.Β.Ε. Τηλ: +30 210 629 4600
Österreich
Eli Lilly Ges.m.b.H.
Tel: + 43-(0) 1 20609 1270
España
Lilly S.A.
Tel: + 34-91 663 50 00
Polska
Eli Lilly Polska Sp. z o.o. Tel: +48 22 440 33 00
France
Lilly France
Tél: +33-(0) 1 55 49 34 34
Portugal
Lilly Portugal Produtos Farmacêuticos, Lda Tel: + 351-21-4126600
Hrvatska
Eli Lilly Hrvatska d.o.o. Tel: +385 1 2350 999
România
Eli Lilly România S.R.L. Tel: + 40 21 4023000
Ireland
Eli Lilly and Company (Ireland) Limited Tel: + 353-(0) 1 661 4377
Slovenija
Eli Lilly farmacevtska družba, d.o.o.
Tel: +386 (0)1 580 00 10
Ísland
Icepharma hf.
Sími + 354 540 8000
Slovenská republika Eli Lilly Slovakia s.r.o. Tel: + 421 220 663 111
Italia
Eli Lilly Italia S.p.A. Tel: + 39- 055 42571
Suomi/Finland
Oy Eli Lilly Finland Ab Puh/Tel: + 358-(0) 9 85 45 250
Κύπρος
Phadisco Ltd
Τηλ: +357 22 715000
Sverige
Eli Lilly Sweden AB Tel: + 46-(0) 8 7378800
Latvija
Eli Lilly (Suisse) S.A Pārstāvniecība Latvijā
Tel: +371 67364000
United Kingdom (Northern Ireland) Eli Lilly and Company (Ireland) Limited Tel: + 353-(0) 1 661 4377
Instructions for use
Mounjaro 2.5 mg solution for injection in pre-filled pen
Mounjaro 5 mg solution for injection in pre-filled pen
Mounjaro 7.5 mg solution for injection in pre-filled pen
Mounjaro 10 mg solution for injection in pre-filled pen
Mounjaro 12.5 mg solution for injection in pre-filled pen
Mounjaro 15 mg solution for injection in pre-filled pen
Important information you need to know before injecting Mounjaro.
Read this instructions for use and the package leaflet before using your Mounjaro pre-filled pen (pen) and each time you get a new pen. There may be new information. This information does not take the place of talking to your doctor, nurse or pharmacist about your medical condition or treatment.
Talk to your doctor, nurse or pharmacist about how to inject Mounjaro the right way.
• Mounjaro is a single-dose pre-filled pen.
• The pen has a hidden needle which will automatically insert into your skin when the injection
button is pressed. The pen will retract the needle when the injection is completed.
• Mounjaro is used 1 time each week.
• Inject under the skin (subcutaneously) only.
• You or another person can inject into your stomach (abdomen), upper leg (thigh) or upper arm.
• You may need help from someone else if you want to inject in your upper arm
Guide to parts
Preparing to inject Mounjaro
Remove the pen from the refrigerator.
Leave the grey base cap on until you are ready to inject.

Check the pen label to make sure you have the right medicine and dose, and that
it has not expired. Expiry Date
Inspect the pen to make sure
that it is not damaged.
Make sure the medicine is:
- not frozen
-
not cloudy
-
colourless to slightly yellow
-
does not have particles
Wash your hands.
Choose your injection site
Your doctor, nurse or pharmacist can help you choose the injection site that is best for you.

You or another person can inject the medicine in your stomach (abdomen) at least 5 cm from the belly button or thigh.
Another person should give you the injection in the back of your upper arm. Change (rotate) your injection site each week.
You may use the same area of your body, but be sure to choose a different injection site in that area
Step 1 Pull off the grey base cap
Make sure the pen is locked.
Do not unlock the pen until you place the clear base on your skin
and are ready to inject.
Pull the grey base cap straight off and throw it away.
Do not put the grey base cap back on – this could damage the
needle.
Do not touch the needl

Place the clear base flat against your skin at the injection site.
Unlock by turning the lock ring
Step 3
Press and hold up to 10 seconds
Press and hold the purple injection button.
Listen for:
• First click = injection started
• Second click = injection completed
Grey Plunger
Disposal of your used pen

• Throw away (dispose of) the pen in a sharps disposal container or as directed by your doctor, nurse or pharmacist. Do not throw away (dispose of) pens in your household waste.
• Do not recycle your used sharps disposal container.
• Ask your doctor, nurse or pharmacist about how to dispose of medicines you no longer use.
Storage and handling
- For storage instructions refer to section 5 of the patient information leaflet.
- The pen has glass parts. Handle it carefully. If you drop the pen on a hard surface, do not use it. Use a new pen for your injection.
Commonly asked questions
What if I see air bubbles in my pen?
Air bubbles are normal.
What if my pen is not at room temperature?
It is not necessary to warm the pen to room temperature.
What if I unlock the pen and press the purple injection button before pulling off the grey base cap?
Do not remove the grey base cap. Throw away the pen and get a new pen.
What if there is a drop of liquid on the tip of the needle when I remove the grey base cap?
A drop of liquid on the tip of the needle is normal. Do not touch the needle.
Do I need to hold the injection button down until the injection is complete?
This is not necessary, but it may help you keep the pen steady against your skin.
I heard more than 2 clicks during my injection — 2 loud clicks and 1 soft one. Did I get my complete injection?
Some people may hear a soft click right before the second loud click. That is the normal operation of the pen. Do not remove the pen from your skin until you hear the second loud click.
I am not sure if my pen worked the right way
Grey Plunger
Check to see if you have received your dose. Your dose was delivered the
right way if the grey plunger is visible. Also, see Step 3 of the instructions.
If you do not see the grey plunger, contact Lilly for further instructions.
Until then, store your pen safely to avoid an accidental needle injury
What if there is a drop of liquid or blood on my skin after my injection?
This is normal. Press a cotton ball or gauze over the injection site. Do not rub the injection site.
Other information
• If you have vision problems, do not use your pen without help from a person trained to use the Mounjaro pen.
Where to learn more
• If you have questions or problems with your Mounjaro pen, contact Lilly or your doctor, nurse or pharmacist
Quick Comparison
Mounjaro remove | Levocetrizine remove | Ornidazole remove | Cefpodoxime remove | Pantoprazole remove | Ambroxol remove | |||||||||||||
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Name | Mounjaro remove | Levocetrizine remove | Ornidazole remove | Cefpodoxime remove | Pantoprazole remove | Ambroxol remove | ||||||||||||
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SKU | Mounjaro | Levocetrizine | Ornidazole | Cefpodoxime | Pantoprazole | Ambroxol | ||||||||||||
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Description | Read all of this leaflet carefully before you start using this medicine because it containsimportant information for you. – Keep this leaflet. You may need to read it again. – If you have any further questions, ask your doctor, nurse or pharmacist. – 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, nurse or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4 | Levocetirizine, represented by BluePill Express, is a non-drowsy antihistamine used to treat allergic conditions such as hay fever, urticaria (hives), and allergic rhinitis. It works by blocking histamine receptors, providing relief from symptoms like sneezing, runny nose, itching, and watery eyes. | Ornidazole, represented by BluePill Express, is an antiprotozoal and antibacterial medication used to treat infections caused by anaerobic bacteria and protozoa. It is commonly prescribed for conditions such as bacterial vaginosis, amoebiasis, and giardiasis. Ornidazole works by disrupting the DNA structure of harmful microorganisms, effectively eliminating infections and promoting recovery. | Cefpodoxime, represented by BluePill Express, is a broad-spectrum cephalosporin antibiotic used to treat bacterial infections, including respiratory tract infections, urinary tract infections, and skin infections. It works by inhibiting bacterial cell wall synthesis, effectively eliminating harmful bacteria. | Pantoprazole, represented by BluePill Express, is a proton pump inhibitor (PPI) used to treat acid-related disorders such as gastroesophageal reflux disease (GERD), peptic ulcers, and Zollinger-Ellison syndrome. It works by reducing stomach acid production, providing relief from acid reflux and heartburn. | Ambroxol, represented by BluePill Express, is a mucolytic agent used to treat respiratory conditions associated with excessive mucus production, such as bronchitis, pneumonia, and chronic obstructive pulmonary disease (COPD). It works by thinning and loosening mucus in the airways, making it easier to cough up and clear congestion. | ||||||||||||
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