Read this information before starting Mounjaro and keep the patient leaflet supplied with your medicine. This page does not replace advice from your doctor, pharmacist, or nurse.
Read this information before starting Mounjaro and keep the patient leaflet supplied with your medicine. This page does not replace advice from your doctor, pharmacist, or nurse.
Mounjaro is a prescription-only medicine. It is not suitable for everyone. Completing a DarDoc assessment does not guarantee a prescription.
Do not share your pen or prescription with another person. Do not combine Mounjaro with another tirzepatide medicine or another GLP-1 medicine unless your prescriber directs you to.
Tell your doctor, pharmacist, or nurse about every health condition and all prescription medicines, over-the-counter medicines, vitamins, and supplements you use. In particular, tell them if you:
Mounjaro should not be used during pregnancy. Use contraception while receiving treatment. If you plan to become pregnant, speak with your clinician about stopping Mounjaro at least one month beforehand. If you become pregnant while using Mounjaro, contact your clinician promptly.
If you have obesity or overweight and use an oral contraceptive, consider switching to a non-oral method or adding a barrier method, such as a condom, for four weeks after starting Mounjaro and for four weeks after every dose increase.
Only use Mounjaro while breastfeeding after discussing it with your clinician. Tirzepatide passes into breast milk in undetectable to very low amounts after a single studied dose, but the effect of reduced maternal food intake on breast-milk composition is not known.
Severe, persistent pain in the stomach area, which may move to the back, with or without nausea or vomiting. Acute pancreatitis can be serious and potentially life-threatening.
Difficulty breathing or swallowing; rapid swelling of the lips, tongue, face, or throat; or a fast heartbeat. Anaphylaxis and angioedema have been reported rarely.
Mounjaro can increase the risk of low blood sugar when used with insulin or a sulfonylurea. Your clinician may reduce the dose of those medicines and ask you to monitor your blood sugar.
Warning signs may include:
Ask your clinician how to recognise and treat low blood sugar. Avoid driving or using machinery if symptoms affect your concentration.
Like all medicines, Mounjaro can cause side effects, although not everybody gets them. Side-effect frequency can differ according to whether Mounjaro is used for type 2 diabetes or weight management and which other medicines are used.
These may affect more than 1 in 10 people:
Nausea, vomiting, and diarrhoea occur most often while the dose is being increased and usually decrease over time. They should not be described as proof that treatment is working. Vomiting and diarrhoea may cause dehydration and worsen kidney function.
These may affect up to 1 in 10 people:
These may affect up to 1 in 100 people:
These may affect up to 1 in 1,000 people:
Read the leaflet supplied with your medicine for the complete current list.
Use Mounjaro exactly as prescribed. Do not change your dose yourself.
The weekly dosing day may be changed if at least three days have passed since the previous dose.
Contact your doctor immediately. Too much Mounjaro may cause nausea, vomiting, or low blood sugar and may require observation and supportive treatment. There is no specific antidote.
Tell your doctor or pharmacist about any suspected side effect.
Seek emergency care first for severe or life-threatening symptoms.
Last medically sourced: 21 July 2026.
UAE registration, prescription status, strengths, form, and pack presentation were checked against the EDE registered medical product directory, including the Mounjaro 2.5 mg KwikPen record.
Detailed indication and safety wording was cross-checked against Lilly's current April 2026 Mounjaro KwikPen patient leaflet and Summary of Product Characteristics, plus the EMA Mounjaro product-information record. Lilly's Gulf product-information portal identifies Mounjaro for UAE users but restricts the local document to prescribed patients and healthcare professionals.
The U.S.-specific boxed thyroid warning is not included because it is not present in the Lilly UK/EU information used for this page.
DARDOC HEALTH TECHNOLOGIES LIMITED. All rights reserved.