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Results vary from person to person
Mounjaro (tirzepatide) is an injectable medicine from Eli Lilly, supplied as a pre-filled pen in six strengths from 2.5 to 15 mg.
Registration 1C 19/67 (NC) was approved on 31 July 2024 and is valid to 30 July 2031. Its status is active. The entry checked in the Thai FDA drug database is MOUNJARO 5 MG.
The licensee and importer is Silic Pharma Co., Ltd., Bangkok. The finished product is made by BSP Pharmaceuticals S.p.A. in Latina, Italy, and the entry names a second manufacturer, ANDERSONBRECON INC. in Illinois, USA.
In Europe the marketing authorisation holder is Eli Lilly Nederland B.V. in Utrecht, the Netherlands.
Per the EMA label, the most frequent side effects are digestive: nausea, diarrhoea, vomiting, abdominal pain and constipation. Most are mild or moderate, and they are more frequent while the doctor is raising the dose.
The label warns about acute pancreatitis, which has been reported in people taking it. It has not been studied in people who have had pancreatitis. If pancreatitis is suspected, the medicine must be stopped and a doctor seen. Contact the prescribing doctor if anything unusual happens.
The EMA label says to keep Mounjaro in a refrigerator at 2-8 C and never to freeze it. An unopened pen has a shelf life of 3 years under that label. A multi-dose KwikPen can be kept for 30 days after first use and must be thrown away after that.
This comes from the European label; a Thai label may differ slightly. Follow the label and leaflet in your box, and ask a pharmacist if unsure.
Tirzepatide is the active substance. Mounjaro is the brand name of the Eli Lilly medicine that contains it. The first name tells you what is inside, and the second tells you which company's product it is. The Thai FDA entry is listed under MOUNJARO.
It is injected under the skin once a week with a pre-filled pen. A patient should not start, raise, lower or stop it alone; follow what the doctor sets.
Tell the doctor about medical conditions, any history of pancreatitis, current medicines and drug allergies. Anyone allergic to tirzepatide or any other ingredient must not use it, and anyone who has had an allergic reaction to it must tell the doctor first.
Open the Thai FDA drug database and search for registration number 1C 19/67 (NC). Compare the drug name, the licensee and the manufacturer with the text on the box. That number belongs to the 5 mg entry.
The price depends on the model and the quantity.
This information is for general knowledge and does not replace a doctor's advice. Every procedure should be performed by a licensed doctor in a medical facility.



Thai label
Thai label
Thai label