Patient Leaflet Updated 28-Sep-2026 | IBSA Pharma
Lubion 25 mg solution for injection Vial
Lubion 25 mg solution for injection
Progesterone
1. What Lubion is and what it is used for
2. What you need to know before you use Lubion
3. How to use Lubion
4. Possible side effects
5. How to store Lubion
6. Contents of the pack and other information
Lubion contains the active ingredient Progesterone. Progesterone is a naturally occurring female sex hormone. The medicine works on the lining of the womb and helps you to become pregnant and to stay pregnant.
Lubion is for women who need extra progesterone while undergoing treatment in an Assisted Reproductive Technology (ART) programme who are unable to use or tolerate vaginal preparations.
Take special care with Lubion
If you experience any of the following during treatment tell your doctor immediately as your treatment may need to be stopped. Also tell your doctor immediately if you experience these a few days after the last dosage:
Before treatment with Lubion
Tell your doctor if you have had or have any of the following before using Lubion:
If any of the above applies to you, your doctor will monitor you carefully during treatment.
The product is not to be used by children or adolescents.
Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription and herbal medicines. Some medicines may interact with Lubion. For example:
Do not administer Lubion at the same time as any other injectable medicine.
Ask your doctor or pharmacist for advice before taking any medicine.
Do not drive or use any tools or machines if you feel drowsy and/or dizzy whilst taking Lubion.
If you have a kidney disease, talk to your doctor before you receive this medicine.
This medicine contains less than 1 mmol sodium (23 mg) per dosage unit, that is to say essentially ‘sodium-free’.
Always use Lubion exactly as your doctor has told you. Remember Lubion should only be used under the supervision of a doctor experienced in treating fertility problems.
The usual dose is a once daily injection of 25 mg usually until 12 weeks of confirmed pregnancy (i.e. 10 weeks of treatment).
Lubion can be given either under your skin (subcutaneous injection) or into a muscle (intramuscular injection).
You will be able to administer 25 mg of Lubion subcutaneously after suitable advice and training by your doctor or healthcare professional.
Subcutaneous injection:
Before you inject Lubion you will receive the following training and advice:
Please read instruction below on preparation and administration of Lubion.
The steps for self-administration are:
A Preparing your injection
B Checking pack
C Preparing the vial and syringe
D Filling the syringe
E Changing the injecting needle
F Removing air bubbles
G Injection by subcutaneous administration
H Disposal of used items.
These steps are explained in full below.
IMPORTANT: each vial should only be used once. The solutions should be used immediately after opening the vial. It should not be stored in the syringe.
A. Preparing your injection
It is important to keep everything as clean as possible, so start by washing your hands thoroughly and drying on a clean towel. Choose a clean area to prepare your medicine:
The following items are not supplied with your medicine. Your doctor or pharmacist will supply these items.
B. Checking pack
C. Preparing the vial and syringe
D. Filling the syringe
E. Changing the injecting needle
This step is only required if you are doing a subcutaneous administration; if your doctor is performing an intramuscular injection they will move on to set the dose and administer the injection.
F. Removing air bubbles
G. Injection by subcutaneous administration
H. Disposal of used items
Injection by intramuscular administration should given only by a doctor or healthcare professional
For all intramuscular injections, your doctor or another healthcare professional will perform the injection.
The Lubion injection will be given into the side of the thigh or bottom. Your doctor or healthcare professional will clean the area of skin to be injected using an alcohol wipe, and allow it to dry. Using a dart-like motion they will insert the large needle into the muscle. They will inject the solution by pushing gently on the plunger in a slow and steady motion until all the solution is injected into the muscle. They will pull the needle straight out and wipe the skin at the injection site with an alcohol wipe.
Tell your doctor or pharmacist. The symptoms of an overdose include drowsiness.
Take the dose as soon as you remember and then carry on as before. Do not take a double dose to make up for a forgotten dose. Tell your doctor what you have done.
Do not stop using Lubion without speaking to your doctor or pharmacists first. Abrupt discontinuation of Lubion may cause increased anxiety, moodiness, and increase your risk of having seizures (fits).
If you have any further questions on the use of this product, ask your doctor or pharmacist.
Like all medicines, Lubion can cause side effects, although not everybody gets them.
Very common: may affect more than 1 in 10 people
Common: may affect up to 1 in 10 people
Uncommon: may affect up to 1 in 100 people
Not known: frequency cannot be estimated from the available data
The following disorders, although not reported by patients in clinical studies using Lubion , have been described with other progestins: inability to sleep (insomnia), premenstrual like syndrome and menstrual disturbances, hives, acne, excessive hair growth, hair loss (alopecia), weight gain..
If you get 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 national reporting system listed in Appendix V. By reporting side effects you can help provide more information on the safety of this medicine.
Keep out of the sight and reach of children.
Store below 25°C.
Do not refrigerate or freeze.
Store in the original package in order to protect from light.
This medicinal product must be used immediately after first opening.
Any remaining solution must be discarded.
Do not use Lubion after the expiry date which is stated on the label after Exp:
If the expiry date is reported as month/year, the expiry date refers to the last day of that month.
Do not use Lubion if you notice particles in the solution or if the solution is not clear.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.
The active substance is Progesterone. Each vial (1.112 ml) contains 25 mg progesterone (theoretical concentration 22.48 mg/ml).
The other ingredients are: Hydroxypropylbetadex, Disodium phosphate, Sodium dihydrogen phosphate dihydrate, Water for injections
Lubion is a clear colourless solution supplied in a colourless glass vial.
Each pack contains 1, 7 or 14 vials. Not all pack sizes may be marketed.
This medicinal product is authorized in the Member States of the EEA under the following names: (The strength and pharmaceutical form are identical in all countries, only the trade name changes)
Austria: Progedex
Belgium: Inprosub
Bulgaria: Prolutex
Cyprus: Prolutex
Czech Republic: Prolutex
Denmark: Prolutex
Estonia: Lubion
Finland: Prolutex
France: Progiron
Germany: Prolutex
Greece: Prolutex
Hungary: Prolutex
Italy: Pleyris
Lithuania: Lubion
Latvia: Lubion
Luxembourg: Inprosub
Norway: Prolutex
Poland: Prolutex
Portugal: Prolutex
Romania: Prolutex
Slovakia: Prolutex
Sweden: Prolutex
Spain: Prolutex
The Netherlands: Prolutex
United Kingdom: Lubion
This leaflet was last revised in 09/2024
For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder via [email protected]
01923233466
01923233466