Find similar products:
This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information.
The text only version may be available in large print, Braille or audio CD. For further information call emc accessibility on 0800 198 5000. The product code(s) for this leaflet is: PLGB 11972/0053.
HEPCLUDEX 2 mg powder for solution for injection
Hepcludex 2 mg powder for solution for injection
bulevirtide
▼This medicine is subject to additional monitoring. This will allow quick identification of new safety information. You can help by reporting any side effects you may get. See the end of section 4 for how to report side effects.
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
1. What Hepcludex is and what it is used for
2. What you need to know before you take Hepcludex
3. How to take Hepcludex
4. Possible side effects
5. How to store Hepcludex
6. Contents of the pack and other information
7. Step-by-step injection guide
Hepcludex contains the active substance bulevirtide, which is an antiviral medicine.
Hepcludex is used to treat long-term (chronic) hepatitis delta virus (HDV) infection in adults with compensated liver disease (when the liver is still working well enough). Infection with hepatitis delta virus causes inflammation of the liver.
HDV uses a particular protein in liver cells to enter the cells. Bulevirtide, the active substance in this medicine blocks the protein and so prevents the HDV from getting into liver cells. This reduces the spread of HDV in the liver and reduces inflammation.
If you are not sure, speak to your doctor before taking this medicine.
Do not stop your treatment with Hepcludex unless your doctor advises you to do so. Stopping the treatment can reactivate the infection and worsen your disease.
Talk to your doctor or pharmacist before taking Hepcludex:
Children and adolescents under 18 years of age should not be treated with Hepcludex.
Please tell your doctor if you are taking, have recently taken, or might take any other medicines.
Some medicines can increase side effects of Hepcludex and you should not take them at the same time. This is why you should tell your doctor if you are taking any of these medicines:
Some medicines can increase or decrease the effects of Hepcludex when taken together. In some cases, you may need to have certain tests or your doctor may change the dose or monitor you regularly:
If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine. You should not use this medicine unless specifically told to by your doctor.
If you are a woman of childbearing potential, you should not take this medicine without using an effective method of contraception.
Talk to your doctor to decide whether you should breastfeed while taking Hepcludex.
It is not known whether Hepcludex can pass into breast milk. Therefore, a decision must be made whether to discontinue breast-feeding or to discontinue Hepcludex.
Dizziness and tiredness are side effects which may impair your ability to drive and use machines. If you have any concerns consult your doctor.
This medicine contains less than 1 mmol sodium (23 mg) per ml, that is to say essentially "sodium-free".
Always take this medicine exactly as your doctor has told you. Check with your doctor if you are not sure.
The recommended dose is 2 mg once daily by subcutaneous injection (just under the skin). Your doctor will say how long you need to take the medicine for.
Your doctor and nurse will show you how to prepare and inject Hepcludex. This package leaflet contains a step-by-step injection guide to help you inject the medicine (see section 7).
The usual dose is 2 mg (1 vial) per day. If you think you may have taken more than you should, tell your doctor immediately.
If less than 4 hours have passed since your missed dose of Hepcludex, take the missing dose as soon as possible and take your next scheduled dose at the usual time.
If more than 4 hours have passed since your missed dose of Hepcludex, do not take the missed dose. Take the next dose the following day at the usual time. Do not take a double dose to make up for the missed dose. Tell your doctor if you have missed a dose of Hepcludex.
If you do not want to take Hepcludex anymore, talk to your doctor before stopping the treatment.
Stopping the treatment can reactivate the infection and worsen your disease. Tell your doctor immediately about any changes in symptoms after stopping treatment.
If you have any further questions on the use of Hepcludex, ask your doctor or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Please tell your doctor if any of the side effects occur, or if you notice any side effects not listed in this leaflet.
The following side effect is very common (this may affect more than 1 in 10 people):
The following side effects are common (these may affect up to 1 in 10 people):
The following side effects are uncommon (these may affect up to 1 in 100 people):
Symptoms of allergic reactions can include:
Symptoms of anaphylactic reaction are like those of allergic reaction, but more severe and require immediate medical care.
Blood tests may also show:
If you get any side effects, talk to your doctor or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme, Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App.
By reporting side effects, you can help to provide more information on the safety of this medicine.
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 carton and vial after EXP. The expiry date refers to the last day of that month.
Store in a refrigerator (2°C -8°C). In order to protect from light, keep the vials in the outer carton.
The reconstituted solution should be used immediately. However, if this is not possible it can be stored for up to 2 hours at a temperature of up to 25°C.
Do not throw away any medicines or used needles via wastewater or household waste. Ask your pharmacist how to safely dispose medicines and used needles.
The active substance is bulevirtide 2 mg. Each vial contains bulevirtide acetate equivalent to 2 mg bulevirtide.
The other ingredients are: sodium carbonate anhydrous, sodium hydrogen carbonate, mannitol, hydrochloric acid, sodium hydroxide.
Bulevirtide is a powder for solution for injection and comes as a white to off-white powder.
Each carton contains 30 single doses.
For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder:
This leaflet was last revised in 05/2023.
Before using Hepcludex, you must first read sections 1 – 6 of this package leaflet.
Before you begin treatment with this medicine at home, your doctor or nurse will show you how to prepare and inject Hepcludex. This guide shows how to inject the medicine yourself. Speak with your doctor or nurse if you are unclear about anything or you have questions or need more information or help. Take your time to carefully prepare and inject Hepcludex.
In order to reduce injection site reactions, you may change the site of bulevirtide injection regularly.
Do not inject bulevirtide into the following areas: knee, groin, the lower or inner buttocks, directly over a blood vessel, around the navel (belly button), on scar tissue, a bruise, a mole, a surgical scar, tattoo or burn site, or where there is an injection site reaction.
Abdomen
Upper thighs
1A Storage
Bulevirtide vials must be stored in the original packaging in the refrigerator (2–8 °C) in order to protect bulevirtide from light.
1B Preparing doses
The following instructions are for dissolving a single dose.
1C Wash hands
Wash your hands well using soap and warm water and dry them with a clean towel.
Once your hands are clean, do not touch anything else other than the medicine, supplies and the area around the injection site.
1D Clean vial
Wipe the vial top with a new alcohol pad and let the top air-dry.
If you touch the rubber top after cleaning it, clean it again with a new alcohol pad.
2A Draw up sterile water
Pick up the syringe. Put the longer needle on.
Important! Be sure the capped needle is tight by pushing it down slightly while twisting it clockwise.
Pull off the plastic cap.
Open the sterile water for injection. Insert the needle in the vial and gently turn the water vial upside down. Make sure the tip of the needle is always below the surface of the water to help keep air bubbles from entering the syringe.
Slowly pull the plunger back to get 1.0 ml of sterile water into the syringe. Carefully remove the needle and syringe from the vial.
2B Inject sterile water into the powder
Gently tap the bulevirtide vial to loosen the powder.
Insert the needle with sterile water into the bulevirtide vial at an angle.
Inject the sterile water slowly, so it can drip down the side of the vial into the bulevirtide powder.
2C Gently mix bulevirtide
Gently tap the bulevirtide vial with your fingertip for 10 sec to start dissolving the powder. Then gently roll the bulevirtide vial between your hands to ensure thorough mixing. Make sure no bulevirtide powder is stuck to the vial wall.
Important! Do not shake the bulevirtide vial. Shaking will make the medicine foam and it will take much longer to dissolve.
2D Inspect bulevirtide
Once the powder starts to dissolve, just set it aside and it completely will dissolve.
After tapping, it could take up to 3 min to dissolve.
2E Bulevirtide ready for injection
When mixed completely, Clean the bulevirtide the bulevirtide solution should be clear.
Important! Completely dissolved bulevirtide should be clear and without foam.
If the bulevirtide solution appears foamy or yellowish, allow more time for it to dissolve.
If you see bubbles, gently tap the vial until they disappear.
If you see any particles in the bulevirtide solution once it is (completely) dissolved, do not use that vial. Contact your doctor or pharmacist that provided it.
Reconstituted bulevirtide must be used immediately.
2F Clean vial
Clean the bulevirtide vial top again, using a new alcohol pad.
Allow it to air dry.
3A Insert needle into vial
Pick up the syringe.
Insert the needle into the vial of liquid bulevirtide.
3B Draw up bulevirtide
Gently turn the vial upside down. Make sure the tip of the needle is always below the surface of the bulevirtide solution to help keep air bubbles from entering the syringe. Slowly pull the plunger to get 1.0 ml of bulevirtide.
3C Finishing preparation
Gently tap or flick the syringe and push/pull the plunger to remove extra air and bubbles.
To be sure you end up with 1.0 ml of bulevirtide in the syringe, you may need to pull the plunger past the 1.0 ml mark.
Carefully remove the needle and syringe from the vial.
3D Change and discard the needle
Remove the longer needle from the syringe and dispose of it properly so that nobody can be injured.
Important! Do not put the plastic cap back on the needle.
3E Attach needle for injection
Place the shorter needle on the syringe.
Important! Be sure the capped needle is tight by pushing it down slightly while twisting it clockwise.
Pull off the plastic cap.
3F Choose the injection site
Choose a site different from the one you used for your last injection. Clean the injection site with a new alcohol pad. Start in the centre, apply pressure and clean in a circular motion, working outward.
Important! Allow site to air-dry.
3G Prepare injection site
Pinch and hold a fold of skin around the injection site.
3H Inject bulevirtide
Pierce the skin at a 45-degree angle. The needle should be inserted most of the way in.
Slowly push the plunger all the way to inject bulevirtide.
Remove the needle from skin.
Remove the needle from the syringe and dispose of both properly so that nobody can be injured (see 3D).
4E015