Package Leaflet: Information for the User
Foscarnet Tillomed24 mg/ml solution for infusion EFG
Foscarnet sodium hexahydrate
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
Contents of the pack
This medicine contains the active substance foscarnet sodium hexahydrate, which belongs to a group of medicines called antivirals. It works by inhibiting the multiplication of certain viruses.
This medicine is used to treat the following infections in patients with AIDS:
Do not useFoscarnet Tillomed:
If you are not sure, talk to your doctor or nurse before you are given foscarnet.
Warnings and precautions
Talk to your doctor or nurse before you start using Foscarnet Tillomed if:
If you are not sure if this applies to you, talk to your doctor or nurse before you are given foscarnet.
Children and adolescents
The safety and efficacy of foscarnet sodium hexahydrate in children have not been established.
Other medicines and Foscarnet Tillomed
Tell your doctor or nurse if you are using, have recently used, or might use any other medicines, including those obtained without a prescription and herbal medicines.
In particular, tell your doctor or nurse if you are taking any of the following medicines:
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before using this medicine.
This medicine is not recommended during pregnancy.
You should not try to become pregnant during treatment with this medicine and for up to 6 months after treatment. You should use effective contraception during or up to 6 months after treatment.
Men who are being treated with this medicine should not father a child during or up to 6 months after treatment.
Do not use this medicine if you are breastfeeding.
Driving and using machines
Foscarnet may affect your ability to drive or use machines. Talk to your doctor before doing so.
Tests before and during your treatment with Foscarnet Tillomed
Your doctor may do blood and urine tests before and during your treatment with Foscarnet Tillomed. This is to check how well your kidneys are working and the level of minerals in your blood.
Foscarnet Tillomed contains sodium
This medicine contains 1.375 mg of sodium (the main component of cooking/table salt) in each 250 ml vial. This is equivalent to 69% of the maximum recommended daily intake of sodium for an adult.
Talk to your doctor or pharmacist if you need to use more than 71 ml daily for a prolonged period, especially if you have been advised to follow a low-salt diet.
Follow the instructions for administration of this medicine exactly as told by your doctor or pharmacist. If you are not sure, talk to your doctor or pharmacist again.
Use of Foscarnet Tillomed for CMV infection
If you are being treated with this medicine for CMV retinitis, treatment will be done in two stages. The first stage is called induction treatment and the second stage is called maintenance treatment.
Induction treatment
Maintenance treatment
Your doctor will tell you if you need to take more or less of this medicine and how often you should take it. This is to make sure you get the right dose for you.
Your doctor may also prescribe a medicine called ganciclovir to make sure you get the right treatment.
Use of Foscarnet Tillomed for Herpes Simplex Virus
Personal hygiene
Wash your genitals carefully after urinating. This will help prevent the development of sores.
If Foscarnet Tillomed solution comes into contact with skin or eyes
If the solution accidentally comes into contact with skin or eyes, wash the affected area immediately with water.
Use in children and adolescents:
The safety and efficacy of this medicine in children and adolescents under 18 years have not been established.
If you use more Foscarnet Tillomed than you should
If you think you have been given too much Foscarnet, tell your doctor immediately.
If you miss a dose of Foscarnet Tillomed
If you think you have missed a dose, talk to your doctor immediately.
If you have any other questions about the use of this medicine, ask your doctor or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Some side effects can be serious and need immediate medical attention:
If you experience any of the above side effects, tell your doctor immediately or go to the nearest emergency department.
Other side effects include:
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)
Frequency not known: cannot be estimated from the available data
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist, even if they are not listed in this leaflet. You can also report side effects directly to the Spanish Medicines Agency's Pharmacovigilance System for Human Use: https://www.notificaRAM.es. By reporting side effects, you can help provide more information on the safety of this medicine.
After opening:
From a microbiological point of view, unless the method of opening precludes the risk of microbial contamination, the product should be used immediately. If not used immediately, in-use storage times and conditions are the responsibility of the user.
After dilution:
Chemical and physical in-use stability has been demonstrated for 36 hours at 2-8°C and 20-25°C, when the solution is diluted from 24 mg/ml to 12 mg/ml of foscarnet sodium hexahydrate in PVC bags. From a microbiological point of view, the product should be used immediately. If not used immediately, storage conditions and times before use are the responsibility of the user and should not exceed 24 hours when stored between 2 and 8°C, unless reconstitution has taken place in controlled and validated aseptic conditions.
Composition ofFoscarnet Tillomed
Appearance of the product and container contents
Foscarnet Tillomed is a clear and colorless infusion solution in glass vials. Each pack contains 1 vial or 10 vials of 250 ml.
Only some pack sizes may be marketed.
Marketing authorization holder
Laboratorios Tillomed Spain, S.L.U.
C/ Cardenal Marcelo Spínola 8
28016 Madrid, Spain
Manufacturer[1]
MIAS Pharma Limited
Suite 2, Stafford House,
Strand Road Portmarnock,
Co. Dublin
Ireland
Siegfried Hameln GmbH
Langes Feld 13
31789 Hameln
Germany
SGS Pharma Magyarorszag Kft.
Derkovits Gyula Utca 53,
Budapest XIX,1193,
Hungary
Tillomed Malta Limited
Malta Life Science Park
LS2.01.06 Industrial Estate
San Gwann, SGN 3000, Malta
This medicinal product is authorized in the Member States of the European Economic Area under the following names:
Austria : Foscarnet Tillomed 24 mg / ml Infusionslösung
Czech Republic : Foscarnet Tillomed
Denmark : Foscarnet “Tillomed”
Estonia : Foscarnet sodium Tillomed
Finland : Foscarnet Tillomed 24 mg/ml infuusioneste, liuos
France : Foscarnet Tillomed 24 mg/ml solution pour perfusion
Germany : Foscarnet Tillomed 24 mg / ml Infusionslösung
Greece : Foscarnet Tillomed 24 mg / ml δι?λυμα για ?γχυση
Ireland : Foscarnet sodium hexahydrate Tillomed 24 mg/ml solution for infusion
Italy : Foscarnet Tillomed
Latvia : Foscarnet sodium Tillomed
Lithuania : “Foscarnet Tillomed” 24 mg / ml infuzinis tirpalas
Netherlands : Foscarnet Tillomed 24 mg / ml oplossing voor infusie
Norway : Foskarnetnatriumheksahydrat Tillomed
Poland : Foscarnet sodium hexahydrate Tillomed
Portugal : Foscarnet Tillomed 24 mg / ml solução para perfusão
Slovakia : Foscarnet Tillomed 24 mg / ml infúzny roztok
Spain : Foscarnet Tillomed 24 mg/ml solución para perfusión EFG
Sweden : Foscarnet Tillomed 24 mg/ml infusionsvätska, lösning
Date of last revision of this leaflet 05/2022
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This information is intended only for healthcare professionals:
Instructions for use and handling
When perfused in peripheral veins, the solution must be diluted from 24 mg/ml to 12 mg/ml of foscarnet sodium hexahydrate before use. Individual doses of this medicinal product must be transferred aseptically to plastic infusion bags (PVC bags) and diluted with equal parts of sodium chloride 9 mg/ml (0.9%) solution or glucose 50 mg/ml (5%) solution.
Storage and validity period of the medicinal product and the diluted solution: see section 5.
Each vial of this medicinal product should only be used to treat a single patient with a single infusion.
Accidental contact with the skin or eyes of the foscarnet sodium hexahydrate solution may cause local irritation and a burning sensation. In case of accidental contact, the affected area should be washed with water.
[1]
1Only the actual manufacturer is indicated in the printed leaflet