


Ask a doctor about a prescription for NOXAFIL 100 mg GASTRO-RESISTANT TABLETS
Package Leaflet: Information for the User
Noxafil 100mg gastro-resistant tablets
posaconazole
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
Noxafil contains a medicine called posaconazole, which belongs to a group of medicines called "antifungals". It is used to prevent and treat many different fungal infections.
This medicine works by killing or stopping the growth of some types of fungi that can cause infections.
Noxafil can be used in adults to treat fungal infections caused by fungi of the Aspergillusfamily.
Noxafil can be used in adults and children aged 2 years and older and weighing more than 40 kg to treat the following types of fungal infections:
This medicine can also be used to prevent fungal infections in adults and children aged 2 years and older and weighing more than 40 kg who are at high risk of getting a fungal infection, such as:
Do not take Noxafil
Do not take Noxafil if you are in any of the above situations. If you are in doubt, consult your doctor or pharmacist before taking Noxafil.
See the section "Taking Noxafil with other medicines" later for more information, including information about other medicines that may interact with Noxafil.
Warnings and precautions
Consult your doctor, pharmacist, or nurse before starting to take Noxafil if:
You should avoid exposure to the sun while taking this treatment. It is important to cover exposed skin areas with protective clothing and use a sunscreen with a high sun protection factor (SPF), as you may be more sensitive to the UV rays of the sun.
If you are in any of the above situations (or in doubt), consult your doctor, pharmacist, or nurse before taking Noxafil.
If you develop severe diarrhoea or vomiting (feel sick) while taking Noxafil, consult your doctor, pharmacist, or nurse immediately, as this condition can prevent the medicine from working properly. For more information, see section 4.
Children
Noxafil should not be given to children under 2 years of age.
Taking Noxafil with other medicines
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
Do not take Noxafil if you are taking any of the following medicines:
Noxafil may increase the amount of these medicines in your blood, which could cause serious changes in your heart rhythm.
Do not take Noxafil if you are in any of the above situations. If you are in doubt, consult your doctor or pharmacist before taking Noxafil.
Other medicines
Consult the list provided earlier with the medicines that you should not use while taking Noxafil. In addition to the medicines mentioned earlier, there are other medicines that may increase the risk of heart rhythm problems, which may be greater when taken with Noxafil. Make sure to inform your doctor of all the medicines you are taking (with or without a prescription).
Some medicines may increase the risk of side effects of Noxafil by increasing the amount of Noxafil in your blood.
The following medicines may decrease the effectiveness of Noxafil by reducing its levels in your blood:
Noxafil may increase the risk of side effects of other medicines by increasing their levels in your blood. These medicines include:
If you are in any of the above situations (or in doubt), consult your doctor or pharmacist before taking Noxafil.
Pregnancy and breast-feeding
Tell your doctor if you are pregnant or think you might be pregnant before you start taking Noxafil.
Do not take Noxafil if you are pregnant, unless your doctor tells you to.
If you are a woman who can become pregnant, you must use effective contraception while taking this medicine. If you become pregnant while taking Noxafil, contact your doctor immediately.
Do not breast-feed while taking Noxafil, as small amounts may pass into breast milk.
Driving and using machines
You may feel dizzy, sleepy, or have blurred vision while taking Noxafil, which may affect your ability to drive or use tools or machines. If this happens, do not drive or use any tools or machines and contact your doctor.
Noxafil contains sodium
This medicine contains less than 1 mmol of sodium (23 mg) per tablet; this is essentially "sodium-free".
Do not switch between Noxafil tablets and Noxafil oral suspension without consulting your doctor or pharmacist, as this may lead to a lack of effectiveness or increase the risk of adverse reactions.
Follow the instructions for taking this medicine exactly as your doctor or pharmacist has told you. If you are in doubt, consult your doctor or pharmacist again.
How much to take
The recommended dose is 300 mg (three 100 mg tablets) twice a day on the first day and then 300 mg (three 100 mg tablets) once a day.
The length of treatment may depend on the type of infection you have and may be adjusted individually for you by your doctor. Do not change your dose yourself before consulting your doctor, or change your treatment schedule.
How to take this medicine
If you take more Noxafil than you should
If you think you may have taken too much Noxafil, inform your doctor immediately or go to the hospital immediately.
If you forget to take Noxafil
If you have any other questions about the use of this medicine, ask your doctor, pharmacist, or nurse.
Like all medicines, this medicine can cause adverse effects, although not all people suffer from them.
Severe Adverse Effects
Inform your doctor, pharmacist, or nurse immediately if you notice any of the following severe adverse effects; you may need urgent medical treatment:
Other Adverse Effects
Inform your doctor, pharmacist, or nurse if you notice any of the following adverse effects:
Frequent: the following may affect up to 1 in 10 patients
Infrequent: the following may affect up to 1 in 100 patients
Rare: the following may affect up to 1 in 1,000 patients
Frequency not known: cannot be estimated from the available data
Inform your doctor, pharmacist, or nurse if you experience any of the adverse effects described above.
Reporting Adverse Effects
If you experience any type of adverse effect, consult your doctor, pharmacist, or nurse, even if it is a possible adverse effect that is not listed in this prospectus. You can also report them directly through the national notification system included in Appendix V. By reporting adverse effects, you can contribute to providing 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 expiration date that appears on the blister pack after EXP. The expiration date is the last day of the month indicated.
No special storage conditions are required.
Medicines should not be thrown away through wastewater or household waste. Ask your pharmacist how to dispose of the packaging and medicines that you no longer need. This will help protect the environment.
Noxafil Composition
Product Appearance and Package Contents
Noxafil gastro-resistant tablets have a yellow coating, are capsule-shaped, and are marked with the digits "100" on one side. They are packaged in blister packs in boxes of 24 (2x12) or 96 (8x12) tablets.
Only some package sizes may be marketed.
Marketing Authorization Holder Merck Sharp & Dohme B.V. Waarderweg 39 2031 BN Haarlem Netherlands | Manufacturer Organon Heist bv Industriepark 30 2220 Heist-op-den-Berg Belgium Merck Sharp & Dohme B.V. Waarderweg 39 2031 BN Haarlem Netherlands |
You can request more information about this medicine by contacting the local representative of the marketing authorization holder:
België/Belgique/Belgien MSD Belgium Tel/Tel: +32(0)27766211 | Lietuva UAB Merck Sharp & Dohme Tel. +370 5 2780 247 |
| Luxembourg/Luxemburg MSD Belgium Tél/Tel: +32(0)27766211 |
Ceská republika Merck Sharp & Dohme s.r.o. Tel: +420 233 010 111 | Magyarország MSD Pharma Hungary Kft. Tel.: +36 1 888 5300 |
Danmark MSD Danmark ApS Tlf.: + 45 4482 4000 | Malta Merck Sharp & Dohme Cyprus Limited Tel: 8007 4433 (+356 99917558) |
Deutschland MSD Sharp & Dohme GmbH Tel.: +49 (0) 89 20 300 4500 | Nederland Merck Sharp & Dohme B.V. Tel: 0800 9999000 (+31 23 5153153) |
Eesti Merck Sharp & Dohme OÜ Tel: +372 614 4200 | Norge MSD (Norge) AS Tlf: +47 32 20 73 00 |
Ελλ?δα MSD Α.Φ.Ε.Ε. Τηλ: +30 210 98 97 300 | Österreich Merck Sharp & Dohme Ges.m.b.H. Tel: +43 (0) 1 26 044 |
España Merck Sharp & Dohme de España, S.A. Tel: +34 91 321 06 00 | Polska MSD Polska Sp. z o.o. Tel: +48 22 549 51 00 |
France MSD France Tél: + 33 (0) 1 80 46 40 40 | Portugal Merck Sharp & Dohme, Lda Tel: +351 21 4465700 |
Hrvatska Merck Sharp & Dohme d.o.o. Tel: + 385 1 6611 333 | România Merck Sharp & Dohme Romania S.R.L. Tel: +40 21 529 29 00 |
Ireland Merck Sharp & Dohme Ireland (Human Health) Limited Tel: +353 (0)1 2998700 | Slovenija Merck Sharp & Dohme, inovativna zdravila d.o.o. Tel: +386 1 520 4201 |
Ísland Vistor ehf. Sími: + 354 535 7000 | Slovenská republika Merck Sharp & Dohme, s. r. o. Tel: +421 2 58282010 |
Italia MSD Italia S.r.l. Tel: 800 23 99 89 (+39 06 361911) | Suomi/Finland MSD Finland Oy Puh/Tel: +358 (0)9 804 650 |
Κ?προς Merck Sharp & Dohme Cyprus Limited Τηλ.: 800 00 673 (+357 22866700) | Sverige Merck Sharp & Dohme (Sweden) AB Tel: +46 77 5700488 |
Latvija SIA Merck Sharp & Dohme Latvija Tel.: + 371 67025300 |
Date of the Last Revision of this Prospectus:<{MM/AAAA}><{month AAAA}>.
Other Sources of Information
Detailed information about this medicine is available on the website of the European Medicines Agency: https://www.ema.europa.eu.
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