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PREVYMIS 240 mg FILM-COATED TABLETS

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About the medicine

How to use PREVYMIS 240 mg FILM-COATED TABLETS

Translated with AI

This page provides general information and does not replace a doctor’s consultation. Always consult a doctor before taking any medication. Seek urgent medical care if symptoms are severe.

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Introduction

Package Leaflet: Information for the Patient

PREVYMIS 240mg film-coated tablets

PREVYMIS 480mg film-coated tablets

letermovir

Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.

  • Keep this leaflet, you may need to read it again.
  • If you have any further questions, ask your doctor, pharmacist, or nurse.
  • This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
  • If you get any side effects, talk to your doctor, pharmacist, or nurse. This includes any possible side effects not listed in this leaflet. See section 4.

Contents of the pack

  1. What is PREVYMIS and what is it used for
  2. What you need to know before you take PREVYMIS
  3. How to take PREVYMIS
  4. Possible side effects
  5. Storing PREVYMIS
  6. Contents of the pack and other information

1. What is PREVYMIS and what is it used for

PREVYMIS is a prescription antiviral medicine that contains the active substance letermovir.

PREVYMIS is a medicine for:

  • adults and children weighing at least 15 kg who have recently undergone a stem cell transplant (bone marrow transplant).
  • adults and children weighing at least 40 kg who have recently undergone a kidney transplant.

The medicine helps to prevent you from getting the disease caused by CMV (cytomegalovirus).

CMV is a virus. For most people, CMV does not cause any harm. However, if your immune system is weakened after receiving a stem cell or kidney transplant, you may be at high risk of getting sick from CMV.

Doctor consultation

Not sure if this medicine is right for you?

Discuss your symptoms and treatment with a doctor online.

2. What you need to know before you take PREVYMIS

Do not take PREVYMIS:

  • if you are allergic to letermovir or any of the other ingredients of this medicine (listed in section 6).
  • if you are taking any of the following medicines:
    • pimozide - used for Tourette's syndrome
    • ergot alkaloids (such as ergotamine and dihydroergotamine) - used for migraine headaches.
  • if you are taking the following herbal medicine:
    • St. John's Wort (Hypericum perforatum)

Do not take PREVYMIS if any of the above applies to you. If you are unsure, consult your doctor, pharmacist, or nurse before taking PREVYMIS.

If you are taking PREVYMIS with cyclosporine, do not take the following medicines:

  • dabigatran - used to prevent blood clots
  • atorvastatin, simvastatin, rosuvastatin, pitavastatin - to treat high cholesterol

Warnings and precautions

If you are also taking a medicine to treat high cholesterol (see list of medicines in the section "Other medicines and PREVYMIS"), you must inform your doctor immediately if you have unexplained muscle pain or weakness, especially if you are feeling unwell or have a fever. Then, it may be necessary to change your medicine or dose. For more information, see the leaflet for your other medicine.

Additional blood tests may be needed to monitor the following medicines:

  • cyclosporine, tacrolimus, sirolimus
  • voriconazole

Children and adolescents

PREVYMIS should not be used in children who weigh less than 5 kg who have received a stem cell transplant (bone marrow transplant) or in children who weigh less than 40 kg who have received a kidney transplant. This is because PREVYMIS has not been studied in these groups.

Other medicines and PREVYMIS

Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines. This is because PREVYMIS may affect the way other medicines work and other medicines may affect the way PREVYMIS works. Your doctor or pharmacist will tell you if it is safe to take PREVYMIS with other medicines.

There are some medicines that you must not takewith PREVYMIS (see list in "Do not take PREVYMIS:").

There are some medicines that you must not takewith PREVYMIS and cyclosporine (see list in “If you are taking PREVYMIS with cyclosporine, do not take the following medicines:”).

Also, tell your doctor if you are taking any of the following medicines. This is because your doctor may need to change your medicines or change the dose of your medicines:

  • alfentanil - for severe pain
  • fentanyl - for severe pain
  • quinidine - for heart rhythm disorders
  • cyclosporine, tacrolimus, or sirolimus - used to prevent transplant rejection
  • voriconazole - for fungal infections
  • statins, such as atorvastatin, fluvastatin, rosuvastatin, simvastatin, pravastatin, pitavastatin - to treat high cholesterol
  • gliburide, repaglinide - for high blood sugar
  • carbamazepine, phenobarbital, phenytoin - for seizures or epilepsy
  • dabigatran, warfarin - used to thin the blood or prevent blood clots
  • midazolam - used as a sedative
  • amiodarone - used to correct irregular heartbeats
  • oral steroid contraceptives - for birth control
  • omeprazole, pantoprazole - for stomach ulcers and other stomach problems
  • nafcillin - for bacterial infections
  • rifabutin, rifampicin - for fungal infections
  • thioridazine - for psychiatric disorders
  • bosentan - for high blood pressure in the blood vessels of the lungs
  • efavirenz, etravirine, nevirapine, lopinavir, ritonavir - for HIV
  • modafinil - to stay awake

You can ask your doctor or pharmacist for a list of medicines that may interact with PREVYMIS.

Pregnancy

If you are pregnant, think you may be pregnant, or are planning to have a baby, ask your doctor for advice before taking this medicine. PREVYMIS should not be used during pregnancy. This is because PREVYMIS has not been studied during pregnancy and it is not known whether PREVYMIS could harm the baby during pregnancy.

Breast-feeding

If you are breast-feeding or plan to breast-feed, ask your doctor for advice before taking this medicine. Breast-feeding is not recommended while taking PREVYMIS. This is because it is not known whether PREVYMIS passes into breast milk and could pass to your baby.

Driving and using machines

PREVYMIS may have a minor influence on your ability to drive and use machines (see section 4 "Possible side effects" later). Some patients have reported fatigue (feeling very tired) or dizziness (feeling like you are spinning) during treatment with PREVYMIS. If you experience any of these effects, do not drive or use machines until the effect disappears.

PREVYMIS contains lactose

PREVYMIS contains lactose monohydrate. If your doctor has told you that you have an intolerance to some sugars, consult your doctor before taking this medicine.

PREVYMIS contains sodium

This medicine contains less than 1 mmol of sodium (23 mg) per tablet; this is, essentially "sodium-free".

3. How to take PREVYMIS

Always take this medicine exactly as your doctor or pharmacist has told you. If you are unsure, check with your doctor or pharmacist.

How much to take

Your dose of PREVYMIS depends on your weight and whether you are also taking cyclosporine. Your doctor will tell you how many tablets to take.

  • Take PREVYMIS once a day.
  • Take PREVYMIS at the same time every day.
  • Take it with or without food.

The recommended oral doses of PREVYMIS are presented in Table 1 and Table 2.

Table 1: Recommended doses of PREVYMIS film-coated tablets without cyclosporine

Weight

PREVYMIS oral daily dose

Number of PREVYMIS tablets once daily

30 kg and above

480 mg

One 480 mg tablet or Two 240 mg tablets

Between 15 kg and less than 30 kg

240 mg

One 240 mg tablet

Table 2: Recommended doses of PREVYMIS film-coated tablets with cyclosporine

Weight

PREVYMIS oral daily dose

Number of PREVYMIS tablets once daily

30 kg and above

240 mg

One 240 mg tablet

Between 15 kg and less than 30 kg

120 mg

See the leaflet for PREVYMIS granules for oral suspension

How to take

  • Swallow the tablet whole with a little water. Do not break, crush, or chew the tablet because these methods have not been studied.

If you take more PREVYMIS than you should

If you take more PREVYMIS than you should, contact your doctor immediately.

If you forget to take PREVYMIS

It is very important that you do not miss or skip any dose of PREVYMIS.

  • If you forget to take a dose, take it as soon as you remember. But if it is almost time for your next dose, skip the missed dose. Take the next dose at the usual time.
  • Do not take a double dose of PREVYMIS at the same time to make up for missed doses.
  • If you are unsure what to do, contact your doctor or pharmacist.

Do not stop taking PREVYMIS

Do not stop taking PREVYMIS without talking to your doctor first. Do not run out of PREVYMIS. This way, the medicine will be more effective in preventing you from getting sick with CMV after receiving a stem cell or kidney transplant.

If you have any further questions on the use of this medicine, ask your doctor, pharmacist, or nurse.

Medicine questions

Started taking the medicine and have questions?

Discuss your symptoms and treatment with a doctor online.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Common:may affect up to 1 in 10 people

  • diarrhea
  • nausea
  • vomiting

Uncommon:may affect up to 1 in 100 people

  • allergic reaction (hypersensitivity) - the signs may include hives, difficulty breathing, rash, swelling, itching
  • loss of appetite
  • change in taste
  • headache
  • feeling like you are spinning (vertigo)
  • stomach pain
  • abnormalities in laboratory tests to check liver function (e.g., elevated liver enzymes)
  • muscle spasms
  • elevated creatinine in blood tests
  • feeling tired (fatigue)
  • swelling of hands or feet

Reporting of side effects

If you experience 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.

5. Storing PREVYMIS

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 blister after EXP. The expiry date is the last day of the month stated.

This medicine does not require any special storage conditions. Store in the original package to protect from moisture.

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 protect the environment.

6. Package Contents and Additional Information

Composition of PREVYMIS

The active ingredient is letermovir. Each film-coated tablet contains 240 mg of letermovir or 480 mg of letermovir.

The other ingredients are:

Tablet core

Microcrystalline cellulose (E460), sodium croscarmellose (E468), povidone (E1201), colloidal anhydrous silica (E551), magnesium stearate (E470b).

Film coating

Lactose monohydrate, hypromellose (E464), titanium dioxide (E171), triacetin, yellow iron oxide (E172), red iron oxide (only in 480 mg tablets) (E172), carnauba wax (E903). See section 2 "PREVYMIS contains lactose" and "PREVYMIS contains sodium".

Appearance and Packaging of the Product

PREVYMIS 240 mg film-coated tablet ("tablet") is presented as a yellow, oval-shaped tablet with "591" engraved on one side and the corporate logo on the other side. The tablet measures 16.5 mm in length and 8.5 mm in width.

PREVYMIS 480 mg film-coated tablet ("tablet") is presented as a pink, biconvex, oval-shaped tablet with "595" engraved on one side and the corporate logo on the other side. The tablet measures 21.2 mm in length and 10.3 mm in width.

The 28x1 tablets are packaged in a box containing unit-dose blister packs of polyamide/aluminum/PVC-aluminum (a total of 28 tablets).

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 medicinal product by contacting the local representative of the marketing authorization holder:

België/Belgique/Belgien

MSD Belgium

Tel: +32(0)27766211

[email protected]

Lietuva

UAB Merck Sharp & Dohme

Tel: + 370 5 2780 247

[email protected]

Text in Bulgarian language with contact information of Merck Sharp and Dohme Bulgaria including phone and email

Luxembourg/Luxemburg

MSD Belgium

Tél/Tel: +32(0)27766211

[email protected]

Ceská republika

Merck Sharp & Dohme s.r.o.

Tel: +420 233 010 111

[email protected]

Magyarország

MSD Pharma Hungary Kft.

Tel.: +36 1 888 5300

[email protected]

Danmark

MSD Danmark ApS

Tlf.: + 45 4482 4000

[email protected]

Malta

Merck Sharp & Dohme Cyprus Limited

Tel: 8007 4433 (+356 99917558)

[email protected]

Deutschland

MSD Sharp & Dohme GmbH

Tel.: +49 (0) 89 20 300 4500

[email protected]

Nederland

Merck Sharp & Dohme B.V.

Tel: 0800 9999000

(+31 23 5153153)

[email protected]

Eesti

Merck Sharp & Dohme OÜ

Tel: +372 614 4200

[email protected]

Norge

MSD (Norge) AS

Tlf: +47 32 20 73 00

[email protected]

Ελλάδα

MSD Α.Φ.Ε.Ε.

Τηλ: +30 210 98 97 300

[email protected]

Österreich

Merck Sharp & Dohme Ges.m.b.H.

Tel: +43 (0) 1 26 044

[email protected]

España

Merck Sharp & Dohme de España, S.A.

Tel: +34 91 321 06 00

[email protected]

Polska

MSD Polska Sp. z o.o.

Tel: +48 22 549 51 00

[email protected]

France

MSD France

Tél: + 33 (0) 1 80 46 40 40

Portugal

Merck Sharp & Dohme, Lda

Tel: +351 21 4465700

[email protected]

Hrvatska

Merck Sharp & Dohme d.o.o.

Tel: + 385 1 6611 333

[email protected]

România

Merck Sharp & Dohme Romania S.R.L.

Tel: +40 21 529 29 00

[email protected]

Ireland

Merck Sharp & Dohme Ireland (Human Health) Limited

Tel: +353 (0)1 2998700

[email protected]

Slovenija

Merck Sharp & Dohme, inovativna zdravila d.o.o.

Tel: +386 1 5204 201

[email protected]

Ísland

Vistor ehf.

Sími: + 354 535 7000

Slovenská republika

Merck Sharp & Dohme, s. r. o.

Tel: +421 2 58282010

[email protected]

Italia

MSD Italia S.r.l.

Tel: 800 23 99 89 (+39 06 361911)

[email protected]

Suomi/Finland

MSD Finland Oy

Puh/Tel: +358 (0)9 804 650

[email protected]

Κύπρος

Merck Sharp & Dohme Cyprus Limited

Τηλ.: 800 00 673 (+357 22866700)

[email protected]

Sverige

Merck Sharp & Dohme (Sweden) AB

Tel: +46 77 5700488

[email protected]

Latvija

SIA Merck Sharp & Dohme Latvija

Tel.: + 371 67025300

[email protected]

Date of the Last Revision of this Leaflet:{MM/YYYY}.

Detailed information on this medicinal product is available on the European Medicines Agency website: https://www.ema.europa.eu.

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Tarek Agami

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Dr. Tarek Agami is a general practitioner registered in both Portugal and Israel, with broad experience in family and preventive medicine. He offers online consultations for adults and children, providing personalised support for primary care needs, chronic disease management, and everyday health concerns.

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Dr. Agami provides medical support for patients using GLP-1 medications (such as Ozempic or Mounjaro) as part of a weight loss strategy. He offers individualised treatment planning, regular follow-up, dose adjustment, and advice on combining medication with sustainable lifestyle changes. Consultations follow the medical standards accepted in Portugal and Israel.

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Dr. Anastasiia Shalko is a general practitioner with a background in both paediatrics and general medicine. She graduated from Bogomolets National Medical University in Kyiv and completed her paediatric internship at the P.L. Shupyk National Medical Academy of Postgraduate Education. After working as a paediatrician in Kyiv, she relocated to Spain, where she has been practising general medicine since 2015, providing care for both adults and children.

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Dermatology 21 years exp.

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Frequently Asked Questions

Is a prescription required for PREVYMIS 240 mg FILM-COATED TABLETS?
PREVYMIS 240 mg FILM-COATED TABLETS requires a prescription in Spain. You can check with a doctor online whether this medicine may be appropriate for your situation.
What is the active substance in PREVYMIS 240 mg FILM-COATED TABLETS?
The active ingredient in PREVYMIS 240 mg FILM-COATED TABLETS is letermovir. This information helps identify medicines with the same composition but different brand names.
Who manufactures PREVYMIS 240 mg FILM-COATED TABLETS?
PREVYMIS 240 mg FILM-COATED TABLETS is manufactured by Merck Sharp & Dohme B.V.. Pharmacy brands and packaging may differ depending on the distributor.
Which doctors can assess the use of PREVYMIS 240 mg FILM-COATED TABLETS online?
Doctors such as Family doctors, Psychiatrists, Dermatologists, Cardiologists, Endocrinologists, Gastroenterologists, Pulmonologists, Nephrologists, Rheumatologists, Hematologists, Infectious disease physicians, Allergists, Geriatricians, Paediatricians, Oncologists may assess whether PREVYMIS 240 mg FILM-COATED TABLETS is appropriate, depending on your situation and local regulations. You can book an online consultation to discuss your symptoms and possible next steps.
What are the alternatives to PREVYMIS 240 mg FILM-COATED TABLETS?
Other medicines with the same active substance (letermovir) include PREVYMIS 240 MG CONCENTRATE FOR INFUSION SOLUTION, PREVYMIS 480 mg FILM-COATED TABLETS, PREVYMIS 480 mg CONCENTRATE FOR INFUSION SOLUTION. These may have different brand names or formulations but contain the same therapeutic ingredient. Always consult a doctor before switching or starting a new medicine.
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