Prevymis

Letermovir · Merck Sharp & Dohme LLC
PRESCRIPTION ONLY (USA)

Prevymis ingredients

Active ingredientStrength
Letermovir120 mg/1, 480 mg/1, 20 mg/mL, 20 mg/1, 240 mg/1

What Prevymis is used for

The FDA lists the approved uses on the official label (below). In the EU, letermovir is approved as Prevymis for:

Prevymis is indicated for prophylaxis of cytomegalovirus (CMV) reactivation and disease in adult and paediatric patients weighing at least 5 kg who are CMV-seropositive recipients [R+] of an allogeneic haematopoietic stem cell transplant (HSCT).Prevymis is indicated for prophylaxis of CMV disease in CMV-seronegative adult and paediatric patients weighing at least 40 kg who have received a kidney transplant from a CMV-seropositive donor [D+/R-].Prevymis is indicated for prophylaxis of cytomegalovirus (CMV) reactivation and disease in adult and paediatric patients weighing at least 15 kg who are CMV-seropositive recipients [R+] of an allogeneic haematopoietic stem cell transplant (HSCT). Consideration should be given to official guidance on the appropriate use of antiviral agents.

EU wording from the European Medicines Agency; US approved uses can differ.

Key facts

Brand
Prevymis
Generic name
Letermovir
Made by
Merck Sharp & Dohme LLC
Forms
Injection, Solution, Pellet, Tablet, Film Coated
Given
Intravenous, Oral
Drug class
Cytomegalovirus DNA Terminase Complex Inhibitor
FDA approval
New drug application (NDA) NDA219104
On the US market since
2017

Official information

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Prevymis?

Prevymis (Letermovir) is a specialist medicine made by Merck Sharp & Dohme LLC, approved by the US FDA.

What are the ingredients of Prevymis?

Prevymis contains Letermovir (120 mg/1, 480 mg/1, 20 mg/mL, 20 mg/1, 240 mg/1).

Is Prevymis approved in Europe?

The same active substance is approved in the EU as Prevymis.

From the FDA National Drug Code directory (open.fda.gov, public domain) and the European Medicines Agency medicines list. Page made 5 November 2026 by Satya Babu.

← All specialty medicines, USA

For information only, not medical advice. This page is a plain-language summary written from standard prescribing information and the public guides linked below. Brands sometimes change their formula, so always check the composition printed on the pack. Doses here are typical adult doses; yours may differ. Do not start, stop or change a medicine without your doctor or pharmacist, and keep all medicines away from children. In an emergency, call 112 (India) or your local emergency number.