promomed
Esperavir
Esperavir
Esperavir (capsules) was developed by Promomed Group using a unique technology and studied in a multicenter clinical trial1.
LP-007856
Name Esperavir
Dosage form Capsules
Nosological classification J05AX27
INN Molnupiravir
Active agent

Formula, per capsule:
200 mg
400 mg

Active ingredient:
Molnupiravir
200,0 mg
400,0 mg 

Excipients:
Microcrystalline cellulose
67,0 mg
134,0 mg
Croscarmellose sodium
15,0 mg
30,0 mg 

Povidone K30
15,0 mg
30,0 mg 

Sodium stearyl fumarate
3,0 mg
6,0 mg 

Capsule body:
Titanium dioxide (E171)
2,0 %
2,0 % 

Gelatin
up to 100.0 %
up to 100.0 % 

Capsule cap:
Indigo carmine (E132)
-
0,1333 % 

Titanium dioxide (E171)
2,0 %
1,0 % 

Gelatin
up to 100.0 %
up to 100.0 %

Esperavir is active against various RNA viruses: ARVI, influenza, SARS-CoV-2 and others.

Esperavir inhibits the reproduction of RNA viruses, exerts its antiviral effect by introducing errors during viral RNA copying:

  • after 5 days of therapy, the virus is completely eliminated from the body, and recovery is achieved in 9 out of 10 patients;

  • after 3 days of therapy, catarrhal-febrile syndrome disappears in 70% of patients.

In a pandemic, even if the test for COVID-19 is negative, which is quite common for infection with the Omicron strain, the use of Esperavir is reasonable to prevent the disease progression and minimize the risk and severity of post-COVID syndrome.

The drug is used2 400 mg twice daily by prescription of a doctor. Treatment should be started no later than the 5th day from the onset of the disease. The duration of treatment is 5 days.

An open, two-stage, multicenter study to evaluate the main pharmacokinetic parameters, safety, and efficacy against COVID-19 of Esperavir (molnupiravir) in capsules (Promomed RUS LLC, Russia) in adult population.

Prescription product. Consult a doctor before use.