Pharmgroup:
Antiviral drug for external use
Pharmic action:
Devirs is an antiviral drug.
Ribavirin triphosphate (RTF) is a potent inhibitor of inosine monophosphate dehydrogenase (IMP dehydrogenase), viral RNA polymerase and viral mRNA guanylyltransferase. Inhibition of the latter stops mRNA capping, resulting in significant depletion of intracellular guanosine triphosphate stores and inhibition of viral RNA and protein synthesis. Ribavirin also integrates into the viral genome, causing lethal mutations, with a subsequent reduction in the pathogenicity of the virus.
Ribavirin inhibits replication of new virions, which ensures reduction of viral load, selectively inhibits viral RNA synthesis without suppressing RNA synthesis in normally functioning cells.
The most sensitive DNA viruses to ribavirin are herpes simplex virus, adenoviruses, CMV, smallpox group viruses, Marek’s disease; RNA viruses – influenza A, B, paramyxoviruses (parainfluenza, mumps, Newcastle disease), reoviruses, arenaviruses (Lassa fever virus, Bolivian hemorrhagic fever virus), bunyaviruses (Rift Valley fever virus, Crimean-Congo hemorrhagic fever virus), hantaviruses (hemorrhagic fever virus with renal or pulmonary syndrome), oncogenic RNA viruses.
Ribavirin-insensitive DNA viruses: Varicella zoster, pseudorabies virus, natural cowpox; RNA viruses: enteroviruses, rhinoviruses, Semliki forest encephalitis virus.
Pharmacokinetics:
When applied to the skin and topically, systemic absorption is minimal and virtually insignificant.
Indications
As monotherapy or in combination with dosage forms of ribavirin for oral and parenteral use for the following diseases:
β infections of the skin and mucous membranes caused by Herpes simplex viruses types 1 and 2, of various localizations, incl. in the genital area;
β herpes zoster (as part of complex therapy).
Pharmacological effect
Pharmaceutical group:
Antiviral drug for external use
Pharmaceutical action:
Devirs is an antiviral drug.
Ribavirin triphosphate (RTP) is a potent inhibitor of inosine monophosphate dehydrogenase (IMP dehydrogenase), viral RNA polymerase, and viral mRNA guanylyl transferase. Inhibition of the latter stops mRNA capping, which leads to a significant depletion of intracellular guanosine triphosphate reserves and inhibition of viral RNA and protein synthesis. Ribavirin is also incorporated into the viral genome, causing lethal mutations, with a subsequent decrease in the pathogenicity of the virus.
Ribavirin inhibits the replication of new virions, which reduces the viral load, and selectively inhibits viral RNA synthesis without suppressing RNA synthesis in normally functioning cells.
The most sensitive DNA viruses to ribavirin are herpes simplex virus, adenoviruses, CMV, smallpox viruses, Marek’s disease; RNA viruses – influenza A, B viruses, paramyxoviruses (parainfluenza, mumps, Newcastle disease), reoviruses, arenaviruses (Lassa fever virus, Bolivian hemorrhagic fever), bunyaviruses (Rift Valley fever virus, Crimean-Congo hemorrhagic fever virus), hantaviruses (hemorrhagic fever virus with renal or pulmonary syndrome), oncogenic RNA viruses.
DNA viruses insensitive to ribavirin: Varicella zoster, pseudorabies virus, vaccinia virus; RNA viruses: enteroviruses, rhinoviruses, Semliki forest encephalitis virus.
Pharmacokinetics:
When applied to the skin and topically, systemic absorption is minimal and practically negligible.
Special instructions
Do not use for the treatment of ophthalmoherpes, do not apply to the eye area.
The drug should be used with extreme caution in patients with renal failure.
Men and women of childbearing age should use effective contraception during treatment and for 7 months after the end of therapy.
Active ingredient
Ribavirin
Composition
Active substance:
ribavirin 7.5 g
Excipients:
glyceryl monostearate (glycerol monostearate 40-45) – 2.0 g,
macrogol 6 cetostearyl alcohol ether (macrogol 6 cetostearyl ether) – 1.5 g, macrogol 25 cetostearyl alcohol ether (macrogol 25 cetostearyl ether) – 1.5 g,
cetostearyl alcohol – 5.0 g,
liquid paraffin (vaseline oil) – 5.0 g,
methyl parahydroxybenzoate (methylhydroxybenzoate, methylparaben, nipagin) – 0.1 g,
propyl parahydroxybenzoate (propylhydroxybenzoate, propylparaben, nipazole) – 0.02 g,
purified water – up to 100.0 g.
Contraindications
β pregnancy;
– period of lactation (breastfeeding);
– children and adolescents up to 18 years of age;
– hypersensitivity to the components of the drug Devirs.
With caution. The drug Devirspry should be used for renal failure in men and women of reproductive age.
Side Effects
Allergic reactions are possible (skin rash, urticaria, exanthema).
Other: hair loss, changes in thyroid-stimulating hormone (TSH), symptoms of autoimmune diseases (extremely rare).
The observed effects are usually reversible, do not affect the effectiveness of treatment and cease after completion of treatment.
Storage conditions
In a dry place, at a temperature not exceeding 25 Β°C
Shelf life
2 years
Manufacturer
Vertex, Russia
Shelf life | 2 years |
---|---|
Conditions of storage | In a dry place, at a temperature not exceeding 25 Β°C |
Manufacturer | Vertex, Russia |
Medication form | exterior cream |
Brand | Vertex |
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Buy Devirs, cream 7.5% 15 g with delivery to USA, UK, Europe and over 120 other countries.