Veklury (remdesivir) vs Lagevrio (molnupiravir)

Veklury (remdesivir) vs Lagevrio (molnupiravir)

Veklury (remdesivir) is an antiviral medication administered intravenously, primarily used in a hospital setting, and is authorized for the treatment of COVID-19 in patients requiring hospitalization. Lagevrio (molnupiravir), on the other hand, is an oral antiviral medication that can be taken at home, intended for the treatment of mild to moderate COVID-19 in adults who are at risk for progressing to severe illness and/or hospitalization. When deciding between the two, a patient should consider factors such as the severity of their COVID-19 symptoms, their risk of severe disease, the convenience of at-home versus in-hospital treatment, and the guidance of their healthcare provider.

Difference between Veklury and Lagevrio

Metric Veklury (remdesivir) Lagevrio (molnupiravir)
Generic name Remdesivir Molnupiravir
Indications Treatment of COVID-19 in hospitalized patients Treatment of mild-to-moderate COVID-19 in adults with risk factors for severe disease
Mechanism of action Adenosine nucleotide analog, which interferes with the action of viral RNA-dependent RNA polymerase Prodrug of the synthetic nucleoside derivative N4-hydroxycytidine, induces viral mutagenesis
Brand names Veklury Lagevrio
Administrative route Intravenous infusion Oral
Side effects Nausea, ALT and AST elevation, hypersensitivity reactions Diarrhea, nausea, dizziness
Contraindications Hypersensitivity to remdesivir or any component of the formulation Hypersensitivity to molnupiravir or any component of the formulation
Drug class Antiviral Antiviral
Manufacturer Gilead Sciences Merck & Co. (known as MSD outside the US and Canada)

Efficacy

Efficacy of Veklury (Remdesivir) for COVID-19

Veklury, known by its generic name remdesivir, is an antiviral medication that has been approved for use in the treatment of COVID-19 in patients requiring hospitalization. Its efficacy was first noted in a landmark study by the National Institute of Allergy and Infectious Diseases (NIAID), which found that remdesivir shortened the time to recovery in adults hospitalized with COVID-19. Subsequent studies have supported these findings, indicating that remdesivir can reduce the severity of the disease in hospitalized patients, particularly when administered early in the course of infection. However, it is important to note that remdesivir is not a cure for COVID-19, and its benefits are most pronounced in a specific subset of patients.

Remdesivir works by inhibiting the replication of the SARS-CoV-2 virus, which causes COVID-19. This antiviral activity is believed to stem from its ability to interfere with the viral RNA polymerase enzyme, thus halting viral replication within host cells. While remdesivir has been shown to be effective in reducing the duration of hospital stays, its impact on mortality rates has been less clear, with some studies showing a reduction in death rates and others finding no significant effect on survival.

Efficacy of Lagevrio (Molnupiravir) for COVID-19

Lagevrio, also known as molnupiravir, is an oral antiviral medication that has been authorized for emergency use in the treatment of mild to moderate COVID-19 in adults who are at risk for progressing to severe disease. Molnupiravir works by introducing errors into the viral RNA, thereby preventing the virus from replicating effectively. Clinical trials have demonstrated that molnupiravir can reduce the risk of hospitalization or death in non-hospitalized patients with mild to moderate COVID-19 when treatment is initiated within five days of symptom onset.

The efficacy of molnupiravir has been particularly noteworthy in unvaccinated individuals and those with underlying health conditions that put them at higher risk of severe outcomes from COVID-19. However, it is crucial to understand that the use of molnupiravir is not recommended for patients who are hospitalized due to COVID-19 or those requiring oxygen therapy due to COVID-19, as the benefits in these populations have not been established. Additionally, molnupiravir is not authorized for use in patients younger than 18 years of age because it may affect bone and cartilage growth.

Regulatory Agency Approvals

Veklury
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
  • Therapeutic Goods Administration (TGA), Australia
Lagevrio
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Therapeutic Goods Administration (TGA), Australia
  • Medicines & Healthcare products Regulatory Agency (MHRA), United Kingdom

Access Veklury or Lagevrio today

If Veklury or Lagevrio are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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