MOLNUPIRAVIR 200MG 40CAP

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Description

MOLNUPIRAVIR 200MG 40CAP

MOLNUPIRAVIR 200MG 40CAP

DESCRIBTION

Treatment of COVID-19 in adults (aged 18 years and older) who do not require initiation of supplemental oxygen
due to COVID-19 and are at increased risk of progression to hospitalization or death

CONTRINCATION

  • Known allergy to Active ingredients or any of the excipients of this medicine (croscarmellose sodium,
    hydroxypropyl cellulose, magnesium stearate, microcrystalline cellulose, hypromellose, titanium dioxide, red
    iron oxide, butyl alcohol, dehydrated alcohol, isopropyl alcohol, potassium hydroxide, propylene glycol,
    purified water, shellac, strong ammonia solution).
  •  The safety and efficacy in children and adolescents aged 18 years and younger have not yet been
    established, therefore use in these patients is not recommended.
  •  See the below section for information on men and women of childbearing potential, and women who are
    pregnant or breastfeeding

Pregnancy, breastfeeding

Pregnancy

  • Molnupiravir is pregnancy category D – it is not recommended during pregnancy and in women of
    childbearing potential not using contraception.
  • There are no data on the use in pregnant women. Studies in animals have shown
    reproductive toxicity.

Breastfeeding

  • Breastfeeding is not recommended during treatment with and for 4 days after the last dose due
    to the potential for adverse reactions in the infant from
  • Animal lactation studies have not been conducted.
  • It is unknown whether molnupiravir or any of the components of molnupiravir; are present in human milk,
    affect human milk production, or have an effect on the breastfed infant.

Storage and stability

Molnupiravir should be stored in its original packaging; in a cool, dry place (< 30oC).

 

 

 

Additional information

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