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Molnupiravir Alvils
Molnupiravir · Ozon (holder Alvils)
1 form: capsule. No registration in force in Georgia.
Forms and doses0 of 1 in force in Georgia
The dose from the product's label, by species and weight. Check the label of the pack you use.
Used for: Feline Infectious Peritonitis, effusive, Feline Infectious Peritonitis, non-effusive, Feline Infectious Peritonitis, ocular, Feline Infectious Peritonitis, neurological, Feline Infectious Peritonitis
| Form | Species | Dose | Frequency | Georgia | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 200 mg, Capsule · Cat | Cat | Feline Infectious Peritonitis, effusive · By mouth: 10–15 mg/kgFeline Infectious Peritonitis, non-effusive · By mouth: 15 mg/kgFeline Infectious Peritonitis, ocular · By mouth: 15–20 mg/kgFeline Infectious Peritonitis, neurological · By mouth: 15–20 mg/kg | every 12 hours, for 84 days |
Georgia
No
Not registered in Georgia
Human (Ministry of Health, RAMA)
Verified on: 30 Oct 2026 |
||||||||||||||
| 200 mg, Capsule · Dog | Dog | Feline Infectious Peritonitis · By mouth: No dose for this species | - |
Georgia
No
Not registered in Georgia
Human (Ministry of Health, RAMA)
Verified on: 30 Oct 2026 |
||||||||||||||
Details: pack, label wording, sources, registrationhard capsule, human medicine Composition / strength
Molnupiravir200 mg
Formulation Type Capsule Administration route By mouth Manufacturer Registration
Georgia
No
Not registered in Georgia
Human (Ministry of Health, RAMA)
Verified on: 30 Oct 2026 Controlled in Georgia
Unknown
Source:
JVIM 2024 (10 cats)
Scientific article A study or review published in a scientific journal. Its findings apply to the animals and conditions it studied. Journal of Veterinary Internal Medicine 38:3087-3094, 2024
Source:
Lagevrio SmPC
Official product label (SPC), MHRA, UK Approved by the UK Medicines and Healthcare products Regulatory Agency (MHRA) as part of the product's authorisation. It applies to that product as authorised there. electronic medicines compendium (emc), UK, 2026 | ||||||||||||||||||
Known Contraindications
-
Critical
(Dog) Dog: no treatment dose exists, and the cat dose must not be transferred. In the safety studies, bone marrow toxicity affecting all blood cell lines appeared at 17 mg/kg a day or more (no-effect level 6 mg/kg a day), with thrombocytopenia and haemorrhage; recovery was partial or full depending on the dose. The usual cat dose is 20-40 mg/kg a day.Source: EMA Sources: Lagevrio SmPC · FDA · EMA · PubMed
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Warning
Do not use in pregnant or lactating animals or animals intended for breeding. In the human label, embryo-fetal death and malformations (eye, kidney, axial skeleton) occurred in rats at 8 times the human exposure, and reduced fetal weight in rabbits; the active metabolite reached nursing pups.Sources: Lagevrio SmPC · FDA
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Warning
Young animals: in young rats it thickened growth cartilage and impaired its change into bone at 500 mg/kg a day or more (5-6 times the human exposure). No such effect was seen in dogs; the meaning for kittens is not known.Source: EMA Sources: Lagevrio SmPC · FDA · EMA
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Warning
Handling: wear gloves; pregnant people should not handle it. The human label says not to open the capsule; cat doses need the powder divided or compounded (off-label). Bacterial mutation tests were positive and one animal test equivocal, while the other animal tests were negative; the human label's low-risk statement refers to a 5-day course, and cat courses run 84 days.Sources: Lagevrio SmPC · FDA
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Warning
(Cat) Cat (off-label): raised liver enzymes (ALT) and gastrointestinal signs are the most reported. Neutropenia and occasional anaemia occur at higher doses, with severe leukopenia reported above 23 mg/kg; folded ears and hair or whisker loss are also reported. Guidelines advise caution above 15 mg/kg every 12 hours and keep it second-line to GS-441524.
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