Molnupiravir
مولنوپیراویر
🦠 Antiinfectives For Systemic UseNucleoside analogue (SARS-CoV-2)
Market / country: 🇺🇸 USA
Lagevrio (US)
🧮 Dose calculator
COVID-19 · Regimen source: FDA Lagevrio (EUA) · 2.1
- • As soon as possible and within 5 days of symptom onset. No renal or hepatic adjustment. Emergency Use Authorization only. FDA Lagevrio (EUA) · 2.1FDA Lagevrio (EUA) · 2.2
Enter age (weight is optional for this regimen).
🛡️ Safety & information
Warnings
- • Embryo-fetal toxicity (not recommended in pregnancy; contraception during and 4 days after); hypersensitivity; bone and cartilage toxicity (not under 18). FDA Lagevrio (EUA) · 5
Formulations
- 200 mg capsule — capsule 🇺🇸 USA FDA Lagevrio (EUA) · 3
👥 Special populations
- 🤰 PregnancyDangerous / avoid
Label: can cause fetal harm. Dangerous in pregnancy. FDA Lagevrio (EUA) · Boxed Warning
“Based on findings from animal reproduction studies, LAGEVRIO may cause fetal harm when administered to pregnant individuals.”
- 🤱 BreastfeedingDangerous / avoid
Label: breastfeeding not recommended, or choose between the drug and breastfeeding. FDA Lagevrio (EUA) · 8.2
“Based on the potential for adverse reactions in the infant from LAGEVRIO, breastfeeding is not recommended during treatment with LAGEVRIO and for 4 days after the final dose.”
- 👶 ChildrenUse with caution
The label has conditions, age limits or notes for children; the label sentence is quoted below. FDA Lagevrio (EUA) · 8.4
“The safety and efficacy of LAGEVRIO have not been established in pediatric patients [see Warnings and Precautions (5.3) and Nonclinical Toxicology (13.2) ] .”
- 👴 Older adultsNo specific problem stated
Label: no specific difference or dose adjustment stated for older adults. FDA Lagevrio (EUA) · 8.5
“No dosage adjustment is recommended based on age.”
- ⚥ Females & males of reproductive potentialUse with caution
Label has advice on pregnancy testing, contraception or fertility for females and males. FDA Lagevrio (EUA) · 8.3
“Contraception Females Advise individuals of childbearing potential to use a reliable method of contraception correctly and consistently, as applicable for the duration of treatment and for 4 days after the last dose of LAGEVRIO [see Warnings and Precautions (5.1) ].”
🔗 Reference links
- FDA (approval record)❌ None
- DailyMed (FDA label)FDA Lagevrio (EUA)
- MedlinePlus (NIH)Molnupiravir
- WHO ATC/DDDJ05AB18
- Darooyab (Iran)Molnupiravir
🇮🇷 Registered in Iran Darooyab · G-4311/Molnupiravir
Dosage forms with Iranian generic codes, per Darooyab.
- 52942 · MOLNUPIRAVIR CAPSULE ORAL 200 mg · کپسول مولنوپیراویر ۲۰۰ میلیگرم
📚 Reference status for this drug
Shows which sources have references recorded for this drug and which do not.
- FDA label (DailyMed)✅ PresentFDA Lagevrio (EUA) · 3FDA Lagevrio (EUA) · 2.1FDA Lagevrio (EUA) · 2.2FDA Lagevrio (EUA) · 5FDA Lagevrio (EUA) · Boxed WarningFDA Lagevrio (EUA) · 8.2FDA Lagevrio (EUA) · 8.4FDA Lagevrio (EUA) · 8.5FDA Lagevrio (EUA) · 8.3
- UK SmPC (eMC / MHRA)❌ Not present
- Published guideline❌ Not present
- Licensed reference (medical school)❌ Not present
- Iranian leaflet (IFDA)❌ Not present
- Pharmacy website (secondary, unreliable)✅ PresentDarooyab · G-4311/Molnupiravir
- Clinical review⚠ Unverified