Does MOLNUPIRAVIR Cause Product use complaint? 206 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 206 reports of Product use complaint have been filed in association with MOLNUPIRAVIR (LAGEVRIO). This represents 4.3% of all adverse event reports for MOLNUPIRAVIR.
206
Reports of Product use complaint with MOLNUPIRAVIR
4.3%
of all MOLNUPIRAVIR reports
2
Deaths
4
Hospitalizations
How Dangerous Is Product use complaint From MOLNUPIRAVIR?
Of the 206 reports, 2 (1.0%) resulted in death, 4 (1.9%) required hospitalization.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MOLNUPIRAVIR. However, 206 reports have been filed with the FAERS database.
What Other Side Effects Does MOLNUPIRAVIR Cause?
Product use issue (706)
No adverse event (614)
Covid-19 (396)
Wrong technique in product usage process (380)
Product use in unapproved indication (296)
Diarrhoea (259)
Accidental underdose (207)
Rash (200)
Underdose (183)
Nausea (180)
What Other Drugs Cause Product use complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
ACETAMINOPHEN (202)
DIMETHICONE\LOPERAMIDE (201)
Which MOLNUPIRAVIR Alternatives Have Lower Product use complaint Risk?
MOLNUPIRAVIR vs MOLSIDOMINE
MOLNUPIRAVIR vs MOMELOTINIB
MOLNUPIRAVIR vs MOMETASONE
MOLNUPIRAVIR vs MOMETASONE FUROATE
MOLNUPIRAVIR vs MOMETASONE FUROATE\OLOPATADINE