Does LETERMOVIR Cause Product prescribing issue? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product prescribing issue have been filed in association with LETERMOVIR (PREVYMIS). This represents 0.9% of all adverse event reports for LETERMOVIR.
13
Reports of Product prescribing issue with LETERMOVIR
0.9%
of all LETERMOVIR reports
1
Deaths
9
Hospitalizations
How Dangerous Is Product prescribing issue From LETERMOVIR?
Of the 13 reports, 1 (7.7%) resulted in death, 9 (69.2%) required hospitalization.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LETERMOVIR. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does LETERMOVIR Cause?
Off label use (277)
Drug ineffective (103)
Product use in unapproved indication (99)
Death (98)
Cytomegalovirus infection reactivation (89)
Cytomegalovirus infection (87)
No adverse event (69)
Hospitalisation (60)
Drug interaction (57)
Pathogen resistance (57)
What Other Drugs Cause Product prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which LETERMOVIR Alternatives Have Lower Product prescribing issue Risk?
LETERMOVIR vs LETROZOLE
LETERMOVIR vs LETROZOLE\RIBOCICLIB
LETERMOVIR vs LEUCOVORIN
LETERMOVIR vs LEUCOVORIN\LEUCOVORIN
LETERMOVIR vs LEUPROLIDE