Does LETERMOVIR Cause Wrong technique in product usage process? 25 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Wrong technique in product usage process have been filed in association with LETERMOVIR (PREVYMIS). This represents 1.8% of all adverse event reports for LETERMOVIR.
25
Reports of Wrong technique in product usage process with LETERMOVIR
1.8%
of all LETERMOVIR reports
0
Deaths
1
Hospitalizations
How Dangerous Is Wrong technique in product usage process From LETERMOVIR?
Of the 25 reports, 1 (4.0%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LETERMOVIR. However, 25 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which LETERMOVIR Alternatives Have Lower Wrong technique in product usage process Risk?
LETERMOVIR vs LETROZOLE
LETERMOVIR vs LETROZOLE\RIBOCICLIB
LETERMOVIR vs LEUCOVORIN
LETERMOVIR vs LEUCOVORIN\LEUCOVORIN
LETERMOVIR vs LEUPROLIDE