Does LENACAPAVIR Cause Wrong technique in product usage process? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Wrong technique in product usage process have been filed in association with LENACAPAVIR (Sunlenca). This represents 1.4% of all adverse event reports for LENACAPAVIR.
7
Reports of Wrong technique in product usage process with LENACAPAVIR
1.4%
of all LENACAPAVIR reports
0
Deaths
1
Hospitalizations
How Dangerous Is Wrong technique in product usage process From LENACAPAVIR?
Of the 7 reports, 1 (14.3%) 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 LENACAPAVIR. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does LENACAPAVIR Cause?
Off label use (95)
Injection site pain (58)
Injection site nodule (53)
Product use issue (49)
Labelled drug-drug interaction medication error (43)
Injection site discharge (41)
Product use in unapproved therapeutic environment (40)
Injection site mass (23)
Viral load increased (21)
Fatigue (20)
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 LENACAPAVIR Alternatives Have Lower Wrong technique in product usage process Risk?
LENACAPAVIR vs LENALIDOMIDE
LENACAPAVIR vs LENIOLISIB
LENACAPAVIR vs LENOGRASTIM
LENACAPAVIR vs LENVATINIB
LENACAPAVIR vs LEPONEX