Does LEMBOREXANT 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 LEMBOREXANT (DAYVIGO). This represents 0.7% of all adverse event reports for LEMBOREXANT.
7
Reports of Wrong technique in product usage process with LEMBOREXANT
0.7%
of all LEMBOREXANT reports
1
Deaths
1
Hospitalizations
How Dangerous Is Wrong technique in product usage process From LEMBOREXANT?
Of the 7 reports, 1 (14.3%) resulted in death, 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 LEMBOREXANT. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does LEMBOREXANT Cause?
Drug ineffective (225)
Suicide attempt (98)
Somnolence (90)
Suicidal ideation (86)
Sleep paralysis (80)
Condition aggravated (74)
Nightmare (71)
Altered state of consciousness (45)
Off label use (45)
Adverse drug reaction (44)
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 LEMBOREXANT Alternatives Have Lower Wrong technique in product usage process Risk?
LEMBOREXANT vs LENACAPAVIR
LEMBOREXANT vs LENALIDOMIDE
LEMBOREXANT vs LENIOLISIB
LEMBOREXANT vs LENOGRASTIM
LEMBOREXANT vs LENVATINIB