Does LIDOCAINE Cause Wrong technique in product usage process? 491 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 491 reports of Wrong technique in product usage process have been filed in association with LIDOCAINE (Burn Relief). This represents 2.2% of all adverse event reports for LIDOCAINE.
491
Reports of Wrong technique in product usage process with LIDOCAINE
2.2%
of all LIDOCAINE reports
0
Deaths
25
Hospitalizations
How Dangerous Is Wrong technique in product usage process From LIDOCAINE?
Of the 491 reports, 25 (5.1%) required hospitalization, and 12 (2.4%) were considered life-threatening.
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 LIDOCAINE. However, 491 reports have been filed with the FAERS database.
What Other Side Effects Does LIDOCAINE Cause?
Drug ineffective (3,706)
Product adhesion issue (3,444)
Product quality issue (3,126)
Off label use (2,563)
Drug ineffective for unapproved indication (1,761)
Toxicity to various agents (1,096)
Pain (809)
Drug hypersensitivity (783)
Hypotension (777)
Product use in unapproved indication (733)
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 LIDOCAINE Alternatives Have Lower Wrong technique in product usage process Risk?
LIDOCAINE vs LIDOCAINE\MENTHOL
LIDOCAINE vs LIDOCAINE\PRILOCAINE
LIDOCAINE vs LIFILEUCEL
LIDOCAINE vs LIFITEGRAST
LIDOCAINE vs LIMAPROST