Does LIDOCAINE Cause Incorrect product administration duration? 58 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 58 reports of Incorrect product administration duration have been filed in association with LIDOCAINE (Burn Relief). This represents 0.3% of all adverse event reports for LIDOCAINE.
58
Reports of Incorrect product administration duration with LIDOCAINE
0.3%
of all LIDOCAINE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Incorrect product administration duration From LIDOCAINE?
Of the 58 reports, 1 (1.7%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LIDOCAINE. However, 58 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which LIDOCAINE Alternatives Have Lower Incorrect product administration duration Risk?
LIDOCAINE vs LIDOCAINE\MENTHOL
LIDOCAINE vs LIDOCAINE\PRILOCAINE
LIDOCAINE vs LIFILEUCEL
LIDOCAINE vs LIFITEGRAST
LIDOCAINE vs LIMAPROST