Does LIDOCAINE Cause Product administration error? 54 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 54 reports of Product administration error have been filed in association with LIDOCAINE (Burn Relief). This represents 0.2% of all adverse event reports for LIDOCAINE.
54
Reports of Product administration error with LIDOCAINE
0.2%
of all LIDOCAINE reports
5
Deaths
21
Hospitalizations
How Dangerous Is Product administration error From LIDOCAINE?
Of the 54 reports, 5 (9.3%) resulted in death, 21 (38.9%) required hospitalization, and 5 (9.3%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LIDOCAINE. However, 54 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which LIDOCAINE Alternatives Have Lower Product administration error Risk?
LIDOCAINE vs LIDOCAINE\MENTHOL
LIDOCAINE vs LIDOCAINE\PRILOCAINE
LIDOCAINE vs LIFILEUCEL
LIDOCAINE vs LIFITEGRAST
LIDOCAINE vs LIMAPROST