Does EPINEPHRINE Cause Wrong product administered? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Wrong product administered have been filed in association with EPINEPHRINE (EPINEPHRINE). This represents 0.3% of all adverse event reports for EPINEPHRINE.
43
Reports of Wrong product administered with EPINEPHRINE
0.3%
of all EPINEPHRINE reports
5
Deaths
14
Hospitalizations
How Dangerous Is Wrong product administered From EPINEPHRINE?
Of the 43 reports, 5 (11.6%) resulted in death, 14 (32.6%) required hospitalization, and 14 (32.6%) were considered life-threatening.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPINEPHRINE. However, 43 reports have been filed with the FAERS database.
What Other Side Effects Does EPINEPHRINE Cause?
Drug ineffective (3,515)
Product quality issue (1,647)
Device failure (1,344)
Off label use (884)
Drug hypersensitivity (844)
Accidental exposure to product (795)
Liquid product physical issue (618)
Hypotension (608)
Dyspnoea (520)
Condition aggravated (470)
What Other Drugs Cause Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which EPINEPHRINE Alternatives Have Lower Wrong product administered Risk?
EPINEPHRINE vs EPINEPHRINE\LIDOCAINE
EPINEPHRINE vs EPIPEN
EPINEPHRINE vs EPIRUBICIN
EPINEPHRINE vs EPLERENONE
EPINEPHRINE vs EPLONTERSEN