Does EPINEPHRINE Cause Device defective? 45 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Device defective have been filed in association with EPINEPHRINE (EPINEPHRINE). This represents 0.3% of all adverse event reports for EPINEPHRINE.
45
Reports of Device defective with EPINEPHRINE
0.3%
of all EPINEPHRINE reports
1
Deaths
5
Hospitalizations
How Dangerous Is Device defective From EPINEPHRINE?
Of the 45 reports, 1 (2.2%) resulted in death, 5 (11.1%) required hospitalization, and 1 (2.2%) were considered life-threatening.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EPINEPHRINE. However, 45 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 Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which EPINEPHRINE Alternatives Have Lower Device defective Risk?
EPINEPHRINE vs EPINEPHRINE\LIDOCAINE
EPINEPHRINE vs EPIPEN
EPINEPHRINE vs EPIRUBICIN
EPINEPHRINE vs EPLERENONE
EPINEPHRINE vs EPLONTERSEN