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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does EPINEPHRINE Cause Product quality issue? 1,647 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,647 reports of Product quality issue have been filed in association with EPINEPHRINE (EPINEPHRINE). This represents 10.9% of all adverse event reports for EPINEPHRINE.

1,647
Reports of Product quality issue with EPINEPHRINE
10.9%
of all EPINEPHRINE reports
17
Deaths
43
Hospitalizations

How Dangerous Is Product quality issue From EPINEPHRINE?

Of the 1,647 reports, 17 (1.0%) resulted in death, 43 (2.6%) required hospitalization, and 60 (3.6%) were considered life-threatening.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for EPINEPHRINE. However, 1,647 reports have been filed with the FAERS database.

What Other Side Effects Does EPINEPHRINE Cause?

Drug ineffective (3,515) 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) Cardiac arrest (456)

What Other Drugs Cause Product quality issue?

ETONOGESTREL (4,651) ALBUTEROL (4,466) TIOTROPIUM (3,821) MOMETASONE FUROATE (3,406) LIDOCAINE (3,126) FLUTICASONE\SALMETEROL (2,986) FORMOTEROL\MOMETASONE FUROATE (2,458) FENTANYL (2,450) NICOTINE (1,987) EXENATIDE (1,839)

Which EPINEPHRINE Alternatives Have Lower Product quality issue Risk?

EPINEPHRINE vs EPINEPHRINE\LIDOCAINE EPINEPHRINE vs EPIPEN EPINEPHRINE vs EPIRUBICIN EPINEPHRINE vs EPLERENONE EPINEPHRINE vs EPLONTERSEN

Related Pages

EPINEPHRINE Full Profile All Product quality issue Reports All Drugs Causing Product quality issue EPINEPHRINE Demographics