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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 EPIPEN 2-PAK Cause Device failure? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Device failure have been filed in association with EPIPEN 2-PAK. This represents 63.2% of all adverse event reports for EPIPEN 2-PAK.

12
Reports of Device failure with EPIPEN 2-PAK
63.2%
of all EPIPEN 2-PAK reports
0
Deaths
2
Hospitalizations

How Dangerous Is Device failure From EPIPEN 2-PAK?

Of the 12 reports, 2 (16.7%) required hospitalization.

Is Device failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for EPIPEN 2-PAK. However, 12 reports have been filed with the FAERS database.

What Other Side Effects Does EPIPEN 2-PAK Cause?

What Other Drugs Cause Device failure?

EPINEPHRINE (1,344) SOMATROPIN (1,141) PEGFILGRASTIM (829) TREPROSTINIL (713) BACLOFEN (691) BUDESONIDE\FORMOTEROL (686) ETANERCEPT (576) GOLIMUMAB (487) LEVONORGESTREL (332) ACLIDINIUM (304)

Related Pages

EPIPEN 2-PAK Full Profile All Device failure Reports All Drugs Causing Device failure EPIPEN 2-PAK Demographics