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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 HUMIRA Cause Device failure? 13 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Device failure have been filed in association with HUMIRA. This represents 0.0% of all adverse event reports for HUMIRA.

13
Reports of Device failure with HUMIRA
0.0%
of all HUMIRA reports
0
Deaths
2
Hospitalizations

How Dangerous Is Device failure From HUMIRA?

Of the 13 reports, 2 (15.4%) required hospitalization.

Is Device failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for HUMIRA. However, 13 reports have been filed with the FAERS database.

What Other Side Effects Does HUMIRA Cause?

Injection site pain (6,005) Drug ineffective (3,506) Arthralgia (2,204) Pain (2,045) Fatigue (1,868) Psoriasis (1,857) Injection site erythema (1,654) Injection site bruising (1,623) Headache (1,582) Nasopharyngitis (1,552)

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)

Which HUMIRA Alternatives Have Lower Device failure Risk?

HUMIRA vs HUMIRA PEN HUMIRA vs HYALURONATE HUMIRA vs HYALURONIC ACID HUMIRA vs HYALURONIC ACID\LIDOCAINE HUMIRA vs HYALURONIDASE

Related Pages

HUMIRA Full Profile All Device failure Reports All Drugs Causing Device failure HUMIRA Demographics