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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 PEN Cause Device malfunction? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Device malfunction have been filed in association with HUMIRA PEN. This represents 2.7% of all adverse event reports for HUMIRA PEN.

7
Reports of Device malfunction with HUMIRA PEN
2.7%
of all HUMIRA PEN reports
0
Deaths
2
Hospitalizations

How Dangerous Is Device malfunction From HUMIRA PEN?

Of the 7 reports, 2 (28.6%) required hospitalization.

Is Device malfunction Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for HUMIRA PEN. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does HUMIRA PEN Cause?

Injection site pain (38) Arthralgia (28) Drug ineffective (28) Pain (19) Headache (18) Nasopharyngitis (18) Psoriasis (16) Fatigue (15) Incorrect dose administered (15) Nausea (15)

What Other Drugs Cause Device malfunction?

PEGFILGRASTIM (6,818) EXENATIDE (3,273) BUDESONIDE\FORMOTEROL (2,771) ABATACEPT (2,459) SOMATROPIN (2,311) GOLIMUMAB (2,293) SECUKINUMAB (2,259) ALBUTEROL (2,257) GUSELKUMAB (1,410) MOMETASONE FUROATE (1,332)

Which HUMIRA PEN Alternatives Have Lower Device malfunction Risk?

HUMIRA PEN vs HYALURONATE HUMIRA PEN vs HYALURONIC ACID HUMIRA PEN vs HYALURONIC ACID\LIDOCAINE HUMIRA PEN vs HYALURONIDASE HUMIRA PEN vs HYALURONIDASE-OCSQ\OCRELIZUMAB

Related Pages

HUMIRA PEN Full Profile All Device malfunction Reports All Drugs Causing Device malfunction HUMIRA PEN Demographics