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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 ADALIMUMAB-ADAZ Cause Device malfunction? 168 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 168 reports of Device malfunction have been filed in association with ADALIMUMAB-ADAZ. This represents 2.4% of all adverse event reports for ADALIMUMAB-ADAZ.

168
Reports of Device malfunction with ADALIMUMAB-ADAZ
2.4%
of all ADALIMUMAB-ADAZ reports
0
Deaths
2
Hospitalizations

How Dangerous Is Device malfunction From ADALIMUMAB-ADAZ?

Of the 168 reports, 2 (1.2%) required hospitalization.

Is Device malfunction Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ADALIMUMAB-ADAZ. However, 168 reports have been filed with the FAERS database.

What Other Side Effects Does ADALIMUMAB-ADAZ Cause?

Drug ineffective (928) Off label use (925) Fatigue (798) Arthralgia (787) Pain (735) Diarrhoea (721) General physical health deterioration (597) Malaise (566) Product dose omission issue (562) Rheumatoid arthritis (506)

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 ADALIMUMAB-ADAZ Alternatives Have Lower Device malfunction Risk?

ADALIMUMAB-ADAZ vs ADALIMUMAB-ADBM ADALIMUMAB-ADAZ vs ADALIMUMAB-AFZB ADALIMUMAB-ADAZ vs ADALIMUMAB-ATTO ADALIMUMAB-ADAZ vs ADALIMUMAB-BWWD ADALIMUMAB-ADAZ vs ADALIMUMAB-FKJP

Related Pages

ADALIMUMAB-ADAZ Full Profile All Device malfunction Reports All Drugs Causing Device malfunction ADALIMUMAB-ADAZ Demographics