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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 ANAKINRA Cause Deafness neurosensory? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Deafness neurosensory have been filed in association with ANAKINRA (Kineret). This represents 0.1% of all adverse event reports for ANAKINRA.

7
Reports of Deafness neurosensory with ANAKINRA
0.1%
of all ANAKINRA reports
0
Deaths
1
Hospitalizations

How Dangerous Is Deafness neurosensory From ANAKINRA?

Of the 7 reports, 1 (14.3%) required hospitalization.

Is Deafness neurosensory Listed in the Official Label?

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

What Other Side Effects Does ANAKINRA Cause?

Off label use (4,317) Drug ineffective (3,368) Pain (1,344) Condition aggravated (1,339) Rheumatoid arthritis (1,300) Drug intolerance (946) Joint swelling (921) Injection site pain (879) Product dose omission issue (864) Arthralgia (850)

What Other Drugs Cause Deafness neurosensory?

METHOTREXATE (224) FENTANYL (202) OXYCODONE (198) ETANERCEPT (171) TEPROTUMUMAB-TRBW (171) TOCILIZUMAB (164) HYDROXYCHLOROQUINE (162) SULFASALAZINE (153) ABATACEPT (149) CELECOXIB (143)

Which ANAKINRA Alternatives Have Lower Deafness neurosensory Risk?

ANAKINRA vs ANAMORELIN ANAKINRA vs ANASTROZOLE ANAKINRA vs ANDEXANET ALFA ANAKINRA vs ANDROGEL ANAKINRA vs ANETHOLTRITHION

Related Pages

ANAKINRA Full Profile All Deafness neurosensory Reports All Drugs Causing Deafness neurosensory ANAKINRA Demographics