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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 Hypokalaemia? 200 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 200 reports of Hypokalaemia have been filed in association with ANAKINRA (Kineret). This represents 1.7% of all adverse event reports for ANAKINRA.

200
Reports of Hypokalaemia with ANAKINRA
1.7%
of all ANAKINRA reports
16
Deaths
199
Hospitalizations

How Dangerous Is Hypokalaemia From ANAKINRA?

Of the 200 reports, 16 (8.0%) resulted in death, 199 (99.5%) required hospitalization, and 81 (40.5%) were considered life-threatening.

Is Hypokalaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ANAKINRA. However, 200 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 Hypokalaemia?

FUROSEMIDE (2,503) HYDROCHLOROTHIAZIDE (1,152) CARBOPLATIN (1,118) PREDNISONE (967) DEXAMETHASONE (876) CYCLOPHOSPHAMIDE (864) OMEPRAZOLE (851) RITUXIMAB (822) AMLODIPINE (815) PANTOPRAZOLE (811)

Which ANAKINRA Alternatives Have Lower Hypokalaemia Risk?

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

Related Pages

ANAKINRA Full Profile All Hypokalaemia Reports All Drugs Causing Hypokalaemia ANAKINRA Demographics