Does ANAKINRA Cause Dyspnoea? 262 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 262 reports of Dyspnoea have been filed in association with ANAKINRA (Kineret). This represents 2.2% of all adverse event reports for ANAKINRA.
262
Reports of Dyspnoea with ANAKINRA
2.2%
of all ANAKINRA reports
11
Deaths
72
Hospitalizations
How Dangerous Is Dyspnoea From ANAKINRA?
Of the 262 reports, 11 (4.2%) resulted in death, 72 (27.5%) required hospitalization, and 8 (3.1%) were considered life-threatening.
Is Dyspnoea Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANAKINRA. However, 262 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 Dyspnoea?
ALBUTEROL (21,856)
TREPROSTINIL (16,348)
AMBRISENTAN (13,367)
PREDNISONE (12,830)
BUDESONIDE\FORMOTEROL (11,158)
TIOTROPIUM (10,863)
ADALIMUMAB (10,547)
DUPILUMAB (10,310)
FLUTICASONE\SALMETEROL (9,783)
MEPOLIZUMAB (9,192)
Which ANAKINRA Alternatives Have Lower Dyspnoea Risk?
ANAKINRA vs ANAMORELIN
ANAKINRA vs ANASTROZOLE
ANAKINRA vs ANDEXANET ALFA
ANAKINRA vs ANDROGEL
ANAKINRA vs ANETHOLTRITHION