Does ANAKINRA Cause Product quality issue? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Product quality issue have been filed in association with ANAKINRA (Kineret). This represents 0.3% of all adverse event reports for ANAKINRA.
35
Reports of Product quality issue with ANAKINRA
0.3%
of all ANAKINRA reports
4
Deaths
19
Hospitalizations
How Dangerous Is Product quality issue From ANAKINRA?
Of the 35 reports, 4 (11.4%) resulted in death, 19 (54.3%) required hospitalization, and 4 (11.4%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANAKINRA. However, 35 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 Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which ANAKINRA Alternatives Have Lower Product quality issue Risk?
ANAKINRA vs ANAMORELIN
ANAKINRA vs ANASTROZOLE
ANAKINRA vs ANDEXANET ALFA
ANAKINRA vs ANDROGEL
ANAKINRA vs ANETHOLTRITHION