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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 IXEKIZUMAB Cause Product quality issue? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product quality issue have been filed in association with IXEKIZUMAB (TALTZ). This represents 0.0% of all adverse event reports for IXEKIZUMAB.

6
Reports of Product quality issue with IXEKIZUMAB
0.0%
of all IXEKIZUMAB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product quality issue From IXEKIZUMAB?

Of the 6 reports, 1 (16.7%) required hospitalization.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for IXEKIZUMAB. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does IXEKIZUMAB Cause?

Injection site pain (3,799) Psoriasis (2,818) Drug ineffective (2,759) Injection site erythema (2,144) Injection site reaction (1,701) Injection site swelling (1,615) Incorrect dose administered (1,032) Covid-19 (861) Product dose omission issue (832) Therapy interrupted (796)

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 IXEKIZUMAB Alternatives Have Lower Product quality issue Risk?

IXEKIZUMAB vs JAKAFI IXEKIZUMAB vs JANUMET IXEKIZUMAB vs JANUVIA IXEKIZUMAB vs JETREA IXEKIZUMAB vs JUXTAPID

Related Pages

IXEKIZUMAB Full Profile All Product quality issue Reports All Drugs Causing Product quality issue IXEKIZUMAB Demographics