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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 AZASITE Cause Product quality issue? 10 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product quality issue have been filed in association with AZASITE. This represents 26.3% of all adverse event reports for AZASITE.

10
Reports of Product quality issue with AZASITE
26.3%
of all AZASITE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product quality issue From AZASITE?

Of the 10 reports.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AZASITE. However, 10 reports have been filed with the FAERS database.

What Other Side Effects Does AZASITE Cause?

Drug dose omission (20) No adverse event (17) Inappropriate schedule of drug administration (12) Off label use (7)

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)

Related Pages

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