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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 TRETINOIN Cause Product quality issue? 170 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 170 reports of Product quality issue have been filed in association with TRETINOIN (Tretinoin). This represents 4.1% of all adverse event reports for TRETINOIN.

170
Reports of Product quality issue with TRETINOIN
4.1%
of all TRETINOIN reports
119
Deaths
78
Hospitalizations

How Dangerous Is Product quality issue From TRETINOIN?

Of the 170 reports, 119 (70.0%) resulted in death, 78 (45.9%) required hospitalization, and 78 (45.9%) 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 TRETINOIN. However, 170 reports have been filed with the FAERS database.

What Other Side Effects Does TRETINOIN Cause?

Off label use (665) Drug ineffective (537) Product use in unapproved indication (466) Vomiting (286) Paraesthesia (284) Pain (270) Drug intolerance (263) Maternal exposure during pregnancy (261) Taste disorder (258) Differentiation syndrome (251)

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 TRETINOIN Alternatives Have Lower Product quality issue Risk?

TRETINOIN vs TRIAMCINOLONE TRETINOIN vs TRIAMCINOLONE ACETONIDE TRETINOIN vs TRIAMCINOLONE HEXACETONIDE TRETINOIN vs TRIAMTERENE TRETINOIN vs TRIATEC

Related Pages

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