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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 TRIFAROTENE Cause Intentional underdose? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Intentional underdose have been filed in association with TRIFAROTENE (AKLIEF). This represents 5.4% of all adverse event reports for TRIFAROTENE.

6
Reports of Intentional underdose with TRIFAROTENE
5.4%
of all TRIFAROTENE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Intentional underdose From TRIFAROTENE?

Of the 6 reports.

Is Intentional underdose Listed in the Official Label?

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

What Other Side Effects Does TRIFAROTENE Cause?

Erythema (25) Skin burning sensation (16) Dry skin (15) Skin exfoliation (13) Acne (12) Skin irritation (12) Skin hyperpigmentation (8) Drug ineffective (7) Pain of skin (7) Application site pain (6)

What Other Drugs Cause Intentional underdose?

BUPRENORPHINE\NALOXONE (1,037) NIRAPARIB (677) FLUTICASONE\SALMETEROL (605) DIMETHYL (364) LEVODOPA (196) TECFIDERA (180) FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (167) DROXIDOPA (163) ICOSAPENT ETHYL (145) FLUTICASONE (144)

Which TRIFAROTENE Alternatives Have Lower Intentional underdose Risk?

TRIFAROTENE vs TRIFLUOPERAZINE TRIFAROTENE vs TRIFLURIDINE TRIFAROTENE vs TRIHEPTANOIN TRIFAROTENE vs TRIHEXYPHENIDYL TRIFAROTENE vs TRILACICLIB

Related Pages

TRIFAROTENE Full Profile All Intentional underdose Reports All Drugs Causing Intentional underdose TRIFAROTENE Demographics