SALICYLIC ACID 17% WART REMOVER

N/A

Manufactured by AAA Pharmaceutical, Inc.

31 FDA adverse event reports analyzed

Last updated: 2026-04-15

About SALICYLIC ACID 17% WART REMOVER

SALICYLIC ACID 17% WART REMOVER is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by AAA Pharmaceutical, Inc.. The most commonly reported adverse reactions for SALICYLIC ACID 17% WART REMOVER include AMNESIA, APATHY, APHASIA, ASTHENIA, CHEST DISCOMFORT. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for SALICYLIC ACID 17% WART REMOVER.

Top Adverse Reactions

AMNESIA1 reports
APATHY1 reports
APHASIA1 reports
ASTHENIA1 reports
CHEST DISCOMFORT1 reports
CONDITION AGGRAVATED1 reports
DECREASED INTEREST1 reports
DEPRESSED LEVEL OF CONSCIOUSNESS1 reports
DIARRHOEA1 reports
DISTURBANCE IN ATTENTION1 reports
DRUG WITHDRAWAL SYNDROME1 reports
DYSPHONIA1 reports
FEELING ABNORMAL1 reports
FEELING OF DESPAIR1 reports
HELPLESSNESS1 reports
IMPAIRED SELF CARE1 reports
INCREASED APPETITE1 reports
INSOMNIA1 reports
LACK OF SATIETY1 reports
LETHARGY1 reports
METHYLENETETRAHYDROFOLATE REDUCTASE GENE MUTATION1 reports
MIGRAINE1 reports
MOOD SWINGS1 reports
NASOPHARYNGITIS1 reports
NEUTROPHIL COUNT DECREASED1 reports
OROPHARYNGEAL PAIN1 reports
PAIN1 reports
PRODUCT AVAILABILITY ISSUE1 reports
PRODUCT SUBSTITUTION ISSUE1 reports
SUICIDAL IDEATION1 reports
WHITE BLOOD CELL COUNT DECREASED1 reports

Report Outcomes

Out of 3 classified reports for SALICYLIC ACID 17% WART REMOVER:

Serious 66.7%Non-Serious 33.3%

The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.

Demographics Breakdown

Reports by Sex

Female2 (66.7%)
Male1 (33.3%)

Reports by Age

Age 281 reports
Age 431 reports

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

Frequently Asked Questions

How many FDA adverse event reports are associated with SALICYLIC ACID 17% WART REMOVER?

This profile reflects 31 FDA FAERS reports that mention SALICYLIC ACID 17% WART REMOVER. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for SALICYLIC ACID 17% WART REMOVER?

Frequently reported terms in FAERS include AMNESIA, APATHY, APHASIA, ASTHENIA, CHEST DISCOMFORT, CONDITION AGGRAVATED. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures SALICYLIC ACID 17% WART REMOVER?

Labeling and FAERS entries often list AAA Pharmaceutical, Inc. in connection with SALICYLIC ACID 17% WART REMOVER. Always verify the specific product and NDC with your pharmacist.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.