SALICYLIC ACID 2%

N/A

Manufactured by Guangzhou Huixue Biotechnology Co., Ltd.

35 FDA adverse event reports analyzed

Last updated: 2026-04-15

About SALICYLIC ACID 2%

SALICYLIC ACID 2% is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Guangzhou Huixue Biotechnology Co., Ltd.. The most commonly reported adverse reactions for SALICYLIC ACID 2% include ABDOMINAL DISTENSION, ARTHRALGIA, ARTHROPATHY, BURNS THIRD DEGREE, CATARACT. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for SALICYLIC ACID 2%.

Top Adverse Reactions

ABDOMINAL DISTENSION1 reports
ARTHRALGIA1 reports
ARTHROPATHY1 reports
BURNS THIRD DEGREE1 reports
CATARACT1 reports
CHRONIC SINUSITIS1 reports
DEPRESSION1 reports
EATING DISORDER1 reports
ERYTHEMA1 reports
FATIGUE1 reports
FOOT FRACTURE1 reports
FUNGAL INFECTION1 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION1 reports
INFECTION1 reports
INFUSION SITE BRUISING1 reports
INFUSION SITE DISCHARGE1 reports
INFUSION SITE HAEMORRHAGE1 reports
INFUSION SITE PAIN1 reports
LIGAMENT SPRAIN1 reports
MIDDLE INSOMNIA1 reports
MULTIPLE ALLERGIES1 reports
NEEDLE ISSUE1 reports
PNEUMONIA1 reports
PRODUCT QUALITY ISSUE1 reports
SCAR1 reports
SINUS DISORDER1 reports
SINUS POLYP1 reports
SINUSITIS1 reports
SKIN DISCOLOURATION1 reports
SKIN INFECTION1 reports
SNEEZING1 reports
THERMAL BURN1 reports
WEIGHT DECREASED1 reports
WEIGHT INCREASED1 reports
WRONG TECHNIQUE IN DRUG USAGE PROCESS1 reports

Report Outcomes

Out of 3 classified reports for SALICYLIC ACID 2%:

Serious 100.0%Non-Serious 0.0%

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

Male2 (66.7%)
Female1 (33.3%)

Reports by Age

Age 371 reports
Age 661 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 2%?

This profile reflects 35 FDA FAERS reports that mention SALICYLIC ACID 2%. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for SALICYLIC ACID 2%?

Frequently reported terms in FAERS include ABDOMINAL DISTENSION, ARTHRALGIA, ARTHROPATHY, BURNS THIRD DEGREE, CATARACT, CHRONIC SINUSITIS. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures SALICYLIC ACID 2%?

Labeling and FAERS entries often list Guangzhou Huixue Biotechnology Co., Ltd. in connection with SALICYLIC ACID 2%. 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.