OCTINOXATE

N/A

Manufactured by ALTONA COSMETICS TECHNOLOGY SANAYI VE TICARET ANONIM SIRKETI

107 FDA adverse event reports analyzed

Last updated: 2026-04-15

About OCTINOXATE

OCTINOXATE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by ALTONA COSMETICS TECHNOLOGY SANAYI VE TICARET ANONIM SIRKETI. The most commonly reported adverse reactions for OCTINOXATE include DIVERTICULITIS, ANAPHYLACTIC REACTION, BRONCHIECTASIS, BURSITIS, DIVERTICULUM INTESTINAL. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for OCTINOXATE.

Top Adverse Reactions

DIVERTICULITIS7 reports
ANAPHYLACTIC REACTION6 reports
BRONCHIECTASIS6 reports
BURSITIS6 reports
DIVERTICULUM INTESTINAL6 reports
HYPERSENSITIVITY6 reports
HYPERTHYROIDISM6 reports
LOWER RESPIRATORY TRACT INFECTION6 reports
MIGRAINE6 reports
POLYP6 reports
PRESBYACUSIS6 reports
PSORIASIS6 reports
ROTATOR CUFF SYNDROME6 reports
SUSPECTED COVID 196 reports
TENDONITIS6 reports
TINNITUS6 reports
UTERINE LEIOMYOMA6 reports
ABDOMINAL PAIN UPPER1 reports
FEELING HOT1 reports
NASOPHARYNGITIS1 reports
RASH1 reports

Report Outcomes

Out of 8 classified reports for OCTINOXATE:

Serious 87.5%Non-Serious 12.5%

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

Female5 (71.4%)
Male2 (28.6%)

Reports by Age

Age 475 reports
Age 541 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 OCTINOXATE?

This profile reflects 107 FDA FAERS reports that mention OCTINOXATE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for OCTINOXATE?

Frequently reported terms in FAERS include DIVERTICULITIS, ANAPHYLACTIC REACTION, BRONCHIECTASIS, BURSITIS, DIVERTICULUM INTESTINAL, HYPERSENSITIVITY. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures OCTINOXATE?

Labeling and FAERS entries often list ALTONA COSMETICS TECHNOLOGY SANAYI VE TICARET ANONIM SIRKETI in connection with OCTINOXATE. 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.