TITANIUM DIOXIDE

N/A

Manufactured by Baxter of California, LLC

566 FDA adverse event reports analyzed

Last updated: 2026-04-15

About TITANIUM DIOXIDE

TITANIUM DIOXIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Baxter of California, LLC. The most commonly reported adverse reactions for TITANIUM DIOXIDE include HYPERSENSITIVITY, ERYTHEMA, RASH, ACNE, ABDOMINAL PAIN UPPER. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for TITANIUM DIOXIDE.

Top Adverse Reactions

HYPERSENSITIVITY18 reports
ERYTHEMA15 reports
RASH15 reports
ACNE13 reports
ABDOMINAL PAIN UPPER12 reports
OFF LABEL USE11 reports
DRUG HYPERSENSITIVITY10 reports
DYSPNOEA10 reports
HEADACHE10 reports
PAIN10 reports
SWELLING FACE10 reports
CONDITION AGGRAVATED9 reports
FATIGUE9 reports
PAIN IN EXTREMITY9 reports
REACTION TO EXCIPIENT9 reports
SUNBURN9 reports
DEATH8 reports
DRY SKIN8 reports
MADAROSIS8 reports
MALIGNANT MELANOMA8 reports
NAUSEA8 reports
PRURITUS8 reports
DIARRHOEA7 reports
DRUG INEFFECTIVE7 reports
DRY MOUTH7 reports
INTENTIONAL PRODUCT MISUSE7 reports
PSORIASIS7 reports
SOMNOLENCE7 reports
ABDOMINAL DISTENSION6 reports
APPLICATION SITE ERYTHEMA6 reports
BASAL CELL CARCINOMA6 reports
CHEST PAIN6 reports
DEPRESSION6 reports
PHOTOSENSITIVITY REACTION6 reports
PRODUCT USE ISSUE6 reports
RASH ERYTHEMATOUS6 reports
RASH MACULAR6 reports
RESTLESS LEGS SYNDROME6 reports
URTICARIA6 reports
ARTHRALGIA5 reports
BLISTER5 reports
DECREASED APPETITE5 reports
DERMATITIS5 reports
DRUG INTOLERANCE5 reports
HYPERTENSION5 reports
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION5 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION5 reports
MALAISE5 reports
SENSITIVE SKIN5 reports
SKIN EXFOLIATION5 reports
SWELLING5 reports
XEROSIS5 reports
ABDOMINAL PAIN4 reports
ANAEMIA4 reports
ANXIETY4 reports
APPLICATION SITE PAIN4 reports
ASCITES4 reports
ASTHENIA4 reports
BACTERIAL INFECTION4 reports
BLOOD PRESSURE INCREASED4 reports
COUGH4 reports
DIABETES MELLITUS4 reports
DRY EYE4 reports
DYSPHAGIA4 reports
NEURALGIA4 reports
PAIN OF SKIN4 reports
PULMONARY EMBOLISM4 reports
SKIN BURNING SENSATION4 reports
SKIN CANCER4 reports
SKIN IRRITATION4 reports
SLEEP DISORDER4 reports
THERAPEUTIC RESPONSE UNEXPECTED4 reports
VISUAL IMPAIRMENT4 reports
WEIGHT DECREASED4 reports
ABDOMINAL DISCOMFORT3 reports
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED3 reports
ADVERSE EVENT3 reports
ALLERGIC REACTION TO EXCIPIENT3 reports
ALLERGY TO CHEMICALS3 reports
BLOOD CHOLESTEROL INCREASED3 reports
BURNING SENSATION3 reports
CHEILITIS3 reports
CHRONIC OBSTRUCTIVE PULMONARY DISEASE3 reports
CONFUSIONAL STATE3 reports
CONSTIPATION3 reports
ECZEMA3 reports
HEART RATE INCREASED3 reports
HOSPITALISATION3 reports
HYPERHIDROSIS3 reports
ILLNESS3 reports
INCORRECT ROUTE OF PRODUCT ADMINISTRATION3 reports
INSOMNIA3 reports
JOINT SWELLING3 reports
LUNG DISORDER3 reports
LUNG NEOPLASM MALIGNANT3 reports
MIGRAINE3 reports
MOOD ALTERED3 reports
MUSCLE SPASMS3 reports
NEOPLASM MALIGNANT3 reports
PIGMENTATION DISORDER3 reports

Report Outcomes

Out of 229 classified reports for TITANIUM DIOXIDE:

Serious 57.2%Non-Serious 42.8%

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

Female117 (58.8%)
Male82 (41.2%)

Reports by Age

Age 8014 reports
Age 476 reports
Age 656 reports
Age 666 reports
Age 505 reports
Age 585 reports
Age 625 reports
Age 695 reports
Age 755 reports
Age 845 reports
Age 244 reports
Age 344 reports
Age 434 reports
Age 554 reports
Age 684 reports
Age 764 reports
Age 313 reports
Age 403 reports
Age 443 reports
Age 523 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 TITANIUM DIOXIDE?

This profile reflects 566 FDA FAERS reports that mention TITANIUM DIOXIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for TITANIUM DIOXIDE?

Frequently reported terms in FAERS include HYPERSENSITIVITY, ERYTHEMA, RASH, ACNE, ABDOMINAL PAIN UPPER, OFF LABEL USE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures TITANIUM DIOXIDE?

Labeling and FAERS entries often list Baxter of California, LLC in connection with TITANIUM DIOXIDE. 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.