POVIDONE IODINE 10%

N/A

Manufactured by Farmacias De Similares TX LLC

1,006 FDA adverse event reports analyzed

Last updated: 2026-04-15

About POVIDONE IODINE 10%

POVIDONE IODINE 10% is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Farmacias De Similares TX LLC. The most commonly reported adverse reactions for POVIDONE IODINE 10% include TOXIC ANTERIOR SEGMENT SYNDROME, ENDOPHTHALMITIS, VISUAL ACUITY REDUCED, POST PROCEDURAL COMPLICATION, OFF LABEL USE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for POVIDONE IODINE 10%.

Top Adverse Reactions

TOXIC ANTERIOR SEGMENT SYNDROME52 reports
ENDOPHTHALMITIS51 reports
VISUAL ACUITY REDUCED51 reports
POST PROCEDURAL COMPLICATION25 reports
OFF LABEL USE24 reports
BLINDNESS21 reports
CONJUNCTIVAL OEDEMA21 reports
INTRAOCULAR PRESSURE INCREASED21 reports
PAROPHTHALMIA20 reports
EXOPHTHALMOS18 reports
EYE INFLAMMATION18 reports
EYE PAIN18 reports
NAUSEA17 reports
WHITE BLOOD CELL COUNT DECREASED17 reports
DRUG HYPERSENSITIVITY16 reports
DIARRHOEA15 reports
PYREXIA15 reports
DETACHMENT OF RETINAL PIGMENT EPITHELIUM14 reports
ERYTHEMA13 reports
VOMITING13 reports
NEUTROPHIL COUNT DECREASED12 reports
PLATELET COUNT DECREASED12 reports
PNEUMONIA12 reports
PRURITUS12 reports
PAIN11 reports
SEPSIS11 reports
BACTERIAL INFECTION10 reports
EYELID OEDEMA10 reports
FEBRILE NEUTROPENIA10 reports
MALAISE10 reports
RASH10 reports
DYSPNOEA9 reports
HYPERSENSITIVITY9 reports
OCULAR HYPERTENSION9 reports
RETINAL PIGMENT EPITHELIAL TEAR9 reports
ANAEMIA8 reports
ANAPHYLACTIC REACTION8 reports
BLINDNESS UNILATERAL8 reports
BLOOD PRESSURE DECREASED8 reports
CONDITION AGGRAVATED8 reports
DRUG EXPOSURE DURING PREGNANCY8 reports
HYPOTENSION8 reports
RETINOGRAM ABNORMAL8 reports
UVEITIS8 reports
ALANINE AMINOTRANSFERASE INCREASED7 reports
BACK PAIN7 reports
CATARACT7 reports
DEATH7 reports
HEPATIC FUNCTION ABNORMAL7 reports
HYPERTENSION7 reports
HYPOTHYROIDISM7 reports
MALIGNANT NEOPLASM PROGRESSION7 reports
MEDICATION ERROR7 reports
NASOPHARYNGITIS7 reports
PLEURAL EFFUSION7 reports
RETINAL HAEMORRHAGE7 reports
RETINAL INJURY7 reports
URTICARIA7 reports
ASPARTATE AMINOTRANSFERASE INCREASED6 reports
CORNEAL ABRASION6 reports
ECZEMA6 reports
FALL6 reports
GAMMA GLUTAMYLTRANSFERASE INCREASED6 reports
GENERAL PHYSICAL HEALTH DETERIORATION6 reports
HAEMATURIA6 reports
HEADACHE6 reports
IRIDOCYCLITIS6 reports
LIVER DISORDER6 reports
LYMPHOCYTE COUNT DECREASED6 reports
MACULAR OEDEMA6 reports
OEDEMA PERIPHERAL6 reports
RETINAL OEDEMA6 reports
SOMNOLENCE6 reports
STAPHYLOCOCCAL INFECTION6 reports
STOMATITIS6 reports
VISION BLURRED6 reports
ABDOMINAL PAIN5 reports
ABSCESS5 reports
ANGIONEUROTIC OEDEMA5 reports
BLOOD ALKALINE PHOSPHATASE INCREASED5 reports
BLOOD BILIRUBIN INCREASED5 reports
DERMATITIS CONTACT5 reports
DISSEMINATED INTRAVASCULAR COAGULATION5 reports
DRUG INEFFECTIVE5 reports
HYPONATRAEMIA5 reports
INFLAMMATION5 reports
INTERSTITIAL LUNG DISEASE5 reports
MASS5 reports
OLIGURIA5 reports
RENAL FAILURE ACUTE5 reports
STEVENS JOHNSON SYNDROME5 reports
WRONG DRUG ADMINISTERED5 reports
ABDOMINAL DISTENSION4 reports
ANOREXIA4 reports
BLOOD PRESSURE INCREASED4 reports
BODY TEMPERATURE DECREASED4 reports
CARDIAC ARREST4 reports
CELLULITIS4 reports
CONSTIPATION4 reports
COUGH4 reports

Report Outcomes

Out of 540 classified reports for POVIDONE IODINE 10%:

Serious 96.1%Non-Serious 3.9%

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

Female289 (58.5%)
Male204 (41.3%)
Unknown1 (0.2%)

Reports by Age

Age 7434 reports
Age 7916 reports
Age 4513 reports
Age 7212 reports
Age 6811 reports
Age 7611 reports
Age 5810 reports
Age 6910 reports
Age 8110 reports
Age 529 reports
Age 629 reports
Age 639 reports
Age 719 reports
Age 598 reports
Age 678 reports
Age 788 reports
Age 848 reports
Age 507 reports
Age 667 reports
Age 737 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 POVIDONE IODINE 10%?

This profile reflects 1,006 FDA FAERS reports that mention POVIDONE IODINE 10%. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for POVIDONE IODINE 10%?

Frequently reported terms in FAERS include TOXIC ANTERIOR SEGMENT SYNDROME, ENDOPHTHALMITIS, VISUAL ACUITY REDUCED, POST PROCEDURAL COMPLICATION, OFF LABEL USE, BLINDNESS. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures POVIDONE IODINE 10%?

Labeling and FAERS entries often list Farmacias De Similares TX LLC in connection with POVIDONE IODINE 10%. 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.