FERRIC OXIDE RED

N/A

Manufactured by Better Living Brands, LLC

1,588 FDA adverse event reports analyzed

Last updated: 2026-04-15

About FERRIC OXIDE RED

FERRIC OXIDE RED is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Better Living Brands, LLC. The most commonly reported adverse reactions for FERRIC OXIDE RED include RASH, DIARRHOEA, FATIGUE, CONSTIPATION, PRURITUS. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for FERRIC OXIDE RED.

Top Adverse Reactions

RASH68 reports
DIARRHOEA59 reports
FATIGUE52 reports
CONSTIPATION43 reports
PRURITUS41 reports
NAUSEA36 reports
SEIZURE34 reports
DIZZINESS33 reports
NEUROPATHY PERIPHERAL32 reports
HEADACHE31 reports
LACRIMATION INCREASED31 reports
DRUG INEFFECTIVE30 reports
OFF LABEL USE29 reports
WEIGHT DECREASED27 reports
ABDOMINAL PAIN25 reports
COUGH25 reports
CHEST PAIN24 reports
URINARY TRACT INFECTION24 reports
MUCOSAL INFLAMMATION22 reports
OROPHARYNGEAL PAIN22 reports
ALOPECIA21 reports
DEPRESSED MOOD21 reports
PALPITATIONS21 reports
INSOMNIA20 reports
MUSCLE SPASMS19 reports
MUSCLE TWITCHING19 reports
NASOPHARYNGITIS19 reports
HICCUPS18 reports
NAIL DISORDER18 reports
NAIL INFECTION18 reports
NEURALGIA18 reports
POOR PERIPHERAL CIRCULATION18 reports
PYREXIA18 reports
CONDITION AGGRAVATED17 reports
LEFT VENTRICULAR DYSFUNCTION17 reports
PAIN17 reports
VAGINAL DISCHARGE17 reports
URTICARIA16 reports
HYPOKALAEMIA15 reports
MEMORY IMPAIRMENT15 reports
PANIC ATTACK15 reports
VOMITING15 reports
ANAPHYLACTIC REACTION14 reports
APPENDICITIS14 reports
DEMENTIA14 reports
DRY SKIN14 reports
CHEST DISCOMFORT13 reports
EJECTION FRACTION DECREASED13 reports
RASH PRURITIC13 reports
AMNESIA12 reports
AXILLARY PAIN12 reports
CATHETER SITE HAEMORRHAGE12 reports
DEATH12 reports
DYSPNOEA12 reports
MALAISE12 reports
NAIL DYSTROPHY12 reports
PRODUCT USE IN UNAPPROVED INDICATION12 reports
DISEASE PROGRESSION11 reports
SKIN EXFOLIATION11 reports
ARTHRALGIA10 reports
CARDIAC ARREST10 reports
DECREASED APPETITE10 reports
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION10 reports
ERYTHEMA10 reports
MATERNAL EXPOSURE DURING PREGNANCY10 reports
ANAEMIA9 reports
BACK PAIN9 reports
CONFUSIONAL STATE8 reports
DRUG INDUCED LIVER INJURY8 reports
GASTROOESOPHAGEAL REFLUX DISEASE8 reports
PAIN IN EXTREMITY8 reports
ASTHENIA7 reports
BLISTER7 reports
DRUG ERUPTION7 reports
FALL7 reports
FOETAL EXPOSURE DURING PREGNANCY7 reports
HYPERSENSITIVITY7 reports
HYPERTENSION7 reports
HYPOAESTHESIA7 reports
NEUTROPENIA7 reports
PRODUCT USE ISSUE7 reports
TOXIC EPIDERMAL NECROLYSIS7 reports
WHEEZING7 reports
ABDOMINAL DISTENSION6 reports
ABDOMINAL PAIN UPPER6 reports
CHILLS6 reports
CROHN^S DISEASE6 reports
DERMATITIS ALLERGIC6 reports
FEBRILE NEUTROPENIA6 reports
HYPOTENSION6 reports
JAUNDICE6 reports
JOINT SWELLING6 reports
PERIPHERAL SWELLING6 reports
PNEUMONIA6 reports
RHINORRHOEA6 reports
SKIN BURNING SENSATION6 reports
SWELLING6 reports
SWOLLEN TONGUE6 reports
TREATMENT FAILURE6 reports
ACUTE KIDNEY INJURY5 reports

Report Outcomes

Out of 427 classified reports for FERRIC OXIDE RED:

Serious 77.5%Non-Serious 22.5%

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

Female237 (59.7%)
Male160 (40.3%)

Reports by Age

Age 5725 reports
Age 7220 reports
Age 5313 reports
Age 7013 reports
Age 5410 reports
Age 6910 reports
Age 329 reports
Age 519 reports
Age 759 reports
Age 408 reports
Age 487 reports
Age 567 reports
Age 647 reports
Age 677 reports
Age 787 reports
Age 316 reports
Age 596 reports
Age 746 reports
Age 615 reports
Age 625 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 FERRIC OXIDE RED?

This profile reflects 1,588 FDA FAERS reports that mention FERRIC OXIDE RED. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for FERRIC OXIDE RED?

Frequently reported terms in FAERS include RASH, DIARRHOEA, FATIGUE, CONSTIPATION, PRURITUS, NAUSEA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures FERRIC OXIDE RED?

Labeling and FAERS entries often list Better Living Brands, LLC in connection with FERRIC OXIDE RED. 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.