MEDICATED CORN REMOVERS

N/A

Manufactured by 111MedCo LLC

11,888 FDA adverse event reports analyzed

Last updated: 2026-04-15

About MEDICATED CORN REMOVERS

MEDICATED CORN REMOVERS is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by 111MedCo LLC. The most commonly reported adverse reactions for MEDICATED CORN REMOVERS include VOMITING, PRURITUS, CONDITION AGGRAVATED, HEADACHE, DRUG INEFFECTIVE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for MEDICATED CORN REMOVERS.

Top Adverse Reactions

VOMITING195 reports
PRURITUS192 reports
CONDITION AGGRAVATED180 reports
HEADACHE177 reports
DRUG INEFFECTIVE169 reports
WEIGHT DECREASED169 reports
DYSPNOEA164 reports
URTICARIA164 reports
PSORIASIS163 reports
WEIGHT INCREASED162 reports
INFECTION161 reports
PAIN161 reports
HYPERTENSION160 reports
TYPE 2 DIABETES MELLITUS158 reports
PAIN IN EXTREMITY157 reports
NAUSEA151 reports
HYPOAESTHESIA147 reports
RASH144 reports
NASOPHARYNGITIS143 reports
PNEUMONIA143 reports
PERIPHERAL SWELLING142 reports
OSTEOARTHRITIS141 reports
HYPERSENSITIVITY139 reports
WHEEZING139 reports
OFF LABEL USE138 reports
PYREXIA137 reports
FATIGUE136 reports
TOXICITY TO VARIOUS AGENTS136 reports
WOUND136 reports
VISUAL IMPAIRMENT134 reports
INFUSION RELATED REACTION133 reports
IRRITABLE BOWEL SYNDROME133 reports
DIZZINESS130 reports
ARTHRALGIA129 reports
JOINT STIFFNESS128 reports
MOBILITY DECREASED128 reports
UPPER RESPIRATORY TRACT INFECTION127 reports
JOINT RANGE OF MOTION DECREASED126 reports
OSTEOPOROSIS126 reports
PRESCRIBED UNDERDOSE126 reports
WOUND INFECTION126 reports
JOINT DISLOCATION125 reports
PSORIATIC ARTHROPATHY124 reports
MUSCULOSKELETAL STIFFNESS120 reports
CONTUSION119 reports
OEDEMA PERIPHERAL118 reports
ROAD TRAFFIC ACCIDENT118 reports
SINUSITIS117 reports
PERICARDITIS116 reports
DECREASED APPETITE113 reports
SCIATICA113 reports
HYPERCHOLESTEROLAEMIA112 reports
PEMPHIGUS112 reports
IMPAIRED HEALING111 reports
OEDEMA111 reports
DIARRHOEA109 reports
INJURY109 reports
ANXIETY108 reports
MUSCULAR WEAKNESS108 reports
COMPLETED SUICIDE107 reports
ABDOMINAL DISCOMFORT106 reports
FIBROMYALGIA106 reports
GAIT INABILITY106 reports
HELICOBACTER INFECTION106 reports
GENERAL PHYSICAL HEALTH DETERIORATION105 reports
ALOPECIA103 reports
ASTHMA103 reports
CHEST PAIN101 reports
GAIT DISTURBANCE101 reports
JOINT SWELLING101 reports
HEPATIC ENZYME INCREASED99 reports
CONFUSIONAL STATE97 reports
SYSTEMIC LUPUS ERYTHEMATOSUS96 reports
MEMORY IMPAIRMENT95 reports
C REACTIVE PROTEIN INCREASED94 reports
LIVER INJURY94 reports
BLOOD CHOLESTEROL INCREASED92 reports
RHEUMATOID ARTHRITIS92 reports
PRESCRIBED OVERDOSE89 reports
PULMONARY FIBROSIS89 reports
SYNOVITIS89 reports
TACHYCARDIA89 reports
LIVER FUNCTION TEST INCREASED88 reports
MUSCLE INJURY88 reports
SWELLING87 reports
KNEE ARTHROPLASTY86 reports
RHEUMATOID FACTOR POSITIVE86 reports
HIP ARTHROPLASTY85 reports
LARYNGITIS85 reports
SWOLLEN JOINT COUNT INCREASED85 reports
DEPRESSION84 reports
LUPUS VULGARIS84 reports
RETINITIS84 reports
SERONEGATIVE ARTHRITIS84 reports
LUPUS LIKE SYNDROME83 reports
RHEUMATIC FEVER83 reports
LOWER LIMB FRACTURE82 reports
FOLLICULITIS81 reports
GRIP STRENGTH DECREASED80 reports
STOMATITIS80 reports

Report Outcomes

Out of 1,748 classified reports for MEDICATED CORN REMOVERS:

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

Female979 (61.8%)
Male597 (37.7%)
Unknown7 (0.4%)

Reports by Age

Age 6566 reports
Age 4349 reports
Age 6042 reports
Age 8140 reports
Age 6436 reports
Age 6836 reports
Age 5635 reports
Age 5334 reports
Age 3832 reports
Age 5831 reports
Age 6330 reports
Age 7223 reports
Age 7321 reports
Age 6720 reports
Age 6920 reports
Age 7820 reports
Age 5719 reports
Age 6619 reports
Age 7019 reports
Age 7119 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 MEDICATED CORN REMOVERS?

This profile reflects 11,888 FDA FAERS reports that mention MEDICATED CORN REMOVERS. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for MEDICATED CORN REMOVERS?

Frequently reported terms in FAERS include VOMITING, PRURITUS, CONDITION AGGRAVATED, HEADACHE, DRUG INEFFECTIVE, WEIGHT DECREASED. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures MEDICATED CORN REMOVERS?

Labeling and FAERS entries often list 111MedCo LLC in connection with MEDICATED CORN REMOVERS. 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.