CHLOROXYLENOL

N/A

109 FDA adverse event reports analyzed

Last updated: 2026-04-15

About CHLOROXYLENOL

CHLOROXYLENOL is a medication tracked in the FDA Adverse Event Reporting System (FAERS). The most commonly reported adverse reactions for CHLOROXYLENOL include ABDOMINAL PAIN UPPER, EYE PAIN, KIDNEY TRANSPLANT REJECTION, LUNG NEOPLASM MALIGNANT, METASTASES TO LIVER. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for CHLOROXYLENOL.

Top Adverse Reactions

ABDOMINAL PAIN UPPER2 reports
EYE PAIN2 reports
KIDNEY TRANSPLANT REJECTION2 reports
LUNG NEOPLASM MALIGNANT2 reports
METASTASES TO LIVER2 reports
PNEUMONIA2 reports
RENAL DISORDER2 reports
RENAL FAILURE2 reports
VOMITING2 reports
ABDOMINAL DISTENSION1 reports
ABDOMINAL PAIN1 reports
ABDOMINAL PAIN LOWER1 reports
ACANTHAMOEBA KERATITIS1 reports
ACUTE MYELOID LEUKAEMIA1 reports
ANAEMIA1 reports
ANAPHYLACTIC REACTION1 reports
ANGIOEDEMA1 reports
ARTERIOSCLEROSIS1 reports
ARTHRALGIA1 reports
ARTHRITIS1 reports
ARTHROPATHY1 reports
BLADDER CANCER1 reports
BLISTER1 reports
BLOOD CREATININE INCREASED1 reports
BLOOD PRESSURE DECREASED1 reports
BONE MARROW FAILURE1 reports
BOVINE TUBERCULOSIS1 reports
C REACTIVE PROTEIN INCREASED1 reports
CARDIAC FAILURE1 reports
CARDIOGENIC SHOCK1 reports
CEREBROVASCULAR ACCIDENT1 reports
CHEST DISCOMFORT1 reports
CHEST PAIN1 reports
CHOLECYSTITIS1 reports
CORNEAL EPITHELIUM DEFECT1 reports
COUGH1 reports
CYSTITIS1 reports
DEMENTIA1 reports
DEPRESSION1 reports
DERMATITIS1 reports
DRUG EFFECT DECREASED1 reports
DRUG HYPERSENSITIVITY1 reports
DRUG INEFFECTIVE1 reports
DRUG INTERACTION1 reports
DRUG LEVEL DECREASED1 reports
DYSPNOEA1 reports
ERYTHEMA1 reports
EYE DISCHARGE1 reports
EYE HAEMORRHAGE1 reports
EYE INFECTION BACTERIAL1 reports
EYE IRRITATION1 reports
EYE SWELLING1 reports
FALL1 reports
FOREIGN BODY SENSATION IN EYES1 reports
GALLBLADDER ADENOCARCINOMA1 reports
GASTRIC DISORDER1 reports
GASTRITIS1 reports
GASTROOESOPHAGEAL REFLUX DISEASE1 reports
GRAFT VERSUS HOST DISEASE1 reports
HAEMODIALYSIS1 reports
HAEMORRHAGE1 reports
HAEMORRHOIDAL HAEMORRHAGE1 reports
HAND FRACTURE1 reports
HEAD INJURY1 reports
HEPATIC ENZYME INCREASED1 reports
HEPATIC FUNCTION ABNORMAL1 reports
HOSPITALISATION1 reports
IMMUNE RECONSTITUTION SYNDROME1 reports
INCORRECT ROUTE OF DRUG ADMINISTRATION1 reports
ISCHAEMIC CEREBRAL INFARCTION1 reports
JOINT SWELLING1 reports
KIDNEY FIBROSIS1 reports
LACRIMATION INCREASED1 reports
LEUKOPENIA1 reports
LIVER DISORDER1 reports
LIVER TRANSPLANT REJECTION1 reports
LOBAR PNEUMONIA1 reports
LYMPHADENITIS1 reports
MALAISE1 reports
MALNUTRITION1 reports
METASTASES TO BONE1 reports
MOUTH ULCERATION1 reports
MULTIPLE SCLEROSIS1 reports
NAUSEA1 reports
NEUROENDOCRINE CARCINOMA OF THE SKIN1 reports
NON SMALL CELL LUNG CANCER1 reports
OCULAR HYPERAEMIA1 reports
OSTEOPOROSIS1 reports
OVARIAN CYST1 reports
PAIN1 reports
PELVIC PAIN1 reports
PLEURAL EFFUSION1 reports
PLEURISY1 reports
PRODUCT DOSE OMISSION ISSUE1 reports
PROPIONIBACTERIUM INFECTION1 reports
PROSTATE CANCER1 reports
PYREXIA1 reports
RENAL HAEMORRHAGE1 reports
SEXUAL ABUSE1 reports
SHOCK HAEMORRHAGIC1 reports

Demographics Breakdown

Reports by Age

Age 502 reports
Age 752 reports
Age 131 reports
Age 201 reports
Age 241 reports
Age 271 reports
Age 281 reports
Age 331 reports
Age 541 reports
Age 621 reports
Age 661 reports
Age 731 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 CHLOROXYLENOL?

This profile reflects 109 FDA FAERS reports that mention CHLOROXYLENOL. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for CHLOROXYLENOL?

Frequently reported terms in FAERS include ABDOMINAL PAIN UPPER, EYE PAIN, KIDNEY TRANSPLANT REJECTION, LUNG NEOPLASM MALIGNANT, METASTASES TO LIVER, PNEUMONIA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

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.