PHENOL

N/A

Manufactured by P & L Development, LLC

755 FDA adverse event reports analyzed

Last updated: 2026-04-15

About PHENOL

PHENOL is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by P & L Development, LLC. The most commonly reported adverse reactions for PHENOL include DRUG INEFFECTIVE, DYSPNOEA, OFF LABEL USE, VOMITING, ACUTE KIDNEY INJURY. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for PHENOL.

Top Adverse Reactions

DRUG INEFFECTIVE24 reports
DYSPNOEA21 reports
OFF LABEL USE21 reports
VOMITING21 reports
ACUTE KIDNEY INJURY18 reports
NAUSEA17 reports
DIARRHOEA16 reports
FATIGUE16 reports
COMPLETED SUICIDE15 reports
PAIN15 reports
ABDOMINAL PAIN14 reports
SEPSIS13 reports
ANXIETY12 reports
ARTHRALGIA12 reports
RESPIRATORY FAILURE12 reports
TOXICITY TO VARIOUS AGENTS12 reports
DYSPHAGIA11 reports
FALL11 reports
CHEST PAIN10 reports
DEATH10 reports
PNEUMONIA10 reports
RENAL FAILURE10 reports
SEIZURE10 reports
DISTURBANCE IN ATTENTION9 reports
LOSS OF CONSCIOUSNESS9 reports
MALAISE9 reports
CHRONIC KIDNEY DISEASE8 reports
DEPRESSION8 reports
DIZZINESS8 reports
HAEMOGLOBIN DECREASED8 reports
MUSCULOSKELETAL DISORDER8 reports
PYREXIA8 reports
RASH8 reports
SOMNOLENCE8 reports
SWELLING FACE8 reports
ASTHENIA7 reports
ATRIAL FIBRILLATION7 reports
CONSTIPATION7 reports
DECREASED APPETITE7 reports
DYSGRAPHIA7 reports
HEADACHE7 reports
HYPOACUSIS7 reports
OVERDOSE7 reports
RENAL DISORDER7 reports
CONVULSION6 reports
COUGH6 reports
CYSTITIS LIKE SYMPTOM6 reports
GENERAL PHYSICAL HEALTH DETERIORATION6 reports
HYPOTENSION6 reports
PRODUCT USE IN UNAPPROVED INDICATION6 reports
SINUS TACHYCARDIA6 reports
STOMATITIS6 reports
ABDOMINAL PAIN UPPER5 reports
ACUTE RESPIRATORY FAILURE5 reports
ANAEMIA5 reports
CARDIAC ARREST5 reports
CHEST DISCOMFORT5 reports
CLAVICLE FRACTURE5 reports
DEEP VEIN THROMBOSIS5 reports
EYE HAEMORRHAGE5 reports
HYPOAESTHESIA5 reports
HYPOGLYCAEMIA5 reports
INTENTIONAL OVERDOSE5 reports
MEDICATION ERROR5 reports
MUSCULAR WEAKNESS5 reports
NEUTROPENIA5 reports
OROPHARYNGEAL PAIN5 reports
OSTEONECROSIS5 reports
PAIN IN EXTREMITY5 reports
PRODUCT USE ISSUE5 reports
PRURITUS5 reports
PULMONARY EMBOLISM5 reports
SINUS CONGESTION5 reports
WOUND INFECTION5 reports
ABDOMINAL DISCOMFORT4 reports
AGGRESSION4 reports
BACTERIAL INFECTION4 reports
BLOOD BILIRUBIN INCREASED4 reports
CELLULITIS4 reports
CONDITION AGGRAVATED4 reports
CONFUSIONAL STATE4 reports
DISEASE PROGRESSION4 reports
FLUSHING4 reports
GASTROINTESTINAL DISORDER4 reports
GASTROINTESTINAL HAEMORRHAGE4 reports
GASTROOESOPHAGEAL REFLUX DISEASE4 reports
HAEMATOCHEZIA4 reports
HEART RATE INCREASED4 reports
HOT FLUSH4 reports
HYPONATRAEMIA4 reports
HYPOXIA4 reports
LYMPHOEDEMA4 reports
MENTAL STATUS CHANGES4 reports
PANIC ATTACK4 reports
PERIPHERAL SWELLING4 reports
PNEUMONIA ASPIRATION4 reports
PRODUCT DOSE OMISSION4 reports
PRODUCT DOSE OMISSION ISSUE4 reports
PRODUCT PACKAGING CONFUSION4 reports
PRODUCTIVE COUGH4 reports

Report Outcomes

Out of 265 classified reports for PHENOL:

Serious 84.9%Non-Serious 15.1%

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

Female148 (60.7%)
Male96 (39.3%)

Reports by Age

Age 1716 reports
Age 7010 reports
Age 35 reports
Age 485 reports
Age 495 reports
Age 565 reports
Age 665 reports
Age 695 reports
Age 765 reports
Age 184 reports
Age 234 reports
Age 274 reports
Age 374 reports
Age 554 reports
Age 614 reports
Age 624 reports
Age 734 reports
Age 83 reports
Age 153 reports
Age 193 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 PHENOL?

This profile reflects 755 FDA FAERS reports that mention PHENOL. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for PHENOL?

Frequently reported terms in FAERS include DRUG INEFFECTIVE, DYSPNOEA, OFF LABEL USE, VOMITING, ACUTE KIDNEY INJURY, NAUSEA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures PHENOL?

Labeling and FAERS entries often list P & L Development, LLC in connection with PHENOL. 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.