PAIN RELIEF

N/A

Manufactured by H E B

202 FDA adverse event reports analyzed

Last updated: 2026-04-14

About PAIN RELIEF

PAIN RELIEF is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by H E B. The most commonly reported adverse reactions for PAIN RELIEF include PAIN, DYSPNOEA, NAUSEA, CONSTIPATION, DEATH. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for PAIN RELIEF.

Top Adverse Reactions

PAIN9 reports
DYSPNOEA6 reports
NAUSEA6 reports
CONSTIPATION5 reports
DEATH5 reports
FATIGUE5 reports
BACK PAIN4 reports
COUGH4 reports
DIZZINESS4 reports
PNEUMONIA4 reports
ACUTE KIDNEY INJURY3 reports
ANXIETY3 reports
ASTHENIA3 reports
DIARRHOEA3 reports
HAEMORRHOIDS3 reports
LOSS OF CONSCIOUSNESS3 reports
NASOPHARYNGITIS3 reports
WEIGHT DECREASED3 reports
ABDOMINAL DISCOMFORT2 reports
ABDOMINAL DISTENSION2 reports
ANAEMIA2 reports
ARTHRALGIA2 reports
BALANCE DISORDER2 reports
BONE DISORDER2 reports
BRONCHITIS2 reports
CHILLS2 reports
CHRONIC KIDNEY DISEASE2 reports
CYSTITIS2 reports
DEVICE OCCLUSION2 reports
DRUG INEFFECTIVE2 reports
DRY MOUTH2 reports
DYSURIA2 reports
ECONOMIC PROBLEM2 reports
EMOTIONAL DISTRESS2 reports
END STAGE RENAL DISEASE2 reports
FALL2 reports
GASTROOESOPHAGEAL REFLUX DISEASE2 reports
HAEMATURIA2 reports
HEART RATE INCREASED2 reports
HYPERTENSION2 reports
INJECTION SITE BRUISING2 reports
INJECTION SITE ERYTHEMA2 reports
INJECTION SITE PAIN2 reports
INJURY2 reports
LOCAL SWELLING2 reports
MALAISE2 reports
OEDEMA PERIPHERAL2 reports
PAIN IN EXTREMITY2 reports
PNEUMONIA ASPIRATION2 reports
PRODUCTIVE COUGH2 reports
RECTAL HAEMORRHAGE2 reports
RENAL CYST2 reports
RENAL FAILURE2 reports
RESPIRATORY TRACT CONGESTION2 reports
RESPIRATORY TRACT INFECTION2 reports
RETCHING2 reports
SECRETION DISCHARGE2 reports
SINUSITIS2 reports
SURGERY2 reports
TREMOR2 reports
URINARY TRACT INFECTION2 reports
VOMITING2 reports
ABASIA1 reports
ABDOMINAL PAIN1 reports
ABDOMINAL PAIN UPPER1 reports
ABSCESS1 reports
ACCIDENT1 reports
ACCIDENTAL OVERDOSE1 reports
ACTIVITIES OF DAILY LIVING IMPAIRED1 reports
ADVERSE EVENT1 reports
ALANINE AMINOTRANSFERASE INCREASED1 reports
AMNESIA1 reports
ANAPHYLACTIC REACTION1 reports
ANHEDONIA1 reports
AORTIC ARTERIOSCLEROSIS1 reports
AORTIC DISORDER1 reports
AORTIC VALVE INCOMPETENCE1 reports
APATHY1 reports
APHAGIA1 reports
APHTHOUS STOMATITIS1 reports
ARRHYTHMIA1 reports
ARTERIOSCLEROSIS CORONARY ARTERY1 reports
ASCITES1 reports
ASPARTATE AMINOTRANSFERASE INCREASED1 reports
ASTHMA1 reports
ATELECTASIS1 reports
AZOTAEMIA1 reports
BASAL CELL CARCINOMA1 reports
BIOPSY GINGIVAL1 reports
BLADDER CANCER1 reports
BLADDER OPERATION1 reports
BLOOD ACID PHOSPHATASE INCREASED1 reports
BLOOD PRESSURE ABNORMAL1 reports
BOWEL MOVEMENT IRREGULARITY1 reports
BRAIN MIDLINE SHIFT1 reports
BRAIN OEDEMA1 reports
CARCINOID TUMOUR1 reports
CARDIAC FAILURE CONGESTIVE1 reports
CARDIAC VALVE DISEASE1 reports
CARDIOMEGALY1 reports

Report Outcomes

Out of 72 classified reports for PAIN RELIEF:

Serious 61.1%Non-Serious 38.9%

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

Female41 (58.6%)
Male29 (41.4%)

Reports by Age

Age 763 reports
Age 392 reports
Age 452 reports
Age 512 reports
Age 602 reports
Age 632 reports
Age 642 reports
Age 712 reports
Age 321 reports
Age 381 reports
Age 431 reports
Age 491 reports
Age 501 reports
Age 531 reports
Age 541 reports
Age 551 reports
Age 581 reports
Age 621 reports
Age 651 reports
Age 661 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 PAIN RELIEF?

This profile reflects 202 FDA FAERS reports that mention PAIN RELIEF. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for PAIN RELIEF?

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

Who manufactures PAIN RELIEF?

Labeling and FAERS entries often list H E B in connection with PAIN RELIEF. 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.