ALLERGY RELIEF

N/A

Manufactured by AAA PHARMACEUTICAL, INC.

1,014 FDA adverse event reports analyzed

Last updated: 2026-04-14

About ALLERGY RELIEF

ALLERGY RELIEF is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by AAA PHARMACEUTICAL, INC.. The most commonly reported adverse reactions for ALLERGY RELIEF include FATIGUE, NAUSEA, DIARRHOEA, HEADACHE, DYSPNOEA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ALLERGY RELIEF.

Top Adverse Reactions

FATIGUE42 reports
NAUSEA32 reports
DIARRHOEA30 reports
HEADACHE28 reports
DYSPNOEA23 reports
PAIN22 reports
CONSTIPATION21 reports
COUGH20 reports
DRUG INEFFECTIVE20 reports
DIZZINESS19 reports
ARTHRALGIA18 reports
DEATH18 reports
WEIGHT DECREASED17 reports
FALL16 reports
PRODUCT DOSE OMISSION ISSUE16 reports
SINUSITIS16 reports
ASTHENIA15 reports
FEELING ABNORMAL15 reports
PRURITUS15 reports
ABDOMINAL PAIN UPPER14 reports
GAIT DISTURBANCE14 reports
PAIN IN EXTREMITY14 reports
VOMITING14 reports
OFF LABEL USE13 reports
RASH13 reports
URINARY TRACT INFECTION13 reports
WEIGHT INCREASED13 reports
NEUROPATHY PERIPHERAL12 reports
ABDOMINAL DISCOMFORT11 reports
DECREASED APPETITE11 reports
HOT FLUSH11 reports
ILLNESS11 reports
MALAISE11 reports
PNEUMONIA11 reports
SEASONAL ALLERGY11 reports
BRONCHITIS10 reports
DEPRESSION10 reports
NASOPHARYNGITIS10 reports
PERIPHERAL SWELLING10 reports
PYREXIA10 reports
RHINORRHOEA10 reports
CHEST PAIN9 reports
COVID 199 reports
FLUSHING9 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION9 reports
MULTIPLE SCLEROSIS RELAPSE9 reports
MUSCLE SPASMS9 reports
SOMNOLENCE9 reports
TREMOR9 reports
BACK PAIN8 reports
DERMATITIS CONTACT8 reports
INFECTION8 reports
MEMORY IMPAIRMENT8 reports
UPPER RESPIRATORY TRACT INFECTION8 reports
ANXIETY7 reports
INSOMNIA7 reports
LIMB DISCOMFORT7 reports
VIRAL INFECTION7 reports
CHILLS6 reports
CHRONIC OBSTRUCTIVE PULMONARY DISEASE6 reports
DEHYDRATION6 reports
DRUG HYPERSENSITIVITY6 reports
ERYTHEMA6 reports
INFLAMMATION6 reports
INFUSION SITE PAIN6 reports
INSURANCE ISSUE6 reports
PARAESTHESIA6 reports
PRODUCT DOSE OMISSION IN ERROR6 reports
PRODUCT USE ISSUE6 reports
RHEUMATOID ARTHRITIS6 reports
WHITE BLOOD CELL COUNT DECREASED6 reports
ALOPECIA5 reports
ANAEMIA5 reports
BALANCE DISORDER5 reports
BURNING SENSATION5 reports
CONDITION AGGRAVATED5 reports
DISEASE PROGRESSION5 reports
DYSPEPSIA5 reports
FLATULENCE5 reports
GASTROOESOPHAGEAL REFLUX DISEASE5 reports
HOSPITALISATION5 reports
HYPERHIDROSIS5 reports
HYPERSENSITIVITY5 reports
INFLUENZA5 reports
INJECTION SITE BRUISING5 reports
JOINT SWELLING5 reports
MUSCULAR WEAKNESS5 reports
POOR QUALITY SLEEP5 reports
PSORIASIS5 reports
SLEEP DISORDER5 reports
SYNCOPE5 reports
ARTHRITIS4 reports
ASTHMA4 reports
BLOOD PRESSURE INCREASED4 reports
CATARACT4 reports
DIVERTICULITIS4 reports
DYSPHONIA4 reports
DYSPNOEA EXERTIONAL4 reports
EYE PAIN4 reports
FLUID RETENTION4 reports

Report Outcomes

Out of 395 classified reports for ALLERGY RELIEF:

Serious 46.3%Non-Serious 53.7%

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

Female276 (72.6%)
Male104 (27.4%)

Reports by Age

Age 6012 reports
Age 6712 reports
Age 5911 reports
Age 6110 reports
Age 7610 reports
Age 569 reports
Age 739 reports
Age 527 reports
Age 537 reports
Age 747 reports
Age 757 reports
Age 636 reports
Age 646 reports
Age 696 reports
Age 786 reports
Age 575 reports
Age 705 reports
Age 725 reports
Age 805 reports
Age 835 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 ALLERGY RELIEF?

This profile reflects 1,014 FDA FAERS reports that mention ALLERGY RELIEF. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for ALLERGY RELIEF?

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

Who manufactures ALLERGY RELIEF?

Labeling and FAERS entries often list AAA PHARMACEUTICAL, INC. in connection with ALLERGY 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.