ALUMINUM CHLORIDE

N/A

Manufactured by Clarion Brands, LLC

317 FDA adverse event reports analyzed

Last updated: 2026-04-15

About ALUMINUM CHLORIDE

ALUMINUM CHLORIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Clarion Brands, LLC. The most commonly reported adverse reactions for ALUMINUM CHLORIDE include RASH, DRUG INEFFECTIVE, DERMATITIS ATOPIC, HEADACHE, NAUSEA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ALUMINUM CHLORIDE.

Top Adverse Reactions

RASH12 reports
DRUG INEFFECTIVE11 reports
DERMATITIS ATOPIC7 reports
HEADACHE7 reports
NAUSEA7 reports
OFF LABEL USE7 reports
PAIN7 reports
PRURITUS7 reports
ANXIETY6 reports
DISCOMFORT6 reports
FATIGUE6 reports
HYPERHIDROSIS6 reports
PRODUCT DOSE OMISSION ISSUE6 reports
DIARRHOEA5 reports
FALL5 reports
VOMITING5 reports
WEIGHT DECREASED5 reports
ARTHRALGIA4 reports
BACK PAIN4 reports
CONDITION AGGRAVATED4 reports
DEPRESSION4 reports
DIZZINESS4 reports
EMOTIONAL DISTRESS4 reports
HYPERTENSION4 reports
INJECTION SITE PAIN4 reports
PAIN IN EXTREMITY4 reports
PRODUCT USE IN UNAPPROVED INDICATION4 reports
SURGERY4 reports
THERAPY NON RESPONDER4 reports
TREATMENT FAILURE4 reports
CONSTIPATION3 reports
COVID 193 reports
ERYTHEMA3 reports
HYPERSENSITIVITY3 reports
HYPOTHYROIDISM3 reports
INJECTION SITE ERYTHEMA3 reports
INTENTIONAL DOSE OMISSION3 reports
MIGRAINE3 reports
PRE EXISTING CONDITION IMPROVED3 reports
PRODUCT ADMINISTRATION INTERRUPTED3 reports
RASH PRURITIC3 reports
SEPSIS3 reports
SLEEP DISORDER3 reports
URINARY TRACT INFECTION3 reports
URTICARIA3 reports
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS3 reports
ABDOMINAL DISCOMFORT2 reports
ANHEDONIA2 reports
APPLICATION SITE BURN2 reports
CHEST DISCOMFORT2 reports
CHILLS2 reports
CONTUSION2 reports
COUGH2 reports
DECREASED APPETITE2 reports
DERMATITIS CONTACT2 reports
DRUG HYPERSENSITIVITY2 reports
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION2 reports
DRY SKIN2 reports
DYSPNOEA2 reports
EAR INFECTION2 reports
ECZEMA2 reports
EPISTAXIS2 reports
FEELING ABNORMAL2 reports
FLUSHING2 reports
GASTROOESOPHAGEAL REFLUX DISEASE2 reports
HYPOAESTHESIA2 reports
INCREASED APPETITE2 reports
INFECTION2 reports
INJECTION SITE BRUISING2 reports
INJECTION SITE SWELLING2 reports
INSOMNIA2 reports
INTENTIONAL PRODUCT USE ISSUE2 reports
JOINT SWELLING2 reports
LIMB INJURY2 reports
MAJOR DEPRESSION2 reports
MEMORY IMPAIRMENT2 reports
MUSCLE SPASMS2 reports
MYALGIA2 reports
NECK PAIN2 reports
NEPHROLITHIASIS2 reports
NO ADVERSE EVENT2 reports
OEDEMA2 reports
PARAESTHESIA2 reports
PERIPHERAL SWELLING2 reports
POOR QUALITY SLEEP2 reports
PRODUCT DOSE OMISSION IN ERROR2 reports
PRODUCT USE ISSUE2 reports
PULMONARY EMBOLISM2 reports
PULMONARY INFARCTION2 reports
PYREXIA2 reports
SINUSITIS2 reports
SKIN INFECTION2 reports
SKIN IRRITATION2 reports
WEIGHT INCREASED2 reports
ABDOMINAL PAIN1 reports
ABDOMINAL PAIN UPPER1 reports
ABNORMAL DREAMS1 reports
ABNORMAL UTERINE BLEEDING1 reports
ACCIDENTAL OVERDOSE1 reports
ACUTE KIDNEY INJURY1 reports

Report Outcomes

Out of 130 classified reports for ALUMINUM CHLORIDE:

Serious 54.6%Non-Serious 45.4%

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

Female75 (63.6%)
Male36 (30.5%)
Unknown7 (5.9%)

Reports by Age

Age 395 reports
Age 524 reports
Age 644 reports
Age 323 reports
Age 733 reports
Age 162 reports
Age 172 reports
Age 402 reports
Age 462 reports
Age 482 reports
Age 492 reports
Age 512 reports
Age 542 reports
Age 682 reports
Age 742 reports
Age 141 reports
Age 181 reports
Age 201 reports
Age 211 reports
Age 221 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 ALUMINUM CHLORIDE?

This profile reflects 317 FDA FAERS reports that mention ALUMINUM CHLORIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for ALUMINUM CHLORIDE?

Frequently reported terms in FAERS include RASH, DRUG INEFFECTIVE, DERMATITIS ATOPIC, HEADACHE, NAUSEA, OFF LABEL USE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures ALUMINUM CHLORIDE?

Labeling and FAERS entries often list Clarion Brands, LLC in connection with ALUMINUM CHLORIDE. 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.