ALUMINUM CHLOROHYDRATE

N/A

Manufactured by The Procter & Gamble Manufacturing Company

148 FDA adverse event reports analyzed

Last updated: 2026-04-15

About ALUMINUM CHLOROHYDRATE

ALUMINUM CHLOROHYDRATE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by The Procter & Gamble Manufacturing Company. The most commonly reported adverse reactions for ALUMINUM CHLOROHYDRATE include EXPIRED PRODUCT ADMINISTERED, MACULE, PRODUCT ADMINISTERED AT INAPPROPRIATE SITE, APPLICATION SITE PAIN, CERVIX CARCINOMA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ALUMINUM CHLOROHYDRATE.

Top Adverse Reactions

EXPIRED PRODUCT ADMINISTERED5 reports
MACULE5 reports
PRODUCT ADMINISTERED AT INAPPROPRIATE SITE5 reports
APPLICATION SITE PAIN4 reports
CERVIX CARCINOMA4 reports
CERVIX HAEMORRHAGE UTERINE4 reports
ERYTHEMA4 reports
PAIN OF SKIN4 reports
SKIN EROSION4 reports
SQUAMOUS CELL CARCINOMA OF SKIN4 reports
APPLICATION SITE ERYTHEMA3 reports
COUGH3 reports
RECALLED PRODUCT ADMINISTERED3 reports
ANAEMIA2 reports
APPLICATION SITE RASH2 reports
DIARRHOEA2 reports
DRUG INEFFECTIVE2 reports
HEADACHE2 reports
INFLAMMATION2 reports
PRODUCT CONTAMINATION CHEMICAL2 reports
PRODUCT FORMULATION ISSUE2 reports
RHINORRHOEA2 reports
ACUTE CORONARY SYNDROME1 reports
APPLICATION SITE IRRITATION1 reports
APPLICATION SITE PRURITUS1 reports
ARTERIOSCLEROSIS CORONARY ARTERY1 reports
ARTERIOVENOUS FISTULA ANEURYSM1 reports
AXILLARY MASS1 reports
AXILLARY PAIN1 reports
BLOOD DISORDER1 reports
BLOOD LOSS ANAEMIA1 reports
BREAST CANCER1 reports
BURNING SENSATION1 reports
BURNS THIRD DEGREE1 reports
CALCINOSIS1 reports
CHILLS1 reports
CONDITION AGGRAVATED1 reports
CONSTIPATION1 reports
CORONAVIRUS INFECTION1 reports
COVID 191 reports
DERMATITIS CONTACT1 reports
DIALYSIS RELATED COMPLICATION1 reports
DISEASE RECURRENCE1 reports
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION1 reports
DYSPNOEA1 reports
EAR PAIN1 reports
ENZYME LEVEL INCREASED1 reports
EYE PAIN1 reports
FEELING ABNORMAL1 reports
GASTRIC ULCER HAEMORRHAGE1 reports
GASTRITIS1 reports
HIATUS HERNIA1 reports
HIDRADENITIS1 reports
HODGKIN^S DISEASE1 reports
HORMONE RECEPTOR POSITIVE HER2 NEGATIVE BREAST CANCER1 reports
HYPERSENSITIVITY1 reports
HYPERTENSION1 reports
HYPERTENSIVE HEART DISEASE1 reports
HYPOACUSIS1 reports
INFECTION1 reports
INVASIVE DUCTAL BREAST CARCINOMA1 reports
LACRIMATION INCREASED1 reports
LARGE INTESTINE POLYP1 reports
LIMB DISCOMFORT1 reports
MANTLE CELL LYMPHOMA1 reports
MYALGIA1 reports
MYELOFIBROSIS1 reports
NECROTISING SOFT TISSUE INFECTION1 reports
NERVE INJURY1 reports
NEUTROPENIA1 reports
NEUTROPHIL COUNT DECREASED1 reports
OFF LABEL USE1 reports
PAIN IN EXTREMITY1 reports
PERICARDIAL EFFUSION1 reports
PLASMA CELL MYELOMA1 reports
PLEURAL EFFUSION1 reports
PNEUMONIA1 reports
POST PROCEDURAL HAEMORRHAGE1 reports
PROCEDURAL PAIN1 reports
PRODUCT LOT NUMBER ISSUE1 reports
PRODUCT ODOUR ABNORMAL1 reports
PRURITUS1 reports
PYREXIA1 reports
REACTION TO DRUG EXCIPIENTS1 reports
RED BLOOD CELL COUNT INCREASED1 reports
RESPIRATORY FAILURE1 reports
SHUNT BLOOD FLOW EXCESSIVE1 reports
SKIN DISORDER1 reports
SKIN IRRITATION1 reports
SKIN ODOUR ABNORMAL1 reports
SKIN SQUAMOUS CELL CARCINOMA METASTATIC1 reports
STAPHYLOCOCCAL SEPSIS1 reports
TACHYCARDIA1 reports
THROMBOCYTOPENIA1 reports
THYROID CANCER1 reports
UMBILICAL HERNIA1 reports
VITAMIN B12 DEFICIENCY1 reports
VOMITING1 reports
WHITE BLOOD CELL COUNT INCREASED1 reports
WHITE MATTER LESION1 reports

Report Outcomes

Out of 38 classified reports for ALUMINUM CHLOROHYDRATE:

Serious 81.6%Non-Serious 18.4%

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

Female25 (69.4%)
Male10 (27.8%)
Unknown1 (2.8%)

Reports by Age

Age 212 reports
Age 302 reports
Age 482 reports
Age 572 reports
Age 672 reports
Age 682 reports
Age 201 reports
Age 251 reports
Age 311 reports
Age 421 reports
Age 431 reports
Age 471 reports
Age 501 reports
Age 521 reports
Age 541 reports
Age 561 reports
Age 581 reports
Age 591 reports
Age 601 reports
Age 621 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 CHLOROHYDRATE?

This profile reflects 148 FDA FAERS reports that mention ALUMINUM CHLOROHYDRATE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for ALUMINUM CHLOROHYDRATE?

Frequently reported terms in FAERS include EXPIRED PRODUCT ADMINISTERED, MACULE, PRODUCT ADMINISTERED AT INAPPROPRIATE SITE, APPLICATION SITE PAIN, CERVIX CARCINOMA, CERVIX HAEMORRHAGE UTERINE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures ALUMINUM CHLOROHYDRATE?

Labeling and FAERS entries often list The Procter & Gamble Manufacturing Company in connection with ALUMINUM CHLOROHYDRATE. 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.