ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE

N/A

Manufactured by Haleon US Holdings LLC

15,305 FDA adverse event reports analyzed

Last updated: 2026-04-15

About ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE

ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Haleon US Holdings LLC. The most commonly reported adverse reactions for ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE include CHRONIC KIDNEY DISEASE, DIARRHOEA, ACUTE KIDNEY INJURY, NAUSEA, VOMITING. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE.

Top Adverse Reactions

CHRONIC KIDNEY DISEASE457 reports
DIARRHOEA402 reports
ACUTE KIDNEY INJURY395 reports
NAUSEA392 reports
VOMITING389 reports
DYSPNOEA372 reports
FATIGUE362 reports
HEADACHE353 reports
MALAISE291 reports
PAIN289 reports
PYREXIA272 reports
RENAL FAILURE263 reports
ABDOMINAL PAIN UPPER261 reports
DRUG INEFFECTIVE255 reports
GASTROOESOPHAGEAL REFLUX DISEASE248 reports
OFF LABEL USE241 reports
DIZZINESS236 reports
CONFUSIONAL STATE217 reports
FALL213 reports
RASH208 reports
ABDOMINAL DISCOMFORT201 reports
ABDOMINAL PAIN192 reports
CONDITION AGGRAVATED190 reports
CHEST PAIN186 reports
WEIGHT DECREASED179 reports
ARTHRALGIA177 reports
PRURITUS177 reports
PALPITATIONS176 reports
DEPRESSION175 reports
ASTHENIA174 reports
PAIN IN EXTREMITY173 reports
DRUG INTERACTION171 reports
BACK PAIN168 reports
DYSPEPSIA165 reports
HYPONATRAEMIA164 reports
ANXIETY158 reports
COVID 19149 reports
INSOMNIA148 reports
SOMNOLENCE148 reports
CONSTIPATION146 reports
COUGH141 reports
FEELING ABNORMAL140 reports
MIGRAINE137 reports
DEHYDRATION134 reports
TINNITUS127 reports
ARTHRITIS126 reports
CEREBROVASCULAR ACCIDENT122 reports
ANAEMIA121 reports
DYSGEUSIA119 reports
HYPERTENSION119 reports
END STAGE RENAL DISEASE117 reports
PNEUMONIA117 reports
TUBULOINTERSTITIAL NEPHRITIS115 reports
DECREASED APPETITE114 reports
RENAL INJURY114 reports
HYPERHIDROSIS112 reports
HYPOTENSION109 reports
INTENTIONAL PRODUCT USE ISSUE106 reports
PERIPHERAL SWELLING104 reports
THROMBOCYTOPENIA101 reports
HAEMATOCHEZIA100 reports
HALLUCINATION100 reports
TREMOR99 reports
HEART RATE INCREASED98 reports
PRODUCT USE IN UNAPPROVED INDICATION98 reports
MYALGIA96 reports
VERTIGO96 reports
TACHYCARDIA95 reports
PULMONARY EMBOLISM94 reports
NEUTROPENIA93 reports
DEEP VEIN THROMBOSIS92 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION92 reports
BLOOD GLUCOSE INCREASED90 reports
RECTAL HAEMORRHAGE89 reports
VISUAL IMPAIRMENT89 reports
STRESS88 reports
ALOPECIA87 reports
MYOCARDIAL INFARCTION86 reports
ECZEMA84 reports
MUSCULAR WEAKNESS83 reports
OSTEOPOROSIS83 reports
DEATH81 reports
DYSPHAGIA81 reports
MEDICATION ERROR81 reports
SWOLLEN TONGUE81 reports
ACCIDENTAL OVERDOSE79 reports
MUSCLE SPASMS79 reports
ABDOMINAL DISTENSION77 reports
MEMORY IMPAIRMENT77 reports
FREQUENT BOWEL MOVEMENTS76 reports
GENERAL PHYSICAL HEALTH DETERIORATION75 reports
NIGHTMARE75 reports
ADVERSE DRUG REACTION74 reports
AMNESIA74 reports
PARAESTHESIA74 reports
HEPATOCELLULAR INJURY73 reports
MUSCLE TWITCHING73 reports
ERYTHEMA72 reports
FLATULENCE72 reports
DRY SKIN71 reports

Report Outcomes

Out of 6,575 classified reports for ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE:

Serious 88.3%Non-Serious 11.7%

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

Female3,693 (60.9%)
Male2,353 (38.8%)
Unknown17 (0.3%)

Reports by Age

Age 70141 reports
Age 71141 reports
Age 67128 reports
Age 77127 reports
Age 69126 reports
Age 72124 reports
Age 75122 reports
Age 65120 reports
Age 66115 reports
Age 76113 reports
Age 79111 reports
Age 68109 reports
Age 64107 reports
Age 73106 reports
Age 82103 reports
Age 81102 reports
Age 6199 reports
Age 6399 reports
Age 5698 reports
Age 5397 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 HYDROXIDE AND MAGNESIUM CARBONATE?

This profile reflects 15,305 FDA FAERS reports that mention ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE?

Frequently reported terms in FAERS include CHRONIC KIDNEY DISEASE, DIARRHOEA, ACUTE KIDNEY INJURY, NAUSEA, VOMITING, DYSPNOEA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE?

Labeling and FAERS entries often list Haleon US Holdings LLC in connection with ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE. 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.