FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE

N/A

Manufactured by CVS Pharmacy

52 FDA adverse event reports analyzed

Last updated: 2026-04-15

About FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE

FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by CVS Pharmacy. The most commonly reported adverse reactions for FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE include FATIGUE, LUNG DISORDER, ABDOMINAL DISCOMFORT, BREAST CANCER, CARDIOPULMONARY FAILURE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE.

Top Adverse Reactions

FATIGUE2 reports
LUNG DISORDER2 reports
ABDOMINAL DISCOMFORT1 reports
BREAST CANCER1 reports
CARDIOPULMONARY FAILURE1 reports
CHRONIC KIDNEY DISEASE1 reports
CONTUSION1 reports
COUGH1 reports
CYSTIC FIBROSIS RESPIRATORY INFECTION SUPPRESSION1 reports
DEATH1 reports
DIARRHOEA1 reports
DIZZINESS1 reports
DYSPEPSIA1 reports
DYSPNOEA1 reports
EXERCISE TOLERANCE DECREASED1 reports
EYE PRURITUS1 reports
FOOT FRACTURE1 reports
GASTRIC CANCER1 reports
HEADACHE1 reports
HYPERTENSION1 reports
INABILITY TO AFFORD MEDICATION1 reports
JOINT STIFFNESS1 reports
KNEE ARTHROPLASTY1 reports
LARYNGOSPASM1 reports
LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES1 reports
MALABSORPTION1 reports
MIGRAINE1 reports
MULTIPLE ORGAN DYSFUNCTION SYNDROME1 reports
MUSCLE SPASMS1 reports
NASAL CONGESTION1 reports
NASAL INFLAMMATION1 reports
NAUSEA1 reports
OCULAR HYPERAEMIA1 reports
PAIN1 reports
PHOTOPHOBIA1 reports
PNEUMONIA1 reports
PRODUCT COMPLAINT1 reports
PRODUCT LABEL ISSUE1 reports
PRODUCT PACKAGING ISSUE1 reports
PRODUCT SIZE ISSUE1 reports
PRODUCT SUBSTITUTION ISSUE1 reports
PRODUCTIVE COUGH1 reports
PRURITUS1 reports
RENAL INJURY1 reports
SLEEP DISORDER1 reports
SOCIAL PROBLEM1 reports
SPHINCTER OF ODDI DYSFUNCTION1 reports
URTICARIA1 reports
VOMITING1 reports
WHEEZING1 reports

Report Outcomes

Out of 12 classified reports for FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE:

Serious 66.7%Non-Serious 33.3%

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

Female8 (80.0%)
Male2 (20.0%)

Reports by Age

Age 612 reports
Age 642 reports
Age 331 reports
Age 521 reports
Age 591 reports
Age 661 reports
Age 681 reports
Age 731 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 FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE?

This profile reflects 52 FDA FAERS reports that mention FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE?

Frequently reported terms in FAERS include FATIGUE, LUNG DISORDER, ABDOMINAL DISCOMFORT, BREAST CANCER, CARDIOPULMONARY FAILURE, CHRONIC KIDNEY DISEASE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE?

Labeling and FAERS entries often list CVS Pharmacy in connection with FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE. 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.