ZINC SULFATE

N/A

Manufactured by American Regent, Inc.

6,021 FDA adverse event reports analyzed

Last updated: 2026-04-15

About ZINC SULFATE

ZINC SULFATE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by American Regent, Inc.. The most commonly reported adverse reactions for ZINC SULFATE include DIARRHOEA, FATIGUE, NAUSEA, DEATH, OFF LABEL USE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ZINC SULFATE.

Top Adverse Reactions

DIARRHOEA216 reports
FATIGUE172 reports
NAUSEA167 reports
DEATH155 reports
OFF LABEL USE147 reports
PAIN146 reports
VOMITING137 reports
DYSPNOEA136 reports
PYREXIA127 reports
HEADACHE99 reports
ASTHENIA97 reports
ANAEMIA95 reports
PNEUMONIA93 reports
BACK PAIN90 reports
FALL89 reports
DRUG INEFFECTIVE88 reports
DIZZINESS86 reports
MALAISE84 reports
NEUTROPENIA84 reports
HYPOTENSION83 reports
URINARY TRACT INFECTION83 reports
ACUTE KIDNEY INJURY82 reports
COUGH80 reports
WEIGHT DECREASED80 reports
CONSTIPATION77 reports
ABDOMINAL PAIN75 reports
COVID 1973 reports
CHILLS70 reports
ALANINE AMINOTRANSFERASE INCREASED68 reports
ARTHRALGIA68 reports
ASPARTATE AMINOTRANSFERASE INCREASED61 reports
PULMONARY EMBOLISM61 reports
PRURITUS60 reports
OEDEMA PERIPHERAL59 reports
RASH59 reports
DECREASED APPETITE57 reports
DEHYDRATION57 reports
CONDITION AGGRAVATED56 reports
THROMBOCYTOPENIA55 reports
CROHN^S DISEASE54 reports
RENAL FAILURE53 reports
SEPSIS53 reports
HAEMOGLOBIN DECREASED51 reports
PLATELET COUNT DECREASED51 reports
FEBRILE NEUTROPENIA50 reports
HYPERTENSION50 reports
ABDOMINAL DISTENSION48 reports
BODY TEMPERATURE INCREASED47 reports
DEPRESSION47 reports
RESPIRATORY FAILURE47 reports
SINUSITIS47 reports
WEIGHT INCREASED47 reports
ANXIETY46 reports
HYPOXIA46 reports
ATRIAL FIBRILLATION45 reports
CHEST PAIN45 reports
GAIT DISTURBANCE45 reports
ABDOMINAL PAIN UPPER43 reports
BLOOD CREATININE INCREASED43 reports
PAIN IN EXTREMITY43 reports
GASTROOESOPHAGEAL REFLUX DISEASE41 reports
INFECTION41 reports
PROCTALGIA40 reports
CONFUSIONAL STATE39 reports
HAEMORRHOIDS39 reports
WHITE BLOOD CELL COUNT DECREASED38 reports
HEPATIC ENCEPHALOPATHY37 reports
HYPERSENSITIVITY37 reports
OSTEOARTHRITIS37 reports
PRODUCT DOSE OMISSION ISSUE37 reports
BLOOD PRESSURE INCREASED36 reports
CHRONIC KIDNEY DISEASE36 reports
PLEURAL EFFUSION36 reports
ANAL INFLAMMATION35 reports
SOMNOLENCE35 reports
ACCIDENT34 reports
CARDIAC ARREST34 reports
DYSPEPSIA34 reports
GASTROINTESTINAL HAEMORRHAGE34 reports
HYPOAESTHESIA34 reports
INSOMNIA34 reports
WHEEZING33 reports
BRADYCARDIA32 reports
DEEP VEIN THROMBOSIS32 reports
LOSS OF CONSCIOUSNESS32 reports
OXYGEN SATURATION DECREASED32 reports
TREMOR32 reports
DYSPNOEA EXERTIONAL31 reports
NECK PAIN31 reports
NEUROPATHY PERIPHERAL31 reports
SARS COV 2 TEST NEGATIVE31 reports
CARDIAC FAILURE CONGESTIVE30 reports
DRUG INTERACTION30 reports
RESPIRATORY TRACT INFECTION30 reports
ACUTE RESPIRATORY FAILURE29 reports
ASTHMA29 reports
HOSPITALISATION29 reports
HOT FLUSH29 reports
SEPTIC SHOCK29 reports
CONTUSION28 reports

Report Outcomes

Out of 2,697 classified reports for ZINC SULFATE:

Serious 76.0%Non-Serious 24.0%

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

Female1,304 (52.1%)
Male1,198 (47.9%)
Unknown1 (0.0%)

Reports by Age

Age 6463 reports
Age 6961 reports
Age 6358 reports
Age 6554 reports
Age 7453 reports
Age 6751 reports
Age 7251 reports
Age 6049 reports
Age 5748 reports
Age 6248 reports
Age 6145 reports
Age 7045 reports
Age 7742 reports
Age 6840 reports
Age 5539 reports
Age 6639 reports
Age 2037 reports
Age 7337 reports
Age 5136 reports
Age 7136 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 ZINC SULFATE?

This profile reflects 6,021 FDA FAERS reports that mention ZINC SULFATE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for ZINC SULFATE?

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

Who manufactures ZINC SULFATE?

Labeling and FAERS entries often list American Regent, Inc. in connection with ZINC SULFATE. 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.