ZINC GLUCONATE

N/A

Manufactured by Wal-Mart Stores,Inc.,

66,089 FDA adverse event reports analyzed

Last updated: 2026-04-14

About ZINC GLUCONATE

ZINC GLUCONATE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Wal-Mart Stores,Inc.,. The most commonly reported adverse reactions for ZINC GLUCONATE include FATIGUE, PAIN, DIARRHOEA, NAUSEA, HEADACHE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ZINC GLUCONATE.

Top Adverse Reactions

FATIGUE2,631 reports
PAIN1,909 reports
DIARRHOEA1,880 reports
NAUSEA1,876 reports
HEADACHE1,791 reports
OFF LABEL USE1,757 reports
DRUG INEFFECTIVE1,497 reports
DYSPNOEA1,416 reports
ARTHRALGIA1,319 reports
DIZZINESS1,294 reports
ASTHENIA1,244 reports
FALL1,238 reports
CONSTIPATION1,102 reports
RASH1,057 reports
VOMITING988 reports
COVID 19971 reports
PRURITUS943 reports
MALAISE934 reports
COUGH924 reports
INSOMNIA886 reports
PAIN IN EXTREMITY878 reports
PRODUCT DOSE OMISSION ISSUE876 reports
WEIGHT DECREASED823 reports
PNEUMONIA821 reports
BACK PAIN769 reports
CONDITION AGGRAVATED745 reports
MUSCLE SPASMS721 reports
ALOPECIA716 reports
FEELING ABNORMAL689 reports
PYREXIA689 reports
NASOPHARYNGITIS681 reports
URINARY TRACT INFECTION663 reports
PERIPHERAL SWELLING646 reports
HYPOTENSION645 reports
WEIGHT INCREASED645 reports
BALANCE DISORDER642 reports
DECREASED APPETITE637 reports
ANXIETY636 reports
GAIT DISTURBANCE614 reports
MOBILITY DECREASED605 reports
DEATH600 reports
DEPRESSION582 reports
ABDOMINAL DISCOMFORT579 reports
ABDOMINAL PAIN UPPER576 reports
SINUSITIS565 reports
HYPERTENSION560 reports
PARAESTHESIA539 reports
PRODUCT USE IN UNAPPROVED INDICATION535 reports
HYPOAESTHESIA528 reports
ABDOMINAL PAIN519 reports
BLOOD PRESSURE INCREASED512 reports
MYALGIA504 reports
MEMORY IMPAIRMENT492 reports
COGNITIVE DISORDER452 reports
MUSCULAR WEAKNESS451 reports
SOMNOLENCE451 reports
DRUG HYPERSENSITIVITY447 reports
HYPERSENSITIVITY441 reports
CONFUSIONAL STATE439 reports
CHEST PAIN435 reports
INJECTION SITE PAIN426 reports
ABDOMINAL DISTENSION421 reports
JOINT SWELLING415 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION413 reports
ANAEMIA396 reports
ILLNESS392 reports
TREMOR385 reports
CHILLS383 reports
ERYTHEMA383 reports
MIGRAINE379 reports
URTICARIA375 reports
DYSPEPSIA374 reports
MUSCULOSKELETAL STIFFNESS374 reports
CONTUSION367 reports
TOXICITY TO VARIOUS AGENTS360 reports
VISION BLURRED359 reports
DEPRESSED LEVEL OF CONSCIOUSNESS355 reports
ORTHOSTATIC HYPOTENSION355 reports
GASTROOESOPHAGEAL REFLUX DISEASE354 reports
BLOOD CALCIUM DECREASED353 reports
HOT FLUSH350 reports
INFECTION348 reports
DRY MOUTH345 reports
SEDATION344 reports
WHITE BLOOD CELL COUNT DECREASED344 reports
NEUROPATHY PERIPHERAL338 reports
OSTEOARTHRITIS335 reports
DEHYDRATION332 reports
CHEST DISCOMFORT331 reports
OROPHARYNGEAL PAIN326 reports
SWELLING319 reports
CREATININE RENAL CLEARANCE DECREASED318 reports
PRODUCT USE ISSUE314 reports
ARTHROPATHY311 reports
SEDATION COMPLICATION310 reports
SLEEP DISORDER305 reports
NECK PAIN302 reports
RHEUMATOID ARTHRITIS301 reports
INFLUENZA296 reports
PALPITATIONS296 reports

Report Outcomes

Out of 24,542 classified reports for ZINC GLUCONATE:

Serious 57.3%Non-Serious 42.7%

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

Female14,974 (65.7%)
Male7,780 (34.2%)
Unknown24 (0.1%)

Reports by Age

Age 77587 reports
Age 68511 reports
Age 65469 reports
Age 70439 reports
Age 63435 reports
Age 66435 reports
Age 60420 reports
Age 64408 reports
Age 73408 reports
Age 72407 reports
Age 67406 reports
Age 62395 reports
Age 71395 reports
Age 74378 reports
Age 61367 reports
Age 69367 reports
Age 75353 reports
Age 59347 reports
Age 58342 reports
Age 76332 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 GLUCONATE?

This profile reflects 66,089 FDA FAERS reports that mention ZINC GLUCONATE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for ZINC GLUCONATE?

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

Who manufactures ZINC GLUCONATE?

Labeling and FAERS entries often list Wal-Mart Stores,Inc., in connection with ZINC GLUCONATE. 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.