SILVER NITRATE

N/A

Manufactured by Boiron

1,031 FDA adverse event reports analyzed

Last updated: 2026-04-15

About SILVER NITRATE

SILVER NITRATE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Boiron. The most commonly reported adverse reactions for SILVER NITRATE include DRUG INEFFECTIVE, FATIGUE, DIARRHOEA, ON AND OFF PHENOMENON, STOMA SITE DISCHARGE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for SILVER NITRATE.

Top Adverse Reactions

DRUG INEFFECTIVE26 reports
FATIGUE26 reports
DIARRHOEA23 reports
ON AND OFF PHENOMENON22 reports
STOMA SITE DISCHARGE21 reports
DYSKINESIA19 reports
STOMA SITE ERYTHEMA19 reports
FIBROMA18 reports
HALLUCINATION18 reports
MEMORY IMPAIRMENT18 reports
MOBILITY DECREASED18 reports
OFF LABEL USE18 reports
PARKINSON^S DISEASE18 reports
MUSCLE RIGIDITY17 reports
VOMITING17 reports
BRADYKINESIA16 reports
COGNITIVE DISORDER16 reports
FALL16 reports
GAIT DISTURBANCE16 reports
WEIGHT DECREASED15 reports
ARTHRALGIA14 reports
MUSCLE SPASMS14 reports
PAIN14 reports
UNEVALUABLE EVENT14 reports
DEVICE ISSUE13 reports
FEELING ABNORMAL13 reports
FREEZING PHENOMENON13 reports
DEVICE DISLOCATION12 reports
DYSPNOEA12 reports
NAUSEA12 reports
TENSION12 reports
URINARY TRACT INFECTION12 reports
CONSTIPATION11 reports
DIZZINESS11 reports
GENERAL PHYSICAL HEALTH DETERIORATION11 reports
INSOMNIA11 reports
OEDEMA PERIPHERAL11 reports
MUSCULOSKELETAL STIFFNESS10 reports
STOMA SITE HAEMORRHAGE10 reports
STOMA SITE PAIN10 reports
TREMOR10 reports
WOUND10 reports
ANAEMIA9 reports
C REACTIVE PROTEIN INCREASED9 reports
MUCOSAL INFLAMMATION9 reports
PRURITUS9 reports
SOMNOLENCE9 reports
SPEECH DISORDER9 reports
STOMA SITE INFLAMMATION9 reports
STOMA SITE IRRITATION9 reports
STOMA SITE REACTION9 reports
ABNORMAL DREAMS8 reports
ASTHENIA8 reports
BONE PAIN8 reports
COUGH8 reports
DYSPHAGIA8 reports
FEAR8 reports
PNEUMONIA8 reports
THERAPEUTIC PRODUCT EFFECT INCOMPLETE8 reports
THERAPEUTIC PRODUCT EFFECT VARIABLE8 reports
WEIGHT INCREASED8 reports
CANCER PAIN7 reports
CONFUSIONAL STATE7 reports
DECREASED APPETITE7 reports
DEMENTIA7 reports
DISEASE PROGRESSION7 reports
EPISTAXIS7 reports
GASTROINTESTINAL HAEMORRHAGE7 reports
HYPERKINESIA7 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION7 reports
LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES7 reports
OSTEONECROSIS OF JAW7 reports
PYREXIA7 reports
RASH7 reports
ANXIETY6 reports
DEATH6 reports
DYSTONIA6 reports
FLUID INTAKE REDUCED6 reports
HALLUCINATION, VISUAL6 reports
HEADACHE6 reports
HYPERHIDROSIS6 reports
MUSCULAR WEAKNESS6 reports
NEUTROPENIC SEPSIS6 reports
POOR QUALITY SLEEP6 reports
STOMA SITE HYPERGRANULATION6 reports
UNDERDOSE6 reports
ABDOMINAL PAIN5 reports
BALANCE DISORDER5 reports
CHOLESTATIC LIVER INJURY5 reports
CONDITION AGGRAVATED5 reports
DEVICE DIFFICULT TO USE5 reports
GASTROINTESTINAL DISORDER5 reports
HYPOTENSION5 reports
INJURY5 reports
LIP ULCERATION5 reports
LOSS OF CONSCIOUSNESS5 reports
LYMPHOCYTIC LEUKAEMIA5 reports
MALAISE5 reports
MEDICAL DEVICE PAIN5 reports
NEUTROPENIA5 reports

Report Outcomes

Out of 235 classified reports for SILVER NITRATE:

Serious 84.3%Non-Serious 15.7%

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

Female119 (54.8%)
Male97 (44.7%)
Unknown1 (0.5%)

Reports by Age

Age 6111 reports
Age 6211 reports
Age 668 reports
Age 67 reports
Age 637 reports
Age 717 reports
Age 787 reports
Age 575 reports
Age 755 reports
Age 775 reports
Age 795 reports
Age 364 reports
Age 404 reports
Age 644 reports
Age 694 reports
Age 724 reports
Age 834 reports
Age 83 reports
Age 593 reports
Age 673 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 SILVER NITRATE?

This profile reflects 1,031 FDA FAERS reports that mention SILVER NITRATE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for SILVER NITRATE?

Frequently reported terms in FAERS include DRUG INEFFECTIVE, FATIGUE, DIARRHOEA, ON AND OFF PHENOMENON, STOMA SITE DISCHARGE, DYSKINESIA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures SILVER NITRATE?

Labeling and FAERS entries often list Boiron in connection with SILVER NITRATE. 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.