NICKEL

N/A

Manufactured by Boiron

344 FDA adverse event reports analyzed

Last updated: 2026-04-15

About NICKEL

NICKEL is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Boiron. The most commonly reported adverse reactions for NICKEL include DRUG HYPERSENSITIVITY, RASH, DYSPNOEA, ALLERGY TO METALS, OFF LABEL USE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for NICKEL.

Top Adverse Reactions

DRUG HYPERSENSITIVITY79 reports
RASH11 reports
DYSPNOEA9 reports
ALLERGY TO METALS8 reports
OFF LABEL USE8 reports
ERYTHEMA6 reports
HYPERSENSITIVITY6 reports
AGEUSIA5 reports
ARTHRALGIA5 reports
COVID 195 reports
HYPERTENSION5 reports
INTENTIONAL PRODUCT USE ISSUE5 reports
PRURITUS5 reports
WEIGHT DECREASED5 reports
WEIGHT INCREASED5 reports
DIARRHOEA4 reports
FATIGUE4 reports
MIGRAINE4 reports
TENSION HEADACHE4 reports
THROAT IRRITATION4 reports
ABDOMINAL PAIN3 reports
ALLERGY TO ARTHROPOD STING3 reports
ALOPECIA3 reports
ANOSMIA3 reports
ATTENTION DEFICIT HYPERACTIVITY DISORDER3 reports
BLOOD PRESSURE INCREASED3 reports
COUGH3 reports
DIZZINESS3 reports
DRUG DEPENDENCE3 reports
DRUG INEFFECTIVE3 reports
ECZEMA3 reports
GIANT CELL ARTERITIS3 reports
GOUT3 reports
HALLUCINATION, VISUAL3 reports
HEADACHE3 reports
HEART RATE INCREASED3 reports
HERPES ZOSTER3 reports
HORMONE LEVEL ABNORMAL3 reports
HOT FLUSH3 reports
HYPERTENSIVE URGENCY3 reports
HYPOAESTHESIA3 reports
INSOMNIA3 reports
MITRAL VALVE PROLAPSE3 reports
OEDEMA3 reports
SEIZURE3 reports
URTICARIA3 reports
CHEST DISCOMFORT2 reports
CONDITION AGGRAVATED2 reports
CYSTITIS2 reports
DECREASED APPETITE2 reports
DEMENTIA2 reports
DEVICE ALLERGY2 reports
DISTURBANCE IN ATTENTION2 reports
DRUG ERUPTION2 reports
DRY SKIN2 reports
FREQUENT BOWEL MOVEMENTS2 reports
GAIT DISTURBANCE2 reports
HAEMATURIA2 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION2 reports
INFECTION2 reports
INFUSION RELATED REACTION2 reports
JOINT SWELLING2 reports
MASS2 reports
NEUROPATHY PERIPHERAL2 reports
PAIN2 reports
PAIN IN EXTREMITY2 reports
PRODUCT STORAGE ERROR2 reports
ROAD TRAFFIC ACCIDENT2 reports
STEVENS JOHNSON SYNDROME2 reports
TROPONIN I INCREASED2 reports
URINARY BLADDER HAEMORRHAGE2 reports
ABDOMINAL ABSCESS1 reports
ADVERSE DRUG REACTION1 reports
ALLERGY TO CHEMICALS1 reports
ANAEMIA1 reports
ANAPHYLACTIC REACTION1 reports
ANGINA PECTORIS1 reports
ANKLE FRACTURE1 reports
ANKLE OPERATION1 reports
ANTINUCLEAR ANTIBODY POSITIVE1 reports
APHASIA1 reports
ASTHMA1 reports
ATRIAL FIBRILLATION1 reports
BLEPHAROSPASM1 reports
BLISTER1 reports
BRAIN INJURY1 reports
BRAIN OEDEMA1 reports
CATARACT1 reports
CELLULITIS1 reports
CHEILITIS1 reports
CHEST PAIN1 reports
COMPLICATION ASSOCIATED WITH DEVICE1 reports
CONTRAINDICATED PRODUCT ADMINISTERED1 reports
CONTRAST MEDIA ALLERGY1 reports
CORONARY ARTERY OCCLUSION1 reports
DEVICE INFUSION ISSUE1 reports
DEVICE LEAKAGE1 reports
DYSGEUSIA1 reports
DYSPEPSIA1 reports
DYSPHAGIA1 reports

Demographics Breakdown

Reports by Sex

Female99 (90.8%)
Male10 (9.2%)

Reports by Age

Age 686 reports
Age 695 reports
Age 765 reports
Age 554 reports
Age 614 reports
Age 634 reports
Age 734 reports
Age 313 reports
Age 403 reports
Age 653 reports
Age 703 reports
Age 743 reports
Age 362 reports
Age 432 reports
Age 502 reports
Age 562 reports
Age 592 reports
Age 622 reports
Age 642 reports
Age 662 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 NICKEL?

This profile reflects 344 FDA FAERS reports that mention NICKEL. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for NICKEL?

Frequently reported terms in FAERS include DRUG HYPERSENSITIVITY, RASH, DYSPNOEA, ALLERGY TO METALS, OFF LABEL USE, ERYTHEMA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures NICKEL?

Labeling and FAERS entries often list Boiron in connection with NICKEL. 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.