SELENIUM

N/A

Manufactured by BM Private Limited

10,707 FDA adverse event reports analyzed

Last updated: 2026-04-15

About SELENIUM

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

Top Adverse Reactions

FATIGUE467 reports
HEADACHE326 reports
DIARRHOEA308 reports
NAUSEA303 reports
PAIN280 reports
ARTHRALGIA257 reports
DIZZINESS250 reports
DRUG INEFFECTIVE234 reports
DYSPNOEA198 reports
INSOMNIA189 reports
PAIN IN EXTREMITY182 reports
OFF LABEL USE176 reports
MUSCLE SPASMS175 reports
ANXIETY174 reports
WEIGHT DECREASED170 reports
ASTHENIA169 reports
PRURITUS157 reports
RASH155 reports
BACK PAIN148 reports
FALL143 reports
COUGH141 reports
VOMITING140 reports
FEELING ABNORMAL136 reports
WEIGHT INCREASED132 reports
MALAISE123 reports
ALOPECIA120 reports
MYALGIA120 reports
PYREXIA117 reports
CONSTIPATION115 reports
DEATH113 reports
PNEUMONIA112 reports
GAIT DISTURBANCE110 reports
PARAESTHESIA106 reports
DECREASED APPETITE105 reports
DEPRESSION103 reports
PERIPHERAL SWELLING101 reports
ABDOMINAL PAIN UPPER99 reports
HYPOAESTHESIA96 reports
COVID 1995 reports
PRODUCT DOSE OMISSION ISSUE92 reports
NEUROPATHY PERIPHERAL90 reports
CONDITION AGGRAVATED89 reports
NASOPHARYNGITIS88 reports
DYSPEPSIA86 reports
ERYTHEMA85 reports
MUSCULAR WEAKNESS85 reports
URINARY TRACT INFECTION85 reports
SINUSITIS84 reports
ABDOMINAL DISCOMFORT82 reports
BLOOD PRESSURE INCREASED82 reports
TINNITUS82 reports
CHEST PAIN81 reports
ABDOMINAL PAIN80 reports
HYPERTENSION79 reports
PALPITATIONS79 reports
ANAEMIA78 reports
JOINT SWELLING76 reports
INFECTION74 reports
SOMNOLENCE73 reports
EMOTIONAL DISTRESS72 reports
OROPHARYNGEAL PAIN71 reports
VISUAL IMPAIRMENT70 reports
CONTUSION68 reports
DISCOMFORT68 reports
FLUSHING68 reports
MIGRAINE68 reports
CHEST DISCOMFORT67 reports
PLATELET COUNT DECREASED66 reports
HYPOTENSION65 reports
BLOOD GLUCOSE INCREASED64 reports
OEDEMA PERIPHERAL64 reports
TREMOR64 reports
HYPERHIDROSIS63 reports
WHITE BLOOD CELL COUNT DECREASED63 reports
ATRIAL FIBRILLATION62 reports
DRY SKIN61 reports
HYPERSENSITIVITY61 reports
VISION BLURRED61 reports
SLEEP DISORDER60 reports
GASTROOESOPHAGEAL REFLUX DISEASE59 reports
BALANCE DISORDER57 reports
MEMORY IMPAIRMENT57 reports
SEIZURE56 reports
CHILLS55 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION55 reports
OSTEOARTHRITIS55 reports
PRODUCT USE ISSUE55 reports
HAEMOGLOBIN DECREASED54 reports
ABDOMINAL DISTENSION53 reports
INFLUENZA53 reports
PRODUCT USE IN UNAPPROVED INDICATION53 reports
CONFUSIONAL STATE51 reports
ARTHRITIS50 reports
DEHYDRATION50 reports
HEART RATE INCREASED50 reports
HOT FLUSH50 reports
BRONCHITIS49 reports
DRUG HYPERSENSITIVITY48 reports
DRUG INTERACTION48 reports
DRY MOUTH48 reports

Report Outcomes

Out of 4,079 classified reports for SELENIUM:

Serious 63.2%Non-Serious 36.8%

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

Female2,485 (65.0%)
Male1,333 (34.9%)
Unknown6 (0.2%)

Reports by Age

Age 6785 reports
Age 7285 reports
Age 6476 reports
Age 5673 reports
Age 7371 reports
Age 7070 reports
Age 6869 reports
Age 6268 reports
Age 6668 reports
Age 7866 reports
Age 6065 reports
Age 6365 reports
Age 7465 reports
Age 6564 reports
Age 7762 reports
Age 7161 reports
Age 5156 reports
Age 5955 reports
Age 6955 reports
Age 7654 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 SELENIUM?

This profile reflects 10,707 FDA FAERS reports that mention SELENIUM. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for SELENIUM?

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

Who manufactures SELENIUM?

Labeling and FAERS entries often list BM Private Limited in connection with SELENIUM. 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.