POTASSIUM DICHROMATE

N/A

Manufactured by BM Private Limited

41 FDA adverse event reports analyzed

Last updated: 2026-04-15

About POTASSIUM DICHROMATE

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

Top Adverse Reactions

DRUG HYPERSENSITIVITY2 reports
FATIGUE2 reports
PAIN2 reports
ABDOMINAL PAIN UPPER1 reports
ANAEMIA1 reports
ANOREXIA1 reports
ANXIETY1 reports
ARTHRALGIA1 reports
ASTHENIA1 reports
BLOOD TRIGLYCERIDES INCREASED1 reports
CHEST PAIN1 reports
DYSKINESIA1 reports
DYSPNOEA1 reports
EAR PAIN1 reports
ERECTILE DYSFUNCTION1 reports
FALL1 reports
FLIGHT OF IDEAS1 reports
HEADACHE1 reports
INAPPROPRIATE AFFECT1 reports
INSOMNIA1 reports
MALIGNANT NEOPLASM PROGRESSION1 reports
MEDICATION ERROR1 reports
MUSCLE CRAMP1 reports
MYALGIA1 reports
NO ADVERSE EVENT1 reports
PAIN IN EXTREMITY1 reports
PERFORMANCE STATUS DECREASED1 reports
PRESSURE OF SPEECH1 reports
PRODUCT FORMULATION ISSUE1 reports
RASH VESICULAR1 reports
RENAL DISORDER1 reports
RHABDOMYOLYSIS1 reports
ROTATOR CUFF SYNDROME1 reports
SENSATION OF FOREIGN BODY1 reports
SENSORY DISTURBANCE1 reports
SINUSITIS1 reports
SPEECH DISORDER1 reports
WEIGHT INCREASED1 reports

Report Outcomes

Out of 6 classified reports for POTASSIUM DICHROMATE:

Serious 50.0%Non-Serious 50.0%

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

Male5 (83.3%)
Female1 (16.7%)

Reports by Age

Age 201 reports
Age 421 reports
Age 601 reports
Age 701 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 POTASSIUM DICHROMATE?

This profile reflects 41 FDA FAERS reports that mention POTASSIUM DICHROMATE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for POTASSIUM DICHROMATE?

Frequently reported terms in FAERS include DRUG HYPERSENSITIVITY, FATIGUE, PAIN, ABDOMINAL PAIN UPPER, ANAEMIA, ANOREXIA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures POTASSIUM DICHROMATE?

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