FERRUM PHOSPHORICUM

N/A

Manufactured by Energique, Inc.

16 FDA adverse event reports analyzed

Last updated: 2026-04-15

About FERRUM PHOSPHORICUM

FERRUM PHOSPHORICUM is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Energique, Inc.. The most commonly reported adverse reactions for FERRUM PHOSPHORICUM include ABDOMINAL PAIN, ATRIAL FIBRILLATION, CONDITION AGGRAVATED, DIARRHOEA, ECZEMA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for FERRUM PHOSPHORICUM.

Top Adverse Reactions

ABDOMINAL PAIN1 reports
ATRIAL FIBRILLATION1 reports
CONDITION AGGRAVATED1 reports
DIARRHOEA1 reports
ECZEMA1 reports
EYE PAIN1 reports
HAEMATOCHEZIA1 reports
NAUSEA1 reports
OCULAR HYPERAEMIA1 reports
PHOTOPHOBIA1 reports
SICKLE CELL ANAEMIA1 reports
SKIN DISORDER1 reports
THROMBOTIC CEREBRAL INFARCTION1 reports
UVEITIS1 reports
VISUAL ACUITY REDUCED1 reports
WEIGHT INCREASED1 reports

Report Outcomes

Out of 4 classified reports for FERRUM PHOSPHORICUM:

Serious 100.0%Non-Serious 0.0%

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

Female3 (75.0%)
Male1 (25.0%)

Reports by Age

Age 451 reports
Age 501 reports
Age 861 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 FERRUM PHOSPHORICUM?

This profile reflects 16 FDA FAERS reports that mention FERRUM PHOSPHORICUM. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for FERRUM PHOSPHORICUM?

Frequently reported terms in FAERS include ABDOMINAL PAIN, ATRIAL FIBRILLATION, CONDITION AGGRAVATED, DIARRHOEA, ECZEMA, EYE PAIN. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures FERRUM PHOSPHORICUM?

Labeling and FAERS entries often list Energique, Inc. in connection with FERRUM PHOSPHORICUM. 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.