FERROUS FUMARATE, FOLIC ACID

N/A

Manufactured by PureTek Corporation

43 FDA adverse event reports analyzed

Last updated: 2026-04-15

About FERROUS FUMARATE, FOLIC ACID

FERROUS FUMARATE, FOLIC ACID is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by PureTek Corporation. The most commonly reported adverse reactions for FERROUS FUMARATE, FOLIC ACID include DIARRHOEA, ALCOHOL ABUSE, ALOPECIA, ARTHRALGIA, ATRIAL FIBRILLATION. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for FERROUS FUMARATE, FOLIC ACID.

Top Adverse Reactions

DIARRHOEA2 reports
ALCOHOL ABUSE1 reports
ALOPECIA1 reports
ARTHRALGIA1 reports
ATRIAL FIBRILLATION1 reports
BLOOD CREATININE INCREASED1 reports
BLOOD UREA INCREASED1 reports
CALCIPHYLAXIS1 reports
CATARACT1 reports
CEREBRAL ISCHAEMIA1 reports
CIRCULATORY COLLAPSE1 reports
CONTUSION1 reports
CYTOMEGALOVIRUS INFECTION1 reports
DEATH1 reports
DEPRESSION1 reports
DIABETIC ULCER1 reports
DIALYSIS1 reports
ECCHYMOSIS1 reports
EPISTAXIS1 reports
ERYTHEMA1 reports
FATIGUE1 reports
FLUSHING1 reports
HAEMATURIA1 reports
HEPATITIS B1 reports
HEPATITIS C1 reports
INFECTION1 reports
INTERNATIONAL NORMALISED RATIO INCREASED1 reports
LIVER FUNCTION TEST ABNORMAL1 reports
NOCTURIA1 reports
OEDEMA PERIPHERAL1 reports
PAIN IN JAW1 reports
PARAESTHESIA1 reports
PLATELET COUNT ABNORMAL1 reports
PLATELET COUNT DECREASED1 reports
RECTAL HAEMORRHAGE1 reports
SUICIDAL IDEATION1 reports
TELANGIECTASIA1 reports
TREMOR1 reports
TUBULOINTERSTITIAL NEPHRITIS1 reports
URINARY TRACT INFECTION1 reports
VIRAL INFECTION1 reports
VISION BLURRED1 reports

Report Outcomes

Out of 8 classified reports for FERROUS FUMARATE, FOLIC ACID:

Serious 75.0%Non-Serious 25.0%

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

Male6 (75.0%)
Female2 (25.0%)

Reports by Age

Age 311 reports
Age 561 reports
Age 751 reports
Age 771 reports
Age 841 reports
Age 851 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 FERROUS FUMARATE, FOLIC ACID?

This profile reflects 43 FDA FAERS reports that mention FERROUS FUMARATE, FOLIC ACID. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for FERROUS FUMARATE, FOLIC ACID?

Frequently reported terms in FAERS include DIARRHOEA, ALCOHOL ABUSE, ALOPECIA, ARTHRALGIA, ATRIAL FIBRILLATION, BLOOD CREATININE INCREASED. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures FERROUS FUMARATE, FOLIC ACID?

Labeling and FAERS entries often list PureTek Corporation in connection with FERROUS FUMARATE, FOLIC ACID. 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.