INFLUENZINUM

N/A

Manufactured by Boiron

31 FDA adverse event reports analyzed

Last updated: 2026-04-15

About INFLUENZINUM

INFLUENZINUM is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Boiron. The most commonly reported adverse reactions for INFLUENZINUM include ANGIOEDEMA, AORTIC DILATATION, BACK PAIN, BLOOD PRESSURE INCREASED, CEREBROVASCULAR ACCIDENT. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for INFLUENZINUM.

Top Adverse Reactions

ANGIOEDEMA1 reports
AORTIC DILATATION1 reports
BACK PAIN1 reports
BLOOD PRESSURE INCREASED1 reports
CEREBROVASCULAR ACCIDENT1 reports
CONTUSION1 reports
DYSPHAGIA1 reports
DYSPHONIA1 reports
EYELID OEDEMA1 reports
FACE OEDEMA1 reports
FALL1 reports
GRIP STRENGTH DECREASED1 reports
HAEMORRHOIDS1 reports
INFUSION RELATED REACTION1 reports
LANGUAGE DISORDER1 reports
LIP OEDEMA1 reports
LOCALISED OEDEMA1 reports
MALAISE1 reports
MALIGNANT NEOPLASM PROGRESSION1 reports
MEMORY IMPAIRMENT1 reports
MOBILITY DECREASED1 reports
OEDEMA1 reports
PAINFUL RESPIRATION1 reports
RASH PRURITIC1 reports
RESPIRATORY RATE INCREASED1 reports
RESPIRATORY TRACT CONGESTION1 reports
SINUSITIS1 reports
URINARY TRACT INFECTION1 reports
VISION BLURRED1 reports
WEIGHT DECREASED1 reports
WEIGHT INCREASED1 reports

Report Outcomes

Out of 2 classified reports for INFLUENZINUM:

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

Female2 (100.0%)

Reports by Age

Age 391 reports
Age 771 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 INFLUENZINUM?

This profile reflects 31 FDA FAERS reports that mention INFLUENZINUM. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for INFLUENZINUM?

Frequently reported terms in FAERS include ANGIOEDEMA, AORTIC DILATATION, BACK PAIN, BLOOD PRESSURE INCREASED, CEREBROVASCULAR ACCIDENT, CONTUSION. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures INFLUENZINUM?

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