Skip to content
Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

MENADIONE: 20 Adverse Event Reports & Safety Profile

Boost Your Natural Energy & Metabolism

Mitolyn — 6 exotic plants to unlock your body's fat-burning power. 90-day guarantee.

Try Mitolyn Now
20
Total FAERS Reports
3 (15.0%)
Deaths Reported
12
Hospitalizations
20
As Primary/Secondary Suspect
1
Life-Threatening
2
Disabilities
Approved Prior to Jan 1, 1982
FDA Approved
Energique, Inc.
Manufacturer
Discontinued
Status

Route: ORAL · Manufacturer: Energique, Inc. · FDA Application: 002139 · HUMAN OTC DRUG · FDA Label: Available

First Report: 201404 · Latest Report: 20210907

What Are the Most Common MENADIONE Side Effects?

#1 Most Reported
Wheezing
7 reports (35.0%)
#2 Most Reported
Therapeutic product effect incomplete
7 reports (35.0%)
#3 Most Reported
Sleep disorder due to a general medical condition
7 reports (35.0%)

All MENADIONE Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Addison's disease 7 35.0% 0 7
Asthma 7 35.0% 0 7
Dyspnoea 7 35.0% 0 7
Infection 7 35.0% 0 7
Productive cough 7 35.0% 0 7
Sleep disorder due to a general medical condition 7 35.0% 0 7
Therapeutic product effect incomplete 7 35.0% 0 7
Wheezing 7 35.0% 0 7
Loss of personal independence in daily activities 6 30.0% 0 6

Who Reports MENADIONE Side Effects? Age & Gender Data

Gender: 59.1% female, 40.9% male. Average age: 52.1 years. Most reports from: CA. View detailed demographics →

Is MENADIONE Getting Safer? Reports by Year

YearReportsDeathsHosp.
2014 1 1 0
2016 1 0 0
2017 3 0 2
2018 1 1 1
2020 1 0 0
2021 1 1 1

View full timeline →

What Is MENADIONE Used For?

IndicationReports
Product used for unknown indication 14

Official FDA Label for MENADIONE

Official prescribing information from the FDA-approved drug label.

FDA Approved Uses (Indications)

INDICATIONS For the temporary relief of diarrhea, gas, cramping, fatigue, minor joint pain or swelling, or occasional headache due to sensitivity to phenolic compounds found in foods or other products.*

Dosage & Administration

DIRECTIONS: Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Warnings

WARNINGS: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Active Ingredient

ACTIVE INGREDIENT: (in each drop): 24.98% of Menadione 12X, 30X, 12C, 30C. 0.10% of Menadione 6X.

Inactive Ingredients

INACTIVE INGREDIENTS: Demineralized water, 20% Ethanol.