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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.

INTERLEUKIN-12 HUMAN RECOMBINANT: 11 Adverse Event Reports & Safety Profile

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11
Total FAERS Reports
0
Deaths Reported
1
Hospitalizations
11
As Primary/Secondary Suspect
1
Life-Threatening
Guna spa
Manufacturer

Route: ORAL · Manufacturer: Guna spa · HUMAN OTC DRUG · FDA Label: Available

First Report: 20170713 · Latest Report: 20170713

What Are the Most Common INTERLEUKIN-12 HUMAN RECOMBINANT Side Effects?

#1 Most Reported
Aspartate aminotransferase increased
4 reports (36.4%)
#2 Most Reported
Alanine aminotransferase increased
4 reports (36.4%)
#3 Most Reported
Lymphopenia
2 reports (18.2%)

All INTERLEUKIN-12 HUMAN RECOMBINANT Side Effects by Frequency

No side effect data available.

Who Reports INTERLEUKIN-12 HUMAN RECOMBINANT Side Effects? Age & Gender Data

Gender: 0.0% female, 100.0% male. Average age: 63.8 years. Most reports from: US. View detailed demographics →

Is INTERLEUKIN-12 HUMAN RECOMBINANT Getting Safer? Reports by Year

YearReportsDeathsHosp.
2017 1 0 1

View full timeline →

Official FDA Label for INTERLEUKIN-12 HUMAN RECOMBINANT

Official prescribing information from the FDA-approved drug label.

FDA Approved Uses (Indications)

Take 15 minutes before meals.

Dosage & Administration

DIRECTIONS Take 15 minutes before meals. Adults and children 12 years and older 20 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow. Children between 12 years and 6 years of age 10 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow. Children under 6 years 5 drops twice a day in a glass of water.

Warnings

WARNINGS Stop use and ask doctor if symptoms worsen or persist more than 3 days

Active Ingredient

ACTIVE INGREDIENTS/PURPOSE INTERLEUKIN-12 4C ANTI-ALLERGY IMMUNE SUPPORT

Inactive Ingredients

Inactive ingredient: Ethyl alcohol 30%.