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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.

CONIUM MACULATUM FLOWERING TOP: 11 Adverse Event Reports & Safety Profile

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11
Total FAERS Reports
11 (100.0%)
Deaths Reported
2
Hospitalizations
11
As Primary/Secondary Suspect
Deseret Biologicals, Inc.
Manufacturer

Route: ORAL · Manufacturer: Deseret Biologicals, Inc. · HUMAN OTC DRUG · FDA Label: Available

First Report: 2017 · Latest Report: 2017

What Are the Most Common CONIUM MACULATUM FLOWERING TOP Side Effects?

#1 Most Reported
Completed suicide
9 reports (81.8%)
#2 Most Reported
Cardio-respiratory arrest
7 reports (63.6%)
#3 Most Reported
Toxicity to various agents
5 reports (45.5%)

All CONIUM MACULATUM FLOWERING TOP Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Completed suicide 9 81.8% 9 2
Cardio-respiratory arrest 7 63.6% 7 1
Toxicity to various agents 5 45.5% 5 0

Who Reports CONIUM MACULATUM FLOWERING TOP Side Effects? Age & Gender Data

Gender: 90.9% female, 9.1% male. Average age: 75.0 years. Most reports from: US. View detailed demographics →

Is CONIUM MACULATUM FLOWERING TOP Getting Safer? Reports by Year

YearReportsDeathsHosp.
2017 4 4 0

View full timeline →

What Is CONIUM MACULATUM FLOWERING TOP Used For?

IndicationReports
Product used for unknown indication 10

Official FDA Label for CONIUM MACULATUM FLOWERING TOP

Official prescribing information from the FDA-approved drug label.

FDA Approved Uses (Indications)

Uses Temporarily relieves occasional throat swelling, elevated body temperature, headaches, loss of appetite, discomfort in the parotid glands, stiff neck, nausea, vomiting, dry mouth, and discomfort when swallowing, talking, chewing, or drinking acidic beverages.* *CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED. This product is not intended to diagnose, treat, cure, or prevent any disease.

Dosage & Administration

Directions Take 15 minutes before meals. Adults and children twelve years and older: 20 drops in a little water, 2 times per day Children between 12 years and 6 years of age: 10 drops in a little water, 2 times per day Children under 6 years: consult a physician

Contraindications

Care & contra-indications: This is a homoeopathic remedy, no contra-indications are established.

Known Adverse Reactions

To Report SUSPECTED ADVERSE REACTIONS, contact Guna Inc at (484) 223-3500 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch

Warnings

Warning If symptoms persist, contact a licensed practitioner. If you have known sensitivity to any of the ingredients, please consult your licensed practitioner before use. If you are pregnant or nursing a baby, seek the advice of a health care professional before use. Keep out of the reach of children. Protect from light and heat.

Tamper

Evident Do not use this product if tamper evident strip is broken or removed from base of cap.

Active Ingredient

Active Ingredients Coneflower 1XHPUS Witch Hazel 2XHPUS Tribasic calcium phosphate 3XHPUS Goldenseal 4XHPUS Milkwort 4XHPUS Silicon dioxide 4XHPUS Poison Hemlock 4XHPUS Sodium tetrachloroaurate 5XHPUS Impure Calcium Carbonate 5XHPUS Bladder-wrack 5XHPUS Bushmaster viper venom 8XHPUS The letters HPUS indicates that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of United Sates. Purpose FOR TEMPORARY RELIEF OF SORE THROATS AND LYMPHATIC INFLAMMATION. Keep out of reach of children.

Dosage

Adults take 1 tablet three times daily, dissolving on the tongue. For severe symptoms, take one tablet every hour until improvement is felt. Children receive 1/2 tablet as above. Warnings If pregnant or breast-feeding, consult a health professional before use. (Read Suggested Use Section)

Inactive Ingredients Faex

Med. and Lactose

Inactive Ingredients

INACTIVE INGREDIENTS Active: As Above; Inactive: ENA 50% v/v and Purified Water q.s.