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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.

COBALT: 22 Adverse Event Reports & Safety Profile

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22
Total FAERS Reports
0
Deaths Reported
2
Hospitalizations
22
As Primary/Secondary Suspect
Boiron
Manufacturer

Drug Class: Allergens [CS] · Route: ORAL · Manufacturer: Boiron · HUMAN OTC DRUG · FDA Label: Available

First Report: 20061023 · Latest Report: 20220101

What Are the Most Common COBALT Side Effects?

#1 Most Reported
Drug hypersensitivity
16 reports (72.7%)
#2 Most Reported
Rash
2 reports (9.1%)
#3 Most Reported
Pruritus
2 reports (9.1%)

All COBALT Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Drug hypersensitivity 16 72.7% 0 0

Who Reports COBALT Side Effects? Age & Gender Data

Gender: 100.0% female, 0.0% male. Average age: 56.6 years. Most reports from: US. View detailed demographics →

Is COBALT Getting Safer? Reports by Year

YearReportsDeathsHosp.
2006 1 0 0
2016 1 0 1
2022 1 0 0

View full timeline →

What Is COBALT Used For?

IndicationReports
Product used for unknown indication 10

Other Drugs in Same Class: Allergens [CS]

Official FDA Label for COBALT

Official prescribing information from the FDA-approved drug label.

FDA Approved Uses (Indications)

Relieves low back pain * Uses: See symptoms on front panel.

Dosage & Administration

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

Active Ingredient

COBALTUM METALLICUM 200CK HPUS Less than 10 -12 mg cobalt per pellet Active ingredient**: See product name on front panel (contains 0.443 mg of the active ingredient per pellet).

Inactive Ingredients

lactose, sucrose