CHLORHEXIDINE\SODIUM FLUORIDE\TRICLOSAN\ZINC: 31 Adverse Event Reports & Safety Profile
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31
Total FAERS Reports
23 (74.2%)
Deaths Reported
31
Hospitalizations
31
As Primary/Secondary Suspect
11
Life-Threatening
11
Disabilities
Active Ingredient: CHLORHEXIDINE\SODIUM FLUORIDE\TRICLOSAN\ZINC CHLORIDE ·
What Are the Most Common CHLORHEXIDINE\SODIUM FLUORIDE\TRICLOSAN\ZINC Side Effects?
#1 Most Reported
Helicobacter infection
25 reports (80.6%)
#2 Most Reported
Type 2 diabetes mellitus
24 reports (77.4%)
#3 Most Reported
Off label use
24 reports (77.4%)
All CHLORHEXIDINE\SODIUM FLUORIDE\TRICLOSAN\ZINC Side Effects by Frequency
| Side Effect | Reports | % of Total | Deaths | Hosp. |
|---|---|---|---|---|
| Helicobacter infection | 25 | 80.7% | 23 | 25 |
| Drug ineffective | 24 | 77.4% | 23 | 24 |
| Drug intolerance | 24 | 77.4% | 23 | 24 |
| Hypertension | 24 | 77.4% | 23 | 24 |
| Off label use | 24 | 77.4% | 23 | 24 |
| Type 2 diabetes mellitus | 24 | 77.4% | 23 | 24 |
| Abdominal discomfort | 23 | 74.2% | 21 | 23 |
| Alopecia | 23 | 74.2% | 21 | 23 |
| Arthralgia | 23 | 74.2% | 21 | 23 |
| Fatigue | 23 | 74.2% | 21 | 23 |
| Hepatic enzyme increased | 23 | 74.2% | 21 | 23 |
| Hypoaesthesia | 23 | 74.2% | 23 | 23 |
| Infusion related reaction | 23 | 74.2% | 21 | 23 |
| Blood cholesterol increased | 22 | 71.0% | 21 | 22 |
| Dizziness | 22 | 71.0% | 21 | 22 |
| Fibromyalgia | 22 | 71.0% | 21 | 22 |
| General physical health deterioration | 22 | 71.0% | 21 | 22 |
| Headache | 22 | 71.0% | 21 | 22 |
| Intentional product use issue | 22 | 71.0% | 21 | 22 |
| Product use in unapproved indication | 22 | 71.0% | 21 | 22 |
Who Reports CHLORHEXIDINE\SODIUM FLUORIDE\TRICLOSAN\ZINC Side Effects? Age & Gender Data
Gender: 100.0% female, 0.0% male. Average age: 43.0 years. Most reports from: CA. View detailed demographics →
What Is CHLORHEXIDINE\SODIUM FLUORIDE\TRICLOSAN\ZINC Used For?
| Indication | Reports |
|---|---|
| Product used for unknown indication | 28 |
Official FDA Label for CHLORHEXIDINE\SODIUM FLUORIDE\TRICLOSAN\ZINC
Official prescribing information from the FDA-approved drug label.