SODIUM AUROTIOSULFATE: 99 Adverse Event Reports & Safety Profile
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99
Total FAERS Reports
89 (89.9%)
Deaths Reported
72
Hospitalizations
99
As Primary/Secondary Suspect
65
Life-Threatening
72
Disabilities
First Report: 20080101 · Latest Report: 20150818
What Are the Most Common SODIUM AUROTIOSULFATE Side Effects?
#1 Most Reported
Drug intolerance
76 reports (76.8%)
#2 Most Reported
Drug ineffective
71 reports (71.7%)
#3 Most Reported
Synovitis
70 reports (70.7%)
All SODIUM AUROTIOSULFATE Side Effects by Frequency
| Side Effect | Reports | % of Total | Deaths | Hosp. |
|---|---|---|---|---|
| Drug intolerance | 76 | 76.8% | 71 | 52 |
| Drug ineffective | 71 | 71.7% | 63 | 46 |
| Synovitis | 70 | 70.7% | 63 | 46 |
| Hypertension | 68 | 68.7% | 61 | 46 |
| Product use issue | 68 | 68.7% | 61 | 44 |
| Intentional product use issue | 67 | 67.7% | 66 | 43 |
| Treatment failure | 67 | 67.7% | 60 | 43 |
| Contraindicated product administered | 65 | 65.7% | 58 | 42 |
| Product use in unapproved indication | 65 | 65.7% | 65 | 41 |
| Vomiting | 65 | 65.7% | 65 | 41 |
| Abdominal discomfort | 64 | 64.7% | 57 | 42 |
| Alopecia | 64 | 64.7% | 57 | 42 |
| Arthropathy | 64 | 64.7% | 58 | 42 |
| Therapeutic product effect incomplete | 63 | 63.6% | 56 | 39 |
| Wound | 62 | 62.6% | 62 | 38 |
| Drug hypersensitivity | 61 | 61.6% | 54 | 38 |
| General physical health deterioration | 61 | 61.6% | 54 | 40 |
| Glossodynia | 61 | 61.6% | 61 | 39 |
| Taste disorder | 61 | 61.6% | 61 | 37 |
| Hand deformity | 60 | 60.6% | 60 | 38 |
Who Reports SODIUM AUROTIOSULFATE Side Effects? Age & Gender Data
Gender: 100.0% female, 0.0% male. Average age: 41.7 years. Most reports from: CA. View detailed demographics →
Is SODIUM AUROTIOSULFATE Getting Safer? Reports by Year
| Year | Reports | Deaths | Hosp. |
|---|---|---|---|
| 2008 | 1 | 0 | 1 |
| 2015 | 4 | 4 | 4 |
What Is SODIUM AUROTIOSULFATE Used For?
| Indication | Reports |
|---|---|
| Product used for unknown indication | 85 |
Official FDA Label for SODIUM AUROTIOSULFATE
Official prescribing information from the FDA-approved drug label.