SOLOSTAR for Device therapy: Side Effects & Safety Data
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There are 89 adverse event reports in the FDA FAERS database where SOLOSTAR was used for Device therapy.
Most Reported Side Effects for SOLOSTAR
| Side Effect | Reports | % | Deaths | Hosp. |
|---|---|---|---|---|
| Blood glucose increased | 253 | 33.6% | 0 | 14 |
| Injection site pain | 99 | 13.1% | 0 | 4 |
| Injection site haemorrhage | 69 | 9.2% | 0 | 1 |
| Drug dose omission | 59 | 7.8% | 0 | 3 |
| Visual impairment | 57 | 7.6% | 0 | 1 |
| Blood glucose decreased | 52 | 6.9% | 0 | 2 |
| Injection site bruising | 52 | 6.9% | 0 | 1 |
| Incorrect product storage | 51 | 6.8% | 0 | 0 |
| Injury associated with device | 51 | 6.8% | 0 | 0 |
| Feeling abnormal | 33 | 4.4% | 0 | 0 |
| Malaise | 31 | 4.1% | 0 | 1 |
| Visual acuity reduced | 31 | 4.1% | 0 | 0 |
| Glycosylated haemoglobin increased | 28 | 3.7% | 0 | 1 |
| Blood glucose abnormal | 27 | 3.6% | 0 | 0 |
| Cataract | 21 | 2.8% | 0 | 1 |