AFINITOR for Tuberous sclerosis: Side Effects & Safety Data
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There are 11 adverse event reports in the FDA FAERS database where AFINITOR was used for Tuberous sclerosis.
Most Reported Side Effects for AFINITOR
| Side Effect | Reports | % | Deaths | Hosp. |
|---|---|---|---|---|
| Death | 192 | 27.1% | 192 | 22 |
| Malignant neoplasm progression | 70 | 9.9% | 47 | 25 |
| Dyspnoea | 58 | 8.2% | 19 | 28 |
| Stomatitis | 57 | 8.1% | 17 | 17 |
| Diarrhoea | 47 | 6.6% | 11 | 27 |
| Fatigue | 44 | 6.2% | 9 | 16 |
| Cough | 34 | 4.8% | 8 | 16 |
| Pyrexia | 34 | 4.8% | 10 | 29 |
| Rash | 29 | 4.1% | 7 | 10 |
| Nausea | 28 | 4.0% | 7 | 15 |
| Drug ineffective | 27 | 3.8% | 5 | 5 |
| Anaemia | 26 | 3.7% | 11 | 14 |
| General physical health deterioration | 26 | 3.7% | 17 | 14 |
| Pneumonitis | 26 | 3.7% | 9 | 10 |
| Asthenia | 25 | 3.5% | 13 | 19 |
Other Indications for AFINITOR
Breast cancer (153)
Breast cancer metastatic (85)
Pancreatic neuroendocrine tumour (41)
Renal cancer (35)
Metastatic renal cell carcinoma (27)
Renal cell carcinoma (27)
Off label use (26)
Neuroendocrine tumour (24)
Angiomyolipoma (17)
Neoplasm malignant (13)