Table 3.
Side Effect | Number of Particular Adverse Events | |
---|---|---|
Everolimus | Sirolimus | |
dyslipidemia (mostly hypertriglicerydemia) | 6 | 3 |
transient lymphopenia | 3 | 0 |
infections | 3 | 1 (sepsis) |
mouth ulcers/mucositis | 2 | 1 |
acne | 2 | 0 |
changes in phosphate levels | 2 | 0 |
increased cholinesterase | 2 | 0 |
transient neutropenia | 2 | 1 |
diarrhea/constipation | 1 | 1 |
transient hypokalemia | 1 | 0 |
transient anemia | 1 | 0 |
pulmonary hemorrhage | 1 | 0 |
elevated liver enzymes | 1 | 0 |
decreased CD4/CD8 ratio | 1 | 0 |
hyponatremia | 1 (association with everolimus is doubtful because the patient also received diuretics) | 0 |
fever without evidence of infection | 0 | 1 |
none reported (no. of patients) | 7 | 4 |
no data (no. of studies) | 7 | 2 |
Patients in whom side effects were monitored (n = 33). There was a possibility of more than 1 adverse event per patient.