Table 4.
Proportional meta-analysis of the frequency of adverse events.
Frequency of AE | 95% CI | Chi-square | p | PI | Included studies (n) | Included patients (n) | |
---|---|---|---|---|---|---|---|
Pasireotide | |||||||
SAE | 0.17 | 0.04, 0.49 | 0.6 | 0.219 | – | 8 | 522 |
Diabetes | 0.21 | 0.15, 0.28 | 2.1 | 0.076 | 0.11, 0.36 | 8 | 522 |
Randomized only | 0.25 | 0.21, 0.30 | 0 | – | – | 2 | 312 |
Hyperglycemia | 0.29 | 0.15, 0.49 | 18.4 | 0 | 0.06, 0.72 | 8 | 522 |
Randomized only | 0.48 | 0.42, 0.53 | 0 | – | – | 2 | 312 |
Diarrhea | 0.3 | 0.16, 0.48 | 17.7 | 0 | 0.08, 0.68 | 5 | 467 |
Cholecystitis | 0.13 | 0.02, 0.54 | 73.2 | 0 | 0, 0.92 | 5 | 467 |
Randomized only | 0.38 | 0.33, 0.44 | 0 | – | – | 2 | 312 |
Nausea | 0.21 | 0.12, 0.33 | 7.8 | 0.003 | 0.06, 0.50 | 5 | 467 |
Randomized only | 0.29 | 0.24, 0.34 | 0 | – | – | 2 | 312 |
Abdominal pain | 0.29 | 0.14, 0.49 | 0.8 | 0.18 | – | 3 | 331 |
Randomized only | 0.21 | 0.16, 0.25 | 0 | – | – | 2 | 312 |
Headache | 0.24 | 0.19, 0.28 | 0 | – | – | 3 | 331 |
Randomized only | 0.23 | 0.18, 0.28 | 0 | – | – | 2 | 312 |
Fatigue | 0.2 | 0.16, 0.25 | 0 | – | – | 4 | 363 |
Cabergoline | |||||||
Escape from treatment | 0.14 | 0.09, 0.21 | 0 | – | – | 6 | 143 |
Vertigo | 0.12 | 0.07, 0.19 | 0 | – | – | 6 | 143 |
Nausea | 0.1 | 0.06, 0.16 | 0 | – | – | 6 | 143 |
Fatigue | 0.07 | 0.03, 0.18 | 0.1 | 0.373 | – | 6 | 143 |
Ketoconazole | |||||||
Elevated transaminasesa | 0.14 | 0.11, 0.18 | 0 | – | – | 8 | 366 |
Diarrhea and/or abdominal pain | 0.08 | 0.04, 0.18 | 2.6 | 0.052 | – | 8 | 366 |
Rash | 0.03 | 0.01, 0.09 | 2.4 | 0.06 | – | 8 | 366 |
Adrenal insufficiency | 0.06 | 0.04, 0.10 | 0.2 | 0.327 | – | 8 | 366 |
Metyrapone | |||||||
Nausea | 0.18 | 0.07, 0.40 | 1.9 | 0.085 | – | 4 | 89 |
Vertigo | 0.17 | 0.10, 0.26 | 0 | – | – | 4 | 89 |
Hirsutism | 0.17 | 0.10, 0.26 | 0 | – | – | 4 | 89 |
Fatigue | 0.07 | 0.01, 0.40 | 0.1 | 0.351 | – | 4 | 89 |
Hypokalemia | 0.09 | 0.05, 0.17 | 0 | – | – | 4 | 89 |
AE, adverse events; CI, confidence interval; Chi-square, heterogeneity; PI, predictive interval; SAE, serious adverse events.
Includes an increase in alanine aminotransferase and alkaline phosphatase.