29. Overview of all interventions in the serious adverse events analysis.
Treatment | RCTs | Participants |
Antidepressants with ≥ 200 participants | ||
Desvenlafaxine high dose | 2 | 691 |
Duloxetine high dose | 12 | 1803 |
Duloxetine low dose | 4 | 473 |
Duloxetine standard dose | 15 | 2507 |
Esreboxetine high dose | 1 | 281 |
Esreboxetine standard dose | 1 | 556 |
Milnacipran high dose | 7 | 1569 |
Milnacipran standard dose | 7 | 1240 |
Milnacipran dose unable to be categorised | 3 | 203 |
Mirtazapine standard dose | 3 | 243 |
Antidepressants with < 200 participants (excluded from summaries) | ||
Amitriptyline high dose | 1 | 96 |
Amitriptyline low dose | 1 | 32 |
Amitriptyline standard dose | 3 | 114 |
Amitriptyline dose unable to be categorised | 1 | 25 |
Bupropion standard dose | 1 | 54 |
Citalopram standard dose | 2 | 34 |
Desipramine low dose | 1 | 38 |
Desipramine + cognitive behavioural therapy | 1 | 37 |
Desvenlafaxine standard dose | 2 | 199 |
Esreboxetine dose unable to be categorised | 1 | 134 |
Imipramine low dose | 1 | 18 |
Imipramine standard dose | 1 | 51 |
Milnacipran standard + cognitive behavioural therapy | 1 | 17 |
Mirtazapine low dose | 1 | 26 |
Nortriptyline low dose | 2 | 137 |
Nortriptyline unable to be categorised | 1 | 56 |
Nortriptyline unable to be categorised + cognitive behavioural therapy | 1 | 41 |
Nortriptyline unable to be categorised + disease management | 1 | 37 |
Paroxetine low dose | 2 | 62 |
Paroxetine dose unable to be categorised | 2 | 152 |
Reboxetine standard dose | 1 | 18 |
Sertraline high dose | 1 | 30 |
Trazadone + gabapentin | 1 | 94 |
Venlafaxine high dose | 1 | 82 |
Venlafaxine low dose | 1 | 82 |
Venlafaxine standard dose | 1 | 86 |
Non‐antidepressant interventions (excluded from summaries) | ||
Carbamazepine | 2 | 99 |
Cognitive behavioural therapy | 3 | 72 |
Coping skills training | 1 | 29 |
Disease management | 1 | 24 |
Gabapentin | 2 | 56 |
Nabilone | 1 | 32 |
Pregabalin | 3 | 643 |
Terbutaline | 1 | 51 |
RCT: randomised controlled trial Participant numbers reflect the total number of participants receiving the antidepressant. |