| Ref (type) | Population | Outcome, Interventions | Results and statistical analysis | Effect size | Favours |
| Adverse effects | |||||
|
RCT Crossover design |
41 people with a proven first episode of PCP |
Major adverse effects
10/20 (50%) with intravenous pentamidine 11/20 (55%) with TMP–SMX |
P = 0.9 |
Not significant | |
|
RCT Crossover design |
187 people with suspected PCP; 163 people with confirmed diagnoses (only those with confirmed diagnoses and who gave consent were evaluated further) |
Proportion of people changing treatment because of adverse effects
17/68 (25%) with intravenous pentamidine 31/92 (34%) with TMP–SMX |
P = 0.23 |
Not significant | |
|
RCT Crossover design |
70 people with confirmed or presumed PCP |
Adverse effects requiring cessation of treatment
with intravenous pentamidine with TMP–SMX |