Oral 5‐ASA vs SASP
The review found no eligible studies for this question.
- Oral 5‐aminosalicylic acid for induction of remission in ulcerative colitis 2020 · Cochrane Headline outcomes onlyno estimate extractedStudies not reportedNo studies found
The review found no eligible studies for this question.
Oral 5‐ASA probably leads to lower adverse events compared with SASP (moderate certainty).
Oral 5‐ASA showed no clear difference in serious adverse events compared with SASP (low certainty).
Oral 5‐ASA probably leads to lower withdrawal due to adverse events compared with SASP (moderate certainty).
Once daily dosing showed no clear difference in failure to induce global or clinical remission compared with conventional dosing (high certainty).
Once daily dosing showed no clear difference in failure to induce global or clinical improvement compared with conventional dosing (moderate certainty).
Once daily dosing showed no clear difference in failure to induce endoscopic remission compared with conventional dosing (high certainty).
Once daily dosing showed no clear difference in failure to adhere to medication regimen compared with conventional dosing (low certainty).
Once daily dosing showed no clear difference in adverse events compared with conventional dosing (moderate certainty).
Oral 5‐ASA probably leads to lower failure to induce global or clinical improvement compared with placebo (moderate certainty).
Once daily dosing showed no clear difference in serious adverse events compared with conventional dosing (low certainty).
Once daily dosing showed no clear difference in withdrawal due to adverse events compared with conventional dosing (low certainty).
Oral 5‐ASA showed no clear difference in failure to induce global or clinical remission compared with comparator 5‐ASA (moderate certainty).
Oral 5‐ASA showed no clear difference in failure to induce global or clinical improvement compared with comparator 5‐ASA (moderate certainty).
The review found no eligible studies for this question.
The review found no eligible studies for this question.
Oral 5‐ASA showed no clear difference in adverse events compared with comparator 5‐ASA (moderate certainty).
Oral 5‐ASA showed no clear difference in serious adverse events compared with comparator 5‐ASA (low certainty).
Oral 5‐ASA showed no clear difference in withdrawal due to adverse events compared with comparator 5‐ASA (moderate certainty).
Oral 5‐ASA probably leads to lower failure to induce endoscopic remission compared with placebo (moderate certainty).