Intervention not reported
- Safety of non‐steroidal anti‐inflammatory drugs, including aspirin and paracetamol (acetaminophen) in people receiving… 2011 · Cochrane Headline outcomes onlyno estimate extracted7 studies · 283 participantsModerate
PGE1 showed no clear difference in adverse events (participants) compared with inositol niacinate (low certainty).
Summary of findings: urate oxidase may leads to higher frequency of adverse events ( compared with allopurinol (low certainty).
It is very uncertain whether probiotics changes withdrawal due to adverse events compared with 5‐aminosalicylic acid (5‐ASA) (mesalazine) (very low certainty).
Azathioprine or 6‐mercaptopurine may leads to higher withdrawal due to adverse events compared with 5‐aminosalicylic acid (low certainty).
Benzbromarone showed no clear difference in withdrawal due to adverse events compared with allopurinol (low certainty).
It is very uncertain whether probiotics changes serious adverse events (52 weeks) compared with 5‐aminosalicylic acid (5‐ASA) (mesalazine) (very low certainty).
The review found no eligible studies for this question.
Oral 5‐ASA showed no clear difference in serious adverse events compared with SASP (low certainty).
Once daily dosing showed no clear difference in serious adverse events compared with conventional dosing (low 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 serious adverse events compared with placebo (low certainty).
Once‐daily dosing showed no clear difference in serious adverse events compared with conventional dosing (moderate certainty).
Alteplase may leads to higher serious adverse events compared with urokinase (low certainty).
Streptokinase showed no clear difference in serious adverse events compared with urokinase (low certainty).
5‐ASAs showed no clear difference in serious adverse events compared with placebo (low certainty).
The review found no eligible studies for this question.
It is very uncertain whether 5‐ASA changes serious adverse events compared with purine antimetabolites (very low certainty).