Non‐serious adverse events · adults with cirrhosis and hepatic encephalopathy
1 finding from 1 review
Non‐serious adverse events · adults with oesophageal varices
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Diarrhoea · exacerbations of COPD
Antibiotics showed no clear difference in adverse events ‐ diarrhoea compared with placebo overall (moderate certainty).
1 finding from 1 review
Non‐serious adverse events · adults with cirrhosis and gastroesophageal varices
It is very uncertain whether carvedilol changes non‐serious adverse events compared with traditional, non‐selective beta‐blockers (very low certainty).
1 finding from 1 review
Systemic adverse events at · adults with centre‐involving diabetic macular oedema
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Systemic adverse events at · adults with centre‐involving diabetic macular oedema
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Systemic adverse events at · adults with centre‐involving diabetic macular oedema
Summary of findings: intravitreal anti‐VEGF plus intravitreal steroid showed no clear difference in systemic adverse events at compared with intravitreal anti‐VEGF (low certainty).
1 finding from 1 review
Frequency of adverse events ( · daytime workers
Morning bright light showed no clear difference in adverse events (frequency) compared with afternoon bright light (low certainty).
1 finding from 1 review
Adverse events 67.7 months · DCM (non‐ischaemic)
1 finding from 1 review
Non‐serious adverse events · people with venous leg ulcers
High frequency ultrasound probably leads to higher non‐serious adverse events compared with no ultrasound (moderate certainty).
1 finding from 1 review
Adverse events: malignancy · kidney transplant recipients
Low dose calcineurin inhibitors (CNI) showed no clear difference in adverse events: malignancy compared with to standard dose CNI (low certainty).
1 finding from 1 review
Adverse events: malignancy · kidney transplant recipients
Calcineurin inhibitor (CNI) withdrawal + mammalian target of… showed no clear difference in adverse events: malignancy compared with standard dose CNI (low certainty).
1 finding from 1 review
Adverse events: lymphocele · kidney transplant recipients
Calcineurin inhibitor (CNI) withdrawal + mammalian target of… showed no clear difference in adverse events: lymphocele compared with standard dose CNI (low certainty).
1 finding from 1 review
Adverse events: malignancy · kidney transplant recipients
Low dose CNI calcineurin inhibitor (CNI) + mammalian target of… showed no clear difference in adverse events: malignancy compared with standard dose CNI (low certainty).
1 finding from 1 review
Adverse events: malignancy · kidney transplant recipients
Calcineurin inhibitor (CNI) withdrawal showed no clear difference in adverse events: malignancy compared with standard dose CNI (low certainty).
1 finding from 1 review
Adverse events, short‐term · people of any age with an existing pressure ulcer of Category/Stage II or above
It is very uncertain whether foam dressing changes adverse events, short‐term compared with hydrogel dressing (very low certainty).
1 finding from 1 review
Adverse events, short‐term · people of any age with an existing pressure ulcer of Category/Stage II or above
It is very uncertain whether hydropolymer foam dressing changes adverse events, short‐term compared with silicone foam dressing (very low certainty).
1 finding from 1 review
Adverse events, short‐term · people of any age with an existing pressure ulcer of Category/Stage II or above
It is very uncertain whether foam dressings changes adverse events, short‐term compared with hydrocolloid dressings (very low certainty).
1 finding from 1 review
Intervention not reported
Non‐serious adverse events · people with pressure ulcers
The intervention may leads to higher non‐serious adverse events (low certainty).
1 finding from 1 review
Adverse events (grade ≥ 3) · previously untreated patients with mRCC
Interferon‐α combined with targeted therapies may leads to higher adverse events (grade ≥ 3) compared with standard targeted therapy (low certainty).
1 finding from 1 review