Serious adverse events (12 weeks) · IBD patients
It is very uncertain whether oral ferric maltol changes serious adverse events (12 weeks) compared with IV ferric carboxymaltose (very low certainty).
1 finding from 1 review
Separation from mother for treatment of hypoglycaemia · newborn infants at risk of neonatal hypoglycaemia
Dextrose gel showed no clear difference in separation from mother for treatment of hypoglycaemia (infant nursed… compared with placebo (low certainty).
1 finding from 1 review
Number of responders ‐ mild to moderate disease (12 weeks) · IBD patients
IV ferric carboxymaltose showed no clear difference in number of responders ‐ mild to moderate disease (16 weeks) compared with oral iron sulphate (low certainty).
1 finding from 1 review
Serious adverse events ‐ mild to moderate disease (16 weeks) · IBD patients
It is very uncertain whether IV ferric carboxymaltose changes serious adverse events ‐ mild to moderate disease (16 weeks) compared with oral iron sulphate (very low certainty).
1 finding from 1 review
Intervention not reported
Low Hb deferral ‐ at first donation visit after commencement of treatment · patients with iron deficiency and/or anaemia in blood donors
The intervention probably leads to lower low Hb deferral ‐ at first donation visit after commencement of… (moderate certainty).
1 finding from 1 review
Intervention not reported
Low Hb deferral ‐ after multiple donation visits · patients with iron deficiency and/or anaemia in blood donors
The intervention probably leads to lower low Hb deferral ‐ after multiple donation visits (moderate certainty).
1 finding from 1 review
Intervention not reported
Hb (g/L) ‐ before further donation Scale from: 123 to 152 · patients with iron deficiency and/or anaemia in blood donors
1 finding from 1 review
Intervention not reported
Hb (g/L) ‐ after subsequent donation(s) Scale from: 127.3 to 129 · patients with iron deficiency and/or anaemia in blood donors
1 finding from 1 review
Intervention not reported
Serum ferritin (ng/mL) ‐ before further donation Scale from: 12.9 to 57.8 · patients with iron deficiency and/or anaemia in blood donors
1 finding from 1 review
Intervention not reported
Serum ferritin (ng/mL) ‐ after subsequent donation(s) Scale from: 18 to 19 · patients with iron deficiency and/or anaemia in blood donors
1 finding from 1 review
Intervention not reported
Adverse effects (any) · patients with iron deficiency and/or anaemia in blood donors
The intervention probably leads to higher adverse effects (any) (moderate certainty).
1 finding from 1 review
Number of responders · IBD patients
It is very uncertain whether IM erythropoietin changes number of responders ‐ active disease (12 weeks) compared with oral placebo (very low certainty).
1 finding from 1 review
Serious adverse events · IBD patients
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Number of responders · IBD patients
Intravenous preparations may leads to higher number of responders compared with oral preparations (low certainty).
1 finding from 1 review
Withdrawals due to adverse events · IBD patients
Intravenous preparations may leads to lower withdrawal due to adverse events compared with oral preparations (low certainty).
1 finding from 1 review
Intervention not reported
Ferritin: final or change (µg/L) · adults and children with CKD
1 finding from 1 review
Intervention not reported
TSAT: final or change (%) · adults and children with CKD
1 finding from 1 review
Intervention not reported
HCT (%) · adults and children with CKD
1 finding from 1 review
Intervention not reported
ESA dose: final or change · adults and children with CKD
1 finding from 1 review
Intervention not reported
eGFR: final or change (mL/min) · adults and children with CKD
1 finding from 1 review