Birthweight (g) · Women receiving supplements in pregnancy
Any intermittent iron regimen (with or without other vitamins and… showed no clear difference in birthweight (g) compared with daily regimen (with same vitamins and minerals)‐infant outcomes (low certainty).
1 finding from 1 review
Gestational age (preterm birth < 37 weeks) · Women receiving supplements in pregnancy
Any intermittent iron regimen (with or without other vitamins and… showed no clear difference in premature birth (less than 37 weeks of gestation) compared with daily regimen (with same vitamins and minerals)‐infant outcomes (low certainty).
1 finding from 1 review
Neonatal mortality · Women receiving supplements in pregnancy
It is very uncertain whether any intermittent iron regimen (with or without other vitamins and… changes neonatal death (within 28 days after delivery) compared with daily regimen (with same vitamins and minerals)‐infant outcomes (very low certainty).
1 finding from 1 review
Congenital anomalies (including neural tube defects) · Women receiving supplements in pregnancy
1 finding from 1 review
Maternal anaemia at term (Hb less than 110 g/L at 37 weeks' gestation or more) (ALL) · Women receiving supplements in pregnancy
It is very uncertain whether any intermittent iron regimen (with or without other vitamins and… changes maternal anaemia at term (Hb less than 110 g/L at 37 weeks'… compared with daily regimen (with same vitamins and minerals)‐maternal outcomes (very low certainty).
1 finding from 1 review
Maternal death · Women receiving supplements in pregnancy
Any intermittent iron regimen (with or without other vitamins and… led to lower maternal death (death while pregnant or within 42 days of… compared with daily regimen (with same vitamins and minerals)‐maternal outcomes; GRADE not reported.
1 finding from 1 review
Number of responders ‐ disease activity not stated (12 weeks) · IBD patients
Oral ferric maltol showed no clear difference in number of responders ‐ disease activity not stated (12 weeks) compared with IV ferric carboxymaltose (low certainty).
1 finding from 1 review
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