Oral iron is slow to rebuild stores, and its side effects, including nausea, abdominal pain and constipation, mean many people struggle to keep taking it. An infusion aims to replace iron stores in a single sitting.
This page sets out the case for your doctor's caution, then the case against it, then the situations where an infusion is a reasonable thing to ask for.
Intravenous iron dispensing in Australia, 2013 to 2024
A 2026 analysis of Pharmaceutical Benefits Scheme dispensing data tracked intravenous iron among Australian women aged 18 to 44. In 2013, 0.3 in every 100 women were dispensed it. By 2024 that had risen to 5.0 in every 100, or one woman in 20, and total spending on the medicine alone rose from $1.1 million to $82.3 million.
A community screening study of 640 women of reproductive age in Western Australia found that a history of iron infusion was common.
The authors of the national analysis also found more than threefold variation in use between states and territories, and concluded that the rapid rise and the degree of variation raise questions about whether intravenous iron is being prescribed appropriately and cost-effectively.
Reason 1: oral iron as first-line treatment
Australian Prescriber describes oral iron as the first-line and safest treatment for iron deficiency, and says most people with iron deficiency can be given oral supplements. Iron studies are then repeated after 60 to 90 days to see whether it has worked.
A separate Australian Prescriber article states that intravenous iron is usually only indicated when oral iron has failed, and that an infusion is rarely urgent.
A general practitioner (GP) who suggests tablets first is following the documents they are expected to follow. Whether the tablets were given a fair trial is covered in why your iron tablets aren't raising your ferritin.
Reason 2: the side effects of intravenous iron
Australian Prescriber states that the use of intravenous iron should be limited because of three adverse effects in particular: permanent skin staining, low blood phosphate, and rarely anaphylaxis.
Low phosphate after the infusion
Some intravenous iron products cause the kidneys to excrete more phosphate, which lowers the level in the blood. Concern about this has grown from reports of osteomalacia, a softening of bone, and fractures. The effect depends heavily on which product is used.
| Study | What it found |
|---|---|
| Meta-analysis of 42 clinical trials, 2021 | Hypophosphataemia in 47 per cent after ferric carboxymaltose, against 4 per cent after iron isomaltoside (now called ferric derisomaltose) |
| Same meta-analysis | Still present at the end of follow-up, up to three months, in up to 45 per cent of those given ferric carboxymaltose |
| Two randomised trials, 245 adults with iron deficiency anaemia, 2020 | Hypophosphataemia in 75.0 and 73.7 per cent after ferric carboxymaltose, against 7.9 and 8.1 per cent after iron isomaltoside |
This matters in Australia because ferric carboxymaltose made up 93.9 per cent of intravenous iron dispensed to women aged 18 to 44 in 2024.
The meta-analysis identified low baseline ferritin, low transferrin saturation and normal kidney function as risk factors. That profile fits many otherwise healthy young women with iron deficiency.
Low phosphate after an infusion is often a laboratory finding with no symptoms, and the trial authors wrote that further research is needed to determine how clinically important the difference between products is.
An analysis of the PREVENTT trial looked at patients given ferric carboxymaltose or placebo before major abdominal surgery. Hypophosphataemia developed in 26 per cent of the iron group against 4.5 per cent on placebo, and in an exploratory analysis of the iron group, patients who developed moderate or severe hypophosphataemia had a longer median hospital stay, 12 days against 9. That is an association in a surgical population, which leaves open whether the infusion caused the longer stay, and it does not translate directly to a healthy woman in general practice.
Skin staining
If iron leaks out of the vein into the surrounding tissue during an infusion, it can leave a brown stain on the skin. Clinical trials have reported skin discolouration in 0.68 to 1.3 per cent of patients.
It features prominently in the guidance because the stain is permanent in many cases, and the best-supported treatment is repeated laser sessions over one to two years. The Medical Board of Australia has reminded doctors to tell patients about this risk before they consent.
Allergic reactions
Serious reactions are uncommon with the modern products. A pooled analysis of randomised trials counted serious or severe hypersensitivity reactions in 29 of 2,683 patients given ferric carboxymaltose and 5 of 3,474 given ferric derisomaltose. The authors noted that head-to-head trials would be needed to confirm the difference between the two.
Australian Prescriber also advises against giving intravenous iron during an active systemic infection.
Reason 3: the evidence in iron deficiency without anaemia
A systematic review and meta-analysis I led of intravenous iron in adults with iron deficiency but no anaemia pooled 21 randomised controlled trials and 3,514 participants. Intravenous iron improved peak oxygen consumption and reduced fatigue compared with placebo, and made no overall difference to quality of life. Mild adverse events were more common in the iron groups.
The quality of the evidence was rated low or very low for every outcome except fatigue, mostly because the included studies carried a high risk of bias.
The IRONWOMAN randomised trial gave 26 recreationally active women with ferritin below 20 ug/L either 1,000 mg of intravenous iron or a saline placebo. The infusion corrected iron status, with a highly variable response between individuals. Running economy and fatigue scores improved at four weeks. Peak oxygen consumption, lactate threshold, haemoglobin mass, mood and quality of life did not differ. The sample was small and was constrained by COVID-19 recruitment problems, which is a real limitation.
Correcting iron deficiency without anaemia does help some outcomes, but the evidence base is thinner than the enthusiasm around infusions suggests. Australian Prescriber makes the same point, noting limited evidence about the benefits of giving iron to people who do not have anaemia.
Reason 4: no Medicare item for giving the infusion
The medicine is subsidised through the Pharmaceutical Benefits Scheme (PBS). The national dispensing analysis points out that there are no Medicare Benefits Schedule items that specifically cover giving intravenous iron, so the cost of the appointment, the nurse, the cannula and the monitoring is either absorbed by public health services or passed on to the woman when it is given in the community.
The authors suggest this creates inequitable access, and they observed that the share of women receiving intravenous iron who held a concession card fell from 30.9 per cent in 2013 to 17.2 per cent in 2024. A general practitioner (GP) who hesitates may also be thinking about what the infusion will cost you.
Women's ratings of infusions and tablets
In a survey study of 403 exercising women who were, or had been, iron deficient, sentiment towards iron infusions was strongly positive, while sentiment towards oral iron was only moderately positive, and many participants felt tablets had done nothing for them.
That is perception from a survey, and it helps explain the gap between what women ask for and what the guidance recommends. The useful question is whether an infusion is right for you, now.
Indications for intravenous iron
Australian Prescriber lists six main indications for intravenous iron, and surgery and pregnancy have their own consensus guidance; all of them, with the ferritin thresholds for each setting, are set out in what iron level you need for an iron infusion.
Questions for your doctor
- Have I had a fair trial of oral iron, about 60 to 90 days taken in a way that gives it a chance?
- Do we know the cause, and is iron still being lost faster than it can be replaced?
- If an infusion is appropriate, which product, and does the risk of low phosphate differ between the options?
- What should I report during the infusion? Pain, swelling, pressure or prickling at the site are the signs that it should be stopped.
- What will it cost me to have it given, and where?
- When will my iron studies be rechecked? Australian Prescriber suggests roughly 60 to 90 days after intravenous iron.
If you have given oral iron a fair trial and are still depleted and unwell, that is a legitimate reason to raise intravenous iron, and a good clinician will take it seriously.
Related articles
- Iron infusion thresholds
- Iron tablets and a stalled ferritin
- A Practical Guide to Iron Deficiency and Anaemia
Sources
The figures on this page come from these papers.
- Kassie GM, Jackson H, Clarke L, et al. Increasing utilisation of intravenous iron among Australian women of reproductive age, 2013-2024: an Australian population-based study. Internal Medicine Journal 2026;56(9):1536-1543. doi:10.1111/imj.70494
- MacLean B, Lim J, Fuller J, et al. Community screening for iron deficiency in reproductive aged women: lessons learnt from Australia. Vox Sanguinis 2025;120(1):22-31. doi:10.1111/vox.13750
- Balendran S, Forsyth C. Non-anaemic iron deficiency. Australian Prescriber 2021;44(6):193-196. doi:10.18773/austprescr.2021.052
- Canning M, Grannell L. A stain on iron therapy. Australian Prescriber 2020;43(5):160-163. doi:10.18773/austprescr.2020.051
- Schaefer B, Tobiasch M, Viveiros A, et al. Hypophosphataemia after treatment of iron deficiency with intravenous ferric carboxymaltose or iron isomaltoside: a systematic review and meta-analysis. British Journal of Clinical Pharmacology 2021;87(5):2256-2273. doi:10.1111/bcp.14643
- Wolf M, Rubin J, Achebe M, et al. Effects of iron isomaltoside vs ferric carboxymaltose on hypophosphatemia in iron-deficiency anemia: two randomized clinical trials. JAMA 2020;323(5):432-443. doi:10.1001/jama.2019.22450
- Richards T, Wijaya LK, Lim J, Dugan C, Dahly D. Intravenous Iron-Induced Hypophosphatemia in Surgical Patients. JAMA Network Open 2025;8(4):e253093. doi:10.1001/jamanetworkopen.2025.3093
- Kennedy NA, Achebe MM, Biggar P, et al. A systematic literature review and meta-analysis of the incidence of serious or severe hypersensitivity reactions after administration of ferric derisomaltose or ferric carboxymaltose. International Journal of Clinical Pharmacy 2023;45(3):604-612. doi:10.1007/s11096-023-01548-2
- Dugan C, Cabolis K, Miles LF, Richards T. Systematic review and meta-analysis of intravenous iron therapy for adults with non-anaemic iron deficiency: An abridged Cochrane review. Journal of Cachexia, Sarcopenia and Muscle 2022;13(6):2637-2649. doi:10.1002/jcsm.13114
- Dugan C, Peeling P, Buissink P, et al. Effect of intravenous iron therapy on exercise performance, fatigue scores and mood states in iron-deficient recreationally active females of reproductive age: a double-blind, randomised control trial (IRONWOMAN Trial). British Journal of Sports Medicine 2025;59(13):921-930. doi:10.1136/bjsports-2024-108240
- Dugan C, Simpson A, Peeling P, et al. The Perceived Impact of Iron Deficiency and Iron Therapy Preference in Exercising Females of Reproductive Age: A Cross-Sectional Survey Study. Patient Preference and Adherence 2023;17:2097-2108. doi:10.2147/PPA.S397122
- Muñoz M, Acheson AG, Auerbach M, et al. International consensus statement on the peri-operative management of anaemia and iron deficiency. Anaesthesia 2017;72(2):233-247. doi:10.1111/anae.13773
- Clarke L, Froessler B, Tang C, et al. Iron optimisation in pregnancy: a Haematology in Obstetric and Women's Health Collaborative consensus statement. Internal Medicine Journal 2025;55(2):300-307. doi:10.1111/imj.16602
This article is educational and not medical advice. Decisions about intravenous iron belong with a qualified clinician who knows your full history.