Iron supplement

Iron supplement

Iron supplement from the late 19th and early 20th century
Clinical data
Trade names Feosol, Feostat, Feratab, others
AHFS/Drugs.com Monograph
Routes of
administration		 by mouth, IV, IM
ATC code
Legal status
Legal status
Identifiers
Synonyms iron pills, iron salts, ferrous salts, ferric salts
CAS Number
ChemSpider
  • none

Iron supplements, also known as iron salts and iron pills, are a number of iron formulations used to treat and prevent iron deficiency including iron deficiency anemia.[1][2] For prevention they are only recommended in those with poor absorption, heavy menstrual periods, pregnancy, hemodialysis, or a diet low in iron.[2][3] Prevention may also be used in low birth weight babies. They are taken by mouth, injection into a vein, or injection into a muscle.[2] While benefits may be seen in days up to two months may be required until iron levels return to normal.[4]

Common side effects include constipation, abdominal pain, dark stools, and diarrhea.[4] Other side effects, which may occur with excessive use, include iron overload and iron toxicity.[3][1] Ferrous salts used as supplements by mouth include ferrous fumarate, ferrous gluconate, ferrous succinate, and ferrous sulfate. Injectable forms include iron dextran and iron sucrose.[3] They work by providing the iron needed for making red blood cells.[4]

Iron has been used medically since at least 1681 with an easy to use formulation being created in 1832.[5] It is on the World Health Organization's List of Essential Medicines, the most effective and safe medicines needed in a health system.[6] Ferrous salts are available as a generic medication and over the counter.[1] The wholesale cost in the developing world is about 0.05 to 0.63 USD per month.[7] In the United States a typical month of treatment costs less than 25 USD.[1] Slow release formulations, while available, are not recommended.[2]

Medical uses

Iron supplements are used to treat iron deficiency and iron-deficiency anemia;[8] parenteral irons can also be used to treat functional iron deficiency, where requirements for iron are greater than the body's ability to supply iron such as in inflammatory states. The main criterion is that other causes of anemia have also been investigated, such as vitamin B12/folate deficiency, drug induced or due to other poisons such as lead, as often the anaemia has more than one underlying cause.

Iron deficiency anemia is classically a microcytic, hypochromic anemia. Generally, in the UK oral preparations are trialled before using parenteral delivery.[9] unless there is the requirement for a rapid response, previous intolerance to oral iron or likely failure to respond. Intravenous iron may decrease the need for blood transfusions however increases the risk of infections when compared to oral iron.[10] A 2015 Cochrane Collaboration review found that daily oral supplementation of iron during pregnancy reduces the risk of maternal anaemia and that effects on infant and on other maternal outcomes are not clear.[11] Another review found that "intermittent regimens (of oral iron supplementation) produced similar maternal and infant outcomes as daily supplementation but were associated with fewer side effects". The quality of evidence was poor, though.[12]

Athletes

There is debate about whether athletes are at an increased risk for iron deficiencies, and whether athletes with low iron, who are not anemic, would benefit from iron supplementation.[13]

Despite these additional sources of iron loss, male athletes have normally been observed to receive adequate amounts of dietary iron at the same levels recommended for the average male.[13] Female athletes, however, have been observed to receive an inadequate supply of iron, but this may be caused more from blood loss from menstruation than from athletic activity.[13] Additionally, pseudoanemia can be observed in athletes with adequate haemoglobin due to an increase in blood plasma in athletes that dilutes their haemoglobin concentration, making it appear as if they are anemic when they actually have an adequate amount of total haemoglobin.

When an athlete should be recommended to take iron supplements is debated, and should generally be judged on an individual basis.[13] While iron supplementation can be a pragmatic treatment for athletes that are anemic, its effects remain unclear in athletes that are nonanemic.[13] Iron supplementation has not been demonstrated to improve athletic performance in individuals who are nonanemic.[13] For athletes who are nonanemic, however, iron supplementation may function to stave off iron-deficient anemia, as well as prevent excess absorption of toxic metal ions of lead and cadmium.[13] Due to risks associated with differing individual tolerances, drug interactions, and overdosing, iron supplementation should be directed by a medical professional based off a clinical assessment of the athlete’s iron parameters and not undertaken as self-medication.[14]

Side effects

Side effects of therapy with oral iron are most often diarrhea or constipation and epigastric abdominal discomfort. Taken after a meal, side effects decrease, but there is an increased risk of interaction with other substances. Side effects are dose-dependent, and the dose may be adjusted.

The patient may notice that his/her stools become black. This is completely harmless, but patients must be warned about this to avoid unnecessary concern. When iron supplements are given in a liquid form, teeth may reversibly discolor (this can be avoided through the use of a straw). Intramuscular injection can be painful, and brown discoloration may be noticed.

Treatments with iron(II) sulfate have higher incidence of adverse events than iron(III)-hydroxide polymaltose complex (IPC)[15][16][17] or iron bis-glycinate chelate.[18][19]

Iron overdose has been one of the leading causes of death caused by toxicological agents in children younger than 6 years.[20]

Iron poisoning may result in mortality or short-term and long-term morbidity.[21]

Infection risk

Because one of the functions of elevated ferritin (an acute phase reaction protein) in acute infections is thought to be to sequester iron from bacteria, it is generally thought that iron supplementation (which circumvents this mechanism) should be avoided in patients who have active bacterial infections. Replacement of iron stores is seldom such an emergency situation that it cannot wait for any such acute infection to be treated.

Some studies have found that iron supplementation can lead to an increase in infectious disease morbidity in areas where bacterial infections are common. For example, children receiving iron-enriched foods have demonstrated an increased rate in diarrhea overall and enteropathogen shedding. Iron deficiency protects against infection by creating an unfavorable environment for bacterial growth. Nevertheless, while iron deficiency might lessen infections by certain pathogenic diseases, it also leads to a reduction in resistance to other strains of viral or bacterial infections, such as Salmonella typhimurium or Entamoeba histolytica. Overall, it is sometimes difficult to decide whether iron supplementation will be beneficial or harmful to an individual in an environment that is prone to many infectious diseases; however this is a different question than the question of supplementation in individuals who are already ill with a bacterial infection.[22]

Children living in areas prone for malarial infections are also at risk of developing anemia. It was thought that iron supplementation given to such children could increase the risk of malarial infection in them. A Cochrane systematic review published in 2016 found high quality evidence that iron supplementation does not increase the risk of clinical malaria in children.[23]

Contraindications

Contraindications often depend on the substance in question. Documented hypersensitivity to any ingredients and anemias without proper work-up (i.e., documentation of iron deficiency) is true of all preparations. Some can be used in iron deficiency, others require iron deficiency anaemia to be present. Some are also contraindicated in rheumatoid arthritis[24]

Haemochromatosis

Individuals may be genetically predisposed to excessive iron absorption, as is the case with those with HFE hereditary haemochromatosis. Within the general population, 1 out of 400 people has the homozygous form of this genetic trait, and 1 out of every 10 people has its heterozygous form.[13] Neither individuals with the homozygous or heterozygous form should take iron supplements.[13]

Interactions

Non-heme iron forms an insoluble complex with several other drugs, resulting in decreased absorption of both iron and the other drug. Examples include tetracycline, penicillamine, methyldopa, levodopa, bisphosphonates and quinolones. The same can occur with elements in food, such as calcium. Absorption of iron is better at a low pH (i.e. an acidic environment), and absorption is decreased if there is a simultaneous intake of antacids.

Many other substances decrease the rate of non-heme iron absorption. Examples are tannins from foods, such as tea and saw palmetto, phytic acid and roughage.[25] Vegetarians and especially vegans are at increased risk of iron deficiency due to the combination of limited amounts of iron in the diet in a form that is poorly absorbed alongside compounds that further limit absorption.

Taken after a meal, there are fewer side effects but there is also less absorption because of interaction and pH alteration. Generally, an interval of 2–3 hours between the iron intake and that of other drugs seems advisable, but is less convenient for patients and can impact on compliance.

History

The first pills were commonly known as Blaud's pills,[26] which were named after P. Blaud of Beaucaire, the French physician who introduced and started the use of these medications as a treatment for patients with anemia.[27]

Administration

By mouth

Iron can be supplemented by mouth using various forms, such as iron(II) sulfate. This is the most common and well studied soluble iron salt sold under brand names such as Feratab, Fer-Iron, and Slow-FE. It is in complex with gluconate, dextran, carbonyl iron, and other salts. Ascorbic acid, vitamin C, increases the absorption of non-heme sources of iron.[28]

Heme iron polypeptide (HIP) (e.g. Proferrin ES and Proferrin Forte) can be used when regular iron supplements such as ferrous sulfate or ferrous fumarate are not tolerated or absorbed. A clinical study demonstrated that HIP increased serum iron levels 23 times greater than ferrous fumarate on a milligram-per-milligram basis.[29]

Another alternative is ferrous glycine sulfate or ferroglycine sulfate, has less gastrointestinal side-effects than standard preparations such as iron fumarate.[30] It is unusual among oral preparations of iron supplements in that the iron in this preparation has very high oral bioavailability, especially in the liquid formulation. This option should be evaluated before resorting to parenteral therapy. It is especially useful in iron deficiency anemia associated with autoimmune gastritis and Helicobacter pylori gastritis, where it generally has satisfactory effect.[31]

Since iron stores in the body are generally depleted, and there is a limit to what the body can process (about 2–6 mg/kg of body mass per day; i.e. for a 100 kg/220 lb man this is equal to a maximum dose of 200–600 mg/per day) without iron poisoning, this is a chronic therapy which may take 3–6 months.[32]

Due to the frequent intolerance of oral iron and the slow improvement, parenteral iron is recommended in many indications.[33][34]

By injection

Iron therapy (intravenously or intramuscular) is given when therapy by mouth has failed (not tolerated by the patient), oral absorption is seriously compromised (by illnesses, or when the patient cannot swallow), benefit from oral therapy cannot be expected, or fast improvement is required (for example, prior to elective surgery).[35] Parenteral therapy is more expensive than oral iron preparations and is not suitable during the first trimester of pregnancy.[36]

There are cases where parenteral iron is preferable over oral iron. These are cases where oral iron is not tolerated, where the haemoglobin needs to be increased quickly (e.g. post partum, post operatively, post transfusion), where there is an underlying inflammatory condition (e.g. inflammatory bowel disease) or renal patients, the benefits of parenteral iron far outweigh the risks. In many cases, use of intravenous iron such as ferric carboxymaltose has lower risks of adverse events than a blood transfusion and as long as the person is stable is a better alternative.[37] Ultimately this always remains a clinical decision based on local guidelines, although National Guidelines are increasingly stipulating IV iron in certain groups of patients.[38][39]

Soluble iron salts have a significant risk of adverse effects and can cause toxicity due to damage to cellular macromolecules. Delivering iron parenterally has utilised various different molecules to limit this. This has included dextrans, sucrose, carboxymaltose and more recently Isomaltoside 1000.

One formulation of parenteral iron is iron dextran which covers the old high molecular weight (trade name DexFerrum) and the much safer low molecular iron dextrans (tradenames including Cosmofer and Infed).[40]

Iron sucrose (trade names including Venofer) has an occurrence of allergic reactions of less than 1 in 1000.[41] A common side effect is taste changes, especially a metallic taste, occurring in between 1 in 10 and 1 in 100 treated patients.[41] It has a maximum dose of 200 mg on each occasion according to the SPC, but it has been given in doses of 500 mg. Doses can be given up to 3 times a week[42]

Iron carboxymaltose is marketed as Ferinject, Injectafer, and Iropremand in various countries.[43][44] The most common side effects are headaches which occur in 3.3%.[45][46]

Iron Isomaltoside 1000 (Trade name Monofer) is a newer formulation of parenteral iron that has a matrix structure that results in very low levels of free iron and labile iron. It can be given at high doses – 20 mg/kg in a single visit – no upper dose limit. This formulation has the benefit of giving a full iron correction in a single visit.[47][44]

Follow-up

Follow-up is needed to ensure compliance and to detect adequate response to therapy. The interval of follow up can widely depend on both the method of administration, and the underlying pathology. For parenteral irons it is recommended that there be a period of 4 weeks before repeating blood test to allow the body to utilise the iron.[8] For oral iron, this can take considerably longer, so waiting 3 months may be appropriate.

See also

References

  1. 1 2 3 4 Hamilton, Richart (2015). Tarascon Pocket Pharmacopoeia 2015 Deluxe Lab-Coat Edition. Jones & Bartlett Learning. p. 217. ISBN 9781284057560.
  2. 1 2 3 4 British national formulary : BNF 69 (69 ed.). British Medical Association. 2015. pp. 660–664. ISBN 9780857111562.
  3. 1 2 3 WHO Model Formulary 2008 (PDF). World Health Organization. 2009. pp. 247–250. ISBN 9789241547659. Retrieved 8 January 2017.
  4. 1 2 3 "Iron Preparations, Oral". The American Society of Health-System Pharmacists. Retrieved 8 January 2017.
  5. ↑ Upfal, Jonathan (2006). Australian Drug Guide. Black Inc. pp. 378–379. ISBN 9781863951746.
  6. ↑ "WHO Model List of Essential Medicines (19th List)" (PDF). World Health Organization. April 2015. Retrieved 8 December 2016.
  7. ↑ "Ferrous Salt". International Drug Price Indicator Guide. Retrieved 8 December 2016.
  8. 1 2 Ferinject (ferric n 2012-12-21.
  9. ↑ Goddard AF, James MW, McIntyre AS and Scott BB (May 2005). Guidelines for the management of iron deficiency anaemia. British Society of Gastroenterology
  10. ↑ Litton, E; Xiao, J; Ho, KM (Aug 15, 2013). "Safety and efficacy of intravenous iron therapy in reducing requirement for allogeneic blood transfusion: systematic review and meta-analysis of randomised clinical trials.". BMJ (Clinical research ed.). 347: f4822. PMC 3805480 Freely accessible. PMID 23950195. doi:10.1136/bmj.f4822.
  11. ↑ Peña-Rosas JP, De-Regil LM, Garcia-Casal MN, Dowswell T (2015). "Daily oral iron supplementation during pregnancy.". Cochrane Database Syst Rev. 7: CD0047361. PMID 26198451. doi:10.1002/14651858.CD004736.pub5.
  12. ↑ Peña-Rosas, Juan Pablo (19 October 2015). "Intermittent oral iron supplementation during pregnancy". Cochrane Database of Systematic Reviews. 10: CD009997. PMID 26482110. doi:10.1002/14651858.CD009997.pub2. Retrieved 14 November 2015.
  13. 1 2 3 4 5 6 7 8 9 Nielson, Peter; Nachtigall, Detlef (Oct 1998). "Iron supplementation in athletes: current recommendations" (PDF). Sports Med. 26 (4): 207–216. PMID 9820921. doi:10.2165/00007256-199826040-00001. Retrieved 7 July 2013.
  14. ↑ Chatard, Jean-Claude; Mujika, Iñigo; Guy, Claire; Lacour, Jean-René (Apr 1999). "Anaemia and Iron Deficiency in Athletes Practical Recommendations for Treatment" (PDF). Sports Med. 4. 27 (4): 229–240. PMID 10367333. doi:10.2165/00007256-199927040-00003. Retrieved 7 July 2013.
  15. ↑ Geisser P (2007). "Safety and efficacy of iron(III)-hydroxide polymaltose complex / a review of over 25 years experience". Arzneimittelforschung. 57 (6A): 439–52. PMID 17691594. doi:10.1055/s-0031-1296693.
  16. ↑ Toblli JE, Brignoli R (2007). "Iron(III)-hydroxide polymaltose complex in iron deficiency anemia / review and meta-analysis". Arzneimittelforschung. 57 (6A): 431–8. PMID 17691593. doi:10.1055/s-0031-1296692.
  17. ↑ Saha L, Pandhi P, Gopalan S, Malhotra S, Saha PK (2007). "Comparison of efficacy, tolerability, and cost of iron polymaltose complex with ferrous sulfate in the treatment of iron deficiency anemia in pregnant women". MedGenMed. 9 (1): 1. PMC 1924983 Freely accessible. PMID 17435611.
  18. ↑ Szarfarc SC, de Cassana LM, Fujimori E, Guerra-Shinohara EM, de Oliveira IM (2001). "Relative effectiveness of iron bis-glycinate chelate (Ferrochel) and ferrous sulfate in the control of iron deficiency in pregnant women". Arch Latinoam Nutr. 51 (1 Suppl 1): 42–7. PMID 11688081.
  19. ↑ Ashmead SD (2001). "The chemistry of ferrous bis-glycinate chelate". Arch Latinoam Nutr. 51 (1 Suppl 1): 7–12. PMID 11688084.
  20. ↑ Iron Toxicity at eMedicine
  21. ↑ Toxicity, Iron (Overview). Tripdatabase.com. Retrieved on 2012-12-21.
  22. ↑ http://jn.nutrition.org/content/131/2/616S.full
  23. ↑ Neuberger, A; Okebe, J; Yahav, D; Paul, M (27 February 2016). "Oral iron supplements for children in malaria-endemic areas.". The Cochrane database of systematic reviews. 2: CD006589. PMC 4916933 Freely accessible. PMID 26921618. doi:10.1002/14651858.CD006589.pub4. Retrieved 16 March 2016.
  24. ↑ CosmoFer – Summary of Product Characteristics (SPC) – (eMC). Medicines.org.uk. Retrieved on 2012-12-21.
  25. ↑ Boosting iron absorption: A guide to for the science-minded. Parentingscience.com. Retrieved on 2012-12-21.
  26. ↑ Blaud's pill – Medical Definition and More from. Merriam-Webster. Retrieved on 2012-12-21.
  27. ↑ Robinson, Victor, ed. (1939). "P. Blaud of Beaucaire, Blaud's Pills for Anemia, Iron pills, Iron". The Modern Home Physician, A New Encyclopedia of Medical Knowledge. WM. H. Wise & Company (New York)., p. 435.
  28. ↑ Lynch, SR; Cook, JD (1980). "Interaction of vitamin C and iron.". Annals of the New York Academy of Sciences. 355: 32–44. doi:10.1111/j.1749-6632.1980.tb21325.x.
  29. ↑ Seligman, Paul A.; Moore, Gary M.; Schleicher, Rhoda B. (2000). "Clinical studies of hip: An oral heme-iron product". Nutrition Research. 20 (9): 1279–86. doi:10.1016/s0271-5317(00)00215-3.
  30. ↑ Aronstam, A.; Aston, D. (1982). "A comparative trial of a controlled-release iron tablet preparation ('Ferrocontin' Continus) and ferrous fumarate tablets". Pharmatherapeutica. 3 (4): 263–267. PMID 7146040.
  31. ↑ Hershko, C.; Ianculovich, M.; Souroujon, M. (2007). "Decreased Treatment Failure Rates following Duodenal Release Ferrous Glycine Sulfate in Iron Deficiency Anemia Associated with Autoimmune Gastritis and Helicobacter pylori Gastritis". Acta Haematologica. 118 (1): 19–26. PMID 17426393. doi:10.1159/000101701.
  32. ↑ Iron Poisoning. Webmd.com (2012-09-27). Retrieved on 2012-12-21.
  33. ↑ National Clinical Guideline Centre (2015). Anaemia Management in Chronic Kidney Disease. NICE Guideline, No. 8. London: Royal College of Physicians. PMID 26065064.
  34. ↑ Mowat, C; Cole, A; Windsor, A; Ahmad, T; Arnott, I; Driscoll, R; Mitton, S; Orchard, T; et al. (2011). "Guidelines for the management of inflammatory bowel disease in adults" (PDF). Gut. 60 (5): 571–607. PMID 21464096. doi:10.1136/gut.2010.224154.
  35. ↑ Kumpf, V. (1996). "Parenteral iron supplementation". Nutrition in Clinical Practice. 11 (4): 139–46. PMID 9070014. doi:10.1177/0115426596011004139.
  36. ↑ https://www.medicines.org.uk/emc/medicine/24167
  37. ↑ Moore, R Andrew; Gaskell, Helen; Rose, Peter; Allan, Jonathan (2011). "Meta-analysis of efficacy and safety of intravenous ferric carboxymaltose (Ferinject) from clinical trial reports and published trial data". BMC Blood Disorders. 11: 4. PMC 3206450 Freely accessible. PMID 21942989. doi:10.1186/1471-2326-11-4.
  38. ↑ "2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure". European Heart Journal. 37: 2129–2200. doi:10.1093/eurheartj/ehw128.
  39. ↑ "European Consensus on the Diagnosis and Management of Iron Deficiency and Anaemia in Inflammatory Bowel Diseases". Journal of Crohn's and Colitis. 9: 211–222. doi:10.1093/ecco-jcc/jju009.
  40. ↑ Chertow, Glenn M.; Mason, Phillip D.; Vaage-Nilsen, Odd; Ahlmén, Jarl (2004). "On the relative safety of parenteral iron formulations". Nephrology Dialysis Transplantation. 19 (6): 1571–5. PMID 15150356. doi:10.1093/ndt/gfh185.
  41. 1 2 Venofer in FASS (drug formulary), translated from Swedish "Allergiska reaktioner (inträffar hos färre än 1 av 1 000 patienter)" and "Vanliga (inträffar hos färre än 1 av 10 patienter): Tillfälliga smakförändringar (speciellt metallsmak)."
  42. ↑ https://www.medicines.org.uk/emc/medicine/24168
  43. ↑ "Summary review: Application number 203565Orig1s000 by Luitpold Pharmaceuticals, Inc." (PDF). FDA. July 24, 2013.
  44. 1 2 Cançado, Rodolfo Delfini; Muñoz, Manuel (2011). "Intravenous iron therapy". Revista Brasileira de Hematologia e Hemoterapia. 33 (6): 461–9. PMC 3459360 Freely accessible. PMID 23049364. doi:10.5581/1516-8484.20110123.
  45. ↑ Ferinject (ferric carboxymaltose) – Summary of Product Characteristics (SPC) – (eMC). Medicines.org.uk. Retrieved on 2012-12-21.
  46. ↑ "Injectafer US label" (PDF). FDA. July 2013. See FDA index page for NDA 203565 for updates and further information.
  47. ↑ Jahn, Markus R.; Andreasen, Hans B.; Fütterer, Sören; Nawroth, Thomas; Schünemann, Volker; Kolb, Ute; Hofmeister, Wolfgang; Muñoz, Manuel; Bock, Klaus; Meldal, Morten; Langguth, Peter (2011). "A comparative study of the physicochemical properties of iron isomaltoside 1000 (Monofer®), a new intravenous iron preparation and its clinical implications". European Journal of Pharmaceutics and Biopharmaceutics. 78 (3): 480–91. PMID 21439379. doi:10.1016/j.ejpb.2011.03.016.
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