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Drug: Iron Sucrose
Brand: Venofer 100mg/5mL
Manufacturer /
TM Owner
American Regent
Origin: USA

Venofer 100mg/5mL Injection

Venofer contains Iron Sucrose, an iron replacement therapy. It restores iron stores to correct iron-deficiency anaemia and improve energy and oxygen delivery. It is used in the treatment of blood disorders. It is supplied as an injection (100mg/5mL). Available on prescription, it forms part of modern, guideline-driven care.
Strength: 100mg/5mL
Pack Size: 1s
Storage: 20°C to 25°C
Form: Injection

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Indications & Clinical Uses

  • Venofer 100mg/5mL is an intravenous iron replacement medicine containing iron sucrose (20 mg/mL) in a single-dose vial.
  • In the US it is indicated for the treatment of iron deficiency anaemia in patients with chronic kidney disease (CKD), including those on haemodialysis, peritoneal dialysis or not on dialysis; use in children is described in a separate paediatric section of the label.
  • It is given only by a healthcare provider in a clinic, dialysis unit or hospital, by slow intravenous injection or intravenous infusion.
  • It must not be given any other way.
  • Typical adult schedules in the US label are 100 mg per haemodialysis session, 200 mg on five occasions over 14 days in non-dialysis CKD, or three divided infusions over 28 days in peritoneal dialysis.

Side Effects

  • Common side effects reported in at least 2% of adults include diarrhoea, nausea, vomiting, headache, dizziness, low blood pressure (hypotension), itching, pain in the arm or leg, joint pain, back pain and muscle cramps.
  • Low blood pressure was most frequent in haemodialysis patients (about 39%).
  • MedlinePlus also lists constipation, tiredness, taste changes, fever and irritation at the injection site.
  • Serious hypersensitivity reactions, including anaphylactic-type reactions, can occur, as can clinically significant hypotension.
  • The label has no boxed warning.
  • Tell your care team immediately if you develop difficulty breathing, swelling of the face or throat, hives, fainting, chest pain or an irregular heartbeat during or after an infusion.

Precautions & Warnings

  • Venofer is contraindicated in anyone with known hypersensitivity to it.
  • Because serious hypersensitivity can occur, you should be observed for at least 30 minutes after each dose.
  • Blood pressure is watched during and after administration because clinically significant hypotension can occur.
  • It must not be given to patients with evidence of iron overload.
  • Venofer must only be given intravenously, by slow injection over 2 to 5 minutes or by infusion.
  • Published data after the first trimester have not shown harm to mother or baby, but data for the first trimester are insufficient; untreated iron deficiency anaemia in pregnancy should be treated, so discuss with your provider.
  • Tell your provider if you are breastfeeding.

Avoid Interactions

  • Medicines that reduce efficacy: Venofer may reduce the absorption of oral iron preparations taken at the same time, so oral iron is usually not needed alongside it unless your provider advises.
  • Do not take other iron products without asking your provider.
  • Medicines that increase risk: the fetched US label lists no other specific drug interactions, but medicines that lower blood pressure could add to the hypotension risk, so mention them to the care team.
  • Do not start or stop any medicine, including over-the-counter iron products, without checking with your care team.
  • Tell your prescriber about all medicines, herbal products and supplements you take.

References

Frequently Asked Questions

Venofer (iron sucrose) is an intravenous iron treatment for iron deficiency anaemia in people with chronic kidney disease, whether or not they are on dialysis. It replaces iron so your body can make red blood cells. A healthcare provider gives it in a clinic, dialysis unit or hospital.

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