Sodium feredetate is an iron chelate rather than a conventional iron salt. The iron is held in a stable, non-ionized complex with the sodium salt of EDTA. This helps prevent the iron from directly contacting the teeth and therefore reduces the possibility of tooth discoloration.
After reaching the gastrointestinal tract, the chelate releases elemental iron, which is then absorbed and utilized by the body. A large proportion of absorbed iron is incorporated into hemoglobin, while much of the remaining iron is stored as ferritin or haemosiderin, mainly within the reticuloendothelial system and, to a lesser extent, the liver. Smaller amounts contribute to myoglobin, heme-containing enzymes, and transferrin-bound iron in the blood.
EDTA itself is poorly absorbed and is largely eliminated from the body without significant metabolic alteration.
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S-Fer Syrup is an oral iron preparation used to prevent and treat iron deficiency anemia in adults, children, and infants. It provides iron in a form that is generally less likely to cause gastrointestinal discomfort than some conventional iron preparations and does not typically cause tooth staining.
It may be used for:
S-Fer Syrup should be taken orally according to the dose prescribed by a healthcare professional.
The appropriate dose for adults and individual patients should be determined according to the severity of iron deficiency and medical advice.
Neonates and infants 1–11 months: 1 mL once daily may be used for prophylactic supplementation in certain low-birth-weight, exclusively breastfed infants. Supplementation may begin around 4–6 weeks after birth and continue until mixed feeding is established, as advised by a healthcare professional.
Oral iron can interact with many medicines and may affect their absorption or effectiveness.
Tell your doctor or pharmacist about all medicines and supplements you are taking. Some medicines may need to be taken at a different time from S-Fer.
S-Fer should not be used in patients with:
S-Fer is generally well tolerated, but allergic reactions may occur rarely. Symptoms requiring immediate medical attention include:
Iron preparations may also cause stools to become darker or black. This is generally harmless but can sometimes interfere with tests designed to detect hidden blood in stool.
The use of medicines during the first trimester of pregnancy should be carefully considered, with the expected benefits weighed against potential risks. No specific harmful effects associated with sodium feredetate use during pregnancy or breastfeeding have been reported.
Pregnant or breastfeeding women should use S-Fer under medical supervision.
Use S-Fer cautiously in patients with:
Long-term or excessive use, particularly in children, can result in iron accumulation and toxicity. The medicine should therefore be used at the recommended dose and duration.
Iron supplementation should generally be continued only when clinically indicated and according to medical advice.
Taking excessive amounts of iron can cause serious poisoning, especially in children. Early symptoms may include:
Severe poisoning may also lead to high blood glucose and metabolic acidosis.
An iron overdose can be a medical emergency. Keep S-Fer safely out of children's reach and seek urgent medical attention if an overdose is suspected.
Oral Iron Preparations
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At ePharma, we’re committed to providing accurate and accessible health information. However, all content is intended for informational purposes only and should not replace medical advice from a qualified physician. Please consult your healthcare provider for personalized guidance. We aim to support, not substitute, the doctor-patient relationship.