Searched over 200M research papers
10 papers analyzed
Some studies suggest intravenous iron treatments are more effective and better tolerated than oral ferrous sulfate for various types of anemia, while other studies indicate potential interactions and adverse effects with ferrous sulfate.
20 papers analyzed
Ferrous sulfate 325 mg is a commonly prescribed oral iron supplement for treating iron deficiency anemia. Studies have shown that it is effective in increasing hemoglobin levels and iron stores in various patient populations. For instance, in a study comparing ferrous sulfate to ferric citrate in patients with chronic kidney disease (CKD), ferrous sulfate was found to significantly increase transferrin saturation (TSAT) and ferritin levels over 12 weeks. Similarly, in cancer patients with mild non-chemotherapy-induced iron deficiency anemia, ferrous sulfate effectively increased hemoglobin and ferritin levels over a two-month period.
While ferrous sulfate is effective, intravenous (IV) iron therapies such as ferric carboxymaltose and ferric gluconate have been shown to offer superior outcomes in certain conditions. For example, in postpartum women with anemia, IV ferric carboxymaltose led to a quicker and more substantial increase in hemoglobin levels compared to oral ferrous sulfate . Additionally, in anemic cancer patients receiving chemotherapy, IV ferric gluconate significantly improved hemoglobin response compared to oral ferrous sulfate or no iron supplementation.
The safety profile of ferrous sulfate is generally acceptable, but it is associated with gastrointestinal side effects such as constipation and nausea. In a study comparing ferrous bisglycinate chelate to ferrous sulfate, the latter was associated with a higher incidence of gastrointestinal toxicity, although both treatments were effective in increasing hemoglobin and ferritin levels. Furthermore, in patients with CKD, oral ferrous sulfate was associated with fewer serious adverse events compared to IV iron sucrose, which had a higher risk of cardiovascular and infectious complications.
Ferrous sulfate can interact with various medications, affecting their bioavailability and efficacy. For instance, it significantly reduces the bioavailability of levodopa, a medication used in Parkinson's disease, by forming strong chemical complexes with it . This interaction can lead to a substantial decrease in the effectiveness of levodopa, necessitating careful management of dosing schedules. Similarly, ferrous sulfate modestly reduces the bioavailability of gemifloxacin, an antibiotic, when taken concurrently. It also affects the absorption and metabolism of methyldopa, a medication used for hypertension, leading to altered blood pressure control.
Ferrous sulfate 325 mg is an effective oral iron supplement for treating iron deficiency anemia, but its efficacy can be surpassed by certain intravenous iron therapies in specific patient populations. While generally safe, it is associated with gastrointestinal side effects and significant drug interactions that require careful management. Understanding these factors is crucial for optimizing treatment outcomes and minimizing adverse effects.
Most relevant research papers on this topic