Overview
Iron deficiency anemia is a large public health concern worldwide, especially in young children, infants, and women of childbearing age. This type of anemia occurs when iron intake, iron stores, and iron loss do not adequately support the formation of erythrocytes, also known as red blood cells. Ferrous sulfate is a synthetic agent used in the treatment of iron deficiency. It is the gold standard of oral iron therapy in the UK and many other countries.
Indication
抗贫血药。用于预防和治疗各种原因引起的缺铁性贫血,包括儿童或婴儿期需铁量增加而食物中供应不足、铁吸收障碍、妊娠中后期以及慢性失血等。
Associated Conditions
- Anaemia folate deficiency
- Anemia
- Folate deficiency
- Iron Deficiency (ID)
- Iron Deficiency Anemia (IDA)
- Hypochromic anemia
Research Report
Ferrous Sulfate (DB13257): A Comprehensive Pharmacological and Clinical Monograph
1.0 Executive Summary
Ferrous sulfate is a small molecule inorganic salt that has served as the cornerstone of oral iron repletion therapy for decades. Identified by DrugBank ID DB13257 and CAS Number 7720-78-7, it is widely regarded as the "gold standard" for the treatment and prevention of iron deficiency anemia (IDA), a condition with significant global public health impact.[1] The therapeutic action of ferrous sulfate is rooted in its ability to supply the body with ferrous iron (
Fe2+), an essential mineral component for the synthesis of hemoglobin in red blood cells and myoglobin in muscle tissue, thereby facilitating systemic oxygen transport.[4]
The pharmacokinetics of ferrous sulfate are characterized by a tightly regulated absorption process in the proximal small intestine, which is significantly enhanced in iron-deficient states but can be inhibited by food and certain medications.[4] This creates a fundamental clinical challenge: the conditions that maximize bioavailability—administration on an empty stomach—are precisely those that precipitate the most common adverse effects.[8] The predominant adverse events are gastrointestinal in nature, including nausea, abdominal pain, and constipation, which are a primary driver of patient non-adherence and subsequent treatment failure.[3]
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2024/08/13 | Phase 4 | Not yet recruiting | |||
2023/01/10 | Not Applicable | Active, not recruiting | |||
2022/04/04 | Not Applicable | Recruiting | |||
2020/12/31 | Phase 3 | Completed | |||
2019/05/21 | Phase 3 | Completed | |||
2016/07/07 | Phase 4 | Terminated | Queen Mary Hospital, Hong Kong | ||
2016/05/17 | Phase 4 | UNKNOWN | |||
2013/11/25 | Phase 4 | Completed | |||
2012/10/05 | Phase 4 | Completed | |||
2012/06/27 | Not Applicable | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
No FDA approvals found for this drug. |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
No TGA approvals found for this drug. |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
No Health Canada approvals found for this drug. |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
No CIMA AEMPS (Spain) approvals found for this drug. |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
---|---|---|---|---|---|
No UK EMC drug information found for this drug. |
Help Us Improve
Your feedback helps us provide better drug information and insights.