Page last updated: 2024-11-11

ferrous succinate

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

ferrous succinate: RN given refers to Fe(+2)(1:1) salt; important as iron supplement [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID10464762
SCHEMBL ID275423
MeSH IDM0079657

Synonyms (22)

Synonym
iron succinate
ferplex (tn)
ferrous succinate
10030-90-7
D08015
818zyk7n91 ,
einecs 233-082-3
butanedioic acid, iron(2+) salt (1:1)
unii-818zyk7n91
iron(ii) succinate
ferrlecit 2
iron succinate (fe(o4c4h4))
ferrous succinate [mi]
succinic acid, iron(2+) salt (1:1)
ferrous succinate [mart.]
ferrous succinate [who-dd]
ferromyn
SCHEMBL275423
succinic acid iron(ii) salt;succinic acid iron(ii) salt
DB14489
butanedioate;iron(2+)
Q27269230

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" Secondary outcomes included the change in the reticulocyte percentage after 2 weeks of treatment, the increase in hemoglobin level after 4 weeks of treatment, the increase in serum ferritin level after 8 weeks of treatment, and adverse events."( The Efficacy and Safety of Vitamin C for Iron Supplementation in Adult Patients With Iron Deficiency Anemia: A Randomized Clinical Trial.
Chen, Q; Li, N; Liu, W; Wang, X; Wu, W; Zhang, M; Zhao, G, 2020
)
0.56
" There were no significant differences between the 2 groups regarding the rates of adverse events (46 [20."( The Efficacy and Safety of Vitamin C for Iron Supplementation in Adult Patients With Iron Deficiency Anemia: A Randomized Clinical Trial.
Chen, Q; Li, N; Liu, W; Wang, X; Wu, W; Zhang, M; Zhao, G, 2020
)
0.56

Bioavailability

ExcerptReferenceRelevance
"Hemoglobin-repletion tests in rats, organoleptic studies, and iron-absorption studies in humans were used to search for Fe sources with high bioavailability that could be added to infant cereals as alternatives to the Fe compounds currently used for fortification."( Iron fortification of infant cereals: a proposal for the use of ferrous fumarate or ferrous succinate.
Burri, J; Cook, JD; Furniss, DE; Hurrell, RF; Lynch, SR; Whittaker, P, 1989
)
0.28
" Determining the bioavailability of iron products is a challenge, because iron is naturally present in the blood and some tissues."( Comparative bioavailability of ferrous succinate tablet formulations without correction for baseline circadian changes in iron concentration in healthy Chinese male subjects: a single-dose, randomized, 2-period crossover study.
Cao, GY; Hu, X; Jin, PF; Li, KX; Yang, C; Yue, XY, 2011
)
0.37
"The aim of the study was to assess the comparative bioavailability of 200-mg of a test (ferrous succinate,100 mg × 2, Hunan Huana Pharmaceutical Co."( Comparative bioavailability of ferrous succinate tablet formulations without correction for baseline circadian changes in iron concentration in healthy Chinese male subjects: a single-dose, randomized, 2-period crossover study.
Cao, GY; Hu, X; Jin, PF; Li, KX; Yang, C; Yue, XY, 2011
)
0.37
" The relative bioavailability of the test-reference preparations was 101."( Comparative bioavailability of ferrous succinate tablet formulations without correction for baseline circadian changes in iron concentration in healthy Chinese male subjects: a single-dose, randomized, 2-period crossover study.
Cao, GY; Hu, X; Jin, PF; Li, KX; Yang, C; Yue, XY, 2011
)
0.37

Dosage Studied

ExcerptRelevanceReference
" groups in terms of sex, age, duration of hemodialysis, dialysis frequency per week, EPO dosage per week, the level of intact parathyroid hormone, serum creatinine, blood urea nitrogen, or hematological parameters at baseline."( Intravenous iron sucrose in Chinese hemodialysis patients with renal anemia.
Li, H; Wang, SX, 2008
)
0.35
" The average weekly EPO dosage used was lower in SXN group than in FS group (P<0."( Effect of Sheng Xue Ning Tablets on Renal Anemia in Patients Subject to Maintenance Hemodialysis and Safety Evaluation: A Multi-setting Prospective Randomized Study.
Guo, ZY; Jiang, GR; Ma, J; Mei, CL; Ni, ZH; Rong, S; Tang, XJ; Wang, NS; Yan, HD; Yuan, WJ; ZHang, LM, 2020
)
0.56
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (21)

TimeframeStudies, This Drug (%)All Drugs %
pre-19908 (38.10)18.7374
1990's0 (0.00)18.2507
2000's5 (23.81)29.6817
2010's6 (28.57)24.3611
2020's2 (9.52)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials12 (57.14%)5.53%
Reviews0 (0.00%)6.00%
Case Studies1 (4.76%)4.05%
Observational0 (0.00%)0.25%
Other8 (38.10%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (9)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Efficacy and Safety of Ferrous Iron on the Prevention of Vascular Cognitive Impairment Among Patients With Cerebral Infarction/TIA,FAVORITE [NCT03891277]Phase 21,006 participants (Anticipated)Interventional2019-04-01Recruiting
The Effects of Ferric Derisomaltose on Postoperative Anemia in Patients Undergoing Spinal Deformity Surgery: A Prospective Randomized Controlled Study [NCT05714007]Phase 4120 participants (Anticipated)Interventional2023-08-31Recruiting
The Efficacy and Safety of Vitamin C for Iron Supplementation Therapy in Adult Patients With Iron Deficiency Anemia(IDA) [NCT02631668]Phase 4440 participants (Actual)Interventional2016-01-01Completed
Randomized, Controlled Study of Iron Supplementation of Infants With Birth Weights 2000-2500 g [NCT00558454]Phase 4380 participants (Actual)Interventional2004-03-31Completed
Efficacy and Safety of Erythropoietin in the Treatment of Anemia in Patients With Lymphoma After Autologous Hematopoietic Stem Cell Transplantation [NCT03010579]Phase 470 participants (Anticipated)Interventional2016-10-31Recruiting
Prospective Study of Iron Deficiency Anemia in Twin Pregnancy [NCT04975074]Phase 41,000 participants (Anticipated)Interventional2021-07-15Not yet recruiting
Long-term Effects of Thalidomide for Recurrent Gastrointestinal Bleeding Due to Vascular Malformation : An Open-label, Randomized, Parallel Controlled Study [NCT00964496]Phase 255 participants (Actual)Interventional2004-11-30Completed
A Multicenter, Randomized, Double-blind, Parallel Controlled Clinical Study on the Efficacy and Safety of Compound E Jiao Jiang(cEJJ)in the Treatment of Postpartum Anemia [NCT06175117]Phase 4360 participants (Anticipated)Interventional2023-12-31Not yet recruiting
A Multicenter Randomized Controlled Study of Shengxuening Tablet in the Treatment of Chemotherapy-related Anemia in Hematologic Tumors [NCT05784870]Phase 3168 participants (Anticipated)Interventional2023-02-07Recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

TrialOutcome
NCT00964496 (7) [back to overview]Cessation of Bleeding
NCT00964496 (7) [back to overview]Change From Baseline in Bleeding Duration at 12 Months
NCT00964496 (7) [back to overview]Change From Baseline in Bleeding Episodes at 12 Months
NCT00964496 (7) [back to overview]Change From Baseline in Hemoglobin (Hb) Level at 12 Months
NCT00964496 (7) [back to overview]Change From Baseline in Total Transfused Red Cell Requirements at 12 Months
NCT00964496 (7) [back to overview]Participants Dependent on Blood Transfusions
NCT00964496 (7) [back to overview]Participants Whose Rebleeds Decreased From Baseline by ≥ 50% at 12 Months

Cessation of Bleeding

The cessation of bleeding was defined as repeated negative faecal occult blood test (FOBT) (monoclonal colloidal gold color technology) during our observation period. Rebleeding was defined based on a positive FOBT at any visit after treatment. (NCT00964496)
Timeframe: 52 months

Interventionparticipants (Number)
Thalidomide Group13
Iron-controlled Group0

[back to top]

Change From Baseline in Bleeding Duration at 12 Months

The change from baseline in bleeding duration at 12 months (NCT00964496)
Timeframe: baseline and 12 months

Interventiondays (Mean)
Thalidomide Group5.2
Iron-controlled Group0.8

[back to top]

Change From Baseline in Bleeding Episodes at 12 Months

The Change from baseline in bleeding episodes at 12 months (NCT00964496)
Timeframe: baseline and 12 months

Interventionbleeding episodes (Mean)
Thalidomide Group-9.36
Iron-controlled Group1.41

[back to top]

Change From Baseline in Hemoglobin (Hb) Level at 12 Months

The change from baseline in average hemoglobin (Hb) level(tested every month) at 12 months. (NCT00964496)
Timeframe: baseline and 12 months

Interventiong/L (Mean)
Thalidomide Group3.06
Iron-controlled Group-0.01

[back to top]

Change From Baseline in Total Transfused Red Cell Requirements at 12 Months

Change of total transfused red cell requirements at 12 months after randomization from one year before baseline in transfusion dependent patients (NCT00964496)
Timeframe: baseline and 12 months

Interventionmilliliter (Mean)
Thalidomide Group-1585.71
Iron-controlled Group-28.57

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Participants Dependent on Blood Transfusions

Numbers of participants dependent on blood transfusions (NCT00964496)
Timeframe: 52 months

Interventionparticipants (Number)
Thalidomide Group3
Iron-controlled Group13

[back to top]

Participants Whose Rebleeds Decreased From Baseline by ≥ 50% at 12 Months

The primary end point was defined as the patients whose rebleeds decreased from baseline by ≥ 50% at 12 months. Reduction of rebleeds = [(total bleeding episode at 12 months - total bleeding episodes at a year before randomization)/total bleeding episodes at a year before randomization(baseline)]*100%. Rebleeding was defined based on a positive fecal occult blood test (FOBT) (monoclonal colloidal gold color technology) at any visit after treatment. (NCT00964496)
Timeframe: baseline and 12 months

Interventionparticipants (Number)
Thalidomide Group20
Iron-controlled Group1

[back to top]