Clinical Research Directory

Inclusion Criteria: * Male or female patients aged 18 years or older. * Diagnosis of mild to moderate iron deficiency anemia (IDA), defined as hemoglobin 70-129 g/L in men or 70-119 g/L in women and ferritin \<30 ng/mL, with laboratory results obtained within 14 days before Visit 0. * Presence of at least 1 chronic CVD, defined as coronary artery disease or congestive heart failure with preserved ejection fraction (left ventricular ejection fraction ≥50%; NYHA Functional Class I-II). * Ability to understand the study requirements and provide written informed consent to participate in the study, including consent for the use and transfer of health information relevant to the study. * The physician has decided to prescribe Ferretab® comp. as IDA treatment of IDA at a dose of 2 capsules per day. * Signed Informed Consent Form. Exclusion Criteria: * Hypersensitivity to any component of Ferretab® comp. * Any contraindication to the use of Ferretab® comp. as specified in the Summary of Product Characteristics. * Use of any other iron-containing medicinal products within 3 months prior to study enrollment (including oral iron preparations, intravenous iron formulations, or mineral/supplement products containing a therapeutic dose of iron). * Severe anemia (hemoglobin concentration \<70 g/L). * Confirmed or suspected diagnosis of anemia of chronic disease. * Pregnancy or breastfeeding. * Surgery planned to be performed during the study period. * CVD or any other chronic disease in the stage of decompensation. * Congestive heart failure with reduced ejection fraction (NYHA Functional Class III-IV (see Appendix 2) and/or ejection fraction \<50%). * Severe chronic kidney disease (Stage IV-V chronic kidney disease, or patients receiving hemodialysis or peritoneal dialysis). * Severe chronic liver disease (Child-Pugh Class B or C liver cirrhosis, active hepatitis, or ALT/AST \>3 × the upper limit of normal). * Active malignancy (patients receiving chemotherapy, radiotherapy, or immunotherapy). * Anemias unrelated to iron deficiency, as well as other chronic hematologic disorders (thalassemia, aplastic anemia, myelodysplastic syndrome, and autoimmune hemolytic anemia). * Evidence of anemia of inflamation. * Gastrointestinal malabsorption disorders (active celiac disease, small bowel resection, short bowel syndrome, or severe flare of Crohn's disease or ulcerative colitis). * Recent bleeding, including gastrointestinal bleeding within 3 months before the study entry, surgery associated with blood loss within 8 weeks before the study entry, hemorrhagic stroke within 3 months before the study entry. * Blood transfusion within 3 months before the study entry. * Severe psychiatric disorders that impair the patient's ability to comply with the Protocol requirements and/or to provide valid informed consent. * Planned use, at the time of the study entry, of any medication or procedure listed as prohibited therapy.