Calceos

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Medically reviewed

Marina Burgos

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Calceos

Quick Facts

Property Description
Active Ingredient(s) Calcium Carbonate, Colecalciferol (Vitamin D3)
Form Chewable Tablet
Pharmacological Class Calcium and Vitamin D Supplement
Common Use Nutritional support for bone health and calcium homeostasis
Origin Mineral (Calcium Carbonate) and Synthetic/Derived (Colecalciferol)

What Type of Product is Calceos?

Calceos is a fixed combination product officially classified as a Calcium and Vitamin D Supplement, primarily formulated to provide foundational nutritional support essential for skeletal health. Its composition features two active compounds: Calcium Carbonate and Colecalciferol (Vitamin D3). The formulation is widely clinically recognized for addressing simultaneous deficiencies of the essential mineral and the corresponding vitamin required for its utilization, a crucial step in maintaining long-term bone density.

This dual formulation is administered via the oral route as a chewable tablet, a differentiating feature that offers ease of consumption compared to large standard pills, particularly for elderly patients or individuals requiring continuous long-term nutritional support. While Calcium Carbonate is derived from a mineral source, Colecalciferol is a synthetic/derived compound necessary for regulating the body's internal mineral processing. This combined nature distinguishes Calceos from supplements containing only a single vitamin or mineral component. Supplemental Vitamin D is crucial for the body's ability to absorb the essential mineral calcium.


Essential Role in Supporting Calcium Metabolism

The general benefit of Calceos is to support calcium-phosphorus metabolism and promote robust bone health by supplementing these two key dietary elements. The combination is fundamental to correcting or preventing nutritional states where the body lacks sufficient quantities of these critical micronutrients for proper physiological maintenance, a typical use scenario being nutritional management in post-menopausal women.

The product's efficacy lies in the synergistic action of its components. The Calcium Carbonate provides the vital elemental calcium needed for bone structure and critical functions like nerve and muscle signaling. Simultaneously, the presence of Colecalciferol significantly enhances the active intestinal absorption of that calcium, ensuring the mineral is effectively utilized and deposited in the bone matrix. The combination is used to manage the underlying nutritional causes of bone fragility. This means the two ingredients work together to ensure the body can efficiently acquire and use the calcium it needs for strong bones.

What side effects are possible with Calceos?

Possible Side Effects and Safety Information

This information describes the documented safety profile of Calceos (Calcium Carbonate/Colecalciferol) as defined in official regulatory documents. It does not contain dosage instructions or treatment advice.

Frequency-Classified Adverse Reactions

Adverse reactions are classified according to how often they occur, based on regulatory conventions:

Frequency Side Effect Category
Uncommon (Affects 1 to 10 users in 1,000) Increased calcium levels in blood (Hypercalcaemia) or urine (Hypercalciuria).
Rare (Affects 1 to 10 users in 10,000) Gastrointestinal symptoms (e.g., Constipation, Flatulence, Nausea, Abdominal pain, Diarrhoea), and skin reactions (Pruritus, Rash, Urticaria).
Frequency Not Known Serious hypersensitivity reactions (e.g., Angioedema, Laryngeal oedema), Milk-alkali syndrome.

Safety Restrictions and Monitoring

The use of Calceos is subject to specific safety limitations defined in official labeling:

  • Contraindications: The medicine must not be used in patients with pre-existing Hypercalcaemia, Hypercalciuria, Nephrolithiasis (kidney stones), severe renal insufficiency, or prolonged immobilisation accompanied by elevated calcium levels.
  • Monitoring Requirements: For individuals on long-term treatment or with pre-existing kidney issues, official documents state that serum (blood) and urinary calcium levels, along with kidney function (serum creatinine), should be monitored regularly.
  • Population-Specific Notes: While use during pregnancy and lactation is permitted, intake must not exceed a specified total daily amount of calcium and vitamin D3. Caution is also noted for patients with sarcoidosis, requiring close calcium monitoring.

Overdose and Emergency Response

Overdose and When to Seek Help

Overdose of Calceos (Calcium Carbonate and Colecalciferol) is officially documented to lead to hypercalcaemia and hypervitaminosis D. The clinical manifestations described in regulatory sources include gastrointestinal symptoms such as nausea, vomiting, and constipation, alongside systemic signs like weakness, apathy, thirst (polydipsia), and increased urination (polyuria).


When to Seek Immediate Medical Attention

Urgent medical attention is required for extreme hypercalcaemia or the development of severe complications. Regulatory documents warn of potentially life-threatening outcomes, including cardiac arrhythmias, coma, and irreversible renal damage (nephrocalcinosis, renal calculi), particularly with chronic overdose. Death is a documented risk in isolated, severe cases.


Required Emergency Actions

If overdose is suspected, the official required action is the immediate discontinuation of all intake of calcium and Vitamin D supplements. A specific antidote does not exist. Management is symptomatic and supportive, demanding strict medical supervision. Treatment may involve measures such as rehydration and pharmacological interventions like bisphosphonates or calcitonin, along with rigorous monitoring of serum electrolytes and renal function. Overdose must also be avoided during pregnancy due to documented risks of fetal harm.

Therapeutic Uses of Calceos

Symptomatic Comfort During Periods of Disruption

Calceos is applied across domains where additional symptomatic support is needed, and is commonly used to help with conditions where functional stability becomes affected. It is often used when symptoms intensify and supportive relief is needed, and may assist with managing symptoms related to systemic imbalance, providing support that helps ease the overall symptom load.


Addressing Episodic Symptom Patterns

This medicine is commonly used across conditions presenting with acute episodes and situations involving recurrent or episodic manifestations. Calceos may assist with managing symptoms that create noticeable physiological strain, supporting the patient during difficult episodes by easing distress and helping maintain a sense of stability when symptoms are more noticeable. This medicine is relevant in conditions characterized by periods of heightened symptoms, including those involving systemic imbalance where supportive management is appropriate.


Support for Daily Stability and Functional Strain

Calceos is applied across domains where additional symptomatic support is needed, particularly for managing symptoms that interfere with daily comfort and may become more disruptive during flare-ups. It is relevant in clinical settings that involve acute or unstable symptom patterns and contributes to improved comfort during periods of heightened symptoms by providing supportive relief when symptoms interfere with routine activities.

Quick Fact: Relief for Functional Strain Calceos supports general well-being during symptomatic phases by assisting with maintaining functional stability when symptoms lead to temporary discomfort.

Eligibility and Restrictions for Use

Eligibility Map: Who Can and Cannot Use Calceos

Official regulatory documents define strict criteria for the use of Calceos (Calcium Carbonate and Colecalciferol).

Eligibility Scope Detail
Populations for whom use is allowed Adults and the Elderly are the established population. Use is permitted during Pregnancy and Lactation only when a calcium and vitamin D deficiency is confirmed.
Populations for whom use is contraindicated Patients with Hypersensitivity to the active substances or excipients (including peanut or soya allergy in some formulas). Absolute contraindications are Hypercalcaemia, Hypercalciuria, Hypervitaminosis D, Nephrolithiasis (kidney stones), and Severe Renal Impairment.
Age-related eligibility rules Use in the Paediatric Population (children and adolescents) is often restricted; some high-strength products are explicitly not intended for use in this group.
Eligibility-related restrictions Use with caution is required for patients with Sarcoidosis, Mild to Moderate Renal Impairment, and those with Prolonged Immobilisation accompanied by hypercalcaemia. Patients with certain hereditary sugar intolerances are not recommended to use the medicine.

These official eligibility statements establish clear, non-negotiable contraindications and specific conditional use requirements (e.g., in pregnancy or renal impairment) that govern who is eligible to use the medicine, according to governmental labeling.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Calceos (Calcium Carbonate and Colecalciferol) has officially documented interactions that primarily fall into three categories: reduced absorption of co-administered medicines, additive effects increasing risk, and altered metabolism of the Vitamin D component.

Reduced Systemic Exposure (Timing Required)

The calcium component can physically bind to other medicinal products in the digestive tract, which officially results in their reduced systemic exposure. A mandatory time separation is required when co-administering certain agents, including:

  • Antibiotics (Tetracyclines, Quinolones): Must be separated by at least three hours.
  • Bone Metabolism Agents (Bisphosphonates, Strontium): Requires timing separation.
  • Thyroid Hormones (Levothyroxine) and Estramustine: Should be administered at least two hours before or after Calceos.

Additive Pharmacodynamic Effects

Co-administration with the following agents increases the risk of hypercalcaemia (excess calcium in the blood), which is officially linked to serious adverse outcomes:

  • Cardiac Glycosides (e.g., digoxin): Increased hypercalcaemia risk leads to a heightened risk of cardiac dysrhythmia (cardiotoxicity).
  • Thiazide Diuretics: These reduce the renal elimination of calcium, resulting in an officially increased risk of hypercalcaemia.

Other Documented Interactions

  • Metabolic Enzyme Inducers (e.g., Phenytoin, Rifampicin): These officially reduce the effect of Colecalciferol by increasing its metabolic breakdown.
  • Food/Supplements: Consumption of foods containing Oxalic Acid (e.g., spinach, rhubarb) or Phytic Acid (e.g., whole cereals) must be separated from Calceos administration by at least two hours to prevent reduced calcium absorption.

Population-Specific Cautions

Official regulatory sources note that close monitoring of calcium levels is particularly important in patients with renal insufficiency and in elderly patients concurrently taking Thiazide Diuretics or Cardiac Glycosides.

Mechanism of Action

Calceos comprises a fixed combination of calcium carbonate and colecalciferol (Vitamin D3). The calcium carbonate component dissociates into calcium ions (Ca^2+) within the acidic environment of the stomach. These Ca^2+ ions are then absorbed primarily via active transport and passive diffusion across the proximal small intestine enterocytes, contributing directly to the systemic calcium pool. Colecalciferol, a prohormone, undergoes hepatic 25-hydroxylation and subsequent renal 1-alpha-hydroxylation to form its biologically active metabolite, calcitriol (1,25-(OH)2D3). Calcitriol functions as a high-affinity agonist at the intracellular Vitamin D Receptor (VDR), a nuclear receptor. Upon binding, the calcitriol-VDR complex forms a heterodimer with the Retinoid X Receptor (RXR) and translocates to the nucleus. This complex interacts with specific DNA sequences (Vitamin D Response Elements, VDREs), modulating the transcription of target genes. Downstream consequences include increased synthesis of calbindin and other transport proteins, leading to a molecular cascade that enhances active transcellular and passive paracellular absorption of Ca^2+ and phosphate in the intestine. The systemic physiological consequence is the coordinated modulation of calcium and phosphate homeostasis across the gastrointestinal tract, renal tubules, and skeletal tissue.

Dosage and Administration Information

How to Use Calceos

Calceos (Calcium Carbonate and Colecalciferol) is approved for oral administration as a chewable tablet.

Standard Administration and Dosing

The standard regimen for adults is one tablet taken twice daily, which provides a total daily intake of 1000 mg of elemental calcium and 800 IU of Vitamin D3. This twice-daily frequency is established for long-term supportive treatment. The official administration method requires the tablet to be chewed or sucked completely before swallowing; it is not intended to be ingested whole.

Timing and Separation Requirements

Proper administration involves adherence to specific timing rules to ensure intended absorption. The dose should be separated by at least two hours from foods high in oxalic acid (such as spinach) or phytic acid (found in whole cereals). This two-hour spacing rule also applies to the use of certain other oral medications, like tetracycline antibiotics and levothyroxine, to prevent reduced drug effectiveness.

Population-Specific Use

The standard adult regimen generally applies to older adults without modification. However, during pregnancy and lactation, the official maximum daily intake is capped at 1500 mg calcium and 600 IU Vitamin D3, which effectively limits the regimen to one tablet per day of the 500 mg/400 IU strength to remain within the established Vitamin D limit.

Recent Clinical Evidence

Overview of Calcium and Vitamin D Supplementation Studies

The components of Calceos (calcium carbonate and cholecalciferol, or Vitamin D3) have been widely investigated in clinical settings, particularly concerning their use as an adjunct therapy for osteoporosis and for the correction of combined calcium and vitamin D deficiencies, especially in older adults.


Efficacy Findings for Fracture Risk

Research on the combined effect of calcium and Vitamin D in reducing fracture risk has yielded mixed findings. While some randomized controlled trials (RCTs), particularly those conducted in institutionalized or frail elderly populations, have reported a statistically significant reduction in hip and non-vertebral fractures, other large community-based studies involving generally healthier, community-dwelling older adults have not consistently demonstrated a benefit in preventing fractures.

Overall meta-analyses suggest that the combination of calcium and Vitamin D may be associated with a small reduction in the risk of total fractures (non-vertebral and hip fractures combined) when compared to placebo.

Population Studied Common Findings Key Context
Institutionalized Elderly Reduction in hip and non-vertebral fractures observed in some trials. Often had lower baseline vitamin D status and calcium intake.
Community-Dwelling Adults Fracture risk reduction not consistently demonstrated in the general population. Results vary depending on study design and participant characteristics.

Safety and Monitoring

Adverse events reported in clinical trials involving calcium and Vitamin D supplementation are typically related to the gastrointestinal tract, such as constipation, flatulence, and abdominal pain. Uncommon adverse effects include hypercalcemia (high calcium levels in the blood) and hypercalciuria (high calcium levels in the urine). Due to the nature of these components, monitoring of serum and urinary calcium levels is often recommended during long-term treatment.

Frequently Asked Questions (FAQ)

Common questions about Calceos (FAQ)


Q: How is Calceos different from regular calcium tablets?

A: Official product information states that Calceos is a fixed-combination product. This means it is specifically formulated to provide both calcium carbonate and Colecalciferol (Vitamin D3) together. It is also supplied as a chewable tablet, which is a differentiating feature from some standard, single-ingredient calcium supplements.


Q: Is it better to take Calceos in the morning or at night?

A: Regulatory information indicates the recommended regimen is one tablet twice daily. While some product guidance suggests taking one in the morning and one in the evening, a key consideration for timing is adhering to the required separation time between the tablet and certain other medicines and foods, as detailed in the official 'Interactions' information.


Q: Is feeling more thirsty a possible side effect of Calceos?

A: Regulatory documents indicate that increased calcium levels in the blood (hypercalcaemia) are an uncommon side effect. Thirst (polydipsia) is a known symptom that may be associated with hypercalcaemia in patients taking this class of medicine.


Q: Are there any signs that a side effect from Calceos is serious?

A: Official information mentions that rare but serious adverse reactions can include severe hypersensitivity events, such as angioedema (swelling). The official product information also highlights that if taken alongside certain heart medications, the risk of high calcium levels is increased, which could potentially lead to serious cardiac effects. Consult the 'Interactions' section for details.


Q: Will drinking coffee or tea affect how Calceos works?

A: Official product information requires a separation of at least two hours between taking Calceos and consuming foods high in oxalic acid or phytic acid. Although coffee and tea are not explicitly listed in the mandatory separation rules, it is important to strictly adhere to the separation from all listed compounds to minimize any risk of reduced calcium absorption.


Q: Is Calceos available over the counter or is it prescription only?

A: In some countries, this medicine, or similar formulations, may be classified as a Pharmacy Medicine or available over the counter (OTC) without a full prescription. However, the exact dispensing status is determined by local regulatory authorities and may vary depending on the strength of the tablet.


Q: Do I need to take extra Vitamin D if I'm taking Calceos?

A: Regulatory sources advise patients to carefully calculate their total daily Vitamin D intake from all sources. This medicine provides a set amount of Vitamin D, and additional supplementation is generally not recommended unless specifically advised by a healthcare professional.


Q: What happens if I take too much Calceos by mistake?

A: Official information regarding overdose states that taking too much Calceos can lead to elevated levels of calcium in the blood (hypercalcaemia) and urine (hypercalciuria). If an overdose is suspected, it is recommended to promptly discontinue the use of Calceos and all other sources of calcium or Vitamin D.


Q: Can Calceos cause skin reactions or itching?

A: Yes, official regulatory documents list various skin reactions as rare adverse effects of the medicine. These reactions can include pruritus (itching), rash, and urticaria (hives).


Q: Does Calceos contain any sugar or artificial sweeteners?

A: The tablet formulation includes several excipients. Regulatory documents list both sucrose (a sugar) and sorbitol, as well as a sweetener like sucralose. Patients with certain hereditary sugar intolerances are cautioned against using this medicine.


Q: Is Calceos recommended for vegans or vegetarians?

A: The suitability of the product for certain diets is based on its ingredients. The Colecalciferol (Vitamin D3) concentrate used is often sourced from lanolin (sheep’s wool), and some ingredients may be derived from gelatin or partially hydrogenated soybean oil, which may not align with strict vegan or vegetarian diets.


Q: Does Calceos affect the results of any medical tests?

A: Yes, the product affects calcium levels. Official warnings require the regular monitoring of serum (blood) and urinary calcium levels during long-term treatment. As this is the therapeutic purpose of the medicine, its components will naturally influence the results of these specific tests.


Q: Does Calceos have a specific flavor?

A: According to the official list of ingredients, the formulation of Calceos includes lemon flavouring.


Q: Can men take Calceos for bone density?

A: Yes. While the medicine is commonly discussed for women’s health, the official posology (dosing) applies to 'Adults and the elderly' in general. The therapeutic indications for deficiency correction and adjunct osteoporosis treatment are applicable to adult men as well as women.


Q: What are the main benefits of taking Calceos long-term?

A: Official documents establish Calceos for long-term supportive treatment. The main benefit is the continuous correction of combined calcium and Vitamin D deficiencies, and its role as an adjunct (supporting) therapy for established osteoporosis (thinning of the bones).


Q: Is it normal to have chalky taste after taking Calceos?

A: The medicine is a chewable tablet that contains calcium carbonate, a naturally chalky substance. As the official instructions require the tablet to be chewed or sucked completely before swallowing, experiencing a chalky or noticeable taste is generally expected.


Q: How does Calceos help in treating osteomalacia?

A: Official regulatory guidance states that the combination of calcium and Vitamin D is indicated for supplementation as a therapeutic treatment in cases of established osteomalacia. Osteomalacia is a condition that causes softening of the bones, often due to severe deficiency.


Q: Is Calceos a lifelong medication or only for a set time?

A: Regulatory documents describe Calceos as a medication for long-term supportive treatment. The medication is generally intended to correct chronic deficiencies or support chronic conditions like osteoporosis, meaning the need for continued treatment is typically evaluated by a healthcare professional over time.


Q: Are there any dietary restrictions needed when taking Calceos?

A: Yes. Official information requires a time separation, but not a full restriction, from certain foods. You must separate the tablet by at least two hours from foods high in oxalic acid (such as spinach) or phytic acid (such as whole cereals) to avoid reducing calcium absorption.


Q: Is Calceos safe to take while on antibiotics?

A: The use of Calceos concurrently with certain antibiotics is subject to mandatory time separation rules. Specifically, antibiotics like tetracyclines and quinolones must be administered at least three hours apart from Calceos. This separation prevents the calcium component from binding to the antibiotic and reducing its effectiveness.


Q: Does Calceos interact with medications for indigestion or heartburn?

A: Calcium salts are found in some indigestion remedies. While no general antacid interaction is listed in all product information, certain other medicines for bone conditions (bisphosphonates) and thyroid hormone (levothyroxine) require a strict two- to three-hour separation. Information regarding specific interactions with common antacids may not be detailed in the official product label, so consultation with a healthcare provider is recommended.


Q: Is the chewable form of Calceos as effective as the tablet?

A: Calceos is officially formulated as a chewable tablet, and this is the specific form on which its approved effectiveness is based. The administration guidelines explicitly require the tablet to be chewed or sucked completely before swallowing.

How should Calceos be stored and disposed of?

How to Store and Dispose of Calceos

The storage and disposal of Calceos 500mg/400IU Chewable Tablets must adhere strictly to official regulatory requirements to ensure product quality and safety.

Storage Conditions

Requirement Official Instruction
Maximum Temperature Do not store above 25°C.
Environmental Protection Store in the original container to protect the tablets from moisture.
Packaging Do not swallow the silica gel desiccant granules in the container stopper.
Child Safety Keep this medicine out of the sight and reach of children.

Disposal Instructions

Official labeling prohibits discarding unused or expired Calceos via wastewater or household waste. To ensure environmentally compliant disposal, patients are instructed to ask their pharmacist how to properly throw away medicines no longer needed.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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