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Dagravit Total 30

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Dagravit Total 30

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Method of action: Mineral, Vitamins

Treatment option: Alcoholism

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.

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Overview of Dagravit Total 30

Quick Facts

Property Description
Active Ingredients 13 Essential Vitamins, 10 Essential Minerals/Trace Elements
Form Dragee (Coated Tablet)
Pharmacological Class Nutritional Supplement / Multivitamin/Mineral Preparation
Common Use General Health Maintenance, Daily Nutritional Support
Origin Primarily Synthetic (micronutrient salts and compounds)

What is Dagravit Total 30 Classified as?

Dagravit Total 30 is an oral preparation classified as a nutritional supplement, belonging to the high-level pharmacological class of Multivitamin/Mineral Supplements. The primary function of this product is to complement the diet by providing foundational micronutrients, rather than to treat, diagnose, cure, or prevent specific diseases. The Dutch distributor, Vemedia B.V., markets this product with a specific focus on daily systemic support for adults, positioning it as a comprehensive broad-spectrum formula. The preparation is generally composed of primarily synthetic compounds, such as various mineral salts and chemically derived vitamin forms, which are engineered for stability and proper absorption.

Comprehensive Composition: Vitamins, Minerals, and Trace Elements

This product contains a broad Essential Micronutrient Matrix, including 13 essential vitamins and 10 essential minerals and trace elements, which are crucial for maintaining human health. Key active ingredients include water-soluble B-complex vitamins (such as Thiamine and Foliumzuur), fat-soluble vitamins (such as Retinyl Acetate and Cholecalciferol), and essential metallic and non-metallic elements like Calcium, Iron, and Zinc. Dagravit Total 30 is notably formulated as a dragee or coated tablet, an oral dosage form that utilizes a solid excipient matrix to ensure the stability and controlled intake of the varied active compounds.

General Purpose: Support for Overall Wellness

The general purpose of Dagravit Total 30 is to support overall wellness and contribute to general health maintenance through the principle of Nutrient Repletion. By ensuring the daily availability of essential cofactors, the supplement is designed to contribute to metabolic efficiency, including the transformation of food into energy to support systemic vitality. This approach is based on the role of multiple vitamins and minerals working synergistically to support the body's metabolic processes.

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What side effects are possible with Dagravit Total 30?

Possible Side Effects and Safety Information

This section outlines the officially documented adverse reactions and safety constraints for Dagravit Total 30, as established by authoritative government regulatory bodies for multivitamin/mineral preparations.


Official Adverse Reactions and Frequencies

Side effects for this type of nutritional supplement are generally limited, with frequency classifications often based on spontaneous reporting rather than controlled trials.

System-Organ Class Adverse Reaction Official Frequency
Immune System Disorders Hypersensitivity reactions (e.g., rash, itching) Not Known
Immune System Disorders Anaphylactic shock (severe allergic reaction) Rare
Gastrointestinal Disorders Mild, transient gastrointestinal discomfort Not Known
Renal and Urinary Disorders Change in urine color (harmless yellowing due to Riboflavin) Common / Expected

Population-Specific Safety Considerations

Safety constraints and cautions exist for specific groups, as detailed in regulatory product information:

  • Known Hypersensitivity: The preparation is contraindicated in individuals with a known allergy to any of the active ingredients or excipients.
  • Renal Impairment: Caution is advised in patients with impaired kidney function, as this may increase the risk of accumulation of certain vitamins and minerals.
  • Kidney Stone History: Use requires caution in individuals with a history of recurrent kidney stones (nephrolithiasis), primarily related to the presence of Calcium and Vitamin C.

Safety-Related Restrictions

Regulatory documents include high-level restrictions to ensure safe use:

  • Dose Limits: The stated daily dose must not be exceeded to prevent potential nutrient toxicity.
  • Co-Administration: The preparation should not be combined with other high-dose products containing Vitamin A or Vitamin D to avoid hypervitaminosis.
  • Laboratory Testing: High intake of certain vitamins, particularly Biotin, may officially interfere with some laboratory test results, potentially causing false readings.
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Overdose and Emergency Response

Overdosage with Dagravit Total 30 is primarily associated with the toxic effects of its high-risk components, particularly Iron and the fat-soluble Vitamins A and D. The regulatory profile for this class of supplement notes that symptoms often involve the gastrointestinal system, presenting with nausea, vomiting, diarrhea, and abdominal pain. Other manifestations can include headache, fatigue, and systemic signs like polyuria and polydipsia, which are indicative of high calcium levels (hypercalcemia) from Vitamin D excess.

Severe outcomes are documented, highlighting the risk of rapidly progressing, life-threatening conditions. These include effects such as metabolic acidosis, hepatic failure, and cardiovascular collapse, particularly following acute, massive ingestion of the Iron component. The official regulatory guidance mandates an immediate emergency response for any suspected overdose. It is required to seek immediate medical attention and contact emergency services without delay, even if symptoms are not yet fully evident.

Management listed in regulatory documents is focused on symptomatic and supportive treatment. This may involve procedures such as fluid and electrolyte balance monitoring, and the potential use of specific chelating agents for severe Iron toxicity. Official labeling further notes that young children are highly vulnerable to the severe and potentially fatal effects of Iron overdose.

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Therapeutic Uses of Dagravit Total 30

What Dagravit Total 30 Treats: Main Uses and Benefits

Dagravit Total 30 generally functions as a comprehensive nutritional support system, focusing on preventing and correcting non-specific discomforts associated with suboptimal micronutrient status rather than treating specific diseases. Essential vitamins and minerals may be vital for energy production, immune function, and overall systemic health, making supplementation relevant when diet alone is insufficient.

It is commonly used to help with symptoms of general tiredness and easy fatigability when these manifestations may be linked to an inadequate diet, particularly gaps in B-vitamins and Iron. The supplement is also applied in addressing contexts marked by restrictive eating patterns or periods of increased physiological demand that may create mild nutritional insufficiency.

Dagravit Total 30 plays a role in managing systemic resilience, specifically supporting the proper function of the immune system and contributing to the supportive foundation for general health maintenance in patient groups such as older adults and individuals with high activity levels.

Quick Fact: Relief for Nutritional Gaps

This preparation assists with maintaining functional stability by addressing marginal nutritional status and contributes to easing the overall symptom load of non-specific malaise.

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Eligibility and Restrictions for Use

Eligibility: Official Regulatory Information

The eligibility for using Dagravit Total 30 is strictly defined by official regulatory labeling, which establishes specific age groups for use, absolute prohibitions, and conditions that require mandatory expert consultation.

Classification Eligibility Status
Approved Age Groups Adults (18 years and older). Children from 4 years up to 17 years (at age-specific regulatory limits).
Absolute Contraindication Individuals with known hypersensitivity to any of the vitamins, minerals, or excipients in the formulation.
Prohibited Use Children under the age of 4 (or up to age 17, depending on dosage) due to regulatory limits on Vitamin B6 content.
Conditional Use Individuals who are pregnant, lactating, suffering from a chronic illness (e.g., diabetes), or taking medication. Expert consultation is mandatory before use in these populations.

The product is categorized for generally healthy adults and requires mandatory professional review for vulnerable or medically complex populations. The use-not-established status applies to those who bypass the mandatory consultation for conditional-use categories.

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What should I know about interactions with other medicines?

Interactions with other medicines and products

Dagravit Total 30 is a multivitamin and mineral preparation. The official interaction profile is structured around the binding properties of the polyvalent cations (Iron, Calcium) and the metabolic effects of Folic Acid, as described in government drug labels and monographs.

Timing-Based Interaction Constraints

Co-administration with the supplement requires mandatory timing separation for certain oral medications. The Iron and Calcium components may reduce the absorption and bioavailability of drugs such as Quinolone antibiotics (e.g., Ciprofloxacin), Tetracycline antibiotics (e.g., Doxycycline), and Thyroid medications (e.g., Levothyroxine) through chelation. Regulatory documents stipulate that these medicines must be administered at least two hours before or two hours after the multivitamin/mineral preparation to minimize reduced drug exposure.

Exposure-Modifying Substances

Official documents note that the Folic Acid component may alter the clearance and reduce the effectiveness of the anti-seizure drug Phenytoin. Additionally, the Iron component may reduce the absorption of Levodopa and certain Bisphosphonates, a significant interaction classified as Major in some regulatory systems.

Food and Supplement Restrictions

Concurrent use with Antacids, Milk, Dairy Products, Tea, or Coffee may reduce the absorption of the Iron component. Furthermore, co-administration with other vitamin/mineral supplements containing high levels of Iron or fat-soluble vitamins (A, D, E, K) must be restricted due to the official risk of additive micronutrient exposure.

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Mechanism of Action

How Dagravit Total 30 Works: Mechanism of Action

Cellular Energy Metabolism

This mechanism centers on the B-group vitamins ( B1, B2, B3, B5, B6) acting as essential coenzymes to participate in key metabolic pathways, including the Krebs cycle and oxidative phosphorylation. By saturating the enzyme systems responsible for converting macronutrients into ATP, the process contributes to ATP generation capacity and cellular maintenance across all tissues.

Integrated Antioxidant and Redox Cascade

The formulation acts by providing direct antioxidants (Vitamins C, E) and cofactors ( Zinc, Selenium) necessary for major endogenous enzymes like Superoxide Dismutase. This combined action functions to quench Reactive Oxygen Species and influence the cellular redox state, influencing the processes related to membrane and DNA structural integrity.

Structural and Hematopoietic Homeostasis

The mechanism includes the hormone-like regulation of Calcium absorption by Vitamin D to facilitate the mineralization of skeletal tissue. Separately, it facilitates blood cell production through the co-dependence of Iron, Folate, and Vitamin B12 in DNA synthesis and oxygen transport, participating in the pathways for tissue synthesis and systemic oxygen transport.

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Dosage and Administration Information

The use of Dagravit Total 30 is governed by explicit instructions detailing the required route, daily quantity, frequency, and administration timing, consistent with global regulatory practices for multivitamin/mineral (MVM) supplements.

Administration Scope

Instruction Detail
Route of administration Oral use (ingestion by mouth).
Dosing schedule Adults (Ages 18+): 1 to 3 dragees per day. Adolescents (Ages 12+): 1 to 2 dragees per day.
Timing in relation to meals The dragee should preferably be taken during meals.
Preparation requirements To be swallowed whole with water. No dilution or reconstitution required.
Age-group administration rules Children (Ages 4-12 years): 1 dragee per day. The product is not suitable for children up to and including 3 years.
Special procedural conditions The recommended daily dosage must not be exceeded. This restriction is a standard administration principle designed to prevent intake above established Tolerable Upper Intake Levels for certain components.

Instruction Classifications (high-level)

Classification Detail
Administration method type Oral (tablet/dragee)
Frequency pattern Daily (intended for continuous consumption).
Regulatory basis National Health Agencies/Official Labeling.
Use-context constraints Must be taken with a meal and must respect the age-specific quantity limits.

Resulting procedural structure

Official step sequence:

  • Take the specified number of dragees once daily.
  • Consume the dragee during a meal.
  • Swallow the dragee whole with water.

Connection to the overall use protocol (2–4 sentences):

The official instructions establish a standardized, non-exceedable daily dose taken through the oral route. This structured approach defines the required frequency and the crucial timing constraint of administration with meals, ensuring the standardized method of use according to regulatory guidelines.

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Recent Clinical Evidence

Research Evidence / Overview of Studies for Dagravit Total 30

This overview summarizes the scientific studies conducted on broad-spectrum multivitamin/mineral preparations, which align with the composition of Dagravit Total 30. This summary focuses only on the structure and findings of scientific research and must not be used as medical advice, personal guidance, or a recommendation for treatment.


Evidence on Nutritional Status and Micronutrient Repletion

Research examined the role of these preparations in contributing to the daily intake of essential nutrients. Studies monitored blood and serum biomarkers for various vitamins and minerals to see how concentrations changed in individuals who reported using supplements. Findings described patterns where those who used multivitamin/mineral preparations were generally associated with a higher prevalence of achieving nutrient adequacy, meaning these individuals were observed to meet the established Recommended Daily Amounts (RDAs) for many micronutrients. A key limitation is the 'healthy user bias' often observed in this type of research, which may complicate the interpretation of findings.

Research on Cognitive Function and Age-Related Changes

The multivitamin/mineral preparation was evaluated in research exploring specific populations, mainly generally healthy older adults aged 65 and over. This area benefits from large-scale, long-term Randomized Controlled Trials (RCTs). These studies monitored outcomes using various cognitive assessment scores, focusing on functions like episodic memory and the rate of cognitive aging. The reported findings described patterns where the rate of change in these assessment scores sometimes was associated with the intervention compared to the control groups. Data for certain groups, such as younger adult populations, remain insufficient.

Studies Investigating General Tiredness and Wellbeing

Research examined multivitamin/mineral preparations in trials assessing short-term or episodic symptom patterns related to general tiredness and perceived energy levels. The findings for this application were mixed, and evidence quality varies across studies. Studies monitored changes in subjective fatigue scale scores. The evidence highlights that the follow-up durations were limited in many interventional trials, providing limited insight into potential sustained changes.

Research on Systemic Support and Immune Function

Multivitamin/mineral use was evaluated in research exploring systemic support and immune function, particularly in older adults. Findings regarding data show patterns related to the frequency of infections were mixed and often inconsistent across different systematic analyses. Certainty remains low for evidence exploring the prevention of infections in generally healthy, non-deficient older adults, and long-term effects are not fully established regarding measures of systemic function.

Key Studies & References

  1. Effect of multivitamin/mineral supplementation on fatigue and mood: a systematic review and meta-analysis of randomized controlled trials
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Frequently Asked Questions (FAQ)

Common questions about Dagravit Total 30 (FAQ)

Q: What should I do if I miss a day of taking the supplement?

If a dose is forgotten, official dosing information indicates that it may be taken as soon as it is remembered. However, if it is close to the time for the next scheduled dose, the missed dose should be skipped. The labeling advises against taking a double dose or two doses at the same time to compensate for a missed dose.


Q: What is the best time of day to take Dagravit Total 30 (morning, afternoon, or evening)?

Official administration instructions specify that the supplement should be taken during a meal once a day. Regulatory documents do not specify whether the morning, afternoon, or evening meal is preferable. The core administration constraint is taking it with a meal, which is consistent with general guidelines for this type of supplement.


Q: Can I split the dragee or chew it instead of swallowing it whole?

The official product information specifies that the dragee (coated tablet) must be swallowed whole with water. Breaking the coating may alter the release characteristics of the components, which is not consistent with the intended method of use described in the regulatory labeling.


Q: Is Dagravit Total 30 safe to take while pregnant or breastfeeding?

Regulatory eligibility documents classify pregnant and lactating individuals as a Conditional Use population. This means the preparation is not for general use in these groups without medical clearance. Consultation is a mandatory step before use for pregnant or lactating individuals.


Q: What is the best way to dispose of expired or unused Dagravit Total 30?

Standard guidelines for disposing of unused supplements often suggest mixing the product (do not crush the tablets) with an unappealing substance, such as used coffee grounds or cat litter. The mixture can be placed in a sealed container or bag for disposal with household trash. This practice helps prevent accidental ingestion.


Q: Where is the Dagravit Total 30 product manufactured or sourced from?

Regulatory labeling requires the name and place of business of the manufacturer, packer, or distributor to be included. The provided product content identifies the distributor as the Dutch company Vemedia B.V., but the provided product information does not specify the exact manufacturing location.


Q: Are there any lifestyle factors (e.g., alcohol, smoking) that interact with the supplement?

Official interaction profiles primarily list known drug, food, and supplement interactions. While alcohol is not typically listed as a direct contraindication, chronic heavy use can interfere with the body's absorption of several B-vitamins. Any concerns regarding lifestyle factors should be discussed with a healthcare provider.


Q: How should Dagravit Total 30 be stored for maximum freshness?

Official documents describe the necessary storage conditions to maintain product stability and effectiveness. These conditions include storing it at room temperature (15-25 C), keeping it in a dry and dark place to protect it from moisture and light, and ensuring the container is kept tightly sealed.

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How should Dagravit Total 30 be stored and disposed of?

Official Storage and Handling Requirements

Regulatory documents define specific conditions for storing Dagravit Total 30 to maintain its stability and effectiveness. The product must be stored within the following constraints, as defined by official labeling.

Storage Requirement Condition
Temperature Room temperature (15-25 C)
Environmental Protection Store dry and dark (protect from moisture and light)
Container Integrity Keep container sealed (Afgesloten)
Child Safety Keep out of reach of young children

Disposal

Official labeling does not provide product-specific instructions for the disposal of unused or expired Dagravit Total 30. Standard health guidelines recommend following local regulations for the safe disposal of medicinal products.

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

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