Гингиум

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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 Гингиум

Quick Facts

Property Description
Active ingredient Ginkgo Bilobae Foliorum Extract
Form Film-coated tablet or Capsule
Pharmacological class Phytomedicine; Neuroprotective / Vasoactive Agent
Common use Supporting age-related cognitive function and peripheral circulation
Origin Natural (from Ginkgo biloba L. leaves), standardized extract

What Type of Medicine is Гингиум (Gingium)?

Гингиум is categorized as an oral phytomedicine, meaning it is a medicinal product derived directly from a botanical source, and specifically manufactured by the pharmaceutical company Hexal AG. This product is a monopreparation, containing only the Ginkgo leaf dry extract as its active substance. The active components are typically linked to the high-level pharmacological actions of supporting neurological function and regulating blood vessel tone. Its classification as a herbal medicinal product is for use in supporting the symptomatic treatment of age-related impairment.

Composition and Pharmaceutical Form of the Extract

The active component in Гингиум is the Ginkgo Bilobae Foliorum Extract (Ginkgo leaf dry extract), which originates from the leaves of the ancient Ginkgo biloba L. tree. This ingredient is a highly standardized extract, meaning the manufacturing process ensures consistent and measured quantities of its key beneficial components: ginkgo flavone glycosides and terpene lactones. Гингиум is primarily provided for the oral route of administration in the form of film-coated tablets or hard capsules. This standardized composition and quality are maintained for defined use.

General Purpose and Supportive Action

The general purpose of Гингиум is to offer support for vascular and cellular health, particularly in tissues reliant on microcirculation, such as the brain and the body’s extremities. This function involves the extract's dual actions as an antioxidant and a substance that supports microcirculation. This means it is typically used in a scenario where an individual seeks to maintain healthy cognitive function or to relieve minor discomforts associated with peripheral circulatory disorders, such as experiencing coldness or a sensation of heaviness in the limbs.

Regulatory References

  1. NIH resources on Ginkgo biloba

What side effects are possible with Гингиум?

Possible side effects and safety information

The safety profile for Ginkgo Bilobae Foliorum Extract, the active substance in Гингиум, is formally documented according to regulatory standards, classifying adverse reactions by frequency and physiological system. This information is derived from official regulatory sources and does not constitute medical advice or instructions for use.


Adverse Reaction Classification

Side effects are primarily categorized into Nervous System Disorders (headache, dizziness), Gastrointestinal Disorders (diarrhoea, nausea, vomiting, abdominal pain), and Immunological/Skin Reactions (allergic skin reactions, hypersensitivity).

Classification Example Reactions (System-Organ Class)
Very Common (ge 1/10) Headache (Nervous System)
Common (ge 1/100 to <1/10) Dizziness (Nervous System); GI disturbances (Gastrointestinal)
Not Known Bleeding events; Allergic Shock (Severe Systemic Reactions)

Serious Adverse Reactions and Safety Restrictions

Official regulatory documents highlight the potential for Serious Adverse Reactions, particularly Bleeding of individual organs, including cerebral or gastrointestinal haemorrhage, the frequency of which is Not Known. The risk of Allergic Shock is also documented.

Several key Safety Restrictions are officially noted:

  • Contraindications include known hypersensitivity to the extract and Pregnancy due to the risk of increased bleeding.
  • Use is Not Recommended in Children and Adolescents (under 18) due to insufficient data, or during Lactation.
  • Specific warnings apply to patients with Epilepsy and those with a pathologically increased bleeding tendency.
  • Discontinuation is officially Recommended 3 to 4 days prior to any planned surgery due to the potential for interference with blood clotting.

Overdose and Emergency Response

The official regulatory profile for overdose of Гингиум (Ginkgo Bilobae Foliorum Extract) is defined by a consistent absence of documented clinical experience in humans. This status is uniformly reported across international regulatory records, including those published by the European Medicines Agency (EMA) and national health authorities.

Overdose Scope and Regulatory Statements

The governing regulatory finding is that no cases of human overdose have been reported with the standardized extract in the official labeling. This foundational statement leads to a defined lack of information regarding clinical presentation or management procedures. Consequently, regulatory documents do not formally list any of the following:

Regulatory Feature Status in Official Labeling
Documented Manifestations No specific clinical signs, symptoms, or laboratory abnormalities are formally described.
Dose-related Factors No toxic dose level for humans is established or referenced in regulatory texts.
Emergency Actions No specific, regulator-mandated emergency action protocols or supportive measures are documented.
Monitoring Requirements No hospital monitoring or continuous observation requirements are specified for an overdose event.

When to Seek Urgent Help

The official labeling does not contain specific instructions or defined criteria for when to seek urgent medical attention for a documented overdose of Гингиум. The entirety of the overdose profile is strictly constrained by this regulatory finding of non-reporting, meaning no adverse outcomes or procedural requirements have been officially established. This description reflects the highest-level regulatory classification.

Therapeutic Uses of Гингиум

The therapeutic application of Гингиум is relevant in contexts involving heightened systemic burden related to age-associated functional decline and minor circulatory concerns.

This phytomedicine is commonly used in situations involving certain distressing symptoms across two core therapeutic domains. Its application includes the symptomatic management of: mild-to-moderate impairment of cognitive function, symptoms of minor circulatory disorders in the limbs, and certain cases of vertigo (dizziness).

This phytomedicine is relevant for managing symptom clusters that interfere with daily comfort, such as memory lapses, difficulty concentrating, and chronic sensations of coldness or heaviness in the extremities. This supportive approach supports the patient during difficult episodes by easing distress when symptoms are more noticeable.

“This supportive therapeutic benefit assists with maintaining functional stability during symptomatic periods.”


Quick Fact: Relief for Functional Discomfort

Domain Core Symptom Management Patient Benefit
Cognitive Memory lapses, concentration difficulty Contributes to easing the overall symptom load
Circulatory Coldness, heaviness in limbs Supports general well-being during symptomatic phases
Neurosensory Symptomatic management of vertigo May assist with comfort

Eligibility and Restrictions for Use

Гингиум (Ginkgo Bilobae Foliorum Extract) is officially indicated for use solely in the adult and elderly population. Its use is subject to specific constraints documented in governmental regulatory sources.

Contraindicated Populations

Use of this medicine is strictly contraindicated for pregnant women due to the risk of increased bleeding. It is also prohibited for any individual with confirmed hypersensitivity to Ginkgo preparations or its excipients.

Age and Physiological Restrictions

Regulatory data is insufficient to establish safety and effectiveness for use in children and adolescents under 18 years of age, and its use is therefore not recommended in this age group. Similarly, use is not recommended for breastfeeding women due to a lack of established data on excretion into human milk.

Conditional Use and Cautions

Patients with pre-existing conditions such as epilepsy or a pathologically increased bleeding tendency must use the product with caution. Furthermore, the official label requires that the product be discontinued 3 to 4 days prior to any planned surgical procedure as a necessary precaution.

What should I know about interactions with other medicines?

Interactions with Other Medicines and Products

Official regulatory documents describe several domains of interaction that may occur with this product, primarily related to altered bleeding risk and changes in drug exposure.

Documented Interaction Domains

Interaction Domain Practical Implication
Anticoagulants and Antiplatelet Drugs (e.g., Warfarin, Aspirin, Clopidogrel) Increased risk of bleeding. Use is sometimes advised against or requires intensified monitoring (e.g., International Normalized Ratio, INR).
P-glycoprotein (P-gp) Substrates (e.g., Dabigatran etexilate) Inhibition of the P-gp transporter may lead to increased plasma levels of the co-administered drug.
CYP450 Enzyme Modulators (e.g., Efavirenz, Nifedipine) Potential for reduced drug effectiveness (due to enzyme induction) or increased exposure (due to inhibition). Concomitant use with Efavirenz is generally not recommended.

Procedural and Contextual Constraints

Due to the documented potential to influence blood clotting, a specific procedural constraint requires the product to be discontinued as a precaution 3 to 4 days prior to any scheduled surgery or dental procedure.

Patients taking medications for conditions such as epilepsy, diabetes, or high blood pressure should consult a healthcare professional before starting treatment, as the product may influence the effectiveness of these concurrent treatments. This is particularly relevant for individuals with an existing pathological bleeding tendency.

Mechanism of Action

Mechanism of Action: Molecular and Physiological Modulation

Гингиум (Gingium), derived from Ginkgo biloba extract, exerts a multi-targeted pharmacodynamic effect involving vascular tone regulation, cellular defense, and signaling pathway modification. The flavonoid glycosides influence vascular smooth muscle, promoting vasodilation via the release of endothelium-derived relaxing factors. This interaction leads to an increase in blood flow, particularly within the microcirculation, affecting tissue perfusion and influencing local blood supply dynamics.

Simultaneously, the extract's components act as antioxidants, neutralizing reactive oxygen species (ROS) and inhibiting lipid peroxidation in cell membranes. This mechanism reduces damage pathways and influences the maintenance of neuronal integrity. Additionally, terpene lactones (ginkgolides) function as antagonists to the Platelet Activating Factor (PAF) receptor, thereby preventing PAF-mediated platelet aggregation and activation. By modifying this specific signaling sequence, the mechanism alters blood fluidity and influences certain localized inflammatory mediators.

Dosage and Administration Information

Official Administration Guidelines

The administration of the Ginkgo Biloba Foliorum Extract contained in Гингиум follows a standardized usage protocol. This medicine is strictly designated for oral administration, typically provided in the form of film-coated tablets or hard capsules.

The standard adult posology outlines a total daily intake of the standardized extract generally ranging from 120 mg to 240 mg. To maintain a consistent systemic concentration, this dose is routinely administered in two or three divided portions throughout the day.

Usage Condition Standardized Parameters
Route of Administration Strictly oral use (swallowing the tablet or capsule whole).
Dosing Schedule Total daily dose is 120 mg to 240 mg, administered in divided doses.
Timing & Intake Must be taken with meals and swallowed whole with water.
Duration for Assessment A course of three months is the standard period before evaluating benefit for cognitive symptoms.
Population Rules The standard dose applies to older adults, but use is not recommended for persons under 18 years of age.

These details define the standardized approach to using the medicine, focusing solely on the manner, amount, and timeframes for administration.

Recent Clinical Evidence

Research evidence / Overview of studies for Гингиум


Evidence for use in Age-Related Cognitive Changes

Research on Гингиум was studied for use in older adult populations used in research exploring how symptoms change over time. These studies, which include randomized controlled trials (RCTs) and systematic reviews, examined outcomes related to systemic or functional imbalance, such as memory recall and attention, which may be affected by age. The findings describe patterns observed in the studies where some trials reported how symptoms evolved in the observed populations, indicating short-term measurement differences in some cognitive scores compared to control groups.

However, the outcomes were not always consistent, and the findings were mixed depending on the specific cognitive test was evaluated in. It is important to note that long-term effects are not fully established. Follow-up durations were limited in most key studies, and certainty remains low regarding how these findings translate broadly.


Evidence for use in Intermittent Claudication (Circulatory Support in Legs)

Research on Гингиум was studied for conditions marked by functional limitations such as intermittent claudication. Studies in this area monitored outcomes reflecting daily functioning or activity level, particularly focusing on the measurement of a participant's pain-free walking distance over defined time intervals. Some trials data show patterns related to measurement differences in the pain-free walking distance among the observed groups compared to those receiving a placebo.

A key limitation is that the available research is limited, and sample sizes were modest in many trials. Comparative evidence is lacking, and the trials generally observed responses over several weeks or months, meaning there is limited information for long-term outcomes related to overall functional limitations.


Evidence for use in Tinnitus and Vertigo

Гингиум was evaluated in individuals experiencing chronic ringing in the ears (tinnitus) and feelings of dizziness (vertigo), which are conditions characterized by fluctuating or episodic manifestations. Research examined these conditions involving periods of heightened symptoms using patient-reported outcomes describing perceived discomfort. For both conditions, reports on the consistency of patterns have been mixed across studies.

Some trials reported how symptoms evolved in the observed populations, while others indicate no clear difference from control groups. The evidence quality varies across studies, and often data are still emerging. The available evidence is considered limited and often relies on study designs that may not provide the highest level of certainty.

Frequently Asked Questions (FAQ)

Common questions about Гингиум (FAQ)


Q: What are the official, approved uses for Гингиум?

Regulatory indications for this medicine include the improvement of age-related cognitive impairment. It is also indicated for the relief of symptoms associated with minor circulation problems, such as the sensation of coldness in the hands and feet.


Q: What is the primary mechanism described for Гингиум's action?

Studies referenced in official regulatory documents indicate that the extract has several pharmacological actions. These include the ability to reduce blood viscosity and promote improved blood flow to certain areas. It is also noted to exhibit an inhibitory action on platelet aggregation.


Q: What is the typical age range of people who use Гингиум?

Official regulatory guidance advises that use is not recommended for children and adolescents under 18 years of age due to insufficient supporting data. The product's regulatory designation applies to adults and the elderly.


Q: Can Гингиум be crushed or mixed with food?

Official regulatory texts describe the medicinal product as a film-coated tablet or capsule intended for oral use. Official instructions describe the medicine as being administered by swallowing the tablet or capsule whole. The guidance provided does not include any information or instructions for crushing or opening the medicine to mix it with food or drink.


Q: Are there any common side effects people report after starting Гингиум?

Official regulatory documents state that common reported side effects include headache, dizziness, abdominal pain, nausea, and vomiting. Less frequently reported events include allergic skin reactions. Additionally, individual cases of organ bleeding have also been noted.


Q: Can Гингиум cause stomach upset or digestive issues?

Gastrointestinal disorders are reported as common side effects in regulatory documents. These common issues can include abdominal pain, diarrhea, nausea, and vomiting.


Q: What is the risk of bleeding associated with Гингиум?

Official warnings indicate that products containing this active ingredient may increase the susceptibility to bleeding. Case reports of bleeding in various organs, such as the eye, nose, and gastrointestinal tract, have been noted, especially in people with a higher risk of bleeding or those using certain blood-thinning medications. Regulatory guidance includes a general recommendation that the medicine be stopped a few days before surgical procedures.


Q: What are the main contraindications for using Гингиум?

The official product information specifies several contraindications. These include known hypersensitivity or allergy to the active substance or its ingredients. Use during pregnancy is also explicitly contraindicated. Additionally, the product is not generally recommended for people with a pathologically increased bleeding tendency.


Q: Are there specific warnings about combining Гингиум with blood thinners?

Official regulatory information contains warnings about co-administering the product with anticoagulant (e.g., warfarin) or antiplatelet drugs (e.g., clopidogrel). Combining these medications may influence their effects. Official guidance indicates that adequate patient monitoring is relevant when these types of medicines are used concurrently.


Q: Does Гингиум interact with common pain relievers like ibuprofen?

Official warnings note a potential interaction with antiplatelet drugs, which includes non-steroidal anti-inflammatory drugs ( NSAIDs) like ibuprofen. Combining Гингиум with these common pain relievers may influence their effect and could potentially increase the overall susceptibility to bleeding.


Q: Can I take Гингиум if I have a history of seizures?

According to regulatory documentation, patients with a history of epilepsy should be aware that the onset of further seizures promoted by Ginkgo preparations cannot be ruled out. This is included as a special warning in the product information.


Q: Is it true that Гингиум helps with tinnitus (ringing in the ears)?

The regulatory monograph for the active ingredient allows for its traditional use for the symptomatic relief of tinnitus of vascular origin in some specific products. However, official use is generally preceded by the need for a medical professional to rule out any serious underlying condition as the cause of the tinnitus.

How should Гингиум be stored and disposed of?

Storage and Disposal Requirements

Гингиум (Gingium), containing Ginkgo Bilobae Foliorum Extract, must be stored and disposed of by strictly adhering to official regulatory instructions to maintain product integrity and ensure safety.

Storage Constraint Regulatory Requirement
Temperature Store at a temperature not exceeding 25^circC
Protection Must be protected from moisture and kept in the original container
Child Safety Keep out of the sight and reach of children
Stability Do not use after the expiration date (EXP)

Official disposal guidelines mandate that unused or expired medicine must be discarded according to local regulations. The product must not be thrown into household waste or flushed down wastewater.

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

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