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Фенилин

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Фенилин

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Medically reviewed

Marina Burgos

Last updated on 10/01/2026

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 Фенилин

What is Phenylin?

Phenylin is an oral medication belonging to the group of indirect-acting anticoagulants. Its active ingredient is phenindione, a synthetic derivative of indandione. The primary function of this medication is to interfere with the normal process of blood coagulation by inhibiting the synthesis of vitamin K-dependent clotting factors.

Mechanism of Action

The medication works by disrupting the production of specific proteins in the liver that are essential for blood clot formation. Unlike direct anticoagulants, Phenylin does not affect existing clots but rather prevents the formation of new ones and limits the extension of established thrombi. Because it acts on the synthesis of new factors, there is a characteristic latent period before the full effect is achieved, and the action continues for a period after the medication is discontinued.

Therapeutic Purpose

Phenylin is used in clinical practice to manage conditions characterized by an increased risk of thrombosis. By reducing the blood's ability to clot, it helps maintain blood flow in various vascular disorders. It is typically utilized for long-term anticoagulation therapy where consistent monitoring of blood parameters is required to ensure the desired level of coagulation inhibition is maintained.

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What side effects are possible with Фенилин?

Possible side effects and safety information

The safety profile of Phenindione (Фенилин) is directly defined by its function as a Vitamin K Antagonist (VKA). The risk profile, as documented in official regulatory sources, centers on the systemic consequences of altered blood clotting and potential organ involvement.

Official Adverse Reactions and System-Organ Classifications

The primary and most frequently documented safety concern is Hemorrhage (bleeding), which is generally classified as a Very Common or Common adverse reaction. Adverse reactions are grouped by System-Organ Class (SOC) in regulatory documents, including:

  • Blood and Lymphatic System Disorders: Encompassing hemorrhage and rare, but serious, effects like Agranulocytosis.
  • Hepatobiliary Disorders: Including the rare occurrence of Jaundice and other signs of hepatic dysfunction.
  • Renal and Urinary Disorders: Documenting potential renal damage, including Acute Renal Failure.
  • Skin and Subcutaneous Tissue Disorders: Such as Dermatitis, rash, and the rare occurrence of Skin Necrosis.

Serious Reactions and Safety Constraints

Regulatory agencies explicitly document events such as Major Hemorrhage (including intracranial bleeding), Agranulocytosis, and severe Hepatic Dysfunction as serious adverse reactions. The risk of serious bleeding is noted to be higher at the initiation of treatment and during dose adjustments.

Safety constraints restrict the use of the medicine in certain populations. Phenindione is Contraindicated in individuals who are pregnant and in patients with severe hepatic or renal disease, as formally stated in prescribing information. Regulatory documents note that older adults may require more frequent monitoring due to increased sensitivity to the anticoagulant effect.

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Overdose and Emergency Response

The regulatory overdose profile for Phenindione (Фенилин) is defined by the risk of haemorrhage resulting from profound systemic anticoagulation. Documented clinical signs that can indicate an overdose include spontaneous bruising, haematomas (lumps of blood), haematuria (blood in the urine), and rectal bleeding. A critical and life-threatening manifestation is the potential for haemorrhage into any internal organ.

Immediate medical attention is officially mandated when any signs of bleeding are observed, regardless of laboratory values, or if the International Normalized Ratio ( INR) is equal to or greater than 8.0 without corresponding bleeding signs. Individuals must be instructed by regulatory guidance to seek emergency medical attention immediately at a hospital casualty department.

Overdose management procedures officially include administering the specific reversal agent, Vitamin K1 ( Phytomenadione). For severe or life-threatening haemorrhage, factor replacement using Prothrombin Complex Concentrate ( PCC) or Fresh Frozen Plasma ( FFP) is described. Following reversal, frequent monitoring of clotting factors and repeated INR estimation are required to assess the therapeutic response. Furthermore, regulatory documents specify that a haematologist should be consulted for all paediatric overdose cases.

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Therapeutic Uses of Фенилин

What Фенилин Treats: Main Uses and Benefits

Фенилин (Fenilin, also known as Phenindione) is an oral medication that is an anticoagulant commonly used to help with symptoms related to systemic imbalance. The primary therapeutic domain of this drug is managing and preventing thromboembolic conditions. Its core action helps address symptoms related to heightened physiological activity and symptoms that create noticeable physiological strain.

This type of medicine may assist in reducing the risk of developing blood clots, providing supportive relief when symptoms interfere with routine activities. It is applied across domains where additional symptomatic support is needed for patients facing conditions characterized by periods of heightened symptoms, such as deep vein thrombosis (DVT), pulmonary embolism (PE), and in prophylaxis for patients with atrial fibrillation or mechanical heart valves. The medicine helps maintain a sense of stability when symptoms are more noticeable. The medication contributes to easing the overall symptom load and assists with maintaining functional stability.

Quick Fact: Relief for symptoms related to systemic imbalance

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Eligibility and Restrictions for Use

The use of Фенилин (Phenindione) is strictly defined by regulatory eligibility criteria, focusing on patient status and specific medical conditions. The medicine is primarily indicated for adults requiring anticoagulation therapy for thromboembolic conditions, but the official label imposes definitive restrictions on many populations.

Contraindicated Populations: Use is absolutely forbidden in patients with known hypersensitivity, haemorrhagic stroke, or clinically significant bleeding risk. It is also explicitly contraindicated in individuals with severe renal disease, severe hepatic disease, uncontrolled hypertension, and bacterial endocarditis.

Age and Status Restrictions: Pregnancy and lactation are absolutely contraindicated. The medicine must not be used within 48 hours postpartum or 72 hours of major surgery. Elderly patients (ge 65 years) are identified as a population requiring caution and potential dosage reduction. Use in the pediatric population is generally not established.

Conditional Use: Patients with non-severe deficient renal function or liver disease require increased monitoring and potential dosage adjustments, reflecting a conditional eligibility status as mandated by regulators.

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What should I know about interactions with other medicines?

Interactions with other medicines and products

The interaction profile for Фенилин (Phenindione) is determined by its potential to alter the blood's clotting activity when combined with other substances, a phenomenon officially classified as Pharmacodynamic Modulation.

Interaction Type Examples of Interacting Products/Substances
Exaggerate Effects (Increased Bleeding Risk) Fibrinolytics, NSAIDs, Heparins, SSRI/SNRI Antidepressants, Allopurinol, Cimetidine, Glucagon, Anticoagulant Agents (Dabigatran, Rivaroxaban)
Reduce Effects (Decreased Anticoagulation) Azathioprine, Amobarbital, Carbamazepine, Griseofulvin, Phenytoin, Increased intake of Dietary Vitamin K, Fats, or Oils

Procedural Constraints and Timing Rules

Official regulatory documents require that co-administration of Heparin must be discontinued for at least six hours before the first INR control test is conducted during the initiation of Фенилин therapy. Furthermore, the label notes that the drug's effect may be significantly exaggerated in elderly patients and those with deficient renal function, factors which officially modify the interaction profile. Concomitant use with agents classified as having adverse effects on haemostasis, such as fibrinolytic drugs, is contraindicated.

Dietary and Non-Medicinal Product Interference

The intake of Dietary Vitamin K and fats or oils is officially documented to interfere with the drug’s activity, potentially reducing its anticoagulant effect. Regulatory advice also states that the regular consumption of Cranberry Juice requires consideration for increased International Normalized Ratio (INR) monitoring.

The regulatory structure emphasizes interactions that directly lead to clinically significant changes in the drug’s primary action, classifying substances based on their effect on the resulting anticoagulation status.

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Mechanism of Action

How Фенилин Works: Mechanism of Action

Фенилин (Phenindione) functions as a Vitamin K Antagonist by interfering with the liver's synthesis of functional coagulation factors, which results in a progressive reduction in the blood's capacity for coagulation.


The primary mechanism involves the drug acting as an inhibitor of the enzyme Vitamin K Epoxide Reductase (VKOR) within hepatic cells. This targeted inhibition functionally antagonizes Vitamin K by preventing it from being recycled back into its active form ( Vitamin K H2). This Vitamin K form is required for factor activation in the coagulation cascade.


The functional consequence of depleting active Vitamin K is the inhibition of gamma-carboxylation of precursor proteins—specifically Coagulation Factors II, VII, IX, and X. The liver synthesizes these proteins, but they are released as biologically inert precursors (PIVKAs) that cannot participate in clot formation, reducing the systemic potential for coagulation.


Since this mechanism targets the synthesis of new factors rather than neutralizing those already circulating, the full physiological effect is achieved only after existing factors naturally clear the bloodstream. This reliance dictates a characteristic delayed onset (36 to 48 hours) and functionally constrains the mechanism, as it does not possess fibrinolytic activity to break down established clots.

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Dosage and Administration Information

How to Use Фенилин (Phenindione) — Official Administration Guidelines

The official route for administering Фенилин is oral, formulated as 10 mg and 25 mg tablets. Treatment begins with a standardized loading regimen over the first two days. The initial loading dose for adults is 200 mg, typically administered in two equal divided doses on the first day, followed by a 100 mg dose on the second day. Maintenance therapy is taken once daily; for optimal consistency, it should be administered at the same time each day. Tablets must be swallowed whole with water, and the score line on the 25 mg tablet is not intended for breaking.

Dose Titration and Monitoring

Dosage adjustment commences from the third day of treatment. The target daily maintenance dose range for most patients is between 50 mg and 150 mg. This precise dose is determined by the results of regular coagulation tests, specifically the International Normalised Ratio (INR). This continuous monitoring is a mandatory procedural condition of the overall use protocol.

Population-Specific and Contextual Rules

Specific administration rules apply to certain patient groups: the tablets are not suitable for use in children, and a dose reduction may be required for older adults or individuals with deficient renal or hepatic function. If a dose is forgotten, it must not be compensated by taking a double dose. Furthermore, the drug's action can be affected by diet; patients are instructed to note that large consumption of alcohol, cranberry juice, and certain Vitamin K-rich foods may interfere with the drug's action.

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Recent Clinical Evidence

Research Evidence / Overview of Studies for Фенилин (Phenindione)


Evidence for Preventing and Managing Blood Clots (Venous Thromboembolism)

The core research for Фенилин (Phenindione) primarily involves historical clinical trials and long-term observational studies that date back to when this class of medication was first widely used. The studies was studied for adult patients diagnosed with established deep vein thrombosis (DVT) or pulmonary embolism (PE), as well as those who needed long-term prevention of these clots. Research examined the drug in contexts where they were observing short-term or episodic symptom patterns.

The main objective monitored in these studies was the ability to record the International Normalized Ratio (INR), a measure of blood thinness. Findings from the available research describe patterns observed in the studies related to how patients maintained that targeted INR over defined time intervals. This evidence contributes to the broader evidence landscape describing how Vitamin K Antagonists (VKAs) were studied and how recurrent clotting events were tracked.


Evidence for Preventing Stroke and Systemic Clotting in Heart Conditions

Research has also explored the use of Фенилин in contexts related to blood clot formation that form in the heart, as these clots may lead to systemic embolic events. These studies primarily involved adults with conditions like atrial fibrillation or those who had undergone mechanical prosthetic heart valve replacement. In these research contexts, the outcomes monitored included the occurrence of stroke and other systemic embolic events, which are outcomes reflecting daily functioning or activity level.

Studies monitored and described patterns regarding the observed frequency of systemic embolic events among the studied populations. The research highlights the changes measured during the study period, focusing on the ability to monitor the intensity of anticoagulation in contexts related to conditions characterized by fluctuating or episodic manifestations.


Key Limitations and Uncertainties in the Research Landscape

One major uncertainty is the lack of contemporary comparative evidence. There have been few recent studies that directly compared it against the newer oral anticoagulants (NOACs) or even against Warfarin, the most common Vitamin K Antagonist. Furthermore, sample sizes were modest in many of the older trials. This means that research provides context, but the findings describe group patterns, not personal outcomes. The evidence is limited regarding its outcomes in diverse subgroups of patients, and there is an ongoing need for research that reflects modern standards of care.

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Frequently Asked Questions (FAQ)

Common questions about Фенилин (FAQ)

Q: Is Фенилин the same kind of blood thinner as Warfarin?

A: According to official regulatory sources, Фенилин (Phenindione) and Warfarin are both classified as Vitamin K Antagonists (VKAs) and share a similar mechanism of action by targeting the blood’s clotting factors. However, the chemical structure is different: Warfarin is a Coumarin derivative, while Фенилин is an Indandione derivative.

Q: What is the main difference between Фенилин and aspirin?

A: Фенилин is an anticoagulant medicine that works by inhibiting the synthesis of clotting factors. Aspirin, in the context of blood thinning, is generally classified as an anti-platelet medicine that affects blood cells. Official guidance advises caution with co-administering aspirin or similar anti-inflammatory painkillers while on Фенилин due to a significantly increased risk of bleeding.

Q: Is it true that Фенилин is an older type of anticoagulant medication?

A: Official sources describe Фенилин as an established medicine in the Vitamin K Antagonist (VKA) class. While it was widely used historically, some authoritative sources note that it is now less commonly employed in many regions compared to newer anticoagulants.

Q: What is the most important information to know about the safety of Фенилин?

A: Hemorrhage (bleeding) and unusual bruising are frequently reported safety concerns described in official product information. This is a direct consequence of the medicine's function. Patients should be informed of the signs of bleeding and should report them to a healthcare provider if they occur.

Q: Does Фенилин interact with pain relievers like Ibuprofen or Paracetamol?

A: Official patient advice states that pain relievers classified as anti-inflammatory medicines (such as NSAIDs, which includes Ibuprofen) are typically advised against co-administration with Фенилин due to increased risk of bleeding. Paracetamol (acetaminophen) is generally permitted, but a doctor should be informed if it is used on a regular basis.

Q: How long does the effect of Фенилин last in the body?

A: The anticoagulant effect of Фенилин is known to last for a significant period. After the last dose, the blood-thinning activity may continue to wane over approximately 48 to 72 hours.

Q: Is it acceptable to drink alcohol in moderation while taking Фенилин?

A: Regulatory guidance addresses alcohol consumption, recommending that intake should be limited to small amounts. Official advice generally recommends limiting intake to a maximum of one to two units in any single day and advises against binge drinking, as alcohol can interfere with the drug’s activity.

Q: Is it safe to take multivitamins while on Фенилин?

A: Official patient information generally states that taking food supplements or vitamin preparations that are not specifically prescribed should be avoided. This is because certain ingredients, like Vitamin K, can alter the drug's intended action.

Q: What should I do if I notice unusual bruising or bleeding while on this medicine?

A: Unusual or severe bruising or bleeding are symptoms that can indicate excessive anticoagulation, requiring attention. Official patient information indicates that if this is noticed, it should be reported to a healthcare provider immediately so the dosage can be assessed.

Q: Does Фенилин have a different name in other countries?

A: The active substance is Phenindione. Like most medicines, it may be sold under various commercial brand names (trade names) that can differ significantly depending on the country or region. One trade name mentioned in official documents is Dindevan.

Q: What should be discussed with a doctor before starting Фенилин?

A: Official documentation lists several factors that must be discussed, including: being pregnant or planning to be, severe kidney or liver disease, a recent major surgery or injury, or a history of stomach ulcers. These conditions are noted in official documents as factors that may require increased caution or dose adjustment.

Q: Are there any known interactions between Фенилин and herbal remedies?

A: Official patient advice recommends checking with a pharmacist about all medicines, including any herbal preparations. Certain herbal remedies and supplements may affect the action of Фенилин and are often advised against co-administration.

Q: Can I stop taking Фенилин suddenly if I feel better?

A: Regulatory documents indicate that treatment status is a clinical decision and should be addressed in consultation with the prescribing physician, rather than stopping suddenly. The dosage is adjusted based on mandatory, regular INR blood tests to maintain controlled anticoagulation.

Q: Can Фенилин be taken at the same time as thyroid medication?

A: Regulatory precautions note that caution is generally required in patients with thyroid disorders. The medicine's anticoagulant activity may be affected by an increase or decrease in thyroid hormone levels. Therefore, any changes to thyroid medication should be discussed with a doctor.

Q: What is the difference between an antiplatelet and an anticoagulant like Фенилин?

A: Anticoagulants such as Фенилин affect the body's clotting factors. Official product information treats anti-platelet drugs as a separate class of medicine, and co-administration with Фенилин is noted as a factor that substantially increases the risk of serious hemorrhage.

Q: Is it true that patients on Фенилин need to avoid contact sports?

A: Due to the effect of the medicine to prevent blood clots, official patient information notes that patients are generally advised to limit activities that carry a risk of cuts or serious bruising, such as contact sports.

Q: What happens if I take too much Фенилин?

A: Taking more than the prescribed amount may result in signs of excessive anticoagulation. These symptoms, described in official product information, include unusual bruising, blood in the urine or stools (rectal bleeding), and hemorrhage (bleeding) into internal organs.

Q: Why is it important to know about all the medicines I take while on Фенилин?

A: This is important because many medicines, vitamins, and supplements can significantly increase or decrease the effect of Фенилин. This can either raise the risk of bleeding or, conversely, the risk of a blood clot. Official sources classify these as pharmacodynamic interactions.

Q: What types of food contain Vitamin K that might affect Фенилин?

A: Official patient information provides examples of foods that contain significant amounts of Vitamin K that may interfere with the drug’s action. These include liver, broccoli, brussels sprouts, and green leafy vegetables.

Q: Does the official evidence indicate a clear benefit of Фенилин in high-risk patients?

A: Official studies examined the drug for its ability to manage and prevent blood clots, which led to its authorization for these uses. The medicine is officially indicated for the prophylaxis and treatment of blood clots and embolization in certain high-risk patient populations.

Q: What is known about the risk of bleeding with Фенилин compared to other similar drugs?

A: The most serious and common side effect is hemorrhage. Regulatory summaries indicate a lack of contemporary comparative evidence against newer agents. Some older sources noted that Phenindione may have a higher incidence of severe adverse effects compared to Warfarin, which contributed to its reduced use.

Q: How does Фенилин fit into current guidelines for preventing stroke?

A: Фенилин is officially indicated for the prophylaxis of systemic embolisation in patients with atrial fibrillation, which is a primary risk factor for stroke. Its specific use in contemporary medical practice is determined by a doctor, based on individual patient characteristics and clinical protocols.

Q: What are the general expectations for someone starting on this treatment?

A: General expectations for starting this treatment, according to official procedures, include the need for a loading regimen, a delayed onset of full effect (36 to 48 hours), and the necessity for mandatory, frequent blood tests (INR) to monitor and adjust the ongoing dose.

Q: Why might a doctor choose Фенилин over another blood thinner for a patient?

A: The drug is authorized for the treatment and prevention of blood clots. The decision is highly dependent on a patient’s unique clinical profile, such as allergies to other anticoagulants or the individual's history of response to medication. Official evidence does not generally dictate the choice over newer agents.

Q: Is Фенилин known to cause changes in weight?

A: While not listed as a side effect, official documents note that a recent loss or gain of a lot of weight is a factor that can potentially alter the medicine's activity. This may require a doctor to assess the dose and make adjustments.

Q: Does Фенилин treat the same conditions as other common anticoagulants?

A: Yes, regulatory documents indicate that Фенилин is intended for the same therapeutic uses as other anticoagulants. It is indicated for the prevention and treatment of conditions such as venous thrombosis, pulmonary embolism, and systemic embolisation in patients with atrial fibrillation.

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How should Фенилин be stored and disposed of?

The storage and disposal of Fenilin ( Phenindione) tablets are subject to specific requirements outlined in official regulatory documents to maintain product quality and ensure safety.

Requirement Official Regulatory Statement
Storage Temperature Store at a temperature not exceeding 25 C (or below 30 C based on regional labeling).
Protection The product must be protected from moisture.
Packaging Rules Storage must be in the original container until the time of use.
Child Safety The medicine must be kept out of the sight and reach of children.

Disposal instructions require that any unused or expired product must be discarded in accordance with local requirements. The product should not be disposed of via wastewater or household waste, as mandated for pharmaceutical products, unless specifically directed by local authority take-back schemes. The stability of the tablets is maintained until the labeled expiry date, provided these official conditions are strictly followed.

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

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