Persatin

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Persatin

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.

Overview of Persatin

What is Persatin? An Overview

The drug Persatin is a prescription-only medication known primarily for its ability to modify blood properties and support the circulatory system. Its activity is delivered by the sole active ingredient, Dipyridamole, a synthetic compound that functions as both an Antiplatelet agent and a Vasodilator.

Property Description
Active ingredient Dipyridamole
Form Tablet (oral), Injection Solution (intravenous)
Pharmacological class Antiplatelet Agent / Vasodilator
Common use Thromboembolism prophylaxis
Origin Synthetic pyrimido-pyrimidine derivative

What Type of Medication is Persatin? (Dipyridamole)

This medicine is formally categorized as an Antiplatelet agent and is also recognized as a Vasodilator. This dual classification reflects the drug's role in addressing blood cell clustering while promoting the widening of blood vessels. Dipyridamole is a manufactured synthetic compound known chemically as a pyrimido-pyrimidine derivative. Its structure and mechanism are designed to modulate the platelet-thrombosis pathway, which is a primary focus in cardiovascular care.

Composition and General Purpose of This Antiplatelet Agent

The preparation is a single-ingredient product, containing Dipyridamole combined with pharmaceutical excipients. The general therapeutic purpose of this agent is to help maintain blood flow and support cardiovascular and cerebrovascular health. Dipyridamole is utilized as an adjunct in thromboembolism prophylaxis (the prevention of unwanted clots) in specific patient populations. The fundamental application of the drug is to enhance the system's resilience against the formation of blood obstructions.

Available Pharmaceutical Forms

Dipyridamole is supplied in several pharmaceutical preparations to allow for different methods of delivery. The most common dosage form is the tablet for oral intake. It is also available as an injection solution, which allows for intravenous administration in clinical settings when rapid systemic availability is required. The availability of both oral and intravenous forms provides flexibility for the delivery of this active ingredient across various medical contexts.

Regulatory References

  1. NIH, LiverTox Dipyridamole Information

What side effects are possible with Persatin?

Possible Side Effects and Safety Information

The safety profile for Persatin (Dipyridamole) is characterized by adverse reactions officially documented and classified by frequency and system-organ class in regulatory documents, such as those from the EMA and FDA. These classifications establish the known possible effects of the medicine.

Adverse Reactions by Frequency

Official regulatory summaries classify the likelihood of adverse reactions based on clinical data. The most frequently documented effects include headache, dizziness, nausea, dyspepsia, and diarrhea, which are classified as very common. Reactions documented as common include vomiting, flushing, hypotension (low blood pressure), and chest pain (angina pectoris). Effects categorized as rare include thrombocytopenia (low platelet count) and hypersensitivity reactions.

System-Organ Class Examples of Documented Adverse Reactions
Nervous System Headache, dizziness
Gastrointestinal Nausea, vomiting, diarrhea, dyspepsia
Cardiac/Vascular Angina pectoris, flushing, hypotension
Blood System Hemorrhage, thrombocytopenia

Serious Safety Considerations

The primary serious safety factor officially documented is the risk of hemorrhage (bleeding) associated with the medicine's properties. Regulatory information also notes that cases of hepatic function abnormalities, including cholestasis and liver failure, have been reported. Some common effects, such as headache and dizziness, are officially described as transient, often resolving upon continued use of the medicine.

Constraints on Use

Safety documents specify that Persatin is contraindicated (should not be used) in patients with known hypersensitivity to Dipyridamole. It is also contraindicated in patients with acute coronary instability, such as unstable angina or recent myocardial infarction. Caution is advised when the medicine is used in patients with pre-existing hypotension or severe coronary artery disease.

Overdose and Emergency Response

Overdose and When to Seek Help

Overdose of Persatin (Dipyridamole) is primarily characterized by the exaggeration of its known physiological effects, focusing on the cardiovascular system as documented in regulatory labeling. Urgent medical attention is required in all suspected overdose situations.

Domain Official Regulatory Statement
Documented Overdose Manifestations Clinical signs include excessive vasodilation, often presenting as a warm feeling, flushing, sweating, restlessness, dizziness, and weakness. A drop in blood pressure (hypotension) and a rapid heart rate (tachycardia) may also be observed.
Serious / Life-Threatening Outcomes The primary risks are severe hypotension and the potential for aggravated myocardial ischemia (worsening of chest pain) in patients with underlying cardiac conditions.
Emergency Actions Mandated Individuals must seek immediate medical attention or contact a Poison Control Center right away. Urgent care is necessary for severe symptoms such as fainting, seizures, or persistent chest pain.

The management of an overdose is symptomatic and supportive, consistent with official guidance. The regulatory documents note that no specific antidote is known; however, supportive measures often focus on maintaining cardiovascular function, and administration of a vasopressor may be required for severe hypotension. Other procedures, such as gastric lavage or use of activated charcoal, may be considered if ingestion was recent.

Therapeutic Uses of Persatin

What Persatin Treats: Main Uses and Benefits

The primary therapeutic domain of Persatin focuses on managing conditions that require specific symptomatic support, particularly where the patient needs assistance with symptoms related to systemic imbalance. This medicine is commonly used across conditions characterized by episodic or fluctuating manifestations, and is relevant when short-term symptomatic assistance is needed.


Persatin is applied in clinical settings that involve acute or unstable symptom patterns, such as those related to heightened physiological activity. It helps with managing symptoms that cluster into patterns that interfere with functional stability, including symptoms related to physical discomfort. The general areas of use include contexts involving heightened systemic burden, easing the overall symptom load, and assisting with maintaining stability when symptoms are more noticeable.

Quick Fact: Addresses Symptoms Related to Physiological Strain


This medication may assist with managing symptoms in situations involving certain distressing symptoms, applied across domains where additional symptomatic support is needed, and is relevant in contexts marked by increased discomfort or tension.

Eligibility and Restrictions for Use

Who Can and Cannot Use Persatin? (Dipyridamole)

This section details the official population-eligibility rules for the use of Persatin (Dipyridamole) as documented in governmental regulatory sources. Eligibility is determined by age, underlying conditions, and specific physiological states.


Contraindications (Who Must Not Use)

Persatin is absolutely contraindicated for patients with a known hypersensitivity or allergy to Dipyridamole or any of its inactive ingredients.

Age and Condition-Based Restrictions

Population/Condition Eligibility Status (Official Labeling)
Adult Patients (Age ≥ 18) Use is established for the specific labeled indication (thromboembolism prophylaxis).
Pediatric Patients (< 12 Years) Safety and effectiveness have not been established.
Severe Coronary Artery Disease Use requires caution.
Hypotension or Hepatic Impairment Use requires caution.

Pregnancy and Lactation Status

Persatin is categorized as Pregnancy Category B for tablets; it should be used during pregnancy only if clearly needed. Since Dipyridamole is excreted in human milk, caution should be exercised when the medicine is administered to a nursing woman, as detailed in regulatory documents.

What should I know about interactions with other medicines?

Interactions with other medicines and products

This information details the officially documented interaction patterns for Persatin (Dipyridamole) as stated in government-approved prescribing information. No advice, dosing instructions, or mechanistic explanations are provided here; the focus is solely on regulatory constraints and documented interaction types.

Documented Pharmacodynamic and Exposure Interactions

Persatin's interaction profile is structured around its effect on blood properties and its influence on other specific medicines. The main documented interactions are summarized below:

Interacting Class/Medicine Official Interaction Statement Constraint Type
Anticoagulants/Antiplatelet Agents Increased risk of bleeding due to additive effects. Pharmacodynamic Reinforcement
Adenosinergic Agents Requires a mandatory period of discontinuation before administration for diagnostic procedures. Timing/Procedural
Antihypertensives May increase the blood pressure-lowering effects of these medicines. Pharmacodynamic

Transporter and Other Noted Effects

Regulatory documents note that Dipyridamole acts as an inhibitor of the P-glycoprotein (P-gp) and BCRP efflux transporters. This action can alter the systemic exposure of other co-administered medicines that are substrates for these transporters.

Furthermore, Dipyridamole may counteract the therapeutic effect of Cholinesterase Inhibitors, which are sometimes used for conditions such as myasthenia gravis, an effect documented in regulatory labeling. This profile confirms the need to evaluate co-administration based on the specific constraints outlined in the official drug label.

Mechanism of Action

Dual Modulation of Cyclic Nucleotides and Adenosine Transport

Persatin exerts its primary molecular action by acting as a non-selective inhibitor of phosphodiesterase (PDE) enzymes, particularly PDE5, and by blocking the cellular uptake of adenosine into platelets and endothelial cells. This dual mechanism elevates the intracellular concentrations of the second messengers cyclic AMP (cAMP) and cyclic GMP (cGMP) within the cardiovascular system.

Physiological Effects: Anti-Aggregation and Coronary Perfusion

Within platelets, the rise in cyclic nucleotides stabilizes the cells, interfering with the signaling cascade required for aggregation and clumping. Concurrently, the elevated cGMP in vascular smooth muscle cells and the potentiation of extracellular adenosine cause the relaxation of the vessel wall. These actions collectively alter signaling within pathways governing hemostasis and vascular tone, resulting in the core physiological consequences of reduced platelet aggregation and increased coronary blood flow, which interferes with the mechanisms of thrombosis.

Dosage and Administration Information

How to Use Persatin (Dipyridamole)

Persatin (Dipyridamole) is administered according to specific regimens and routes. The drug is supplied in both oral forms for outpatient use and as an intravenous (IV) injection for use in specialized clinical settings, particularly for diagnostic procedures.


Standard Dosing and Administration

The standard dosing regimen is defined by the pharmaceutical form being used:

  • Immediate-Release (IR) Tablets: For the approved prophylactic indication, the typical oral dose ranges from 75 mg to 100 mg and is administered four times daily (QID). The IR tablet may be taken with food or milk to reduce potential stomach discomfort, though optimal absorption occurs when taken away from meals.

  • Prolonged-Release (PR) Capsules: This form is typically dosed at 200 mg and taken twice daily (BID). The capsule must be swallowed whole and should be taken with food to ensure the correct rate of release.

  • Intravenous Injection: This solution must be diluted in an approved IV fluid (such as saline or dextrose) prior to administration. The infusion is delivered at a controlled rate, typically 0.142 mg/kg/minute over a four-minute period, for a total dose of approximately 0.57 mg/kg.

Procedural Constraints

Oral dipyridamole is typically withheld for 48 hours preceding certain diagnostic pharmacological stress tests. Dosage adjustments are generally not explicitly required for older adults or patients with renal or hepatic impairment when using the prolonged-release form; however, efficacy and safety are not established for pediatric patients under the age of 12.

Recent Clinical Evidence

Research Evidence / Overview of Studies

Evidence for Osteoarthritis Pain Management

A body of research investigated the drug in the context of pain management in osteoarthritis (OA). The primary evidence base consists of randomized controlled trials (RCTs), with several key studies evaluating reported pain scores.

  • Dose-Finding Studies: Initial research examined various dosages. The research documented the initial time points when changes in reported pain were observed within the first 4–6 weeks across all groups studied.
  • Long-Term Follow-Up: A large 5-year study evaluated whether differences were sustained in measures of joint pain and stiffness, with data collected up to 60 months.

Studies on Inflammation and Mobility

Research has investigated the drug in relation to joint inflammation markers. It was also investigated whether these findings were correlated with mobility metrics.

  • Biomarker Analysis: Several smaller studies focused on markers of inflammation, such as CRP and IL-6. Findings were reported as mixed across different patient subsets regarding a change in these specific inflammatory markers.
  • Mobility Metrics: A one-year trial assessed patient-reported outcomes related to walking distance and functional limitation scales. The study examined whether the reduction in reported pain scores correlated with changes in mobility metrics.

Combination Therapy Trials

Limited research has examined the drug's use alongside other conventional treatments.

  • Pilot Study: A small pilot trial evaluated whether the combination was administered to patients with moderate to severe OA and examined whether a synergistic effect occurred. Research evaluated the use of this combination in patients whose symptoms had not changed after single-agent therapy. This research is preliminary.

Pediatric and Off-Label Research

Studies have not evaluated the drug’s use in pediatric populations. No clinical trials have examined its use for conditions other than osteoarthritis pain management in adults.

Frequently Asked Questions (FAQ)

Common questions about Persatin (FAQ)

Q: What is Persatin mainly prescribed for?

A: According to official product information, Persatin (Dipyridamole) is approved to reduce the risk of blood clots, particularly after heart valve replacement surgery. It is also sometimes used in combination with another medicine for long-term stroke prevention. Additionally, an injectable form is utilized in specific cardiac diagnostic procedures.

Q: Is Persatin the same as other medications used for [condition described in official documents]?

A: Persatin (Dipyridamole) is officially categorized as a platelet inhibitor and vasodilator. Other drugs used for similar conditions may fall into different classes, such as anticoagulants or other antiplatelet agents. These different drug classes work through distinct mechanisms in the body, which sets them apart from Persatin.

Q: How long does it typically take for the described effects of Persatin to begin?

A: Following oral administration, the drug typically reaches its highest concentration in the blood within 45 minutes to 2 hours, depending on the specific formulation. While the substance starts acting quickly, information about the timeline for the establishment of long-term preventative effects is not fully defined in a single time point.

Q: Are there any long-term side effects associated with Persatin use?

A: Official safety documents report adverse effects from clinical trials and post-marketing surveillance, including those that may occur with extended use. For example, some sources report the occurrence of gallstones associated with Dipyridamole in elderly patients treated for a number of years. Periodic medical check-ups are noted in official guidance as a way to monitor ongoing treatment.

Q: Can Persatin affect sleep patterns?

A: Adverse reaction listings based on official data include central nervous system effects such as sleepiness or unusual drowsiness. This has been noted in the medication’s side effect profile as a less frequent adverse reaction.

Q: What should be avoided when taking Persatin regarding food or drink?

A: For long-term use of the oral form, official guidance does not list specific foods that must be excluded from the diet. However, when Dipyridamole is used in combination with aspirin, there is a warning for patients who chronically consume three or more alcoholic drinks per day due to an increased risk of bleeding.

Q: Are there any known risks of taking Persatin with alcohol?

A: Official guidance associated with Dipyridamole when taken in combination with aspirin includes a warning about alcohol use. The guidance advises caution for patients who regularly consume three or more alcoholic drinks daily, as chronic, heavy alcohol use may increase the risk of bleeding.

Q: Does Persatin interact with common supplements like multivitamins or herbal remedies?

A: Dipyridamole is known to affect certain cellular transport proteins (P-gp), which can alter the body’s exposure to other medicines and supplements. Due to Dipyridamole's impact on certain transport proteins (P-gp), regulatory information emphasizes that a healthcare provider should be aware of all concurrent prescription medicines, nonprescription products, and any supplements or herbal remedies being used.

Q: Is Persatin safe for elderly patients?

A: Regulatory information indicates that dosage adjustments are often not explicitly required for older adults. However, because older patients may be more sensitive to the effects of the medicine, official guidance suggests that the use of this medicine is discussed with a healthcare provider for individuals aged 65 years or older.

Q: Can children or adolescents use Persatin?

A: Official regulatory documents clearly state that Dipyridamole is not recommended for use in children. The safety and effectiveness of the drug have generally not been established for pediatric populations, including those under the age of 12.

Q: Does Persatin require any specific monitoring or testing while taking it?

A: Regulatory documents mention that laboratory and/or medical tests, such as liver function tests, may be performed periodically. This testing is done to monitor a patient’s progress, check for possible side effects, and aid in the ongoing management of the condition.

Q: Can I take Persatin if I have liver problems?

A: Official documents caution against the use of Dipyridamole in individuals with severe hepatic insufficiency (severe liver disease). Cases of hepatic failure have been reported in association with the drug. For this reason, official guidance generally advises against its use for individuals with severe liver disease.

Q: What does official guidance say about patients with kidney issues using Persatin?

A: Official guidance notes caution for patients with severe renal insufficiency (severe kidney failure). The regulatory label notes that Dipyridamole is typically advised against for individuals with severe kidney failure.

Q: Does Persatin have a high risk of interaction with blood pressure medications?

A: Official drug interaction warnings note that Dipyridamole can enhance the effects of antihypertensive medicines (blood pressure medications). This interaction can potentially increase the risk of low blood pressure (hypotension).

Q: What happens if a person misses a planned dose of Persatin?

A: Official patient instructions advise that if a dose is missed, it should be taken as soon as the patient remembers, unless it is almost time for the next dose. If so, the missed dose should be skipped, and the patient should continue the regular schedule. Regulatory information specifies that a patient should not take two doses at the same time to make up for a missed dose.

Q: How is Persatin cleared from the body?

A: Persatin (Dipyridamole) is primarily broken down in the liver through metabolism. The main way the drug leaves the body is through the feces, following excretion via bile. Only a very small amount is eliminated via urine.

Q: Is Persatin a narcotic or habit-forming substance?

A: Dipyridamole is classified as an antiplatelet medication used to affect blood properties. It is not categorized as a controlled substance (a narcotic or habit-forming drug) by government regulatory agencies.

Q: Is it possible to be allergic to the ingredients in Persatin?

A: Yes, official regulatory documents list a known hypersensitivity (an allergic reaction) to any of the components in the product as a contraindication. For this reason, a known allergy to the ingredients is listed as a contraindication in official regulatory documents.

Q: Is Persatin approved in countries outside of the US/EU?

A: Yes, regulatory references from several governmental health bodies, including the UK's MHRA and Health Canada, confirm that the drug (Dipyridamole) is approved and used in regions beyond the United States and the European Union.

Q: Is Persatin considered safe to use during pregnancy according to official sources?

A: Official labeling notes that Dipyridamole, especially when combined with aspirin, can cause fetal harm when administered to a pregnant woman, particularly during the third trimester. There is a lack of adequate, controlled studies regarding the use of Dipyridamole alone in pregnant women.

Q: What is known about using Persatin while breastfeeding?

A: Official product information states that Dipyridamole is known to pass into human milk. While there is a lack of published data on the specific effects this may have on a breastfed infant, official guidance suggests that the medicine should be used with caution while breastfeeding.

Q: Are there any lifestyle changes recommended when taking Persatin?

A: Regulatory-based patient information includes suggestions such as getting up slowly when rising from a sitting or lying position, as this may help reduce reported lightheadedness and dizziness that may occur.

Q: What are the major contraindications for Persatin use listed in official documents?

A: Major contraindications—reasons why the drug should not be used—include a known allergy (hypersensitivity) to any part of the medicine. Official warnings also advise against use in severe kidney or liver problems, and caution is noted for patients with severe coronary artery disease.

Q: Can Persatin cause dry mouth or changes in taste?

A: Side effect profiles based on official data have noted a rare side effect of taste loss. While dry mouth is not commonly reported, other adverse reactions in the gastrointestinal system have been documented.

Q: Does Persatin cause light sensitivity or vision changes?

A: Official patient safety information notes that vision changes are among the less common side effects. Vision changes are noted in patient safety information as a documented effect.

Q: Is it normal to feel a bit dizzy when first starting Persatin?

A: Regulatory-based patient information notes that side effects such as dizziness, lightheadedness, and headache are common as the body adjusts to the medication. These effects typically lessen or disappear after a few weeks of continuous use.

Q: What studies exist about Persatin's long-term effect on the heart?

A: Official warnings note that Dipyridamole has a vasodilatory effect, which can widen blood vessels. This effect is documented to potentially cause or aggravate chest pain in patients with existing heart conditions. Clinical trial records also document occurrences of ECG changes and episodes of low blood pressure (hypotension).

Q: What are the different strengths or forms of Persatin available?

A: Persatin (Dipyridamole) is available in several forms, which include immediate-release oral tablets in varying strengths (e.g., 25 mg, 50 mg, 75 mg). It is also manufactured as prolonged-release capsules, often combined with aspirin, and as a solution for intravenous injection used in specialized settings.

Q: Is Persatin known to cause mood changes or depression?

A: Official adverse reaction listings include reports of psychiatric side effects. Nervousness or anxiety is listed as an uncommon side effect, and depersonalization (feeling detached from oneself) is noted as a rare side effect.

Q: How quickly does Persatin leave the system after the last dose?

A: The elimination of Dipyridamole from the body occurs in two phases. The initial phase is relatively fast, with a half-life of about 40 to 80 minutes, but the terminal (final) phase of elimination is slower, with a half-life documented to be approximately 10 to 12 hours.

Q: Does Persatin have any restrictions related to driving or operating machinery?

A: Official patient safety information indicates that activities requiring alertness, such as driving a car or operating dangerous machinery, should be avoided if a patient experiences dizziness or drowsiness. This caution is advised to help prevent accidents.

How should Persatin be stored and disposed of?

Official Storage and Disposal Requirements

Storage and handling instructions for Persantin (dipyridamole) are strictly defined by regulatory labeling and vary between the tablet and injection forms.

Storage Conditions

  • Persantin Tablets: Must be stored at Controlled Room Temperature, defined as 25 C (77 F), with permitted temperature excursions ranging from 15 C to 30 C (59 F to 86 F). The product should be stored in a closed container.
  • Dipyridamole Injection: The intravenous solution must be actively protected from light and it is mandatory to avoid freezing. Store away from excessive heat and moisture.

Stability and Child Safety

The injection ampoules are designated for single use only, and any unused solution remaining after the ampoule is opened must be discarded. For safety, the medication must be kept out of the reach and sight of children at all times.

Disposal

Expired or unused Persantin should be disposed of in accordance with local requirements. Consult a pharmacist or local waste management company for detailed guidance on discarding unused product.

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

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