Rivarin

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Medically reviewed

Laura Arias

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 Rivarin

Property Description
Active Ingredient (INN) Rivaroxaban
Form Oral film-coated tablets
Pharmacological Class Direct Factor Xa Inhibitor (Anticoagulant)
Common Use Treatment and prevention of venous blood clots
Origin Synthetic
Regulatory Status Prescription-only (Rx)

Rivarin is the trade name for an oral, prescription-only medication whose active ingredient is rivaroxaban, a synthetic compound used to manage and prevent blood clotting. It is most commonly supplied as oral film-coated tablets for daily administration.

Unlike older forms of blood thinners, rivaroxaban is an oral direct-acting anticoagulant (DOAC). It is utilized in long-term patient management to maintain blood flow and reduce the risk of harmful clot formation.


What Class of Medicine is Rivarin?

Rivarin belongs to a category of medications known as Direct Factor Xa Inhibitors, which is a modern, targeted class of anticoagulants. This classification indicates that the drug is selective, focusing on blocking one specific protein in the blood-clotting process, Factor Xa.

The active ingredient, rivaroxaban, is the specific chemical that produces the therapeutic effect. Rivaroxaban inhibits Factor Xa to reduce the risk of thromboembolic events. This means the medicine works by blocking a step required for blood clot formation.


What is Rivarin Used For?

Rivarin's primary therapeutic purpose is to prevent and treat blood clots in the veins and arteries, which can lead to health complications like stroke and pulmonary embolism. The drug is used in managing scenarios where abnormal clotting poses a risk.

A typical use scenario involves its prescription to reduce the risk of stroke in patients diagnosed with nonvalvular atrial fibrillation, a heart rhythm disorder that increases the chance of clot formation. It is also used to treat existing clots, such as deep vein thrombosis (DVT) in the legs. This class of drug is used for the long-term prevention of recurrent clotting episodes.

Regulatory References

  1. National Institutes of Health (NIH)

What side effects are possible with Rivarin?

Possible Side Effects and Safety Information

The official safety profile for Rivarin (rivaroxaban), an anticoagulant medication, is characterized by risks related to its intended function of inhibiting blood clotting. All documented adverse reactions and safety statements are based on official government regulatory documents.

Adverse Reactions and Frequency Classification

The most prominent safety characteristic is the risk of haemorrhage (bleeding), which is consistently classified across regulatory documents as a very common adverse reaction. Other documented effects are grouped by frequency:

  • Common: Includes anaemia (often due to blood loss), dizziness, headache, nausea, and elevations in liver transaminases.
  • Uncommon: May include hypersensitivity reactions (allergic oedema), tachycardia, and signs of impaired hepatic function.

Serious Safety Concerns

Specific serious adverse reactions are highlighted in regulatory labeling. These include the risk of fatal haemorrhage and intracranial haemorrhage. Additionally, the U.S. FDA label contains specific caution regarding the risk of spinal or epidural haematoma when the medicine is used in patients undergoing neuraxial anesthesia or spinal puncture procedures.


Population-Specific Safety Considerations

Safety limitations exist for specific patient groups. The medicine is contraindicated in individuals with hepatic disease associated with coagulopathy and clinically relevant bleeding risk (e.g., severe hepatic impairment). Use is generally not recommended during pregnancy, lactation, or in patients with prosthetic heart valves, due to safety and efficacy not being fully established in these contexts. The risk of thrombotic events is also noted to increase upon the premature discontinuation of treatment.

Overdose and Emergency Response

Overdose and When to Seek Help

Overdosage of Rivarin (rivaroxaban) is officially documented to result primarily in excessive anti-Factor Xa activity, which manifests clinically as an elevated risk of hemorrhage (bleeding). This potential for significant blood loss is the defining characteristic of overexposure to this medication, and it carries the risk of serious and potentially fatal bleeding complications.

Documented Manifestations and Emergency Action

Category Official Regulatory Statements
Documented Presentation Manifests as hemorrhage and prolongation of coagulation parameters (PT) due to excessive anti-Factor Xa activity.
Severity Classified by the risk of serious and potentially fatal bleeding.
Required Action Immediate medical attention is required upon any suspected or known overdosage, or upon the development of signs of blood loss.

Management and Considerations

Management of overdosage centers on addressing the increased risk of bleeding. The medication should be discontinued, and the severity of blood loss must be promptly evaluated. Official regulatory labeling confirms that a specific reversal agent to counteract the anti-Factor Xa activity is available. Supportive measures include the consideration of activated charcoal if the ingestion was recent, and the use of plasma products for coagulation support. Rivaroxaban is confirmed to be not dialyzable due to its high protein binding.

Therapeutic Uses of Rivarin

Main Uses and Therapeutic Indications

Rivarin is an anticoagulant medication primarily used to manage and prevent various conditions related to blood clot formation. It belongs to a class of drugs known as direct oral anticoagulants (DOACs), which work by targeting specific proteins involved in the blood's clotting process.

Prevention of Stroke and Systemic Embolism

One of the primary uses of Rivarin is to reduce the risk of stroke and systemic embolism in patients with non-valvular atrial fibrillation. Atrial fibrillation is a heart rhythm disorder that can cause blood to pool in the heart, leading to the formation of clots. If these clots travel to the brain or other organs, they can cause a stroke or significant tissue damage.

Treatment and Prevention of Venous Thromboembolism

Rivarin is indicated for the treatment of deep vein thrombosis (DVT) and pulmonary embolism (PE). DVT occurs when a blood clot forms in a deep vein, usually in the leg, while a PE occurs when a clot breaks free and travels to the lungs. Beyond initial treatment, the medication is also used to prevent these conditions from recurring in the long term.

Prophylaxis Following Major Surgery

Patients undergoing hip or knee replacement surgery are at an increased risk of developing blood clots due to reduced mobility and the nature of the procedure. Rivarin is utilized in these clinical settings to prevent the development of venous thromboembolism during the recovery period.

Cardiovascular Risk Reduction

In specific patient populations with chronic coronary artery disease (CAD) or peripheral artery disease (PAD), Rivarin may be used in combination with other medications to reduce the risk of major cardiovascular events, such as myocardial infarction (heart attack) or cardiovascular-related death.

Benefits and Clinical Impact

Consistent Anticoagulation

Rivarin provides a predictable level of anticoagulation by inhibiting Factor Xa, an enzyme essential for the formation of thrombin and subsequent blood clots. This mechanism allows for a stable therapeutic effect without the need for the frequent laboratory monitoring often associated with older anticoagulant therapies.

Impact on Long-term Outcomes

By effectively managing clot formation, Rivarin helps mitigate the risk of debilitating complications such as permanent neurological damage from strokes or respiratory failure from pulmonary emboli. Its use in chronic vascular conditions aims to improve overall cardiovascular stability and prevent limb-threatening events in patients with circulatory disorders.

Eligibility and Restrictions for Use

Who Can and Cannot Use Rivarin? (Rivaroxaban)

The eligibility profile for Rivarin (Rivaroxaban) is defined by regulatory agencies and is based on criteria that manage bleeding risk and organ function. The medicine is primarily approved for the adult population for its labeled indications, including the prevention and treatment of venous blood clots.

Contraindications and Restrictions

Rivarin is contraindicated (must not be used) in several patient populations, notably:

  • Individuals with active, clinically significant bleeding or any lesion/condition that carries a substantial risk of major bleeding, such as recent intracranial hemorrhage or active gastrointestinal ulceration.
  • Patients with hepatic disease associated with coagulopathy and clinically relevant bleeding risk, typically corresponding to Child-Pugh B and C classifications.
  • Women who are pregnant or breastfeeding.

Use is not recommended or restricted in patients with End-Stage Renal Disease (Creatinine Clearance <15 mL/min), triple-positive Antiphospholipid Syndrome (APS), or those with prosthetic heart valves. While the medicine is approved for the treatment of blood clots in specific pediatric patients from birth to less than 18 years, its use for other indications or in younger ages is restricted. The administration of Rivarin requires special caution relative to spinal or epidural procedures.

What should I know about interactions with other medicines?

Interactions with other medicines and products

The interaction profile for Rivarin (rivaroxaban) is defined by its clearance pathways and its effect on blood clotting factors. Co-administration with other systemic anticoagulants is contraindicated due to a significantly heightened risk of major hemorrhage.


Pharmacokinetic and Transporter Interactions

The most critical drug-drug interactions are classified by their combined effect on two primary routes: the CYP3A4 enzyme and the P-glycoprotein (P-gp) transporter. Medicinal products that are strong inhibitors of both pathways, such as certain antifungal agents (e.g., ketoconazole) and HIV antivirals (e.g., ritonavir), are also contraindicated because they cause a documented and unacceptable increase in Rivarin's systemic exposure.

Conversely, strong inducers of both CYP3A4 and P-gp, including certain antibiotics (e.g., rifampicin) and the herbal product St. John's Wort, must be avoided as they significantly reduce the drug's plasma concentration.


Pharmacodynamic and Administration Constraints

A separate interaction category involves pharmacodynamic effects on bleeding risk. The co-administration of Rivarin with antiplatelet agents (e.g., aspirin) or Nonsteroidal Anti-inflammatory Drugs (NSAIDs) increases the documented risk of bleeding. Furthermore, the 15 mg and 20 mg tablet strengths have an official administration requirement to be taken with food to ensure intended drug exposure. Use is also avoided in patients with moderate to severe hepatic impairment, as this condition heightens the interaction risk and may increase drug exposure.

Mechanism of Action

Selective Inhibition of Factor Xa: The Core Molecular Target

The active ingredient rivaroxaban functions as a highly selective, direct inhibitor of the enzyme Factor Xa (FXa). Its action involves binding precisely to the active site of Factor Xa, neutralizing the enzyme's ability to participate in coagulation. This mechanism immediately interrupts the common pathway of blood clotting, leading to a state of reduced physiological coagulability.

Interruption of the Coagulation Cascade and Thrombin Generation

By halting the function of Factor Xa, the drug stops the crucial conversion of Prothrombin ( Factor II) into Thrombin ( Factor IIa). This systemic suppression of Thrombin generation prevents the final step of converting Fibrinogen into the Fibrin polymer mesh. The result is a fundamental reduction in the physiological capacity of the blood to form and stabilize new clots, creating a state of reduced blood coagulability.

Mechanistic Boundary and Dynamic Constraints

The drug's mechanism is defined by a rapid onset of action and is strictly concentration-dependent. The resulting physiological effect is constrained by situations that affect drug levels in the circulation, such as severe organ impairment. In these specific physiological scenarios, the clearance is compromised, causing the Factor Xa inhibition to functionally exceed the therapeutic level, leading to a state of pathologically excessive hypocoagulability.

Dosage and Administration Information

How to Use Rivarin

Rivarin (rivaroxaban) is administered exclusively by the oral route, available as film-coated tablets in strengths of 2.5 mg, 10 mg, 15 mg, and 20 mg, or as a reconstituted oral suspension. The usage protocol is defined by specific rules governing dose, timing, and frequency, as outlined in the official prescribing information.

The medication’s regimen often follows a time-phased schedule. For the treatment of acute blood clots, for instance, a patient may be instructed to take a 15 mg dose twice daily for an initial period before transitioning to a 20 mg dose taken once daily for maintenance. For stroke prevention in nonvalvular atrial fibrillation, the standard dosage is 20 mg once daily, which is often recommended to be taken with the evening meal.

A critical administration rule is tied to tablet strength: the higher doses of 15 mg and 20 mg must be taken with food to ensure correct drug absorption. Conversely, the 2.5 mg and 10 mg strengths may be taken independent of meals. The label also outlines required population-based dose adjustments, such as reducing the NVAF dose to 15 mg once daily for patients with moderate kidney impairment.

If a dose on a once-daily regimen is missed, the instruction specifies taking the dose immediately on the same day and resuming the regular schedule the next day, with explicit instructions to not double the dose. The tablets may also be crushed and mixed with liquid or applesauce for administration via the mouth or a nasogastric/gastric tube.

Recent Clinical Evidence

Research Evidence: Overview of Studies for Rivarin

This section provides an overview of the official research that led to the clinical evaluation of Rivarin (rivaroxaban), describing the types of studies conducted and what the findings reported. It is a neutral summary of the evidence landscape and is not intended as medical advice or instruction.


Evidence for Preventing Stroke in Atrial Fibrillation

Research has explored the use of Rivarin in settings involving the risk of stroke and other clot-related events in people who have nonvalvular atrial fibrillation (NVAF), a common condition where an irregular heart rhythm may increase the risk of blood clot formation.

The research framework includes large, international Randomized Controlled Trials (RCTs) where Rivarin was evaluated against a standard anticoagulant (Vitamin K Antagonist). The primary outcomes that research examined included the occurrence of all types of stroke and systemic embolism (clot events outside the brain). Findings describe patterns observed in the studies related to thrombotic events where Rivarin was evaluated alongside the established VKA regimen in the patient populations studied. Long-term outcomes extending beyond the observation period of the primary trials are not fully characterized by controlled research. Furthermore, evidence remains limited for patients with severe kidney impairment and for those who have prosthetic heart valves.

Evidence for Treating and Preventing Venous Blood Clots (VTE)

Research has explored the use of Rivarin in settings involving venous thromboembolism (VTE). This includes research examining acute VTE events such as clots in the leg (Deep Vein Thrombosis, DVT) or in the lungs (Pulmonary Embolism, PE), and continued research to observe the recurrence of these events (secondary prevention).

The research was based on a program of Phase 3 Randomized Controlled Trials (RCTs) (the EINSTEIN program). Research examined the principal outcome of symptomatic, recurrent VTE and monitored how these events evolved in the observed populations. Findings describe patterns observed in studies where Rivarin was studied alongside conventional treatment regimens. Data for patients with certain complex medical situations, such as end-stage renal disease (ESRD) requiring dialysis, are insufficient.

What Remains Uncertain About Rivarin Research

Official scientific literature highlights several areas where data are still emerging or evidence is limited: Comparative evidence is lacking for certain rare conditions. While research has explored short-term symptom changes, the long-term effects are not fully established beyond the follow-up durations of the major trials, and research is ongoing in this area.

Key Studies & References Rivaroxaban versus Warfarin in Nonvalvular Atrial Fibrillation (ROCKET AF Trial)

Frequently Asked Questions (FAQ)

Common questions about Rivarin (FAQ)

Q: How quickly does Rivarin start to work after I begin taking it?

Studies in the clinical pharmacology sections of official product information indicate that the drug begins to work quickly. Maximum inhibition of the Factor Xa enzyme, which is its intended anti-clotting effect, generally occurs within 2 to 4 hours after a person takes the dose.


Q: Does Rivarin affect how long it takes for a wound to stop bleeding?

The main function of this drug is to reduce the blood's ability to form and stabilize clots. Because of this, the official warnings mention that the medication is associated with an increased risk of bleeding. This means that if a person sustains a cut or wound, the bleeding may last longer than usual.


Q: Can Rivarin be taken with common pain relievers like Tylenol or ibuprofen?

Regulatory documents warn that taking this medication alongside non-steroidal anti-inflammatory drugs (NSAIDs), such as ibuprofen, increases the risk of bleeding. Regarding acetaminophen (Tylenol), official reviews generally find no direct drug interaction. However, caution is typically advised for patients who may have liver issues, as the drug's safety profile is linked to liver function.


Q: Are there any specific foods or drinks that should be avoided while on Rivarin?

Official patient leaflets state that, unlike older medications in this class, there are generally no known interactions with specific foods. However, strong combined inhibitors of certain enzymes, such as the herbal product St. John's Wort, is advised to be avoided. Official guidance also indicates that excessive or chronic alcohol consumption may interfere with the drug's effect and potentially increase the risk of bleeding.


Q: Is Rivarin generally considered a short-term or long-term medication?

The duration of treatment with this medication is defined by the condition it is prescribed to manage. It is used both for an initial, short-term treatment phase to manage acute blood clots, and for longer-term maintenance to prevent the recurrence of clotting episodes over time. The prescribing information for some indications suggests continuous, long-term use.


Q: Can Rivarin cause any change in energy levels or fatigue?

Fatigue is not explicitly mentioned as a direct common side effect in official documents. However, one common adverse reaction documented is anaemia, which is often related to blood loss. Anaemia is a condition that is frequently associated with symptoms such as unusual tiredness or reduced energy levels.


Q: What are the signs of a serious side effect related to Rivarin that people talk about online?

The official safety profile is characterized by the risk of bleeding. Signs of serious bleeding complications mentioned in patient information include the observation of unusual or heavy bruising. This also includes passing blood in the urine or stool (which may appear black or tarry), or coughing up or vomiting blood.


Q: Does the time of day matter when taking Rivarin?

Official patient information advises that the medication should generally be taken at the same time(s) each day to maintain consistent drug levels. For some specific uses, such as reducing stroke risk, the dose is typically administered specifically with the evening meal.


Q: Is Rivarin the same type of medicine as warfarin?

No, these are different classes of medications. Rivarin is a Direct Factor Xa Inhibitor, belonging to the newer class of blood thinners called DOACs. Warfarin is a Vitamin K Antagonist (VKA). The two differ in their mechanism of action and the need for frequent blood testing to monitor their effect.


Q: What is the risk of having a drug interaction with Rivarin?

The drug has a defined and critical interaction profile detailed in the prescribing information. Co-administration with several types of medications and supplements, such as NSAIDs and strong inhibitors of specific liver enzymes, significantly increases the risk of bleeding. Because of this high risk, many combinations of drugs are either strictly avoided or formally contraindicated.


Q: Is Rivarin something that is usually stopped abruptly, or is there a taper process?

Official safety warnings advise against abruptly stopping the drug without the instruction of a healthcare provider. Stopping the medication early can lead to an increased risk of blood clots. For planned medical procedures, a specific discontinuation protocol is typically required, which usually involves stopping the medication at least 24 hours before the procedure.


Q: What steps are generally advised if a person develops a rash while on Rivarin?

Rashes and allergic oedema are listed as uncommon adverse reactions in regulatory documents, and these can be signs of a hypersensitivity reaction. Patient safety information advises that severe rash or symptoms of an allergic reaction should be reported to a healthcare provider promptly.


Q: Are there any known interactions between Rivarin and herbal supplements?

Yes, the official prescribing information notes a specific interaction with the herbal product St. John's Wort, which is advised to be avoided. Due to the way the drug is processed in the body, individuals should share information with their doctor and pharmacist about all herbal and nutritional supplements being taken, as many have the potential to cause interactions.


Q: What does 'Factor Xa inhibitor' mean in simple terms?

This term simply means the drug works by blocking the action of one specific protein in the blood called Factor Xa. By blocking this single step, the medication prevents the final stage of the blood clotting process. This mechanism is how the drug reduces the overall risk of clot formation in the body.


Q: What are the key findings from the major clinical trials of Rivarin?

Official clinical study sections describe that major trials compared the drug against established anticoagulants. Findings indicated the drug was non-inferior in preventing stroke and systemic embolism in patient populations with nonvalvular atrial fibrillation. The studies reported a similar overall rate of major bleeding, with noted differences in the types of bleeding that occurred.


Q: Can Rivarin be affected by cold and flu medicines?

Many over-the-counter cold and flu medicines contain ingredients, such as Non-Steroidal Anti-inflammatory Drugs (NSAIDs), that significantly increase the risk of bleeding when taken with this medication. Due to these potential interactions, information about all over-the-counter products should be shared with a healthcare provider or pharmacist.


Q: What evidence exists about Rivarin's effectiveness compared to placebo in studies?

Clinical trial data is available from large cardiovascular studies where the drug was evaluated in combination with aspirin against a regimen of placebo plus aspirin. Studies such as the COMPASS trial provided evidence to help establish the drug's role in the reduction of major cardiovascular and thrombotic vascular events in certain patient populations.


Q: Do older adults typically need different monitoring when using Rivarin?

Pharmacokinetic studies, which track how the body handles the medication, indicate that the drug remains in the system for a longer period in older adults. The terminal elimination half-life is longer in elderly subjects (11 to 13 hours) compared to younger adults (5 to 9 hours). This information is used by healthcare providers when managing the medication in this population.


Q: Does Rivarin have a known effect on laboratory blood test results (other than the primary ones)?

Yes, the official documentation of adverse reactions notes that the drug can cause elevations in liver transaminases. These are markers that may be monitored via routine laboratory blood tests. In such cases, close monitoring of the patient's liver function is typically required.


Q: What happens if a person taking Rivarin has to have minor surgery or dental work?

Official safety guides require that a person inform the doctor or dentist they are taking this drug before any surgery or procedure, including routine dental surgery. The healthcare provider will then determine if the drug needs to be temporarily stopped beforehand and when it should be safely resumed.


Q: Do official documents mention any connection between Rivarin and hair loss?

Hair loss, also known as alopecia, is not documented as a common, uncommon, or serious adverse reaction in the key sections of the regulatory prescribing information for this drug. The official adverse reaction lists do not mention any connection to hair loss.


Q: How does the half-life of Rivarin compare to similar medicines?

The estimated duration is measured by its terminal elimination half-life, which is typically 5 to 9 hours in younger adults. This is extended to 11 to 13 hours in elderly subjects. This pharmacokinetic data is used by clinicians for comparative purposes with other anticoagulants that have different durations of effect.


Q: Does Rivarin interact with any common vitamins like Vitamin K or C?

Regulatory information on the drug’s mechanism states that, unlike older anticoagulant classes, Vitamin K is not expected to affect the anticoagulant activity of this drug. The official prescribing information does not specify an interaction with Vitamin C.


Q: What kind of monitoring or follow-up is generally involved when taking Rivarin?

According to official clinical guidance, routine monitoring of the anticoagulant effect using blood clotting tests (like PT or INR) is generally not recommended. However, frequent monitoring of kidney function is generally recommended. Healthcare providers also routinely monitor patients for any signs of bleeding or neurological impairment.


Q: How is Rivarin different from heparin?

This medication is a Factor Xa inhibitor, which is an oral medication that directly blocks one specific clotting factor. Heparin, by contrast, is an injectable anticoagulant that works differently by enhancing the activity of the body’s natural anti-clotting protein, antithrombin.


Q: Are there any specific warnings for people with a history of bleeding disorders?

Yes, patient safety information indicates that individuals should share information with their doctor regarding any history of bleeding or bleeding disorders. This is a crucial factor that a healthcare provider must evaluate when determining the appropriate course of treatment.


Q: What is the estimated duration of Rivarin's effect in the body?

The duration of the drug’s physiological effect in the body is estimated by its terminal elimination half-life. This is typically between 5 to 9 hours in younger adults, but it can be longer, extending up to 11 to 13 hours, in elderly subjects.


Q: What are the official recommendations if a person accidentally takes too much Rivarin?

Official patient information states that the most likely symptom of taking too much of the drug is unusual bleeding. Treatment involves prompt medical evaluation, where the healthcare team will consider the administration of a specific reversal agent or other specialized procoagulant agents to stop the anti-clotting effect.


Q: Can I take Rivarin if I have a history of allergies to other medicines?

Official documents indicate that individuals should provide a complete allergy history before starting treatment. This includes informing the doctor or pharmacist if they are allergic to the drug itself, any of its components, or any other drugs, foods, or substances they have reacted to in the past.


Q: What level of alcohol consumption is mentioned in official guidelines for those on Rivarin?

Official clinical guidance states that excessive or chronic alcohol consumption may interfere with the drug’s anticoagulant effects and could potentially increase the risk of bleeding. Consultation with a healthcare provider is generally advised to discuss individual risk profiles and alcohol consumption.


Q: Does Rivarin interact with any common anti-depressant medications?

Yes, the official prescribing information notes a potential for interaction with certain classes of antidepressants. Concomitant use with Selective Serotonin Reuptake Inhibitors (SSRIs) and Serotonin Norepinephrine Reuptake Inhibitors (SNRIs) is noted to increase the risk of bleeding.

How should Rivarin be stored and disposed of?

Rivaroxaban (Rivarin) must be stored and disposed of according to strict regulatory guidelines to maintain stability and ensure safety.

Detail Official Requirement
Storage Temperature Controlled room temperature: 20 C to 25 C (68 F to 77 F), away from excess heat.
Environmental Protection Keep from freezing and protect from moisture and direct light.
Container Rule Must be kept in the tightly closed, original container.
Stability Note Any prepared oral suspension formulation must be discarded 60 days after reconstitution.
Child Protection Mandatory to keep out of the sight and reach of children.
Disposal Rule Unused or expired medicine must be disposed of correctly. It must not be disposed of via wastewater or flushed down the toilet.

These constraints define the required conditions for product quality and public safety, specifying proper temperature, protection, and container integrity. Disposal must follow regulated methods, such as drug take-back programs or safe household trash disposal.

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

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