Buy Plaquenil
Plaquenil

0.53
Used to treat autoimmune diseases and prevent or treat malaria infections.


Availability
In Stock
Delivery
Airmail (14-21 days) | EMS trackable (5-9 days)
Product is shipped in a fully discreet envelope with no content disclosure, including all required documentation inside

Product Sheet

Alternative/Local Brand
Plaquenil
Active Ingredient(s)
Hydroxychloroquine
Primary Category
Rheumatoid Arthritis Treatment, Antimalarial
Therapeutic Class
Antiprotozoals, Antimalarials, Aminoquinolines
Pharmacological Class
Disease-Modifying Anti-Rheumatic Drugs (DMARDs)
Indications
Rheumatoid arthritis, Systemic lupus erythematosus, Malaria prevention, Malaria treatment
Contraindications
Maculopathy, Hypersensitivity to quinolines, Myasthenia gravis
Minor Side Effects
Stomach cramps, Diarrhoea, Loss of appetite
Moderate Side Effects
Skin rash, Headache, Nervousness
Serious Side Effects
Blurred vision, Ringing in ears, Muscle weakness, Irregular heartbeat
Dosage Forms
Film-coated tablet
Administration Route
Oral
Mechanism of Action
It reduces inflammation and modifies the underlying disease process in autoimmune conditions. It also interferes with the growth of parasites in the red blood cells to treat or prevent malaria.
Prescription Status
Rx
Manufacturer
Sanofi
Patient Summary
Used to treat autoimmune diseases and prevent or treat malaria infections.
Onset Time
Several weeks for arthritis
Duration
Several weeks
Storage Instructions
Store below 25°C in the original packaging.
Drug Interactions
Digoxin, Insulin, Tamoxifen, Amiodarone
Age Restrictions
Children over 31kg and adults
Pregnancy Use
Consult a doctor; only used if benefits outweigh risks.
Alternative Drugs
Quinoric, Chloroquine

What is Plaquenil?

Plaquenil is a brand-name medication that contains hydroxychloroquine as its active ingredient. Hydroxychloroquine belongs to a class of drugs known as antimalarials, which are also used to modulate the immune system in certain autoimmune disorders. In Hong Kong, Plaquenil is a prescription-only product (approved by the Department of Health) and is available in tablet form at strengths of 200 mg and 400 mg.

How Plaquenil Works in the Body

Hydroxychloroquine exerts several pharmacologic actions that are relevant to its therapeutic uses:

  • Immune modulation: The drug interferes with antigen presentation and reduces the activity of certain immune cells (T-lymphocytes and B-lymphocytes). This dampening effect helps control inflammation in autoimmune conditions such as rheumatoid arthritis and systemic lupus erythematosus.
  • Antiparasitic activity: Hydroxychloroquine raises the pH within intracellular vesicles, creating an environment that is hostile to the malaria parasite Plasmodium spp. and to certain other protozoa.
  • Antiviral hypothesis (off-label): Laboratory studies have shown that hydroxychloroquine can impair viral entry and replication by altering cellular endosomal pH. Clinical evidence for this effect, particularly against SARS-CoV-2, remains inconclusive.

After oral administration, hydroxychloroquine is well absorbed. Its onset of action in autoimmune diseases can take several weeks, whereas antiparasitic effects begin within a few days. The drug has a long elimination half-life (approximately 40-50 days), which contributes to its once-daily dosing schedules.

Conditions Treated by Plaquenil

Plaquenil is FDA- and EMA-approved for the following indications, which are also recognized by Hong Kong health authorities:

  • Systemic lupus erythematosus (SLE): Used to reduce disease activity and prevent flares.
  • Rheumatoid arthritis (RA): Often prescribed as part of combination therapy to control joint inflammation.
  • Malaria prophylaxis and treatment: Particularly for chloroquine-sensitive strains.

These approved uses are based on clinical trials demonstrating efficacy in reducing disease activity scores and preventing malaria infection after travel to endemic regions.

Evidence-Based Off-Label Uses

Hydroxychloroquine for COVID-19 Support

Hydroxychloroquine has been investigated as a potential treatment or preventive agent for COVID-19. Large, well-controlled randomized trials have not confirmed a clear benefit, and major health agencies (e.g., WHO, FDA) consider its use for COVID-19 to be not approved. Off-label prescription for this purpose should only occur under close medical supervision, with acknowledgment of the limited efficacy data and possible safety concerns.

Other Investigational Applications

Research continues to explore hydroxychloroquine in diseases such as certain dermatologic conditions (e.g., cutaneous lupus) and as an adjunct in oncologic protocols. These investigations remain experimental; the medication is not formally approved for these purposes.

Who Should Use Plaquenil? Contraindications and Special Considerations

Absolute Contraindications

  • Known hypersensitivity to hydroxychloroquine or any of the tablet’s excipients.
  • Pre-existing retinopathy or other serious eye disease.

Relative Contraindications

  • Significant renal or hepatic impairment (dose adjustments may be required).
  • History of cardiac arrhythmias, especially prolonged QT interval.
  • Pregnancy: Hydroxychloroquine crosses the placenta. While some rheumatology guidelines consider it relatively safe in pregnancy, risk-benefit assessment is essential.
  • Breastfeeding: Small amounts are secreted in breast milk; clinicians evaluate infant exposure.

Special Populations

  • Elderly: Age-related decline in renal function may necessitate lower initial doses.
  • Patients with G6PD deficiency: Increased risk of hemolysis, though the risk is lower than with chloroquine.

If any of these conditions apply, a healthcare professional should evaluate suitability before initiating therapy.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Gastrointestinal upset: Nausea, abdominal discomfort, or mild diarrhea are frequently reported.
  • Skin reactions: Rashes or mild itching may occur, typically early in treatment.
  • Headache or dizziness: Usually transient and mild.

Most of these effects are reversible upon dose reduction or discontinuation.

Serious Adverse Events

  • Retinal toxicity: A rare but potentially irreversible condition that can lead to vision loss. Regular ophthalmologic screening is recommended after six months of therapy and annually thereafter.
  • Cardiac toxicity: Hydroxychloroquine can prolong the QT interval, increasing the risk of ventricular arrhythmias. Patients with existing heart disease or those taking other QT-prolonging agents require cardiac monitoring.
  • Severe cutaneous reactions: Stevens-Johnson syndrome or toxic epidermal necrolysis, though extremely uncommon, demand immediate medical attention.

Drug Interactions

  • Major interactions:
  • Azithromycin, quinidine, or other QT-prolonging drugs - may heighten arrhythmia risk.
  • Cytochrome P450 (CYP) inhibitors (e.g., ketoconazole) - can increase hydroxychloroquine plasma levels.
  • Moderate interactions:
  • Antacids containing aluminum or magnesium - may reduce absorption; spacing doses by at least 2 hours is advised.
  • Digoxin - hydroxychloroquine can raise digoxin concentrations; serum levels should be monitored.

Because interaction data are continually updated, patients should provide a complete medication list-including over-the-counter products and herbal supplements-to their prescriber.

Food and Lifestyle Interactions

  • Food: Hydroxychloroquine can be taken with or without food; taking it with meals may lessen gastrointestinal upset.
  • Alcohol: Moderate consumption is generally acceptable, but excessive alcohol can exacerbate liver toxicity.
  • Driving: The drug does not typically impair cognition, but dizziness in early treatment may affect driving; patients should assess their own response.
  • Sun exposure: Hydroxychloroquine may increase photosensitivity; use sunscreen and protective clothing when outdoors.

How to Take Plaquenil

Standard Dosing (Based on Available Strengths)

  • Rheumatoid arthritis / Lupus:
  • Initial: 200 mg once daily.
  • Titration: May increase to 400 mg daily (usually split as 200 mg twice daily) based on clinical response and tolerability.
  • Malaria prophylaxis: 400 mg once weekly, starting 1-2 weeks before travel and continuing for 4 weeks after leaving the endemic area.
  • Malaria treatment: 800 mg on day 1 (usually as two 400 mg tablets), followed by 400 mg daily for 2 days.

The exact regimen should be individualized by a prescriber. Tablet splitting is acceptable for the 200 mg strength but not recommended for the 400 mg tablet unless the manufacturer indicates it is scored.

Special Populations

  • Renal impairment (eGFR < 30 mL/min): Consider reducing the daily dose by 50 % and monitor plasma levels if available.
  • Hepatic impairment: No formal dose reduction is required, but close monitoring for toxicity is prudent.
  • Elderly: Start with the lower end of the dosing range (200 mg daily) and titrate slowly.

Administration Tips

  • Swallow tablets whole with a full glass of water.
  • If gastrointestinal upset occurs, taking the dose with food may help.
  • Do not crush or chew tablets unless advised by a pharmacist.

Missed Dose

If a dose is missed and the next scheduled dose is more than 12 hours away, take the missed dose as soon as remembered. Do not double the dose to make up for a missed one.

Overdose

Signs of acute overdose may include severe nausea, vomiting, visual disturbances, and cardiac arrhythmias. Seek emergency medical care immediately; supportive care and cardiac monitoring are the mainstays of treatment. No specific antidote exists.

Discontinuation

Long-term therapy can be tapered gradually to minimize the risk of disease flare in autoimmune conditions. Abrupt cessation is discouraged without medical guidance.

Monitoring and Follow-Up

  • Baseline assessments: Complete blood count, liver function tests, renal function, and an ophthalmologic exam before starting therapy.
  • Ongoing monitoring:
  • Every 3-6 months: Visual acuity and retinal examination, especially after six months of continuous use.
  • Quarterly labs: Liver enzymes and renal function, particularly in patients with pre-existing organ impairment.
  • Cardiac evaluation: ECG monitoring for patients on concurrent QT-prolonging medications or with known cardiac disease.

Patients should report new visual symptoms (blurred vision, difficulty reading) or cardiac symptoms (palpitations, syncope) promptly.

Storage and Handling

  • Store Plaquenil tablets at room temperature (20 °C-25 °C) away from excess heat, moisture, and direct sunlight.
  • Keep the container tightly closed and out of reach of children.
  • Do not use tablets beyond the printed expiration date; discard expired medication according to local pharmaceutical waste guidelines.

Medication-Specific Glossary

Retinopathy
Damage to the retina that can lead to vision loss; a known risk with long-term hydroxychloroquine use, requiring regular eye examinations.
QT Prolongation
Extension of the heart’s electrical repolarization interval, which can predispose to dangerous arrhythmias; monitored via electrocardiogram (ECG).
Half-Life
The time required for the plasma concentration of a drug to decrease by 50 %; hydroxychloroquine’s long half-life (≈ 40-50 days) influences dosing frequency and steady-state kinetics.

Medical Disclaimer

This article provides educational information about Plaquenil and is not a substitute for professional medical advice. Treatment decisions, including use for unapproved indications, must be made under the guidance of a qualified healthcare provider. The content is intended for informational purposes and does not constitute medical recommendations. Always consult a physician before starting, stopping, or changing any medication regimen.

Plaquenil FAQ

Can Plaquenil be used for COVID-19 prevention?

Current evidence from large randomized trials does not support hydroxychloroquine for COVID-19 prevention. Health authorities in Hong Kong and internationally consider this an off-label use that should only be undertaken within a clinical trial or under strict medical supervision.

How long does it take to see improvement in lupus symptoms?

Patients often notice a gradual reduction in disease activity over several weeks to months. Full therapeutic effect may require up to 6 months of consistent therapy.

What should I do if I develop a rash while taking Plaquenil?

Stop the medication and contact a healthcare professional promptly. A rash can be an early sign of hypersensitivity or a more serious skin reaction that requires medical assessment.

Is it safe to take Plaquenil while pregnant?

Hydroxychloroquine is sometimes continued during pregnancy for lupus or rheumatoid arthritis when the benefits outweigh potential risks. A specialist should evaluate each case individually.

How often should I have eye exams while on Plaquenil?

Baseline eye testing is recommended before starting therapy, followed by a screening at six months, then annually thereafter, especially after five years of continuous use.

Can I take Plaquenil with over-the-counter antihistamines?

Most antihistamines do not interact with hydroxychloroquine. However, it is advisable to inform your pharmacist or doctor about all medications you are using.

What distinguishes Plaquenil from generic hydroxychloroquine tablets?

Plaquenil is a branded formulation that contains the same active ingredient as generic hydroxychloroquine. Differences may exist in inactive fillers or tablet coating, which can affect tolerability for some patients.

Will taking Plaquenil affect my blood test results?

Hydroxychloroquine can cause mild alterations in liver enzymes and blood counts. Your clinician may order periodic labs to monitor any changes.

Is it necessary to avoid sunlight while on Plaquenil?

The medication can increase photosensitivity in some individuals. Using sunscreen and protective clothing when outdoors is recommended.

How should Plaquenil be disposed of when it is no longer needed?

Do not flush tablets down the toilet. Return unused medication to a pharmacy waste program or follow the Hong Kong Department of Health’s guidelines for safe disposal.

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