Product image of Hydroxychloroquinesulfaat Teva (Hydroxychloroquine Sulfate) supplied by GNH India

Hydroxychloroquinesulfaat Teva

Active Ingredient:
Hydroxychloroquine Sulfate
Origin:
EU

Hydroxychloroquinesulfaat Teva (Hydroxychloroquine Sulfate)

Hydroxychloroquine sulfate, the active ingredient in Hydroxychloroquinesulfaat Teva, is an antimalarial presented as an oral dosage form for systemic use. It is employed in the prevention and treatment of malaria and in managing autoimmune disorders such as rheumatoid arthritis and systemic lupus erythematosus.

GNH India supplies Hydroxychloroquinesulfaat Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Hydroxychloroquine sulfate is used in diseases where it modulates immune activity or treats parasitic infection.

  • Malaria prophylaxis and treatment: Prevents infection and treats acute episodes of Plasmodium malaria in adults and children.
  • Rheumatoid arthritis: Reduces joint inflammation and slows disease progression in patients with active disease.
  • Systemic lupus erythematosus: Controls disease activity and decreases flare frequency in affected individuals.

How It Works

  • Hydroxychloroquine sulfate accumulates in lysosomes, raising intralysosomal pH and inhibiting enzymatic activity, which disrupts autophagy and antigen processing. By interfering with Toll‑like receptor signaling, it reduces cytokine production and modulates the immune response. The drug also interferes with parasite heme polymerization, contributing to its antimalarial effect.

Side Effects

Hydroxychloroquine sulfate may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Nausea or vomiting
  • Diarrhea
  • Abdominal discomfort
  • Headache
  • Skin rash or itching
  • Visual disturbances such as blurred vision

Serious or Rare Side Effects

  • Retinal toxicity leading to vision loss
  • Cardiac arrhythmias including QT prolongation
  • Severe hypoglycemia
  • Hemolytic anemia in G6PD‑deficient patients
  • Severe cutaneous adverse reactions (e.g., Stevens‑Johnson syndrome)

Precautions & Warnings

Hydroxychloroquine requires careful monitoring in several clinical situations.

  • Pregnancy: Use only if potential benefit justifies potential risk; safety data are limited.
  • Renal impairment: Adjust dosing and monitor plasma levels in patients with reduced kidney function.
  • Hepatic impairment: Use cautiously; monitor liver function tests.
  • G6PD deficiency: Assess risk of hemolysis before initiating therapy.
  • Ophthalmologic monitoring: Perform baseline and periodic eye examinations to detect retinal changes.
  • Store at ambient temperature: Keep below 25 °C, in the original container, protected from moisture and light.

Avoid Interactions

Hydroxychloroquine can interact with several medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Concomitant use with other QT‑prolonging agents (e.g., quinidine, macrolide antibiotics) may increase risk of cardiac arrhythmia.
  • Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine) can markedly reduce hydroxychloroquine plasma concentrations.
  • Antacids containing aluminum or magnesium may decrease absorption if taken simultaneously.

Moderate Interactions (Monitor Closely)

  • Digoxin: Hydroxychloroquine may increase serum digoxin levels; monitor for toxicity.
  • Insulin or oral hypoglycemics: May potentiate hypoglycemic effect; check blood glucose regularly.
  • Cyclosporine: Potential for increased nephrotoxicity; monitor renal function.
  • Warfarin: May enhance anticoagulant effect; monitor INR.

Frequently Asked Questions

Hydroxychloroquinesulfaat Teva contains hydroxychloroquine sulfate, which is prescribed for the prevention and treatment of malaria and for managing autoimmune conditions such as rheumatoid arthritis and systemic lupus erythematosus. It works by modulating immune responses and interfering with the life cycle of malaria parasites, providing therapeutic benefit in these distinct disease areas.

Hydroxychloroquine accumulates in lysosomes, raising their pH and inhibiting enzymes involved in antigen processing and autophagy. This dampens Toll‑like receptor signaling and reduces cytokine production, which moderates autoimmune activity. In malaria parasites, the drug disrupts heme polymerization, leading to toxic accumulation of heme and parasite death.

The appropriate dose of hydroxychloroquine is determined by the prescribing clinician based on the specific indication, patient weight, renal and hepatic function, and other individual factors. Dosage regimens differ for malaria prophylaxis, acute malaria treatment, rheumatoid arthritis, and systemic lupus erythematosus, and should be followed exactly as prescribed.

Safety data for hydroxychloroquine in pregnancy are limited, and the drug is classified as pregnancy category unknown. It may be used only when the potential benefit outweighs any risk to the fetus. Breastfeeding mothers should consult their healthcare provider, as the drug can be excreted in breast milk and may affect the infant.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, and will request verification of trade or institutional credentials. After confirmation, the team provides pricing, availability, shipping details (including any cold‑chain requirements) and assists with import documentation.

Compared with chloroquine, hydroxychloroquine has a similar mechanism but a better safety profile, especially regarding retinal toxicity. Relative to disease‑modifying antirheumatic drugs such as methotrexate, it offers a milder immunomodulatory effect and is often used when patients cannot tolerate stronger agents. Choice of therapy depends on disease severity, comorbidities and individual response.

The product should be stored at ambient temperature, preferably below 25 °C, in its original packaging to protect it from moisture and light. Keep the tablets away from excessive heat and humidity, and ensure the container is tightly closed when not in use. Do not store in the bathroom or near a kitchen stove.

Hydroxychloroquinesulfaat is taken orally, usually with or without food, as directed by the prescribing clinician. Tablets should be swallowed whole with a glass of water and not crushed or chewed unless specifically instructed. Adherence to the prescribed schedule is important to maintain therapeutic levels and reduce the risk of resistance or disease flare.

The most serious adverse events include retinal toxicity that can lead to irreversible vision loss, cardiac arrhythmias such as QT prolongation, severe hypoglycemia, and hemolytic anemia in patients with glucose‑6‑phosphate dehydrogenase deficiency. Prompt reporting of visual changes, cardiac symptoms, or unexplained fatigue is essential, and regular monitoring may be required to mitigate these risks.

Hydroxychloroquine is contraindicated in patients with known hypersensitivity to the drug or any of its excipients. Individuals with pre‑existing retinal disease, severe cardiac conduction disorders, or confirmed G6PD deficiency should avoid therapy unless a specialist determines that benefits outweigh risks. Pregnant or breastfeeding women should use only under strict medical supervision, and patients with significant hepatic or renal impairment require careful assessment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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