Product image of Hydroxycarbamid Teva (Hydroxycarbamide) supplied by GNH India

Hydroxycarbamid Teva

Active Ingredient:
Hydroxycarbamide
Origin:
EU

Hydroxycarbamid Teva (Hydroxycarbamide)

Hydroxycarbamide, the active ingredient in Hydroxycarbamid Teva, is a ribonucleotide reductase inhibitor presented as an oral tablet for oral use. It is employed in the management of sickle cell disease, chronic myelogenous leukemia, polycythemia vera, essential thrombocythemia and melanoma, helping to control disease‑related complications in appropriate patient populations.

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

Manufacturer / TM Owner

Teva Pharmaceuticals Polska Sp. Z O.O.

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Indications & Clinical Uses

Hydroxycarbamide acts on rapidly dividing cells by inhibiting DNA synthesis, making it useful in several hematologic and oncologic conditions.

  • Sickle cell disease: reduces frequency of vaso‑occlusive crises and related pain episodes.
  • Chronic myelogenous leukemia: helps achieve cytogenetic remission when combined with targeted therapy.
  • Polycythemia vera: lowers elevated red blood cell mass and decreases thrombotic risk.
  • Essential thrombocythemia: controls platelet overproduction and reduces clotting complications.
  • Melanoma: used as part of combination regimens to limit tumor growth.

How It Works

  • Hydroxycarbamide inhibits ribonucleotide reductase, the key enzyme responsible for converting ribonucleotides to deoxyribonucleotides. This blockade reduces the intracellular pool of deoxyribonucleotides, impairing DNA synthesis and replication in rapidly proliferating cells, leading to cell cycle arrest and apoptosis in malignant or abnormal hematopoietic cells.

Side Effects

Hydroxycarbamide may cause a range of adverse reactions, from mild to severe, that require monitoring during therapy.

Common Side Effects

  • Nausea and vomiting: mild to moderate gastrointestinal upset.
  • Fatigue: persistent tiredness affecting daily activities.
  • Hair thinning or loss: reversible with discontinuation.
  • Skin discoloration: darkening of the skin or nails.
  • Mild cytopenias: slight reductions in white blood cells or platelets.

Serious or Rare Side Effects

  • Severe bone marrow suppression: profound pancytopenia requiring transfusion.
  • Acute tumor lysis syndrome: rapid cell breakdown leading to metabolic disturbances.
  • Pulmonary hypertension: rare but potentially life‑threatening lung vascular disease.
  • Renal impairment: worsening kidney function in susceptible individuals.
  • Secondary malignancies: increased risk of developing other cancers with long‑term use.

Precautions & Warnings

Before initiating Hydroxycarbamide, clinicians should assess baseline health status and monitor patients regularly.

  • Monitor blood counts: perform complete blood count (CBC) weekly during dose escalation.
  • Assess renal function: check serum creatinine and adjust dose in renal impairment.
  • Evaluate hepatic status: monitor liver enzymes for potential toxicity.
  • Counsel on contraception: advise effective birth control for patients of reproductive potential.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Hydroxycarbamide can interact with other medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Azathioprine: additive myelosuppression may lead to severe pancytopenia.
  • Live vaccines: increased risk of infection due to immunosuppression.
  • Allopurinol: may potentiate hydroxycarbamide toxicity and require dose reduction.

Moderate Interactions (Monitor Closely)

  • NSAIDs: can affect renal function, especially in patients with pre‑existing kidney disease.
  • Phenytoin: may increase hydroxycarbamide metabolism, reducing therapeutic effect.
  • Antacids containing aluminum or magnesium: may decrease absorption if taken simultaneously.

Frequently Asked Questions

Hydroxycarbamid Teva, containing hydroxycarbamide, is indicated for sickle cell disease, chronic myelogenous leukemia, polycythemia vera, essential thrombocythemia and melanoma. It helps control disease‑related complications by targeting rapidly dividing cells in these hematologic and oncologic disorders.

Hydroxycarbamide inhibits the enzyme ribonucleotide reductase, which is essential for converting ribonucleotides to deoxyribonucleotides. This reduces the supply of building blocks needed for DNA synthesis, leading to decreased replication of rapidly proliferating cells such as malignant or abnormal blood cells.

The dosage of Hydroxycarbamid Teva is individualized by the prescribing clinician based on the specific indication, patient weight, renal function and response to therapy. Patients should follow the dose prescribed by their healthcare professional and not adjust it without medical guidance.

Safety data for hydroxycarbamide in pregnancy and lactation are limited. It is generally advised to avoid use during pregnancy unless the potential benefit justifies the risk, and breastfeeding is not recommended because the drug may be excreted in milk. Consultation with a specialist is essential.

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, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and necessary import documentation.

Hydroxycarbamide is a cytoreductive agent that differs from targeted therapies such as tyrosine‑kinase inhibitors used in chronic myelogenous leukemia. While it offers broad activity across several hematologic disorders, newer agents may provide more specific mechanisms with distinct safety profiles. Choice of therapy depends on disease characteristics and patient factors.

Hydroxycarbamid Teva should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, excessive heat and direct sunlight to maintain stability throughout its shelf life.

Hydroxycarbamid Teva is taken orally, usually as a tablet, with or without food as directed by the prescribing clinician. The exact administration schedule, including frequency and timing, is determined by the healthcare provider based on the individual treatment plan.

The most serious risks include severe bone marrow suppression leading to pancytopenia, pulmonary hypertension, acute tumor lysis syndrome and potential secondary malignancies with long‑term use. Patients should be monitored closely for signs of infection, bleeding, respiratory symptoms and abnormal blood counts.

Hydroxycarbamid Teva is contraindicated in patients with known hypersensitivity to hydroxycarbamide or any of its excipients. It should also be avoided in individuals with severe active infections, uncontrolled pulmonary hypertension, or significant bone marrow failure unless specifically directed by a specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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