Product image of Hydroxyurea Medac (Hydroxycarbamide) supplied by GNH India

Hydroxyurea Medac

Active Ingredient:
Hydroxycarbamide
Origin:
EU

Hydroxyurea Medac (Hydroxycarbamide)

Hydroxycarbamide, the active ingredient in Hydroxyurea Medac, is an antineoplastic agent presented as an oral formulation for oral use. It is employed to manage sickle cell disease, chronic myelogenous leukemia, polycythemia vera and essential thrombocythemia by modulating DNA synthesis in rapidly dividing cells. The drug is indicated for patients with these hematologic disorders.
GNH India supplies Hydroxyurea Medac as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies, clinics and research institutions worldwide with consistent quality and regulatory compliance.

Manufacturer / TM Owner

Medac Gesellschaft Für Klinische Spezialpräparate Mbh (Wedel)

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Indications & Clinical Uses

  • Hydroxyurea Medac is used in hematologic disorders where abnormal cell proliferation is a key feature.
  • Sickle cell disease: reduces frequency of painful crises and transfusion requirements.
  • Chronic myelogenous leukemia: helps control leukemic cell growth.
  • Polycythemia vera: lowers elevated red blood cell mass.
  • Essential thrombocythemia: decreases platelet counts and thrombotic risk.
  • Myeloproliferative disorders: improves overall disease management.

How It Works

  • Hydroxycarbamide inhibits the enzyme ribonucleotide reductase, the key catalyst for conversion of ribonucleotides to deoxyribonucleotides. By limiting deoxyribonucleotide pools, DNA synthesis is slowed, particularly in rapidly dividing hematopoietic cells. This cytostatic effect reduces abnormal proliferation of sickled erythrocytes, leukemic blasts, and megakaryocytes, thereby moderating disease activity. The drug’s action is dose‑dependent and reversible, allowing normal marrow recovery when treatment is paused.

Side Effects

Hydroxyurea can cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Fatigue: general tiredness and reduced energy.
  • Low white blood cell count: mild neutropenia detectable on routine labs.

Serious or Rare Side Effects

  • Severe bone marrow suppression: pancytopenia requiring medical intervention.
  • Aplastic anemia: rare but potentially life‑threatening.
  • Liver toxicity: elevated transaminases or hepatitis.

Precautions & Warnings

Before initiating therapy, clinicians should assess baseline laboratory values and monitor patients regularly.

  • Monitor blood counts: perform regular CBC to detect myelosuppression.
  • Assess renal and hepatic function: obtain baseline and periodic labs.
  • Avoid use in patients with known hypersensitivity to hydroxyurea.
  • Use caution with concomitant myelosuppressive therapies.
  • Pregnancy and lactation: contraindicated unless benefits outweigh risks; discuss with physician.
  • Store at ambient temperature below 25°C: keep in original container, protect from moisture and light.

Avoid Interactions

Hydroxyurea may interact with several medicines, requiring careful evaluation.

Major Interactions (Avoid)

  • Concurrent use with other myelosuppressive agents (e.g., azathioprine, cyclophosphamide) may cause profound bone‑marrow depression.
  • Combination with antiretroviral drugs such as didanosine can increase toxicity.
  • Co‑administration with live vaccines may reduce vaccine efficacy.

Moderate Interactions (Monitor Closely)

  • Allopurinol: may increase hydroxyurea plasma levels; monitor for toxicity.
  • NSAIDs: may exacerbate renal effects; check renal function.
  • Phenytoin: may reduce hydroxyurea effectiveness; adjust dose if needed.

Frequently Asked Questions

Hydroxyurea Medac is prescribed for several hematologic conditions, including sickle cell disease, chronic myelogenous leukemia, polycythemia vera, and essential thrombocythemia. In each case, the drug helps control abnormal cell proliferation and reduces disease‑related complications.

Hydroxycarbamide (hydroxyurea) blocks ribonucleotide reductase, an enzyme essential for making deoxyribonucleotides, the building blocks of DNA. By limiting these building blocks, DNA synthesis slows, especially in rapidly dividing blood‑forming cells, leading to reduced abnormal cell growth.

Dosing of Hydroxyurea Medac is individualized. The prescribing clinician determines the appropriate dose based on the patient’s condition, weight, laboratory values, and response to therapy. No fixed dose can be stated without a medical prescription.

The pregnancy safety category for hydroxyurea is unknown, and the drug is generally avoided in pregnancy and lactation because of potential fetal and infant risks. Use only if the potential benefit justifies the risk and after thorough discussion with a healthcare professional.

To 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 (including any cold‑chain needs), and import documentation.

Hydroxyurea is a first‑line oral myelosuppressive agent for the listed indications. Compared with other cytoreductive drugs such as busulfan or interferon, hydroxyurea offers oral administration, a well‑characterised safety profile, and ease of dose adjustment, though each therapy must be matched to individual patient factors.

Store the product at ambient temperature below 25 °C, in its original packaging, protected from moisture and direct light. Keep the container tightly closed and out of reach of children. No refrigeration is required for this oral formulation.

Hydroxyurea Medac is taken orally, usually as a tablet swallowed whole with water. The exact timing (e.g., with or without food) should follow the prescribing clinician’s instructions.

The most critical risks include severe bone‑marrow suppression leading to pancytopenia, aplastic anemia, and significant liver toxicity. Patients should be monitored regularly with blood counts and liver‑function tests to detect these complications early.

Hydroxyurea should be avoided in individuals with known hypersensitivity to the drug, those with severe pre‑existing bone‑marrow failure, uncontrolled infections, or in pregnant or breastfeeding women unless the benefits outweigh the risks. A thorough medical evaluation is required before initiation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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