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

Hydroxycarbamid Devatis

Active Ingredient:
Hydroxycarbamide
Origin:
EU

Hydroxycarbamid Devatis (Hydroxycarbamide)

Hydroxycarbamide, the active ingredient in Hydroxycarbamid Devatis, is an antimetabolite presented as an oral tablet for oral use. It is used to manage sickle cell disease, chronic myelogenous leukemia, polycythemia vera and essential thrombocythemia in adult patients.

GNH India supplies Hydroxycarbamid Devatis as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution. Clients benefit from comprehensive regulatory support and consistent product availability across multiple markets.

Manufacturer / TM Owner

Devatis Gmbh

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Indications & Clinical Uses

Hydroxycarbamide is employed in hematologic disorders that involve abnormal cell proliferation or sickling of red blood cells.

  • Sickle cell disease: reduces frequency of painful vaso‑occlusive crises and lowers need for blood transfusions.
  • Chronic myelogenous leukemia: helps achieve cytogenetic remission when used in combination with other agents.
  • Polycythemia vera: controls elevated red blood cell mass and decreases risk of thrombosis.
  • Essential thrombocythemia: lowers platelet counts and reduces thrombotic complications.

How It Works

  • Hydroxycarbamide inhibits ribonucleotide reductase, the enzyme responsible for converting ribonucleotides to deoxyribonucleotides. This restriction limits the intracellular pool of deoxyribonucleotides, suppressing DNA synthesis and repair. The resulting decrease in cell proliferation particularly affects rapidly dividing hematopoietic cells, providing therapeutic benefit in myeloproliferative disorders and sickle cell disease.

Side Effects

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

Common Side Effects

  • Nausea and vomiting: gastrointestinal upset occurring early in therapy.
  • Alopecia: temporary hair thinning or loss.
  • Skin hyperpigmentation: darkening of the skin, especially on the face and hands.
  • Mild neutropenia or anemia: modest reductions in white or red blood cells.

Serious or Rare Side Effects

  • Severe bone marrow suppression: profound pancytopenia requiring transfusion or treatment interruption.
  • Hepatic toxicity: elevated liver enzymes or hepatitis.
  • Renal impairment: acute kidney injury or worsening of pre‑existing renal disease.
  • Cutaneous ulceration or necrosis: painful skin ulcers, particularly on the lower legs.

Precautions & Warnings

When prescribing hydroxycarbamide, clinicians should observe several safety measures.

  • Blood count monitoring: perform complete blood counts regularly to detect myelosuppression.
  • Renal function assessment: evaluate serum creatinine before initiation and periodically during therapy.
  • Hepatic function assessment: monitor liver enzymes for signs of toxicity.
  • Pregnancy risk: avoid use during pregnancy unless benefits outweigh risks; discuss contraception.
  • Drug interactions: review concomitant medications for potential additive myelosuppressive effects.
  • Store at below 25°C: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Hydroxycarbamide can interact with other medicines, altering its safety profile.

Major Interactions (Avoid)

  • Concurrent myelosuppressive chemotherapy: may cause excessive bone marrow suppression.
  • Zidovudine (AZT): combined use can intensify hematologic toxicity.

Moderate Interactions (Monitor Closely)

  • Allopurinol: may increase hydroxycarbamide plasma levels.
  • Penicillins and sulfonamides: can enhance myelosuppression.
  • Live vaccines: reduced efficacy and increased risk of infection.

Frequently Asked Questions

Hydroxycarbamid Devatis, containing hydroxycarbamide, is indicated for the treatment of sickle cell disease, chronic myelogenous leukemia, polycythemia vera and essential thrombocythemia. These are hematologic disorders where the drug helps control abnormal cell growth or red‑cell sickling.

Hydroxycarbamide blocks ribonucleotide reductase, an enzyme needed to produce deoxyribonucleotides for DNA synthesis. By limiting DNA building blocks, it slows the replication of rapidly dividing cells such as malignant blood‑cell precursors and sickled erythrocytes, thereby reducing disease activity.

The specific dose of Hydroxycarbamid Devatis is determined by the prescribing clinician based on the patient’s diagnosis, disease severity, laboratory values and overall health. Dosage regimens are individualized and should follow the prescriber’s instructions and local treatment guidelines.

The safety of hydroxycarbamide in pregnancy and lactation is not well established. It is generally avoided unless the potential benefit justifies the risk. Women of child‑bearing potential should use effective contraception, and breastfeeding decisions should be made in consultation with a healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Hydroxycarbamide is a well‑established oral antimetabolite that offers a convenient, non‑injectable option compared with some newer targeted agents or biologics. While it may be less specific than newer kinase inhibitors, it remains effective for many patients and is often used when cost, accessibility or disease stage favor a broader‑acting therapy.

Hydroxycarbamid Devatis should be stored at temperatures below 25 °C, in its original packaging, protected from moisture and direct sunlight. Keeping the product in a dry, cool environment helps maintain its stability and potency throughout its shelf life.

The medication is taken orally, usually as a tablet, with or without food as directed by the prescriber. Patients should follow the dosing schedule provided by their healthcare professional and avoid crushing or chewing the tablet unless specifically instructed.

The most serious risks include severe bone‑marrow suppression leading to pancytopenia, hepatic toxicity, renal impairment and rare but serious skin ulceration. Patients should be monitored regularly for blood‑count changes, liver and kidney function, and any signs of infection or unusual skin lesions.

Hydroxycarbamid Devatis is contraindicated in patients with known hypersensitivity to hydroxycarbamide, those with severe pre‑existing bone‑marrow failure, and individuals who are pregnant unless the therapeutic benefit outweighs the risk. It should also be used with caution in patients with significant liver or kidney disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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