Buy Hydroxyurea
Hydroxyurea

2.17
A chemotherapy drug used to treat certain cancers and blood conditions like sickle cell disease.


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
Hydrea
Active Ingredient(s)
Hydroxycarbamide
Primary Category
Cancer Treatment, Blood Disorders
Therapeutic Class
Antineoplastic agents, Other antineoplastic agents
Pharmacological Class
Antimetabolites
Indications
Chronic myeloid leukaemia, Cervical cancer, Polycythaemia vera, Sickle cell disease
Contraindications
Severe anaemia, Low white blood cell count, Low platelet count, Known hypersensitivity
Minor Side Effects
Loss of appetite, Nausea, Vomiting, Constipation
Moderate Side Effects
Hair loss, Skin changes, Mouth ulcers, Drowsiness
Serious Side Effects
Bone marrow suppression, Severe lung toxicity, Gangrene of the skin, Secondary malignancy
Dosage Forms
Capsule
Administration Route
Oral
Mechanism of Action
It interferes with the replication of DNA in cancer cells, preventing them from growing and multiplying. In sickle cell disease, it increases fetal haemoglobin, which prevents red blood cells from misshaping.
Prescription Status
Rx
Manufacturer
Bristol-Myers Squibb
Patient Summary
A chemotherapy drug used to treat certain cancers and blood conditions like sickle cell disease.
Onset Time
Several days to weeks
Duration
24 hours
Storage Instructions
Store in a cool, dry place; wash hands after handling capsules.
Drug Interactions
Live vaccines, Didanosine, Stavudine, Uricosuric agents
Age Restrictions
Prescribed to children and adults under specialist supervision
Pregnancy Use
Avoid during pregnancy due to risk of harm to the fetus.
Alternative Drugs
Busulfan, Imatinib

What is Hydroxyurea?

Hydroxyurea (active ingredient hydroxycarbamide) is an oral chemotherapy agent classified as an oncology support medication. It is supplied as a 500 mg pill and is prescribed by a qualified healthcare provider. In Hong Kong, hydroxyurea is a prescription-only product regulated by the Department of Health and the Hospital Authority.

The drug is used to modify disease processes in certain blood-related conditions and certain cancers. It is not an over-the-counter medication and should only be taken under medical supervision.

How Hydroxyurea Works in the Body

Hydroxyurea interferes with the synthesis of DNA by inhibiting the enzyme ribonucleotide reductase. This enzyme is essential for converting ribonucleotides to deoxyribonucleotides, the building blocks of DNA. By limiting the supply of deoxyribonucleotides, hydroxyurea slows the proliferation of rapidly dividing cells, such as malignant white-blood cells and abnormal erythrocytes in sickle-cell disease.

Key pharmacologic points:

  • Onset of action: Effects on blood counts can be observed within 1-2 weeks of starting therapy.
  • Peak effect: Maximum myelosuppressive activity generally occurs after 4-6 weeks.
  • Duration: The drug’s half-life is approximately 3-4 hours, but its biological effects persist due to lasting inhibition of ribonucleotide reductase.

By reducing the number of sickled red cells and decreasing leukocyte counts, hydroxyurea improves oxygen delivery and mitigates complications in sickle-cell disease and certain leukemias.

Conditions Treated with Hydroxyurea

Hydroxyurea is approved in many jurisdictions, including Hong Kong, for the following indications:

  • Chronic myelogenous leukemia (CML) - as a second-line agent when newer tyrosine-kinase inhibitors are unavailable or contraindicated.
  • Polycythemia vera (PV) - to control elevated red-cell mass and reduce thrombotic risk.
  • Essential thrombocythemia (ET) - for patients at high risk of thrombosis.
  • Sickle-cell disease (SCD) - to increase fetal hemoglobin (HbF) production, lower vaso-occlusive crises, and reduce the need for transfusions.

These uses are supported by regulatory approvals and clinical guidelines. Hydroxyurea is not indicated for solid tumors, non-malignant infections, or routine pain management.

Patient Suitability and Contraindications

Who Should Consider Hydroxyurea?

  • Adults diagnosed with the approved conditions above who have active disease requiring cytoreduction or disease-modifying therapy.
  • Patients who can adhere to regular laboratory monitoring (e.g., complete blood counts).
  • Individuals without contraindicating medical conditions.

Absolute Contraindications

  • Known hypersensitivity to hydroxyurea or any of its excipients.
  • Pregnancy - hydroxyurea is teratogenic and classified as Pregnancy Category D. It should be discontinued before conception and avoided throughout gestation.
  • Severe bone-marrow suppression (e.g., neutrophils < 0.5 × 10⁹/L, platelets < 25 × 10⁹/L) before starting therapy.

Relative Contraindications

  • Breast-feeding (potential drug transfer to infant).
  • Significant hepatic impairment (elevated transaminases > 3 × ULN).
  • Renal dysfunction (creatinine clearance < 30 mL/min) - dose adjustments may be required.
  • Concomitant use of other myelosuppressive agents (e.g., azathioprine, methotrexate) - increased risk of severe cytopenias.

Special Populations

  • Elderly patients may require lower initial doses and closer monitoring.
  • Pediatric use is limited to sickle-cell disease; dosing is weight-based and must be prescribed by a pediatric hematologist.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Bone-marrow suppression - lowered white-blood cells, red-cells, or platelets; most frequent reason for dose reduction.
  • Gastrointestinal upset - nausea, mild abdominal discomfort, or loss of appetite.
  • Skin changes - mild rash or hyperpigmentation of the nails and skin.
  • Mouth ulcers - occasional painful lesions that resolve with oral hygiene and dose adjustment.

Serious Adverse Events

  • Severe myelosuppression - may lead to infections, anemia, or bleeding; requires immediate medical evaluation.
  • Teratogenicity - birth defects reported when exposure occurs during pregnancy.
  • Renal toxicity - rare but possible; monitor serum creatinine in at-risk patients.
  • Pulmonary toxicity - interstitial pneumonitis has been reported; discontinue if respiratory symptoms develop.

Drug Interactions

  • Antiretrovirals (e.g., zidovudine) - additive bone-marrow toxicity; monitor blood counts closely.
  • Azathioprine, methotrexate, or other cytotoxics - synergistic myelosuppression; dose reductions often needed.
  • Allopurinol - may increase hydroxyurea plasma levels; consider dose adjustment.
  • Enzyme inducers (e.g., rifampin, carbamazepine) - may reduce hydroxyurea exposure, potentially decreasing efficacy.

Food and Lifestyle Interactions

  • Hydroxyurea can be taken with or without food; however, consistent administration (same relation to meals) helps maintain stable blood levels.
  • Alcohol does not directly interact, but excess intake can worsen hematologic toxicity.
  • Patients should avoid unprotected sun exposure if photosensitivity develops; protective clothing and sunscreen are advisable.
  • No known effects on driving or operating machinery, but severe anemia or infection may impair alertness.

How to Take Hydroxyurea

  • Standard dosing: The 500 mg pill is the most common strength. Starting doses typically range from 15 mg/kg once daily (often rounded to a convenient tablet count) and are adjusted based on laboratory response.
  • Administration: Swallow the tablet whole with a glass of water. Do not crush or chew unless directed by a pharmacist.
  • Dose adjustments: If blood counts fall below target thresholds, the prescriber may reduce the dose by 100-200 mg increments or hold therapy temporarily.
  • Missed dose: Take the missed dose as soon as remembered if the next scheduled dose is more than 12 hours away. Do not double the dose.
  • Overdose: Symptoms may include severe nausea, vomiting, diarrhea, and profound bone-marrow suppression. Seek emergency care; supportive care and possible administration of leucovorin rescue are recommended under medical direction.
  • Discontinuation: Abrupt cessation is generally safe, but patients with sickle-cell disease may experience a rebound of crises; tapering is not required but follow-up monitoring is essential.

All dosing decisions must be individualized by the treating physician, taking into account weight, organ function, disease severity, and concomitant medications.

Monitoring and Follow-Up

  • Complete blood count (CBC) with differential - at baseline, then weekly for the first 2 months, followed by at least monthly monitoring.
  • Renal and hepatic panels - every 1-3 months, or more frequently if pre-existing dysfunction exists.
  • Fetal hemoglobin (HbF) level - for patients with sickle-cell disease, measured every 3-6 months to assess therapeutic response.
  • Clinical assessment - patients should report signs of infection, bleeding, or new skin lesions promptly.
  • Pregnancy testing - mandatory before initiating therapy in women of child-bearing potential and periodically during treatment.

Regular follow-up visits with a hematologist or oncologist ensure that dosing remains optimal and safe.

Storage and Handling

  • Store hydroxyurea tablets at room temperature (20-25 °C), away from excess heat, moisture, and direct sunlight.
  • Keep the container tightly closed and out of reach of children.
  • Do not use the medication beyond the expiration date printed on the package.
  • Unused tablets should be disposed of according to local pharmacy or government hazardous-medicine guidelines.

Glossary (Medication-Specific)

Ribonucleotide reductase
An enzyme needed for DNA synthesis; hydroxyurea blocks this step, limiting cell replication.
Myelosuppression
Decrease in the production of blood cells by the bone marrow, leading to anemia, neutropenia, or thrombocytopenia.
Teratogenicity
The capability of a substance to cause birth defects when exposure occurs during pregnancy.
Fetal hemoglobin (HbF)
A form of hemoglobin that hydroxyurea induces in sickle-cell disease, reducing red-cell sickling.

Medical Disclaimer

This article provides educational information about Hydroxyurea 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.

Hydroxyurea FAQ

Can hydroxyurea be used to treat cancer in children?

Hydroxyurea is occasionally employed in pediatric oncology protocols for specific leukemias, but its use is highly protocol-dependent and requires specialist oversight. Dose calculations are weight-based, and close laboratory monitoring is mandatory.

What should I do if I miss a dose while traveling abroad?

If a dose is missed and the next scheduled dose is more than 12 hours away, take the missed tablet as soon as you remember. Do not double the dose. Keep a supply of the medication in your carry-on luggage and inform customs that it is a prescription drug.

Does hydroxyurea interact with over-the-counter vitamins or supplements?

Most vitamins do not interfere with hydroxyurea, but certain supplements that affect bone-marrow function (e.g., high-dose folic acid) should be discussed with your provider, as they may mask blood-count changes.

Is there a specific brand imprint on the 500 mg hydroxyurea tablet?

In Hong Kong, generic hydroxyurea tablets are often imprinted with “500 MG” and the manufacturer's logo. Imprint details can vary by supplier, so verify with your pharmacist.

Can hydroxyurea affect my ability to pass airport security with liquid restrictions?

Hydroxyurea is a solid pill, not a liquid, so it does not fall under liquid restrictions. Carry it in its original labeled container and have a copy of the prescription available if requested.

How long does it take for fetal hemoglobin levels to rise in sickle-cell disease?

HbF levels typically begin to increase within 2-4 weeks of starting hydroxyurea, with maximal elevations observed after 3-6 months of stable dosing.

Are there any dietary restrictions while taking hydroxyurea?

No specific foods must be avoided, but maintaining a balanced diet supports overall blood-cell health. Excessive alcohol may exacerbate hematologic toxicity and should be limited.

After a dose reduction, CBC should be repeated within 1-2 weeks to ensure recovery of blood counts before considering further adjustments.

Is hydroxyurea safe for patients with mild liver disease?

Mild hepatic impairment does not usually require dose changes, but liver function tests should be monitored regularly. Severe liver disease may necessitate dose reduction.

Can I store hydroxyurea tablets in a bathroom medicine cabinet?

It is best to keep the tablets in a cool, dry place away from humidity and heat; a bathroom cabinet may be too humid. A bedroom drawer or kitchen cabinet at room temperature is preferable.

Categories