DOXLIEVA-L 50 MG is an Injection medication used for treatment purposes. It is manufactured by Allieva Pharma Private Limited.
| Brand Name | DOXLIEVA-L 50 MG |
|---|---|
| Composition | Doxorubicin Hydrochloride Liposomal Injection 50 mg/25 mL |
| Manufacturer | Allieva Pharma Private Limited |
| Dosage Form | Injection |
| Packaging | Vial |
| Country of Origin | India |
DOXLIEVA-L 50 MG (Doxorubicin Hydrochloride Liposomal Injection 50 mg/25 mL) is a widely used Injection medicine manufactured by Allieva Pharma Private Limited. It is commonly prescribed for...
DOXLIEVA-L 50 MG (Doxorubicin Hydrochloride Liposomal Injection 50 mg/25 mL) is a prescription anticancer medicine containing Doxorubicin Hydrochloride 50 mg in a liposomal formulation. It belongs to the Anthracycline class of anticancer medicines and is used in the treatment of several cancers.
The liposomal formulation encapsulates doxorubicin within microscopic lipid particles called liposomes. This formulation alters the distribution of the medicine in the body and allows doxorubicin to reach tumor tissues while potentially reducing some of the toxicity associated with conventional doxorubicin.
Doxorubicin works primarily by interfering with DNA replication and repair and by inhibiting topoisomerase II, an enzyme required for cancer cell division. It can also generate free radicals that contribute to cancer cell damage. These actions inhibit the growth and multiplication of cancer cells.
DOXLIEVA-L 50 MG may be used in the treatment of ovarian cancer, AIDS-related Kaposi's sarcoma, multiple myeloma in combination therapy, and certain other cancers, depending on the approved indication and treatment protocol.
The medicine is administered by intravenous infusion under the supervision of qualified healthcare professionals experienced in oncology treatment.
DOXLIEVA-L 50 MG is commonly used in:
Patients receiving liposomal doxorubicin require regular monitoring of blood counts, liver function, cardiac health, and overall clinical condition.
DOXLIEVA-L 50 MG (Doxorubicin Hydrochloride Liposomal Injection 50 mg/25 mL) is used as part of specific oncology treatment regimens.
Liposomal doxorubicin may be used for advanced ovarian cancer, particularly when the disease has progressed following previous chemotherapy.
It is an established treatment option for AIDS-related Kaposi's sarcoma.
Liposomal doxorubicin may be used in combination with other medicines for selected patients with multiple myeloma.
It may be incorporated into treatment protocols for selected advanced or metastatic malignancies according to the treating oncologist's recommendation.
The medicine may be administered with other anticancer medicines when clinically appropriate.
Doxorubicin is an Anthracycline Anticancer Agent.
DOXLIEVA-L works through several mechanisms:
The liposomal formulation changes the distribution and circulation of doxorubicin in the body and is designed to modify its delivery to tissues.
Like all anticancer medicines, DOXLIEVA-L 50 MG may cause side effects. Their severity and frequency vary from patient to patient.
Tiredness and weakness may occur during treatment.
Some patients may experience nausea or digestive discomfort.
Treatment can reduce white blood cells, red blood cells, or platelets.
Oral ulcers or inflammation of the mouth may occur.
Redness, swelling, tenderness, pain, or peeling of the palms and soles may occur.
Hair thinning or hair loss may occur in some patients.
Changes in bowel habits may develop.
Rash, redness, or other skin changes may occur.
Some patients may experience reduced appetite during treatment.
Seek immediate medical attention if you experience:
Patients should promptly report unusual or severe symptoms to their healthcare provider.
The dosage of DOXLIEVA-L 50 MG must be determined by a qualified oncologist based on the indication, treatment protocol, body surface area, organ function, previous treatments, and individual patient response.
The 50 mg/25 mL presentation does not mean that the entire vial should automatically be administered to every patient. The required dose and infusion schedule are individualized by the treating healthcare professional.
Different cancers require different dosing schedules.
Dosage may be calculated according to body surface area for the relevant indication.
Dose modification may be required in patients with hepatic impairment.
Previous chemotherapy and cumulative anthracycline exposure may influence treatment decisions.
Treatment may need to be delayed or adjusted if blood cell counts are too low.
The oncologist may modify treatment according to effectiveness and adverse effects.
Before treatment, inform your doctor if you have:
Patients receiving liposomal doxorubicin may require:
Tell your healthcare professional about all prescription medicines, over-the-counter medicines, supplements, and herbal products you use.
Pregnancy should be avoided during treatment because doxorubicin may cause fetal harm. Breastfeeding is generally not recommended during treatment; discuss appropriate precautions with your healthcare professional.
DOXLIEVA-L is used in specific treatment regimens for ovarian cancer, AIDS-related Kaposi's sarcoma, and selected multiple myeloma treatment protocols.
Liposomal doxorubicin is a formulation in which doxorubicin is enclosed within lipid-based particles called liposomes. This changes the medicine's distribution and pharmacokinetic properties.
Yes. Doxorubicin is an anthracycline chemotherapy medicine.
It is administered by intravenous infusion under the supervision of trained healthcare professionals.
Yes. It can cause decreases in blood cell counts, which is why regular blood monitoring is important.
Anthracyclines can cause cardiac toxicity. Your doctor may assess cardiac function based on your medical history and cumulative treatment exposure.
Yes. Palmar-plantar erythrodysesthesia, commonly called hand-foot syndrome, can occur with liposomal doxorubicin.
Yes. It should only be administered by qualified healthcare professionals experienced in oncology treatment.