Veneta 10 mg (Tablet)

Unit Price: ৳ 50.00 (3 x 10: ৳ 1,500.00)
Strip Price: ৳ 500.00

Medicine Details

Indications

  • Treatment of chronic lymphocytic leukemia (CLL) in adult patients
  • Monotherapy for CLL in adult patients with specific genetic mutations
  • Indicated for CLL patients unsuitable for or failed B-cell receptor pathway inhibitor
  • Indicated when patients have failed both chemoimmunotherapy and B-cell receptor pathway inhibitor

Pharmacology

  • Selective and orally bioavailable small-molecule inhibitor of BCL-2
  • Restores process of apoptosis by displacing pro-apoptotic proteins
  • Triggers mitochondrial outer membrane permeabilization
  • Demonstrated cytotoxic activity in tumor cells overexpressing BCL-2

Dosage & Administration

  • Starting dose: 20 mg once daily for 7 days
  • Gradual increase to daily dose of 400 mg over 5 weeks
  • Recommended post-titration dose for combination therapy
  • Recommended post-titration dose for monotherapy

Interaction

  • Contraindicated with strong CYP3A inhibitors at initiation and during titration phase
  • Use with moderate CYP3A inhibitors requires dose reduction
  • Avoid concomitant use with P-gp and BCRP inhibitors during dose-titration phase
  • Dose reductions required when used with CYP3A inducers

Contraindications

  • Hypersensitivity to active substance or excipients
  • Concurrent use of strong CYP3A inhibitors
  • Concurrent use of preparations containing St. John's wort

Side Effects

  • Common side effects include neutropenia, diarrhea, and upper respiratory tract infection
  • Serious side effects may include pneumonia, febrile neutropenia, and tumor lysis syndrome (TLS)

Pregnancy & Lactation

  • Women of childbearing potential must use highly effective contraception
  • Avoid becoming pregnant while taking Venetoclax and for at least 30 days after treatment
  • Not recommended during pregnancy and in women not using contraception
  • Breast-feeding should be discontinued during treatment

Precautions & Warnings

  • High risk of tumor lysis syndrome (TLS) in initial dose-titration phase
  • Monitoring and management of electrolyte abnormalities required
  • Dose reductions or interruptions recommended for severe neutropenia
  • Immunization with live attenuated vaccines not studied
  • Highly effective contraception required for women of childbearing potential

Use in Special Populations

  • No specific dose adjustment for elderly patients
  • No dose adjustment for patients with mild or moderate renal impairment
  • Safety in severe renal impairment or on dialysis not established
  • No specific dose adjustment for patients with mild or moderate hepatic impairment

Overdose Effects

  • No specific antidote available
  • Close monitoring and supportive treatment recommended
  • Treatment interruption and careful monitoring for TLS symptoms during overdose

Therapeutic Class

  • Cytotoxic Chemotherapy

Storage Conditions

  • Store below 30°C
  • Protect from moisture and light
  • Keep out of the sight and reach of children

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