Veenat

✅ Treats leukemia
✅ Manages gastrointestinal stromal tumors
✅ Inhibits cancer cell growth
✅ Increases survival rates
✅ Improves quality of life

Veenat contains Imatinib.

Product Overview

Veenat is an anticancer medication containing Imatinib as its active component. As a tyrosine kinase inhibitor, it is clinically proven to treat multiple malignancies including chronic myeloid leukemia (CML), acute lymphoblastic leukemia (ALL), gastrointestinal stromal tumors (GISTs), and dermatofibrosarcoma protuberans (DFSP). The therapeutic action involves targeting specific proteins responsible for cancer cell proliferation. Available in oral tablet form, Veenat requires professional medical prescription tailored to individual cancer types, disease stages, and patient health profiles.

Therapeutic Applications

Veenat demonstrates clinical efficacy across various cancer indications:
• Chronic myeloid leukemia (all phases: chronic, accelerated, blast crisis)
• Philadelphia chromosome-positive acute lymphoblastic leukemia
• Unresectable/metastatic gastrointestinal stromal tumors
• Recurrent or metastatic dermatofibrosarcoma protuberans
The medication significantly improves survival outcomes by impeding malignant cell growth and proliferation.

Administration Guidelines

For optimal therapeutic outcomes:
• Take tablets whole with 240ml water
• May be administered with or without food
• Strictly adhere to prescribed dosing regimen
• Never crush, chew, or split tablets
Dosage parameters are determined by oncologists based on:
– Cancer type and progression
– Patient anthropometrics
– Treatment response
– Comorbid conditions

Mechanism of Action

Imatinib mesylate exerts its antineoplastic effects through:
1. Selective tyrosine kinase inhibition
2. Blockade of BCR-ABL fusion protein (in CML)
3. Disruption of oncogenic signaling pathways
4. Induction of apoptosis in malignant cells
This targeted molecular interference results in:
✓ Tumor size reduction
✓ Disease symptom alleviation
✓ Improved hematological parameters

Dosage Protocol

Therapeutic regimens are individualized with standard guidelines:
• CML: 400-600mg daily
• GIST: 400mg daily
• ALL: 600mg daily
Dosage adjustments may be required based on:
– Hematological monitoring
– Treatment tolerance
– Disease progression
– Concomitant medications

Therapeutic Advantages

Veenat offers significant clinical benefits:
• High response rates in CML patients
• Improved progression-free survival
• Enhanced quality of life metrics
• Reduced tumor burden
• Favorable safety profile compared to conventional chemotherapy

Adverse Effects

Common treatment-emergent reactions include:
• Gastrointestinal disturbances (nausea, diarrhea)
• Musculoskeletal complaints (cramps, pain)
• Constitutional symptoms (fatigue, edema)
• Dermatological manifestations (rash)
Most adverse events are manageable and dose-dependent.

Important Precautions

Critical safety considerations:
• Requires regular hematological monitoring
• Potential for hepatotoxicity
• May cause QT prolongation
• Significant drug interaction potential
• Teratogenic risk (Pregnancy Category D)

Storage Conditions

Proper medication handling:
• Store at 20-25°C (68-77°F)
• Protect from moisture and light
• Keep in original packaging
• Maintain out of children’s reach
• Dispose expired medication properly

Medical Disclaimer

The information provided herein represents carefully curated, evidence-based data intended for educational purposes only. This content does not substitute professional medical advice, diagnosis, or treatment. Always consult qualified healthcare providers regarding:
– Potential drug interactions
– Complete safety profile
– Individualized treatment plans
– Emerging side effects
Our mission is to facilitate informed patient-provider discussions, not to replace clinical judgment.

Strength

100 mg

Quantity

120 Capsule/s, 240 Capsule/s, 360 Capsule/s

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