Vinlieva 1mg Injection

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Vinlieva 1mg Injection

1 Injection in 1 Vial
₹ 64
1 Injection | 1 Vial
₹ 64
0 people have bought this recently
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Vinlieva Information

Vinlieva is consists of Vincristine is a chemotherapy medication derived from the Madagascar periwinkle plant (Catharanthus roseus). It belongs to the vinca alkaloid class and is widely used in the treatment of various cancers, including leukemias, lymphomas, solid tumors, and pediatric malignancies. Vincristine exerts its antineoplastic effects by inhibiting microtubule formation, thereby preventing cancer cell division. It is a cornerstone in combination chemotherapy regimens such as CHOP (for Non-Hodgkin’s Lymphoma) and ALL treatment protocols (for Acute Lymphoblastic Leukemia). Despite its high therapeutic efficacy, Vincristine is associated with dose-limiting neurotoxicity, particularly peripheral neuropathy. Careful dose adjustments and monitoring are essential for optimizing its benefits while minimizing adverse effects.

Mechanism of Action

Vincristine is a mitotic inhibitor that binds to tubulin, a key protein responsible for microtubule assembly. By preventing microtubule polymerization, Vincristine disrupts mitotic spindle formation, leading to cell cycle arrest at the metaphase and subsequent apoptosis in rapidly dividing cancer cells.

Key Mechanisms:

Microtubule Inhibition – Blocks mitotic spindle formation, preventing cell division.
Apoptosis Induction – Triggers programmed cell death in rapidly dividing cancer cells.
Inhibition of Angiogenesis – Reduces the formation of new blood vessels that support tumor growth.

Indications and Uses

1. Hematologic Malignancies (Blood Cancers)

Acute Lymphoblastic Leukemia (ALL) – Used in induction, consolidation, and maintenance phases.
Non-Hodgkin’s Lymphoma (NHL) – Part of CHOP regimen (Cyclophosphamide, Doxorubicin, Vincristine, Prednisone).
Hodgkin’s Lymphoma (HL) – Component of ABVD (Adriamycin, Bleomycin, Vinblastine, Dacarbazine) regimen.
Multiple Myeloma (MM) – Used in combination therapies.

2. Pediatric Cancers

Wilms' Tumor
Neuroblastoma
Rhabdomyosarcoma
Ewing’s Sarcoma

3. Solid Tumors

Small Cell Lung Cancer (SCLC)
Breast Cancer
Ovarian Cancer

4. Other Indications

Immune Thrombocytopenic Purpura (ITP) – Occasionally used in refractory cases.

Vincristine remains one of the most effective chemotherapy agents for hematologic and pediatric cancers. It has significantly improved survival rates for leukemia, lymphoma, and neuroblastoma patients. However, neurotoxicity remains a major limitation, requiring careful dosing and monitoring. With ongoing research into liposomal formulations and targeted drug delivery, the future of Vincristine in oncology continues to evolve. Always administer intravenously, NEVER intrathecally, Monitor for neuropathy, constipation, and drug interactions and dose capping at 2 mg reduces toxicity risks.

Dosage and Administration

Vincristine is administered via intravenous (IV) injection.

Indication Typical Dose Frequency
ALL (Induction) 1.4 mg/m² IV Once weekly
NHL (CHOP Regimen) 1.4 mg/m² IV Day 1 of each cycle
HL (ABVD Regimen) 1.4 mg/m² IV Every 2 weeks
Wilms’ Tumor, Neuroblastoma 1.5 mg/m² IV Weekly
Maximum Dose 2 mg per dose (to limit neurotoxicity)  

Pediatric Dosing is adjusted based on Body Surface Area (BSA).
Dose Capping at 2 mg per administration is recommended to reduce neurotoxicity risk.

Administration Warning: Vincristine is NEVER given intrathecally (into the spinal cord) as it can cause fatal neurotoxicity.

Efficacy and Clinical Studies

1. Acute Lymphoblastic Leukemia (ALL)

Studies show 80–90% remission rates when Vincristine is combined with corticosteroids and asparaginase.
Maintenance therapy with Vincristine + Methotrexate + Mercaptopurine improves survival.

2. Lymphomas (Hodgkin’s and Non-Hodgkin’s)

CHOP and ABVD regimens show high remission rates (~70-80%).
Survival benefits when combined with radiation therapy in advanced stages.

3. Pediatric Tumors

Neuroblastoma and Wilms' tumor respond well to Vincristine + Cyclophosphamide + Doxorubicin combinations.

Side Effects and Toxicity

Common Side Effects:

Peripheral Neuropathy – Tingling, numbness, foot drop, wrist drop.
Gastrointestinal Issues – Constipation, nausea, vomiting.
Alopecia (Hair Loss) – Temporary but significant.
Fatigue – Generalized weakness.

Serious Side Effects:

Severe Neurotoxicity – Dose-limiting, may cause paralytic ileus, vocal cord paralysis, or motor dysfunction.
Myelosuppression – Less severe than other chemotherapy agents but still requires monitoring.
SIADH (Syndrome of Inappropriate ADH Secretion) – Can cause hyponatremia (low sodium levels).
Tumor Lysis Syndrome (TLS) – Can occur in aggressive leukemias and lymphomas.

Fatal Toxicity:

Intrathecal Administration – Always contraindicated; causes irreversible CNS damage and death.

Contraindications and Precautions

Contraindications:
Severe neuropathy.
Hypersensitivity to vinca alkaloids.
Pregnancy & Breastfeeding – Teratogenic effects reported.

Precautions:
Neuropathy Monitoring: Reduce dose if severe neuropathy occurs.
Liver Dysfunction: Dose adjustments needed.
Gastrointestinal Paralysis: Monitor for constipation or paralytic ileus.

Drug Interactions

Vincristine is metabolized by the CYP3A4 enzyme, leading to multiple drug interactions.

CYP3A4 Inhibitors (Ketoconazole, Erythromycin, Fluconazole) – Increase Vincristine toxicity.
CYP3A4 Inducers (Rifampin, Carbamazepine, Phenytoin) – Reduce Vincristine efficacy.
Azole Antifungals (Itraconazole, Voriconazole) – Exacerbate neurotoxicity.
Other Chemotherapy Drugs (Cisplatin, Doxorubicin) – Increase myelosuppression risk.

Storage and Handling

Storage Conditions:
Keep at 2-8°C (Refrigerated).
Protect from light exposure.
Avoid freezing.

Safe Handling:
Vincristine is a cytotoxic drug. Wear gloves and protective clothing when handling.
Proper Disposal: Dispose of per local hazardous waste guidelines.



Vinlieva Benefits & Uses

Vinlieva is used to treat the following -

Main Benefits

Other Benefits

Vinlieva Dosage & How to Take

This is the usual dosage recommended in most common treatment cases. Please remember that every patient and their case is different, so the dosage can be different based on the disease, route of administration, patient's age and medical history.

Find the right dosage based on disease and age

Age Group Dosage
Adult
  • Disease: Blood Cancer
  • Before or After Meal: As advised by a physician
  • Single Maximum Dose: 30 mcg/kg
  • Dosage Route: Parenteral
  • Frequency: 1 Weekly
  • Course Duration: As directed by the doctor
  • Special Instructions: As prescribed by the doctor
Geriatric
  • Disease: Blood Cancer
  • Before or After Meal: As advised by a physician
  • Single Maximum Dose: 30 mcg/kg
  • Dosage Route: Parenteral
  • Frequency: 1 Weekly
  • Course Duration: As directed by the doctor
  • Special Instructions: As prescribed by the doctor
13 - 18 years (Adolescent)
  • Disease: Blood Cancer
  • Before or After Meal: As advised by a physician
  • Single Maximum Dose: 3 mg
  • Dosage Route: Parenteral
  • Frequency: 1 Weekly
  • Course Duration: As directed by the doctor
  • Special Instructions: As prescribed by the doctor
2 - 12 years (Child)
  • Disease: Blood Cancer
  • Before or After Meal: As advised by a physician
  • Single Maximum Dose: 50 mcg/kg
  • Dosage Route: Parenteral
  • Frequency: 1 Weekly
  • Course Duration: As directed by the doctor
  • Special Instructions: As prescribed by the doctor

Vinlieva Related Warnings

  • Is the use of Vinlieva safe for pregnant women?


    Pregnant women may get severe side effects after taking Vinlieva. If you are pregnant, do not take Vinlieva without a doctor's advice.

    Severe
  • Is the use of Vinlieva safe during breastfeeding?


    Vinlieva should not be taken without taking your doctor's advice, as it may have severe side effects on breastfeeding women.

    Severe
  • What is the effect of Vinlieva on the Kidneys?


    Very few cases of side effects of Vinlieva on kidney have been reported.

    Mild
  • What is the effect of Vinlieva on the Liver?


    The liver can be affected by Vinlieva. If you experience any unwanted effects of this drug, stop taking it and consult your doctor. You should restart Vinlieva only after medical advice.

    Moderate
  • What is the effect of Vinlieva on the Heart?


    You can take Vinlieva without any fear of damage to the heart.

    Safe


Severe Interaction of Vinlieva with Other Drugs

Vinlieva should not be taken with following medicines due to severe side effects it may cause to patients -

Severe



Vinlieva Contraindications

If you are suffering from any of the following diseases, you should not take Vinlieva unless your doctor advises you to do so -



Frequently asked Questions about Vinlieva

  • Is this Vinlieva habit forming or addictive?


    No, there is no any evidence that Vinlieva is addictive.

    No
  • Is it safe to drive or operate heavy machinery when consuming?


    No, you should do not do anything that requires concentration and attention as the Vinlieva can make you feel drowsy.

    Dangerous
  • Is it safe?


    Yes, but consume Vinlieva only on doctor's advice.

    Safe, but take only on Doctor's advise
  • Is it able to treat mental disorders?


    No, the use of Vinlieva in mental disorders is not effective.

    No

Vinlieva Interactions with Food and Alcohol

  • Interaction between Food and Vinlieva


    You can take Vinlieva with food.

    Safe
  • Interaction between Alcohol and Vinlieva


    Due to lack of research, nothing can be said about side effects of consuming alcohol while taking Vinlieva.

    Unknown


See all substitutes for Vinlieva


This medicine data has been created by -

Vikas Chauhan

B.Pharma, Pharmacy
5 Years of Experience


References

US Food and Drug Administration (FDA) [Internet]. Maryland. USA; Package leaflet information for the user; Vincristine Sulfate

KD Tripathi. [link]. Seventh Edition. New Delhi, India: Jaypee Brothers Medical Publishers; 2013: Page No 865

April Hazard Vallerand, Cynthia A. Sanoski. [link]. Sixteenth Edition. Philadelphia, China: F. A. Davis Company; 2019: Page No 1269-1271



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