Lemtrada 12mg Infusion
Lemtrada 12mg Infusion

Lemtrada 12mg Infusion

Price 620000.0 INR/ Pack

MOQ : 1 Pack

Lemtrada 12mg Infusion Specification

  • Drug Type
  • Injection
  • Physical Form
  • Liquid
  • Recommended For
  • Doctor
  • Dosage Guidelines
  • As per Instructions
  • Suitable For
  • Adults
  • Storage Instructions
  • Cool & Dry Place
 

Lemtrada 12mg Infusion Trade Information

  • Minimum Order Quantity
  • 1 Pack
  • Payment Terms
  • Cash Advance (CA), Cash in Advance (CID), Telegraphic Transfer (T/T)
  • Supply Ability
  • 5 Packs Per Week
  • Delivery Time
  • 6 Days
  • Sample Available
  • No
  • Sample Policy
  • If order is confirmed we will reimburse the sample cost
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • Main Domestic Market
  • All India
 

About Lemtrada 12mg Infusion

1. Technical Specifications

Attribute Details
Brand Name Lemtrada 12 mg Infusion
Generic Name Alemtuzumab
Strength 12 mg/1.2 mL (concentrate for infusion)
Dosage Form Intravenous Infusion (IV)
Packaging Size Single-use vial (1.2 mL concentrate, to be diluted before infusion)
Packaging Type Glass vial with rubber stopper and flip-off seal
Medicine Type Monoclonal Antibody (Immunotherapy)
Manufacturer Sanofi Genzyme
Distributed By Authorized specialty distributors / infusion centers

2. Product Description

Lemtrada (Alemtuzumab) is a humanized monoclonal antibody directed against the CD52 antigen present on the surface of T and B lymphocytes.
It causes depletion of these immune cells, leading to immune system rebalancing, which reduces inflammation and prevents relapses in autoimmune disease.

It is primarily indicated for the treatment of Relapsing forms of Multiple Sclerosis (MS) in adults.


3. Product Highlights

Attribute Details
Therapeutic Category Immunotherapy / Monoclonal Antibody
Application Area Multiple Sclerosis (MS) relapsing-remitting forms
Mechanism of Action Binds to CD52 antigen on lymphocytes causes antibody-dependent lysis and depletion of T & B cells immune reset reduces autoimmune attack on myelin
Administration IV infusion over 4 hours (requires dilution and premedication) given in 2 treatment courses:
  • Course 1: 12 mg/day for 5 consecutive days (total 60 mg)

  • Course 2: 12 mg/day for 3 consecutive days (total 36 mg), 12 months after first course
    Storage Conditions | Store at 28 C (refrigerated); do not freeze; protect from light


4. Therapeutic Uses

  • Relapsing-Remitting Multiple Sclerosis (RRMS)

    • Reduces relapse rate

    • Slows progression of disability

    • Shown effective in patients who have failed 1 disease-modifying therapy


5. Side Effects

Common:

  • Rash, pruritus

  • Headache, fever, fatigue

  • Nausea, diarrhea

  • Infections (respiratory, urinary tract, herpes reactivation)

  • Infusion-related reactions (flushing, chills, hypotension)

Serious / Severe:

  • Autoimmune conditions: thyroid disorders, idiopathic thrombocytopenic purpura (ITP), nephropathies

  • Serious infections (opportunistic, hepatitis, TB reactivation, herpes, fungal infections)

  • Malignancy risk: thyroid cancer, melanoma, lymphoproliferative disorders

  • Cytopenias: prolonged lymphopenia, anemia, neutropenia

  • Infusion-related anaphylaxis (rare but life-threatening)


6. Precautions

  • Premedication: Corticosteroids, antihistamines, antipyretics before infusion to reduce infusion reactions.

  • Infection Risk: Screen for hepatitis, TB, HIV before therapy; prophylactic antivirals recommended for herpes prevention.

  • Autoimmunity Monitoring: Regular thyroid function, CBC, renal function, urinalysis for 4 years after last dose.

  • Cancer Risk: Long-term monitoring for malignancies.

  • Pregnancy & Breastfeeding: Contraindicated (teratogenic and immunosuppressive effects).

  • Vaccination: Avoid live vaccines during and for several months after treatment.

  • Hospital/Clinic Setting: Must be administered under supervision with emergency resuscitation support available.



Comprehensive Treatment Option

Lemtrada 12mg Infusion offers a robust therapeutic choice, especially favored by healthcare providers for managing specific medical conditions in adults. With a precise dosage format and convenient liquid injection, it is tailored to meet high efficacy standards. The product is accessible in India through reliable distribution networks including traders and wholesalers.


Proper Storage and Handling

To retain its therapeutic potency, Lemtrada 12mg Infusion should always be stored in a cool and dry environment. Vendors and healthcare professionals must carefully adhere to these instructions to guarantee optimal storage conditions and safeguard product quality from manufacturer to patient.

FAQs of Lemtrada 12mg Infusion:


Q: How should Lemtrada 12mg Infusion be administered?

A: Lemtrada 12mg Infusion is administered as an intravenous injection and strictly given under the supervision of a qualified healthcare professional, typically a doctor.

Q: What is the recommended storage method for Lemtrada 12mg Infusion?

A: This medication should be stored in a cool and dry place to preserve its efficacy and prevent degradation of its liquid form.

Q: When is Lemtrada 12mg Infusion prescribed?

A: Lemtrada 12mg Infusion is prescribed to adults as per a doctors assessment and is administered according to specific medical guidelines provided by a healthcare provider.

Q: Where can Lemtrada 12mg Infusion be sourced in India?

A: The product is available through authorized distributors, exporters, suppliers, traders, and wholesalers across India, ensuring nationwide availability to licensed medical practitioners.

Q: What is the process for using Lemtrada 12mg Infusion?

A: A healthcare professional will prepare the prescribed dosage and administer the infusion intravenously, following all safety and procedural protocols as per medical instructions.

Q: What are the benefits of receiving Lemtrada 12mg Infusion?

A: This treatment can offer significant benefits when used as directed by a doctor, including targeted management of eligible medical conditions and controlled administration in a clinical setting.

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