Blenrep (Belantamab Mafodotin-blmf)
- Medicine Name: Blenrep
- Generic Name: Belantamab Mafodotin-blmf
- Dosage Form & Strength: Injection: 100mg/Vial
- Manufactured By: GlaxoSmithKline
- Conduct ophthalmic evaluations (visual acuity and slit lamp) at baseline, before each dose, and promptly for worsening signs/symptoms.
- Perform baseline evaluations within three weeks before the first dose. Each follow-up examination needs to be performed at least 1 week after the last dose and within two weeks before the next dose.
- Withhold the BLENREP 100 mg injection until improvement and resume at same or reduced dose, or consider permanently discontinuing on behalf of severity.
- Advise patients to consider preservative-free lubricant eye drops at least 4 times daily starting with the first infusion and continuing until the end of treatment. Do not use contact lenses unless instructed by an ophthalmologist.
- Changes in visual acuity may be linked with difficulty for driving and reading. Advise patients to consider caution while driving or operating machinery.
- Monitor patients for infusion-related reactions. For Grade 2/3 reactions, interrupt the infusion and offer supportive treatment. Once symptoms resolve, resume at a reduced infusion rate.
- On behalf of mechanism of action, Belantamab Mafodotin can cause fetal harm if administered to a pregnant woman because it contains a genotoxic compound (the microtubule inhibitor, monomethyl auristatin F) and it targets actively dividing cells.
- Women should not breastfeed during treatment with Belantamab Mafodotin-blmf and for three months after the last dose.
What documents are required to import BLENREP to India?
BLENREP (Belantamab Mafodotin-blmf) can be imported by patients or government hospitals on the name of the patients only.
The following documentation required to import the product:
- Valid prescription from a qualified doctor.
- Patients diagnostic reports
- Patients id proof (issued by government of India)
How does order be confirmed?
The order will be confirmed only after the receipt of:
- Valid prescription of Doctor
- Import permit if applicable
Is BLENREP available in India?
BLENREP (Belantamab Mafodotin Injection) is a (prescription drug, prescription medication or prescription medicine) pharmaceutical drug that legally requires a medical prescription to be dispensed.
Urgent Meds helps import cancer medicines on the named patient supply (NPS). Urgent Meds is a facilitator providing input on:
- Availability in India (Mumbai, Kolkata, Hyderabad, Chennai, Ahmedabad, Delhi, Bangalore, and Pune, etc.)
- Medicine Price.
- Finding genuine and reliable sources from Canada, Europe, USA, and Australia.
- Ensuring 100% transparency.
BLENREP can be made available to patients, doctors, and hospitals in Mumbai, Kolkata, Hyderabad, Chennai, Ahmedabad, Delhi, Bangalore, Srinagar, Jammu, Jaipur, Chandigarh, Ludhiana, Noida, Gurgaon, Lucknow, and Pune and other cities in India. The order will be confirmed only after the receipt of a valid prescription from the doctor and import permit.
Urgent Meds can facilitate the supply of BLENREP (prescription medicines) to all locations in the world and in India after fulfilling the legal requirement (if applicable).
Please contact +1-647-818-4196 or write us at info@urgentmeds.in for Blenrep price in India.
We take guarantee of quality and delivery anywhere in the world as per the buyer’s requirements
Urgent Meds is proficient in sourcing BLENREP (Medicines from around the world and has the capability to supply it. We offer global access to the best available treatment for our customers worldwide.
Urgent Meds is committed to dispensing any valid prescription promptly. All prescriptions are dispensed and verified by registered pharmacists and are dispatched only to the patient’s address from New Delhi, India. Your health and well-being are our top priorities.
What is the Generic Name for the trade name drug Blenrep®?
Belantamab Mafodotin-blmf is the Generic Name for the trade name drug Blenrep®.
What is the Manufacturer Name of Blenrep®?
Blenrep® is manufactured by GlaxoSmithKline.
Is Blenrep® approved by the FDA?
Yes, Blenrep® is approved by the FDA. Date of approval: August 5, 2020.
What is Blenrep® injection?
The Blenrep® injection is the FDA-approved medication for the treatment of patients with relapsed or refractory multiple myeloma (RRMM).
What is the dosage and form of Blenrep® supplied?
Blenrep® is supplied for injection: 100 mg as a lyophilized powder in a single-dose vial for reconstitution and further dilution.
What are the most common side effects due to Blenrep®?
Most common side effects due to Blenrep® include nausea, keratopathy (corneal epithelium change on eye exam), decreased visual acuity, pyrexia, infusion-related reactions, blurred vision, and fatigue.
What are the storage conditions of Blenrep®?
Store vials of Blenrep® refrigerated at 36°F to 46°F (2°C to 8°C). It is a hazardous agent. Follow the applicable special handling as well as disposal procedures.
How much does Blenrep® cost in India?
The Blenrep® cost in India is competitive. In order to procure this medication authentically, kindly connect to any WHO-GDP and ISO certified pharmaceutical wholesaler, distributor, or supplier.
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