(LARTRUVO is registered trademarks Eli Lilly & Company)
What is LARTRUVO:
LARTRUVO is a medicine that contains the active substance Olaratumab and is available as Single-dose vial
Generic Name: Olaratumab
Strength: 500 mg/50 mL (10 mg/mL)
Company: Eli Lilly & Company
Packing: Single-dose vial
In how many countries LARTRUVO is approved for marketing?
LARTRUVO is available/approved in USA and Europe. We can help you to access it in India.
What is LARTRUVO used for?
LARTRUVO is indicated, in combination with doxorubicin, for the treatment of adult patients with soft tissue sarcoma (STS) with a histologic subtype for which an anthracycline-containing regimen is appropriate and which is not amenable to curative treatment with radiotherapy or surgery.
How can I get LARTRUVO in India?
LARTRUVO is a prescription only drug and is not approved for marketing in India.
The Indian Pharma (IP) is a consulting pharmaceutical company which assists Patients in accessing medicines in India. The Indian Pharma facilitates such access only against valid prescriptions in conformity with all local laws and regulations.
Patients/ Clinicians / Researchers can contact IP at +91-120-4080562 or write to at –email@example.com
We facilitate by-
• Helping in documentation to import the medicine for personal use
• Finding Genuine and reliable source in USA, Europe and Japan
• Ensuring 100% transparency.
LARTRUVO can be shipped to Mumbai, Kolkata, Hyderabad, Chennai, Ahmedabad, Delhi, Bangalore, Jaipur, Lucknow, Cochin and Pune and other cities in India.
The Indian Pharma can facilitate the supply of LARTRUVO (prescription medicines) to all locations in the world and in India after fulfilling the legal requirement.
The Indian Pharma does not manufacture, supply, re-sell or retail any drugs or medicines. All trademarks and other intellectual property in relation to drugs and medicines supplied to you by suppliers are owned by their respective manufacturers or licensees
Can I get LARTRUVO even if I am not based in India?
Almost all countries across the world have provisions for granting access to drugs prior to marketing approval for personal use for patients who have exhausted all other treatment options available in their country
The Indian Pharma (IP) can help patients in accessing/importing LARTRUVO, unapproved in their home country against a legitimate prescription and in conformity with all local laws and regulations of their home country.
Send your enquiry to find –
LARTRUVO in South East Asia – China, Cambodia, Indonesia, Malaysia, the Philippines, Singapore, Thailand, Vietnam, Hong Kong.
LARTRUVO in United Arab Emirates – Iraq, Iran, Saudi Arabia, Jordan.
LARTRUVO in North America – Mexico.
LARTRUVO in South America – Argentina, Brazil, Chile, Colombia, Peru, Venezuela.
LARTRUVO in Europe – Romania, Switzerland, Georgia, Turkey, Italy, UK, Ukraine, Azerbaijan, Latvia, Poland, Slovakia.
LARTRUVO in Russia CIS – Armenia, Kazakhstan, Moldova, Tajikistan, Turkmenistan, Uzbekistan, Mongolia.
LARTRUVO in African Countries – Algeria, Mauritius, Uganda, Zimbabwe.
LARTRUVO in Australia and New Zealand.
How is LARTRUVO used?
LARTRUVO should be administered under the guidance of specialist doctor having experience in managing cancer treatments.
Recommended dose: 15 mg/kg as an intravenous infusion over 60 minutes on Days 1 and 8
of each 21-day cycle until disease progression or unacceptable toxicity.
If the patient develops certain serious side effects then doctor may interrupt or stop treatment, or reduce the dose. See the summary of product characteristics on company official website for more information
Are there any side-effects/ adverse reactions/precautions associated with treatment with LARTRUVO?
It is recommended to seek your doctor’s medical advice about side effects
How do I contact The Indian Pharma?
You can use different channel to contact The Indian Pharma (IP)
Tele & Mobile: You can reach us on +91 8826990915 or +91-120-4080562 on any working days.
Email: We can also address your enquiries if sent directly to firstname.lastname@example.org. We will respond within 24 hours after receiving your mail. Please mention detailed enquiry, your contact number with ISD code while sending your mail. We will respond within 1 working days after receiving your query form.
What information do you need to help patient in assisting documentation for LARTRUVO import for personal use?
We will require the following documents to help in documentation for Named-Patient import
- Doctor’s Prescription – We would require prescription from Registered Medical Practitioner Stating Product name, dosage, duration of treatment and diagnosis
- Patient’s Medical history – We would require all test reports and Medical reports of the patient for last 3 months.
- Patient’s Identity card – We will require scan copy of Patient’s identity card and proof of residence to initiate documentation process. You can use copy of Passport, Driving License, Employee ID card or any Photo ID document as your Identity card.