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REGISTRATION FORM 1st GULF MULTIDISCIPLINARY MEETING ON UROLOGICAL CANCER 11 & 12 JANUARY 2017 (13 & 14 ARABIA AL THAN 1438) Please print CLEARLY in BLOCK CAPITALS and return this form with payment.
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01
Obtain the required patient information, including their medical history, current medications, and any known allergies.
02
Assess the patient's eligibility for eribulin based on the approved indications and contraindications.
03
Calculate the appropriate dosage of eribulin based on the patient's body surface area.
04
Administer eribulin intravenously over a specified period according to the recommended infusion schedule.
05
Monitor the patient closely for any adverse reactions or side effects during and after eribulin administration.
06
Adjust the dosage or discontinue eribulin if significant toxicity or intolerability occurs.
07
Educate the patient about the potential risks and benefits of eribulin treatment, including the importance of adherence to the prescribed regimen.
08
Follow up with the patient regularly to evaluate the effectiveness of eribulin and manage any treatment-related issues.

Who needs eribulin in male patients?

01
Eribulin may be considered for male patients who have been diagnosed with advanced or metastatic breast cancer.
02
It is typically reserved for those who have already received prior treatment with other chemotherapy agents.
03
The decision to use eribulin in male patients should be made on an individual basis in consultation with a healthcare professional.
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Eribulin is a chemotherapy medication used to treat advanced breast cancer and liposarcoma in male patients.
Oncologists or prescribing physicians are required to file eribulin in male patients.
Eribulin should be administered intravenously according to the prescribed dosage and schedule.
The purpose of eribulin in male patients is to help shrink tumors and slow the progression of cancer.
Information such as patient demographics, dosage administered, side effects, and treatment response must be reported on eribulin in male patients.
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