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Center for Drug Evaluation and Research List of Licensed Biological Products with (1) Reference Product Exclusivity and (2) Biosimilarity or Interchangeability Evaluations to Date BLA STN 125118 103575 125274 125057 761024 125427 125387 103979 125431 103293 103948 125141 125291 125559 103172 103950 125513 101063 125359 761034 761049 103764 103691 125288 125370 125085 761046 125557 125388 761032 125319 103608 761052 125160 125084 101995 125338 103749 761029 761036 103951 103767 125320 125516...
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Start by gathering all the necessary materials for filling out ado-emtansine, including the medication vials, syringes, and sterile needles.
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Remove the cap from the medication vial and clean the rubber stopper with an alcohol swab.
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Who needs ado- emtansine?

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Ado-emtansine is typically prescribed to patients with HER2-positive breast cancer that has spread to other parts of the body.
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It is usually given to individuals who have already received treatment with trastuzumab and chemotherapy but have experienced disease progression.
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Your healthcare provider will determine if ado-emtansine is suitable for your specific condition and medical history.
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Ado-emtansine is a drug used in the treatment of certain types of cancer, specifically breast cancer.
Healthcare providers and facilities are required to file ado-emtansine when administering the drug to patients.
Ado-emtansine should be filled out by providing patient information, dosage details, administration dates, and any adverse reactions experienced.
The purpose of ado-emtansine is to track the usage and outcomes of the drug in order to monitor its effectiveness and safety.
The information reported on ado-emtansine should include patient demographics, treatment details, and any side effects or complications.
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