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MEDICARE FORM For Michigan MMP: FAX: 18442412495 PHONE: 18556765772TMHerceptin (), Hylecta ( and hyaluronidaseoysk), Herzuma (trastuzumabpkrb), Kadcyla (adotrastuzumab), Kanjinti (trastuzumabanns),
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To fill out the product pertuzumab, follow these steps:
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Make sure you have a sterile syringe and vial of pertuzumab.
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Wash your hands thoroughly with soap and water.
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Remove the vial of pertuzumab from the packaging and check for any signs of damage or contamination.
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Clean the rubber stopper on the vial with an alcohol swab.
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Withdraw the required amount of pertuzumab into the syringe according to the prescribed dosage.
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Remove any air bubbles from the syringe by gently tapping on it and pushing the plunger until all air is expelled.
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Prepare the injection site by cleaning it with an alcohol swab.
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Insert the needle into the injection site at a proper angle and slowly inject the pertuzumab.
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Once the injection is complete, properly dispose of the syringe and vial as per the guidelines.

Who needs products pertuzumab and phesgo?

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The products pertuzumab and phesgo are typically used for patients with certain types of cancer, specifically:
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- Pertuzumab is indicated for HER2-positive breast cancer that has spread to other parts of the body or has come back after initial treatment.
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- Phesgo is a combination treatment used for HER2-positive breast cancer in early stage and metastatic stage.
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It is important to note that these products should only be used under the supervision and prescription of a qualified healthcare professional.
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Pertuzumab is a medication used to treat certain types of breast cancer, specifically HER2-positive breast cancer. Phesgo is a combination product that includes pertuzumab and trastuzumab, used for the same indication in a subcutaneous formulation.
Healthcare providers and pharmaceutical companies involved in the distribution or administration of pertuzumab and Phesgo are typically required to file relevant information about these products.
To fill out the filing for pertuzumab and Phesgo, relevant documentation must include details such as dosage, administration guidelines, patient information, and adverse effects. Healthcare providers must comply with regulatory guidelines specific to their jurisdiction.
The purpose of pertuzumab and Phesgo is to treat HER2-positive breast cancer, aiming to inhibit cancer cell growth and improve patient outcomes through targeted therapy.
Information reported must include product identification details, usage instructions, clinical trial data, side effects, and any changes to the drug's status or efficacy.
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