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CLINICAL POLICY PembrolizumabClinical Policy: Pembrolizumab (Katrina) Reference Number: PA.CP.PAR.322 Effective Date: 01/18 Last Review Date: 07/2021Coding Implications Revision Description Pembrolizumab
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Consult with a healthcare provider to determine if Keytruda (pembrolizumab) is the appropriate treatment option for your condition.
02
Follow the dosing instructions provided by your healthcare provider or as directed on the prescription label.
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Keytruda is usually given once every 3 weeks through an IV infusion. Make sure to schedule and attend all appointments as recommended.
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Report any side effects or changes in your health to your healthcare provider immediately.
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Continue to take Keytruda for as long as your healthcare provider recommends, even if you start to feel better.

Who needs keytruda pembrolizumab - official?

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Keytruda (pembrolizumab) is typically prescribed for patients with certain types of cancer, such as melanoma, non-small cell lung cancer, head and neck squamous cell carcinoma, and classical Hodgkin lymphoma.
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Patients who have not responded to other treatments or who have cancer that has spread to other parts of the body may be candidates for Keytruda.
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Keytruda (pembrolizumab) is an immunotherapy medication used to treat various types of cancer.
Healthcare providers and medical facilities are required to file information about the administration of Keytruda (pembrolizumab).
The necessary information can be filled out electronically on the designated reporting platform provided by the relevant health authorities.
The purpose of reporting on Keytruda (pembrolizumab) is to monitor its usage, effectiveness, and any potential side effects in patients.
Information such as patient demographics, dosage administered, treatment outcome, and any adverse reactions must be reported.
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