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4 95 CI 0 to 2. 2 for placebo Diagnosis for GIST only Documentation of prior treatments required Physician Specialty Oncologist For use in clinical trial If yes provide trial name and registration number Drug Name Brand Name and Scientific Name /Strength Dose Quantity Route Number of Refills Product will be delivered to Patient s Home Frequency Physician Office Other Date Prescriber or Authorized Signature Dispensing Pharmacy Name and Phone Number Approved Denied If denied provide reason for...
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How to fill out regorafenib patient information:

01
Start by gathering all the necessary personal and medical information of the patient. This includes their full name, date of birth, address, and contact details.
02
Fill out the section that requires the patient's medical history. Provide details about any previous or existing medical conditions, surgeries, allergies, and medications they are currently taking. It is important to be accurate and thorough in this section to ensure the safe administration of regorafenib.
03
The patient information form may also require information about the patient's healthcare provider or primary physician. Include their name, contact information, and any additional details requested.
04
If the patient has any known drug interactions or sensitivities, it is crucial to include this information in the appropriate section. This will help healthcare professionals to determine the suitability and potential risks of prescribing regorafenib.
05
In some cases, the patient information form might ask for demographic information such as gender, race, or ethnicity. Provide this information if requested.
06
Lastly, ensure that all the required fields are completed accurately. Double-check the form for any errors or missing information before submitting it. It is essential to be transparent and honest when filling out the regorafenib patient information to ensure the best possible treatment and care for the patient.

Who needs regorafenib patient information?

01
Patients who have been prescribed or are considering regorafenib as part of their treatment plan need to provide regorafenib patient information. This information helps healthcare professionals make informed decisions about the safety, dosage, and administration of the medication.
02
Healthcare providers and physicians responsible for the patient's care also require regorafenib patient information. It allows them to assess the patient's eligibility, monitor their medical history, and identify any potential risks or contraindications.
03
Additionally, clinical researchers and experts studying regorafenib may require patient information for research purposes, evaluating the drug's efficacy, side effects, and overall impact on patient outcomes.
In summary, filling out regorafenib patient information involves providing accurate personal, medical, and demographic details of the patient. This information is necessary for healthcare professionals to make informed decisions regarding the medication's administration and to ensure patient safety. Patients, healthcare providers, and researchers all have a role in the collection and use of regorafenib patient information.

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What came out of that study of the results we presented here at ASCOT 2012 which is a much longer progression-free survival in the group initially randomized to reg Arafat NEM about 5 months compared to less than a month for those patients who initially were randomized to placebo you means practically is once we get this drug approved we believe it will set a new standard of care for patients who had and failed had and had that failed to control their disease and now this gives them a third option where should a drug this powerful fifth should it stay in the third line should it move earlier I think that's going to be an interesting question for clinicians and future clinical research to work on also might this drug combined with other interesting drugs that target different pathways we know that gist can be controlled sometimes very long term by shutting down the kit or PDF receptor kinases, but we're not curing these patients how can we continue to push towards cure and my trigger after nib give us a new tool to do that you, but it has certain known and expected side effects high blood pressure hand-foot syndrome some more diarrhea, so these things in our trial were highly manageable very few patients less than seven percent had to come off study because of adverse events you

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Regorafenib patient information includes details about the patient's medical history, current health status, and any treatment plans involving regorafenib.
Healthcare providers and facilities that are prescribing or administering regorafenib are required to file patient information.
Regorafenib patient information can be filled out by healthcare providers by documenting all relevant details about the patient and their treatment.
The purpose of regorafenib patient information is to ensure that healthcare providers have accurate and up-to-date information about the patient's treatment with regorafenib.
Information such as the patient's name, age, medical history, current health status, dosage of regorafenib, and any side effects experienced must be reported on regorafenib patient information.
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