Genentech XOLAIR Access Solutions Form
This file provides detailed instructions for supporting patients using XOLAIR (omalizumab) through Genentech's Access Solutions. It includes essential information for healthcare providers and patient consent forms. Utilize this file to ensure proper submission and compliance with Genentech's protocols.
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How do I fill this out?
To fill out this form, start by entering the patient's information, including their name, date of birth, and contact details. Next, provide insurance information and complete the diagnosis and clinical details accurately. Finally, ensure the prescriber information and necessary certifications are filled out correctly and submit the completed form.

How to fill out the Genentech XOLAIR Access Solutions Form?
1
Gather and fill in the patient's personal information.
2
Complete the insurance details and any related insurance forms.
3
Specify the diagnosis with accurate codes and descriptions.
4
Provide prescriber and healthcare provider information.
5
Review the form for completeness and submit it.
Who needs the Genentech XOLAIR Access Solutions Form?
1
Patients diagnosed with allergic asthma who require treatment.
2
Healthcare providers prescribing XOLAIR for chronic idiopathic urticaria.
3
Individuals seeking insurance reimbursement for XOLAIR.
4
Patients needing initial or ongoing therapy for nasal polyps.
5
Prescribers who need to ensure compliance with Genentech's protocols.
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What are the instructions for submitting this form?
To submit this form, fax it to Genentech at (800) 704-6612, or send it via email to Genentech-Access@genentech.com. You can also opt for online submission at Genentech’s Access Solutions web portal. Ensure that all fields are filled out accurately to facilitate quick processing.
What are the important dates for this form in 2024 and 2025?
Important dates regarding the XOLAIR Access Form in 2024 include January 15 for initial submission deadlines and April 20 for updates. In 2025, continue to refer to these dates, adjusted for any policy changes from Genentech. It’s essential to stay informed about these dates to ensure timely submissions.

What is the purpose of this form?
The purpose of this form is to facilitate the treatment of patients prescribed XOLAIR by collecting necessary patient, insurance, and clinical information. It ensures compliance with Genentech’s protocols while providing the essential data required for therapy initiation. By streamlining the process for healthcare providers, the form helps improve patient outcomes and ensure access to necessary treatments.

Tell me about this form and its components and fields line-by-line.

- 1. First Name: The patient's first name.
- 2. Last Name: The patient's last name.
- 3. Date of Birth: The patient's date of birth in MM/DD/YYYY format.
- 4. Insurance Information: Details about the patient's insurance provider.
- 5. Diagnosis Codes: Specific diagnosis codes related to the patient's condition.
- 6. Prescriber Information: Information about the healthcare provider prescribing XOLAIR.
- 7. Patient Consent: A section for the patient's signature to authorize treatment.
What happens if I fail to submit this form?
Failure to submit this form accurately may lead to delays in patient treatment and reimbursement processes. It's vital to ensure all sections are filled out completely to avoid complications.
- Incomplete Information: Missing fields can result in rejection of the form.
- Inaccurate Diagnoses: Incorrect codes may cause complications with insurance claims.
- Lack of Signature: No signature can delay approval for therapy.
How do I know when to use this form?

- 1. Patient Initiation: Use the form when starting a new therapy for a patient.
- 2. Insurance Verification: Submit for verification of benefits with the patient’s insurance.
- 3. Compliance Documentation: To maintain compliance with Genentech’s healthcare protocols.
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