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This document has been approved for use at [Click here to enter text.] OFFLABEL USE OF RITUXIMABPATIENT CONSENT FORMPharmaceutical companies need approval from the Therapeutic Goods Administration
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Off-label use refers to the practice of prescribing medications for purposes or in patient populations that are not specifically approved by regulatory authorities.
Healthcare providers who prescribe off-label medications may be required to document and report their off-label use, depending on local regulations and institutional policies.
To fill out off-label use documentation, providers should include the patient's information, medication details, rationale for the off-label use, and any relevant clinical data.
The purpose of off-label use is to provide treatment options based on clinical judgment and emerging evidence, especially when approved treatments are ineffective.
Information that must be reported includes the medication name, dosage, reason for off-label use, patient outcomes, and any adverse effects.
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