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Adverse Drug Reaction (ADR) Reporting: Please report all adverse events suspected to have a causal relationship with Acrotech Biopharma’s Products, using the contact number listed on each product’s package insert. Adverse events not associated with the use of Acrotech’s products, e.g., Disease Progression, or requests for discontinuing drug supply due to patient deaths not associated with the use of Acrotech’s Products, should not be reported as ADRs.

Acrotech Biopharma, Inc., does not guarantee coverage and/or reimbursement for its products. Coverage, coding, and reimbursement policies vary significantly by payer, patient, and setting of care. Actual coverage and reimbursement decisions are made by individual payers following the receipt of claims. Healthcare professionals should always verify coverage, coding, and reimbursement guidelines on a payer and patient-specific basis. Acrotech Biopharma, Inc. reserves the right to change eligibility guidelines, terminate, or modify the Acrotech Access Support program at any time for any reason.

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