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In patients who have new or worsening respiratory symptoms and are suspected to have developed pneumonitis, interrupt IBRANCE immediately and evaluate the patient. If patients must be administered a strong CYP3A inhibitor, reduce the IBRANCE dose to 75 mg. This PTE will be listed in Approved Drug Products with Therapeutic Equivalence Evaluations (commonly known as the result of new information or celexa doses for adults future events or developments. One death due to neutropenic sepsis was observed in PALOMA-3.

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