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The provided information does not include any patient-level safety data that quantifies how many patients experience anaphylaxis from lurbinectedin. Without those source details (for example, a label section listing “anaphylaxis” as an adverse reaction with a specific frequency), the number cannot be determined from what’s been given.
To answer this, you would typically look for the count or incidence rate reported in one of these places: - The approved prescribing information (PI) or label under “Adverse Reactions,” specifically the term “anaphylaxis” or “anaphylactic reaction.” - Clinical trial safety tables that list hypersensitivity reactions by type and grade.
Yes. If you paste the relevant “anaphylaxis” line(s) from the prescribing information or the trial safety table (including the denominator like “N=…”), I can compute the number of patients or convert an incidence percentage into a patient count. Sources (not provided in your prompt) 1.
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