I am wondering what is the strategy to determine first excited state in the case of small oscillator strengths.

For instance, assume that I have solved Casida equation for a molecule and all 20 first oscillator strength values are smaller than 0.002,  and after phenomenological broadening, I have a small peak on S_5.

Now If I want to talk about fluorescence in this system I should consider the S_5 as the first excited state?  or TDDFT obtained S_1 (with f_I

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