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Use is restricted to trained professionals operating in laboratory or research settings, following appropriate safety and handling protocols

These reports are submitted through the FDA Adverse Event Reporting System (FAERS) by healthcare professionals, patients, and manufacturers to document any potential safety concerns that arise during the use of these treatments after they have been approved

Acta Crystallogr D Biol Crystallogr

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A complex karyotype including 22q monosomy, recurrent losses involving chromosomes 1, 2, 21, and 17p, trisomy 6p, and ring chromosome 11 have been described in MMNST [3, 4, 10, 17]