Comment from Chrissy Terry
AnonymousSupportIndividual
Summary: A patient with complex medical conditions and chronic pain is requesting that the FDA regulate NarxCare as Software as a Medical Device. The commenter argues that these AI tools need oversight to ensure they account for individual comorbidities and situational conditions when determining treatment eligibility.
Please regulate NarxCare as Software as a Medical Device so it can be properly reviewed and regulated by the FDA as it should be. These tools directly impact patient care and must meet standards for safety, transparency, and accountability.Disabled CRPS patient in need ACDF procedure C23456 inability proceed as spouse diagnosed aggressive cancer inwhich recently succumbed to disease. Recently changed providers as MD retired as has four MD's previously in six years. Upon new patient establishment signed medical record release my personal filing as turnover rate hcare professionals seen Narx score 5 high risk. Oversight needed as already met with refusal treatment any break thru pain RX after deer ran front vehicle July 2025 gaving swelling both feet asked fluid pill having had heart failure from cortisone injection between scapula,spine hit ling causing filled fluid,heart enlargment, afib was full code arrival ER 2019 admitted ICU 7days heart ablation 2week later EF 10-15% stress spouse diagnosis, minor chldrn, non existent outside help have been left suffer from Hcare retiring as DEA seizing assets MD's prescribing opiod epidemic 2016 ongoing has scared hcare field.Writing ask Narx score have oversight as AI has refused treatment upon not knowing my comorbidity's,situational conditions, affects physical ADL's without use full aganost opiod been able receive which taken multiple years suffering with no lack MRI supporting comorbiditys preceding need opiods to have quality of life.