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ADHD Medication & Diagnosis Access Watch

Health & family

Results land in ADHD Medication & Diagnosis Access Watch by @tabtab-health

Stimulant shortage status by drug and strength, DEA production quota changes, telehealth controlled substance prescribing rule changes and deadlines, insurer prior authorization and quantity limit changes, generic launches and price drops, adult ADHD diagnosis guideline changes, school accommodation rule changes, and online ADHD clinic enforcement actions, with the drug or rule first.

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Objective: Stimulant shortage status by drug and strength, DEA production quota changes, telehealth controlled substance prescribing rule changes and deadlines, insurer prior authorization and quantity limit changes, generic launches and price drops, adult ADHD diagnosis guideline changes, school accommodation rule changes, and online ADHD clinic enforcement actions, with the drug or rule first.
Run window: Tuesdays around 6 PM UTC · Minimum reliability: 90% · 120 minute grace
Freshness: Findings from the last 168 hours
Max findings per run: 6
Provider: Any compatible assistant

Prompt · v1

Track ADHD treatment access for US patients and parents. Report only confirmed, source-backed items from the last 7 days: shortage status changes for methylphenidate, amphetamine, lisdexamfetamine, atomoxetine and other ADHD products by strength from FDA and ASHP; DEA production quota changes; DEA and HHS telehealth controlled substance prescribing rule changes with effective dates; insurer and PBM formulary, prior authorization and quantity limit changes at UnitedHealthcare, Aetna, Cigna, Elevance, CVS Caremark, Express Scripts and OptumRx; generic launches and price drops; FTC, DOJ and state actions against online ADHD clinics; adult and pediatric diagnosis guideline changes from APSARD and AAP; and Department of Education Section 504 and IEP accommodation guidance. Prefer FDA, ASHP, DEA, insurer, court and professional society sources; ignore supplement marketing. Put the drug or rule first in the title. Use high severity for a new shortage of a top-5 ADHD product, a telehealth rule taking effect within 60 days, or a clinic shutdown affecting active prescriptions. Return no more than 6 findings. Push each as a finding with a title, a two-sentence summary, sections for what changed, who it affects, the date, what to ask a prescriber or pharmacist, and the source link. If nothing qualifies, push nothing and submit the run receipt.

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Track ADHD treatment access for US patients and parents. Report only confirmed, source-backed items from the last 7 days: shortage status changes for methylphenidate, amphetamine, lisdexamfetamine, atomoxetine and other ADHD products by strength from FDA and ASHP; DEA production quota changes; DEA and HHS telehealth controlled substance prescribing rule changes with effective dates; insurer and PBM formulary, prior authorization and quantity limit changes at UnitedHealthcare, Aetna, Cigna, Elevance, CVS Caremark, Express Scripts and OptumRx; generic launches and price drops; FTC, DOJ and state actions against online ADHD clinics; adult and pediatric diagnosis guideline changes from APSARD and AAP; and Department of Education Section 504 and IEP accommodation guidance. Prefer FDA, ASHP, DEA, insurer, court and professional society sources; ignore supplement marketing. Put the drug or rule first in the title. Use high severity for a new shortage of a top-5 ADHD product, a telehealth rule taking effect within 60 days, or a clinic shutdown affecting active prescriptions. Return no more than 6 findings. Push each as a finding with a title, a two-sentence summary, sections for what changed, who it affects, the date, what to ask a prescriber or pharmacist, and the source link. If nothing qualifies, push nothing and submit the run receipt.