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Rishi Consultative Care · Clinical reference

The in-person pharmacist consult

A credentialed pharmacist, physically present at the dispensary, delivers the consultation Pennsylvania already requires — form, dose, titration, route and interaction screening — for a patient who already holds a medical card.

What it is

Pennsylvania § 1181a.27(c)(7) makes a form/dosage/modality/product-selection consult mandatory where the certifying practitioner did not specify form and dosage. This service supplies the professional who delivers it: a PharmD or physician, contracted to the door, working from an approved protocol library with citations the reviewer can check.

The dispensary is the customer. The patient is the recipient, never the account. The one sentence the whole arrangement rests on: Rishi supplies the professional, the protocol and the paperwork; the dispensary keeps the patient, the product and the PHI.

What it is not

The four things the consult produces

  1. 01

    A form and a starting dose

    Route-first, potency-second. Oral oil is the titration backbone; inhaled is a rescue route with no validated dosing and it is said so.

  2. 02

    A titration plan with stop rules

    Verbatim increments and intervals from the protocol — and the reassessment window, so the patient knows when he is allowed to judge it.

  3. 03

    A named interaction finding

    Not a clearance. The honest statement is a flag and a referral: “your INR needs checking, your cardiologist needs to know.”

  4. 04

    The products actually on that door’s shelf today

    Drawn from this location’s observed shelf inside a freshness window, ranked on measured cannabinoid ratio and form. Never on strain name, indica/sativa or terpenes.

The evidence posture

Every recommendation carries a grade. Grade D is never recommended — it is not a discouragement but a structural impossibility: a grade-D protocol can never reach approved status, and the recommender returns NO_APPROVED_PROTOCOL for its condition code. The formulary is published in full below, including the eighteen exclusions it refuses and the rows of the interaction screen where the honest answer is no evidence of interaction. Where a figure could not be verified against the on-disk corpus it is omitted or marked UNVERIFIED — never carried from memory.

A — Systematic review / meta-analysis or RCT-backed (multiple consistent RCTs or consistent SR).
B — Guideline-supported or consistent observational / expert consensus with caveats (e.g. BMJ guideline positioning for third-line use; Delphi consensus).
C — Mechanistic, observational-only, or limited evidence; the recommendation is defensible only as a cautious, titrated trial with explicit stop rules.
DNot established — evidence absent or negative. No entry graded D may be recommended. Grade D appears in the exclusion section only.

Read the document

Also: the consolidated interaction screen — eleven medication rows, the documented magnitudes, and the two rows where no signal was found.