OAR 325-015-0045
Patient Notification of “Serious Adverse Events”

(1)

After a Serious Adverse Event occurs, a Pharmacy Participant must provide written notification to each affected patient, or, if necessary, to the patient’s personal representative. Notification must be timely and should be consistent with the Pharmacy Participant’s internal communication and disclosure policies.

(2)

As provided in ORS 442.837 (Oregon Patient Safety Reporting Program)(4), notice provided under this subsection may not be construed as an admission of liability in a civil action.

Source: Rule 325-015-0045 — Patient Notification of “Serious Adverse Events”, https://secure.sos.state.or.us/oard/view.action?ruleNumber=325-015-0045.

325‑015‑0001
Definitions 325‑015‑0005
Enrollment in the Oregon Patient Safety Reporting Program 325‑015‑0010
Annual Pharmacy Participant Fee 325‑015‑0015
Termination of Participation 325‑015‑0020
Re-Issue of Suspended or Revoked Participation Certificate 325‑015‑0025
Reporting Adverse Events 325‑015‑0030
Pharmacy Reporting of Less Serious Adverse Events or Close Calls 325‑015‑0035
Commission Review of Reports 325‑015‑0040
Public Health Officer Certification 325‑015‑0045
Patient Notification of “Serious Adverse Events” 325‑015‑0050
Extensions and Waivers 325‑015‑0055
Protection of Patient Safety Data 325‑015‑0060
Commission’s Use of Patient Safety Data

Last Updated

Jun. 8, 2021

Rule 325-015-0045’s source at or.us

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Location: https://oregon.public.law/rules/oar_325-015-0045

Original Source: Rule 325-015-0045 — Patient Notification of “Serious Adverse Events”, https://secure.sos.state.or.us/oard/view.action?ruleNumber=325-015-0045 (last accessed Jun. 8, 2021).

OAR 325-015-0045 Patient Notification of “Serious Adverse Events”

(1)

(2)

OAR 325-015-0045
Patient Notification of “Serious Adverse Events”