F 0757
Ensure each resident’s drug regimen must be free from unnecessary drugs.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review, for one of three sampled residents (Resident 1), the facility failed to ensure
Resident 1 was administered buspirone (treats anxiety) with adequate monitoring of adverse effects from
the medication.
Residents Affected - Few
This failure had the potential to result in delayed management of adverse effects and unnecessary use of
medication.
Findings:
Review of Resident 1's admission Record indicated Resident 1 was admitted to the facility on [DATE] with
diagnoses that included generalized anxiety disorder (excessive and overwhelming worry about ordinary
issues like work, money and family) and anoxic brain damage (brain is deprived of oxygen, symptoms
include changes in sleep pattern, trouble speaking and swallowing).
Review of Resident 1's Order Summary Report for September 2022 indicated an order for Resident 1 to
receive buspirone 5 milligrams via PEG (percutaneous endoscopic gastrostomy, a flexible tube is placed
through the abdominal wall into the stomach to receive nutrition and/or medication) two times daily for
agitation, restlessness and falling tendency.
During a concurrent interview and review of Medication Administration Record (MAR) for August 2022 with
Assistant Director of Nursing (ADON) on 7/25/23 at 11:59 a.m., ADON stated, Resident 1's MAR indicated
monitoring for antipsychotic (medication that treats psychosis, a severe mental illness) adverse effects was
done. ADON stated, Resident 1 was given buspirone, which was an anti anxiety and not an antipsychotic,
and had different adverse effects.
Review of Resident 1's Medication Administration Record (MAR) for September 2022 indicated Resident 1
was monitored for the presence of tardive dyskinesia (facial tongue movement), cognitive impairment
(decreased mental status), akathisia (inability to sit still), parkinsonism (tremors, rigidity, drooling).
According to Dailymed, a nationally-recognized publication of the National Institute of Health in the U.S.
National Library of Medicine and includes references to drug information submitted to the Food and Drug
Administration, buspirone adverse events include; dizziness, insomnia, nervousness, drowsiness,
lightheadedness, nausea, headache and fatigue.
Review of the facility's policy and procedure titled Psychotropic Medication Management last revised
10/24/17 indicated, Medication effects will be monitored and documented on the medication
(continued on next page)
Any deficiency statement ending with an asterisk (*) denotes a deficiency which the institution may be excused from correcting providing it is determined that other
safeguards provide sufficient protection to the patients. (See instructions.) Except for nursing homes, the findings stated above are disclosable 90 days following the
date of survey whether or not a plan of correction is provided. For nursing homes, the above findings and plans of correction are disclosable 14 days following the date
these documents are made available to the facility. If deficiencies are cited, an approved plan of correction is requisite to continued program participation.
LABORATORY DIRECTOR'S OR PROVIDER/SUPPLIER
REPRESENTATIVE'S SIGNATURE
TITLE
(X6) DATE
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Facility ID:
If continuation sheet
Page 1 of 2
Event ID:
055885
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
055885
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Country Drive Post Acute
2500 Country Drive
Fremont, CA 94536
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0757
administration record, to include target behavior monitoring, and monitoring for adverse effects when the
medications are used.
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055885
If continuation sheet
Page 2 of 2