Medication Administration Errors with Insulin and Pantoprazole
Summary
The deficiency involves a failure to maintain a medication error rate below 5%, with surveyors identifying 3 errors out of 25 observed medication administration opportunities, resulting in a 12% error rate. One resident with chronic kidney disease and aftercare for joint replacement had a physician order for pantoprazole 40 mg packet to be dissolved in 5 milliliters of apple juice and given once daily. During observation, a Certified Medication Aide (CMA) poured the pantoprazole packet into a cup of water and administered it, rather than using apple juice as ordered and as required by FDA instructions for pantoprazole delayed-release oral suspension. The Executive Director confirmed that the electronic MAR did not specify administration in apple juice or applesauce, and FDA guidance indicated pantoprazole granules must be given only in apple juice or applesauce due to pH requirements and specific preparation instructions. Another resident, admitted and readmitted with diagnoses including metabolic encephalopathy and type 2 diabetes, had a care plan addressing potential for unmanaged blood sugar and an order for Lantus insulin 18 units twice daily. During observation, an RN drew up Lantus in an insulin syringe, and when asked to verify the dose, the syringe’s black stopper was at the 20-unit mark. The RN initially asserted that the surveyor was looking at the wrong side of the syringe and claimed that one side showed 1-unit increments and the other 2-unit increments, stating she had drawn up 18 units. Upon further questioning, the RN rechecked the syringe and adjusted the plunger to the 18-unit mark. The DON later verified that the insulin syringe was marked in 1-unit increments on both sides, confirming that the RN had initially prepared an incorrect dose. A third resident with a fracture of the left femur and type 2 diabetes had a care plan for altered endocrine function and an order for Humalog insulin 19 units before every meal. During observation, the CMA removed a new Humalog KwikPen from the medication cart, dialed it directly to 19 units, and prepared to administer it. When the surveyor asked whether the pen needed to be primed, the CMA stated she did not understand the question and again indicated she did not know what priming was before entering the resident’s room to administer the insulin. Manufacturer instructions for the Humalog KwikPen specified that the pen must be primed before each injection by selecting 2 units, holding the pen needle-up, tapping to collect air bubbles, and pushing the dose knob until zero appears, to ensure proper function and accurate dosing. These events occurred despite facility policies and the medication aide job description requiring staff to follow medication labels, verify orders, and administer medications in accordance with established nursing standards, facility policies, and state requirements.
Penalty
Resources
Below are regulatory guidelines relevant to this citation:
Medication error rate exceeded the 5% threshold when an RN administered two insulin doses to a resident with DM without priming the Lantus and NovoLog pens before each injection. Surveyors observed the RN give the ordered subcutaneous doses without completing the manufacturer-required safety test, and the RN stated she believed priming was only needed before first use. The DON and consultant pharmacist confirmed the pens should be primed before each dose.
Medication administration errors exceeded the allowed rate when an MA gave late doses, administered a BP medication outside ordered parameters, and gave an incorrect dose of a PPI. One resident with metabolic encephalopathy, cognitive communication deficit, and HTN received Metoprolol late, and another resident with seizures, stroke, GERD, and HTN received Levetiracetam late, Lisinopril despite BP below the hold parameter, and Pantoprazole at 20 mg instead of the ordered 30 mg.
Medication Error Rate Exceeded 5 Percent: The facility had a 7.41% medication error rate after two errors were identified. A resident ordered acetaminophen and Refresh Tears received acetaminophen and artificial tears instead of the ordered eye drops, and the CMA reported giving the meds with the morning pass and not notifying an LN that they were late. The pharmacist confirmed the eye drops and artificial tears were not the same medication, and the regional RN stated meds should be given within one hour before or after the scheduled time.
Medication Administration Error Rate Exceeded: The facility had a 7% medication error rate during observation. An LPN gave a resident sucralfate as a tablet with water instead of as a slurry 1 hour before meals, and an RN administered only one Senna Plus tablet instead of two while lidocaine patches were unavailable and on order. The resident involved in the sucralfate error had anxiety, depression, muscle weakness, and moderate cognitive impairment.
Medication administration errors exceeded the allowed rate when surveyors observed 4 errors in 27 opportunities. An LPN gave one resident's Keppra, Lexapro, and metformin late despite orders for 9 AM administration, and another LPN gave a resident's metoprolol without breakfast even though the order required it with breakfast. The DON confirmed the facility policy required medications to be given within one hour of the ordered time, and staff acknowledged the orders were not followed.
Late Administration of Scheduled Morning Medications: Surveyors found an 11.11% med error rate after an MA gave three residents their 6:30 a.m. meds well after the scheduled time. One resident with dementia and DM received metformin late and initially refused it, while two other residents with GERD or indigestion-related orders received Protonix or omeprazole late while one was sleeping and another was resting in bed. Interviews with the MA, RN, and DON confirmed late administration was considered a med error and should be reported to nursing.
Medication Error Rate Exceeded Due to Unprimed Insulin Pen Administration
Penalty
Summary
The facility failed to maintain a medication error rate of less than 5% after surveyors identified 2 medication errors out of 30 opportunities, resulting in a 6.67% medication error rate for 1 of 3 residents observed during medication pass. The errors involved incorrect administration of insulin pens for a resident with type 2 diabetes mellitus without complications who had orders for Lantus Solostar U-100 insulin 13 units subcutaneous each morning and NovoLog FlexPen U-100 insulin 8 units before meals. During a continuous medication pass observation, Nurse #1 prepared the resident’s Lantus and NovoLog insulin pens and administered both subcutaneous doses without priming either pen as required by the manufacturer instructions. The instructions for both insulin pens stated that a safety test/priming step should be completed prior to each injection to ensure insulin comes out of the needle. In interview, Nurse #1 stated she did not know the pens should be primed before each dose and believed priming was only needed before first use. The Consultant Pharmacist stated the manufacturer instructions required priming before each dose, and the DON stated the pens should be primed prior to each dose to ensure the correct dose was administered.
Medication Administration Errors Exceeded Allowed Rate
Penalty
Summary
The facility failed to keep its medication error rate below 5 percent. Based on observation, interview, and record review, surveyors found a medication error rate of 15.38 percent, with 4 errors out of 26 opportunities involving 2 of 3 residents reviewed for medication administration. The errors involved late administration of Metoprolol Tartrate for one resident and late administration of Levetiracetam for another resident, along with administration of Lisinopril outside ordered vital sign parameters and administration of an incorrect Pantoprazole dose. Resident #107 was a female with diagnoses including metabolic encephalopathy, cognitive communication deficit, and hypertension. Her quarterly MDS showed a BIMS score of 10, indicating moderate cognitive impairment. Her physician ordered Metoprolol Tartrate 12.5 mg twice daily for hypertension, with the July 2026 MAR showing an 8:00 AM administration time. During medication administration observation, MA A gave the Metoprolol at 9:35 AM, which was after the ordered time. Resident #45 was a female with diagnoses including unspecified convulsions, cerebral infarction, GERD, and hypertension. Her annual MDS showed a BIMS score of 12, indicating moderate cognitive impairment. Her orders included Levetiracetam 500 mg twice daily, Lisinopril 10 mg daily to be held if blood pressure was less than 100/60 or heart rate less than 55, and Pantoprazole 30 mg daily. During observation, MA A administered Levetiracetam at 9:49 AM instead of the ordered time, gave Lisinopril when the resident's blood pressure was 99/72, and administered Pantoprazole 20 mg instead of the ordered 30 mg dose.
Medication Error Rate Exceeded 5 Percent
Penalty
Summary
The facility failed to ensure a medication error rate of less than five percent after two medication errors were identified, resulting in a 7.41 percent error rate. One error involved R22, whose physician orders included acetaminophen 325 mg, 2 tablets by mouth three times daily for chronic pain at 07:00 AM, 11:00 AM, and 05:00 PM, and Refresh Tears ophthalmic solution, 1 drop in both eyes three times daily for dry eye syndrome at 07:00 AM, 01:00 PM, and 08:00 PM. On 07/07/2026 at 09:03 AM, CMA R prepared R22's medications and reported that she administered the 07:00 AM medications with her other morning medications, stating she had always done it that way. She administered artificial tears, one drop in each eye, and acetaminophen at that time, and reported that she did not tell an LN that the medications were given late. Later that day, CMA R stated that R22 had always used artificial tears and did not have Refresh eye drops, and after reviewing the EMR and the label she reported the artificial tears were not the same ingredients as Refresh Tears. A medication substitution formulary had been requested the day before, but the facility did not provide one. The pharmacist reported that Refresh eye drops and the artificial tears administered were not the same medication, and both the pharmacist and the regional RN stated medications scheduled at a specific time were to be passed within one hour before or after the scheduled time. The regional RN also indicated that if a different medication was being used, the physician order would be changed.
Medication Administration Error Rate Exceeded
Penalty
Summary
The facility failed to ensure a medication error rate less than 5 percent when a medication administration observation resulted in a 7 percent error rate. Resident #42’s record showed diagnoses of anxiety, depression, and muscle weakness, with a BIMS score of 8 out of 15 indicating moderate cognitive impairment. The June 2026 MAR listed an order for sucralfate 1 gram by mouth twice daily, to be made into a slurry and given 1 hour prior to meals. During an observation, an LPN administered the sucralfate as a tablet with water instead of making it into a slurry, and the resident’s unit dinner time was listed as 5:45 p.m. while the DON stated the unit did not eat until 6:00 p.m. Resident #21’s physician orders included Senna Plus 8.6-50 mg, two tablets by mouth twice daily, and a lidocaine 4 percent patch to be applied daily at 8:00 a.m. and removed at 8:00 p.m. During a medication pass observation, an RN prepared medications for the resident but placed only one Senna Plus tablet in the pill cup and reported she was looking for lidocaine patches, which were not available because more had to be ordered from the pharmacy. The RN administered the medications without including the ordered two Senna Plus tablets, and the MAR documented a code of 9 for the lidocaine patch, with progress notes stating the patch was on order.
Medication Administration Errors Exceeded Allowed Rate
Penalty
Summary
The facility failed to keep its medication error rate below 5 percent. Surveyors identified 4 medication errors out of 27 observed medication administration opportunities, resulting in an overall error rate of 14.81 percent for two sampled residents. The errors involved Resident 23 and Resident 2 during observed medication administration and record review. Resident 23 had diagnoses including type 2 diabetes, major depressive disorder, and epilepsy. The physician's orders showed Keppra 750 mg twice daily, Lexapro 10 mg daily, and metformin 500 mg daily, all scheduled for 9 AM. During a concurrent observation and interview, LVN 3 was preparing to administer these medications at 10:12 AM and stated they were due at 9 AM but would be given late. LVN 3 stated medications can be given one hour after they are due and that it had been over an hour since the medications were due. The DON later confirmed the facility's medication administration policy required medications to be given within one hour before or after the ordered time. Resident 2 had diagnoses including muscle weakness, hypertension, and atherosclerotic heart disease. The physician's order for metoprolol extended release 25 mg specified that it be given by mouth once daily for hypertension, hold for systolic blood pressure less than 110 and heart rate less than 60, and give with breakfast. During observation, LVN 2 administered metoprolol at 9:44 AM without breakfast or any food. LVN 2 stated she did not give the medication with breakfast and did not offer food or a snack. RN 2 and the RNS stated the medication should have been given with breakfast, and the facility policy indicated medications were to be administered following the scheduled routine unless otherwise specified by the doctor.
Late Administration of Scheduled Morning Medications
Penalty
Summary
The facility failed to ensure the medication error rate remained below 5 percent. Surveyors found an 11.11% medication error rate, based on 3 errors out of 27 opportunities, involving three residents and one medication aide. The errors involved late administration of scheduled 6:30 a.m. medications for three residents on the same morning, and each medication was given after the scheduled time while the eMAR was marked red. Resident #69 was an older female with dementia and Type 2 diabetes with hyperglycemia. Her physician ordered Metformin HCL 500 mg twice daily for diabetes, scheduled for 6:30 a.m. and 4:30 p.m. During observation, she was in her room eating breakfast when the medication aide attempted to administer the 6:30 a.m. dose at 7:56 a.m. The aide stated the medication was scheduled for 6:30 a.m., attempted to give it using the language line, and the resident refused. The aide then notified the RN, who notified the physician. Resident #40 had diagnoses including Type 2 diabetes, cellulitis of the right lower limb, and dysphagia. She had an order for Protonix 40 mg in the morning for heartburn/indigestion, scheduled for 6:30 a.m. During observation, she was in her room sleeping with her breakfast tray untouched when the medication aide administered the dose at 8:04 a.m. Resident #38 had diagnoses including GERD and dysphagia, with an order for Omeprazole 20 mg in the morning for GERD, scheduled for 6:30 a.m. During observation, she was resting in bed when the medication aide administered the dose at 8:12 a.m. Interviews with the medication aide, RN, and DON confirmed that medications were expected to be given within an hour before or after the scheduled time, that late medications were to be reported to nursing, and that giving a medication late was considered a medication error.
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