FDA Adverse Event Injury Summary report: N

ZYNO PUMPS

MDR report key: 19373297 · Received May 21, 2024

Report

Report Number
MW5155207
Event Type
Injury
Date Received
May 21, 2024
Date of Event
May 17, 2024
Report Date
May 17, 2024
Manufacturer
ZYNO MEDICAL, LLC
Product Code
FRN
Adverse Event
Yes
Report Source
Voluntary report
Reporter Occupation
NURSE
Health Professional
*

Narratives

Description of Event or Problem · 0

1239- PATIENT HAD RIGORS/ SHAKING ALL OVER HER BODY. 1239- BP (BLOOD PRESSURE )-147/94 HR (HEARTRATE)-78 R-16 TEMP-96.7 O2-97% 1240- (B)(6) FNP (FAMILY NURSE PRACTIONER) NOTIFIED AND FNP INSTRUCTED TO GIVE BENADRYL 25MG, PEPCID 20MG, QUZYTTIR 10MG IV, AND TYLENOL 1000MG 1240-TYLENOL 1000MG GIVEN PO 1246- BENADRYL 25MG IV, PEPCID 20MG , QUZYTTIR V 10MG GIVEN 1249- BP-160/100 HR-92 O2-98 % R-18 1253- BP-131/100 HR-88 O2-98 R-16 1303- BP0163/91 HR-80 O2-98 R-16 1315- PATIENT RIGORS/SHAKING RESOLVED AND PATIENT STATED THEY DO NOT WANT TO RECONTINUE DUE TO BEING IN EMOTIONAL DISTRESS. 1316- MEDICATION WASTED 76MLS AND PATIENT RECEIVED 124MLS 1325- PATIENT BP-156/80 HR-79 O2-98 TEMP-97 PATIENT FAMILY MEMBER PICKED UP PATIENT. FNP (B)(6). INSTRUCTED PATIENT TO GO TO THE ER (EMERGENCY ROOM) IF ANY SIGNS AND SYMPTOMS OF A REACTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2305033 ZYNO PUMPS PUMP, INFUSION FRN ZYNO MEDICAL, LLC

Patients

Seq Age Sex Outcome Treatment
1 78 YR Female Required Intervention BENADRYL.| PANZYGA.| PEPCID.| QUZYTTIR.| TYLENOL.