Does DEVICE Cause Pulseless electrical activity? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Pulseless electrical activity have been filed in association with DEVICE. This represents 0.1% of all adverse event reports for DEVICE.
9
Reports of Pulseless electrical activity with DEVICE
0.1%
of all DEVICE reports
4
Deaths
5
Hospitalizations
How Dangerous Is Pulseless electrical activity From DEVICE?
Of the 9 reports, 4 (44.4%) resulted in death, 5 (55.6%) required hospitalization, and 2 (22.2%) were considered life-threatening.
Is Pulseless electrical activity Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does DEVICE Cause?
Blood glucose increased (2,114)
Device issue (1,417)
Product use issue (1,076)
Intercepted product preparation error (1,033)
Wrong technique in product usage process (935)
Device leakage (795)
Injection site pain (751)
Syringe issue (634)
Product quality issue (567)
Drug ineffective (488)
What Other Drugs Cause Pulseless electrical activity?
METFORMIN (140)
PROPRANOLOL (136)
BUPROPION (135)
OXYCODONE (111)
LORAZEPAM (106)
PROPOFOL (104)
CITALOPRAM HYDROBROMIDE (101)
EPINEPHRINE (87)
FENTANYL (87)
AMLODIPINE (82)
Which DEVICE Alternatives Have Lower Pulseless electrical activity Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN