Does REGADENOSON Cause Product administration error? 5 Reports in FDA Database
Lower Your Cholesterol — The Natural Way
The Oxidized Cholesterol Strategy: a science-backed plan for heart health.
According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product administration error have been filed in association with REGADENOSON (Regadenoson). This represents 0.2% of all adverse event reports for REGADENOSON.
5
Reports of Product administration error with REGADENOSON
0.2%
of all REGADENOSON reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From REGADENOSON?
Of the 5 reports.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REGADENOSON. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does REGADENOSON Cause?
Nausea (311)
Dyspnoea (271)
Seizure (247)
Vomiting (233)
Injection site extravasation (226)
Hypotension (200)
Headache (190)
Cardiac arrest (183)
Dizziness (160)
Blood pressure decreased (143)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which REGADENOSON Alternatives Have Lower Product administration error Risk?
REGADENOSON vs REGORAFENIB
REGADENOSON vs REGORAFENIB\REGORAFENIB
REGADENOSON vs RELATLIMAB
REGADENOSON vs RELPAX
REGADENOSON vs RELUGOLIX