Does REGADENOSON Cause Incorrect product storage? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Incorrect product storage have been filed in association with REGADENOSON (Regadenoson). This represents 0.3% of all adverse event reports for REGADENOSON.
9
Reports of Incorrect product storage with REGADENOSON
0.3%
of all REGADENOSON reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product storage From REGADENOSON?
Of the 9 reports.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REGADENOSON. However, 9 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 Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
Which REGADENOSON Alternatives Have Lower Incorrect product storage Risk?
REGADENOSON vs REGORAFENIB
REGADENOSON vs REGORAFENIB\REGORAFENIB
REGADENOSON vs RELATLIMAB
REGADENOSON vs RELPAX
REGADENOSON vs RELUGOLIX