Does PERFLUTREN Cause Product administration error? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Product administration error have been filed in association with PERFLUTREN (DEFINITY RT). This represents 0.9% of all adverse event reports for PERFLUTREN.
30
Reports of Product administration error with PERFLUTREN
0.9%
of all PERFLUTREN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From PERFLUTREN?
Of the 30 reports.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PERFLUTREN. However, 30 reports have been filed with the FAERS database.
What Other Side Effects Does PERFLUTREN Cause?
Back pain (1,350)
Muscle spasms (604)
Dyspnoea (551)
Pain in extremity (397)
Flushing (263)
Chest pain (254)
Neck pain (249)
Headache (248)
Dizziness (232)
Nausea (177)
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 PERFLUTREN Alternatives Have Lower Product administration error Risk?
PERFLUTREN vs PERICIAZINE
PERFLUTREN vs PERINDOPRIL
PERFLUTREN vs PERINDOPRIL ARGININE
PERFLUTREN vs PERINDOPRIL ERBUMINE
PERFLUTREN vs PERJETA