Does PERFLUTREN Cause Product preparation error? 76 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 76 reports of Product preparation error have been filed in association with PERFLUTREN (DEFINITY RT). This represents 2.2% of all adverse event reports for PERFLUTREN.
76
Reports of Product preparation error with PERFLUTREN
2.2%
of all PERFLUTREN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product preparation error From PERFLUTREN?
Of the 76 reports, 1 (1.3%) required hospitalization.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PERFLUTREN. However, 76 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 preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
Which PERFLUTREN Alternatives Have Lower Product preparation error Risk?
PERFLUTREN vs PERICIAZINE
PERFLUTREN vs PERINDOPRIL
PERFLUTREN vs PERINDOPRIL ARGININE
PERFLUTREN vs PERINDOPRIL ERBUMINE
PERFLUTREN vs PERJETA