Does PERFLUOROHEXYLOCTANE Cause Product dose omission in error? 25 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Product dose omission in error have been filed in association with PERFLUOROHEXYLOCTANE (MIEBO). This represents 2.9% of all adverse event reports for PERFLUOROHEXYLOCTANE.
25
Reports of Product dose omission in error with PERFLUOROHEXYLOCTANE
2.9%
of all PERFLUOROHEXYLOCTANE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission in error From PERFLUOROHEXYLOCTANE?
Of the 25 reports.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PERFLUOROHEXYLOCTANE. However, 25 reports have been filed with the FAERS database.
What Other Side Effects Does PERFLUOROHEXYLOCTANE Cause?
Inappropriate schedule of product administration (135)
Vision blurred (132)
Product delivery mechanism issue (122)
Eye irritation (110)
Product use issue (110)
Product complaint (87)
Product use complaint (86)
Circumstance or information capable of leading to medication error (85)
Ocular hyperaemia (82)
Accidental exposure to product (75)
What Other Drugs Cause Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which PERFLUOROHEXYLOCTANE Alternatives Have Lower Product dose omission in error Risk?
PERFLUOROHEXYLOCTANE vs PERFLUTREN
PERFLUOROHEXYLOCTANE vs PERICIAZINE
PERFLUOROHEXYLOCTANE vs PERINDOPRIL
PERFLUOROHEXYLOCTANE vs PERINDOPRIL ARGININE
PERFLUOROHEXYLOCTANE vs PERINDOPRIL ERBUMINE