Does PERFLUOROHEXYLOCTANE Cause Intentional dose omission? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Intentional dose omission have been filed in association with PERFLUOROHEXYLOCTANE (MIEBO). This represents 0.7% of all adverse event reports for PERFLUOROHEXYLOCTANE.
6
Reports of Intentional dose omission with PERFLUOROHEXYLOCTANE
0.7%
of all PERFLUOROHEXYLOCTANE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Intentional dose omission From PERFLUOROHEXYLOCTANE?
Of the 6 reports, 2 (33.3%) required hospitalization.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PERFLUOROHEXYLOCTANE. However, 6 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 Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which PERFLUOROHEXYLOCTANE Alternatives Have Lower Intentional dose omission Risk?
PERFLUOROHEXYLOCTANE vs PERFLUTREN
PERFLUOROHEXYLOCTANE vs PERICIAZINE
PERFLUOROHEXYLOCTANE vs PERINDOPRIL
PERFLUOROHEXYLOCTANE vs PERINDOPRIL ARGININE
PERFLUOROHEXYLOCTANE vs PERINDOPRIL ERBUMINE