Does PERFLUOROHEXYLOCTANE Cause Product complaint? 87 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 87 reports of Product complaint have been filed in association with PERFLUOROHEXYLOCTANE (MIEBO). This represents 10.0% of all adverse event reports for PERFLUOROHEXYLOCTANE.
87
Reports of Product complaint with PERFLUOROHEXYLOCTANE
10.0%
of all PERFLUOROHEXYLOCTANE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product complaint From PERFLUOROHEXYLOCTANE?
Of the 87 reports, 1 (1.1%) required hospitalization.
Is Product complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PERFLUOROHEXYLOCTANE. However, 87 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 use complaint (86)
Circumstance or information capable of leading to medication error (85)
Ocular hyperaemia (82)
Accidental exposure to product (75)
Exposure via skin contact (75)
What Other Drugs Cause Product complaint?
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417)
ALBUTEROL (2,291)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826)
FLUTICASONE\SALMETEROL (1,601)
MEPOLIZUMAB (1,296)
FLUTICASONE (1,112)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108)
BELIMUMAB (1,079)
SUMATRIPTAN (718)
NICOTINE (700)
Which PERFLUOROHEXYLOCTANE Alternatives Have Lower Product complaint Risk?
PERFLUOROHEXYLOCTANE vs PERFLUTREN
PERFLUOROHEXYLOCTANE vs PERICIAZINE
PERFLUOROHEXYLOCTANE vs PERINDOPRIL
PERFLUOROHEXYLOCTANE vs PERINDOPRIL ARGININE
PERFLUOROHEXYLOCTANE vs PERINDOPRIL ERBUMINE