Does PERFLUOROHEXYLOCTANE Cause Product container issue? 45 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Product container issue have been filed in association with PERFLUOROHEXYLOCTANE (MIEBO). This represents 5.2% of all adverse event reports for PERFLUOROHEXYLOCTANE.
45
Reports of Product container issue with PERFLUOROHEXYLOCTANE
5.2%
of all PERFLUOROHEXYLOCTANE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product container issue From PERFLUOROHEXYLOCTANE?
Of the 45 reports, 1 (2.2%) required hospitalization.
Is Product container issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PERFLUOROHEXYLOCTANE. However, 45 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 container issue?
CYCLOSPORINE (910)
MINOXIDIL (556)
MOMETASONE FUROATE (450)
FORMOTEROL\MOMETASONE FUROATE (375)
LIFITEGRAST (244)
ALBUTEROL (192)
LATANOPROST (158)
CARBOXYMETHYLCELLULOSE\GLYCERIN (123)
BRIMONIDINE (121)
ACETAMINOPHEN (118)
Which PERFLUOROHEXYLOCTANE Alternatives Have Lower Product container issue Risk?
PERFLUOROHEXYLOCTANE vs PERFLUTREN
PERFLUOROHEXYLOCTANE vs PERICIAZINE
PERFLUOROHEXYLOCTANE vs PERINDOPRIL
PERFLUOROHEXYLOCTANE vs PERINDOPRIL ARGININE
PERFLUOROHEXYLOCTANE vs PERINDOPRIL ERBUMINE