Does DIFLUPREDNATE Cause Product container issue? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product container issue have been filed in association with DIFLUPREDNATE (Difluprednate). This represents 0.4% of all adverse event reports for DIFLUPREDNATE.
6
Reports of Product container issue with DIFLUPREDNATE
0.4%
of all DIFLUPREDNATE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product container issue From DIFLUPREDNATE?
Of the 6 reports.
Is Product container issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIFLUPREDNATE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does DIFLUPREDNATE Cause?
Intraocular pressure increased (478)
Drug ineffective (139)
Therapy partial responder (100)
Vision blurred (94)
Eye irritation (92)
Eye pain (87)
Visual impairment (84)
Treatment failure (58)
Blindness (49)
Cataract (48)
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 DIFLUPREDNATE Alternatives Have Lower Product container issue Risk?
DIFLUPREDNATE vs DIGITOXIN
DIFLUPREDNATE vs DIGOXIN
DIFLUPREDNATE vs DIHYDRALAZINE
DIFLUPREDNATE vs DIHYDROCODEINE
DIFLUPREDNATE vs DIHYDROERGOTAMINE