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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DIFLUPREDNATE Cause Product administration error? 13 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product administration error have been filed in association with DIFLUPREDNATE (Difluprednate). This represents 0.8% of all adverse event reports for DIFLUPREDNATE.

13
Reports of Product administration error with DIFLUPREDNATE
0.8%
of all DIFLUPREDNATE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product administration error From DIFLUPREDNATE?

Of the 13 reports.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DIFLUPREDNATE. However, 13 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 administration error?

HYDROXYPROGESTERONE CAPROATE (972) ACETAMINOPHEN (666) CENEGERMIN-BKBJ (613) LEUPROLIDE (595) EVOLOCUMAB (565) ADALIMUMAB (543) METHYLPHENIDATE (414) OLMESARTAN MEDOXOMIL (314) ASPIRIN (241) SECUKINUMAB (225)

Which DIFLUPREDNATE Alternatives Have Lower Product administration error Risk?

DIFLUPREDNATE vs DIGITOXIN DIFLUPREDNATE vs DIGOXIN DIFLUPREDNATE vs DIHYDRALAZINE DIFLUPREDNATE vs DIHYDROCODEINE DIFLUPREDNATE vs DIHYDROERGOTAMINE

Related Pages

DIFLUPREDNATE Full Profile All Product administration error Reports All Drugs Causing Product administration error DIFLUPREDNATE Demographics