Does LATANOPROST Cause Product administration error? 33 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Product administration error have been filed in association with LATANOPROST (IYUZEH). This represents 0.2% of all adverse event reports for LATANOPROST.
33
Reports of Product administration error with LATANOPROST
0.2%
of all LATANOPROST reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product administration error From LATANOPROST?
Of the 33 reports, 2 (6.1%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LATANOPROST. However, 33 reports have been filed with the FAERS database.
What Other Side Effects Does LATANOPROST Cause?
Treatment failure (5,781)
Drug ineffective (1,338)
Eye irritation (1,165)
Eye pain (668)
Hypersensitivity (668)
Ocular hyperaemia (587)
Intraocular pressure increased (579)
Vision blurred (564)
Cataract (546)
Visual impairment (382)
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 LATANOPROST Alternatives Have Lower Product administration error Risk?
LATANOPROST vs LATANOPROSTENE BUNOD
LATANOPROST vs LATANOPROST\NETARSUDIL
LATANOPROST vs LATANOPROST\TIMOLOL
LATANOPROST vs LATISSE
LATANOPROST vs LATUDA