Does LATANOPROST\NETARSUDIL Cause Product container issue? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product container issue have been filed in association with LATANOPROST\NETARSUDIL. This represents 1.3% of all adverse event reports for LATANOPROST\NETARSUDIL.
8
Reports of Product container issue with LATANOPROST\NETARSUDIL
1.3%
of all LATANOPROST\NETARSUDIL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product container issue From LATANOPROST\NETARSUDIL?
Of the 8 reports.
Is Product container issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LATANOPROST\NETARSUDIL. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does LATANOPROST\NETARSUDIL Cause?
Conjunctival hyperaemia (98)
Ocular hyperaemia (96)
Eye irritation (76)
Vision blurred (76)
Lacrimation increased (53)
Eye pruritus (50)
Eye pain (37)
Intraocular pressure increased (36)
Product dose omission issue (31)
Conjunctival haemorrhage (28)
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 LATANOPROST\NETARSUDIL Alternatives Have Lower Product container issue Risk?
LATANOPROST\NETARSUDIL vs LATANOPROST\TIMOLOL
LATANOPROST\NETARSUDIL vs LATISSE
LATANOPROST\NETARSUDIL vs LATUDA
LATANOPROST\NETARSUDIL vs LAZERTINIB
LATANOPROST\NETARSUDIL vs LEBRIKIZUMAB-LBKZ