Does LATANOPROST\NETARSUDIL Cause Product storage error? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product storage error have been filed in association with LATANOPROST\NETARSUDIL. This represents 1.3% of all adverse event reports for LATANOPROST\NETARSUDIL.
8
Reports of Product storage error with LATANOPROST\NETARSUDIL
1.3%
of all LATANOPROST\NETARSUDIL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product storage error From LATANOPROST\NETARSUDIL?
Of the 8 reports.
Is Product storage error 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 storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which LATANOPROST\NETARSUDIL Alternatives Have Lower Product storage error Risk?
LATANOPROST\NETARSUDIL vs LATANOPROST\TIMOLOL
LATANOPROST\NETARSUDIL vs LATISSE
LATANOPROST\NETARSUDIL vs LATUDA
LATANOPROST\NETARSUDIL vs LAZERTINIB
LATANOPROST\NETARSUDIL vs LEBRIKIZUMAB-LBKZ