Does NETARSUDIL Cause Product storage error? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product storage error have been filed in association with NETARSUDIL (Rhopressa). This represents 0.9% of all adverse event reports for NETARSUDIL.
11
Reports of Product storage error with NETARSUDIL
0.9%
of all NETARSUDIL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product storage error From NETARSUDIL?
Of the 11 reports.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NETARSUDIL. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does NETARSUDIL Cause?
Conjunctival hyperaemia (240)
Vision blurred (129)
Off label use (114)
Ocular hyperaemia (109)
Corneal oedema (94)
Visual acuity reduced (86)
Eye irritation (75)
Intraocular pressure increased (64)
Lacrimation increased (64)
Cornea verticillata (59)
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 NETARSUDIL Alternatives Have Lower Product storage error Risk?
NETARSUDIL vs NETUPITANT\PALONOSETRON
NETARSUDIL vs NEULASTA
NETARSUDIL vs NEUPOGEN
NETARSUDIL vs NEUPRO
NETARSUDIL vs NEURONTIN