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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 NETARSUDIL Cause Condition aggravated? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Condition aggravated have been filed in association with NETARSUDIL (Rhopressa). This represents 0.6% of all adverse event reports for NETARSUDIL.

7
Reports of Condition aggravated with NETARSUDIL
0.6%
of all NETARSUDIL reports
0
Deaths
0
Hospitalizations

How Dangerous Is Condition aggravated From NETARSUDIL?

Of the 7 reports.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NETARSUDIL. However, 7 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which NETARSUDIL Alternatives Have Lower Condition aggravated Risk?

NETARSUDIL vs NETUPITANT\PALONOSETRON NETARSUDIL vs NEULASTA NETARSUDIL vs NEUPOGEN NETARSUDIL vs NEUPRO NETARSUDIL vs NEURONTIN

Related Pages

NETARSUDIL Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated NETARSUDIL Demographics