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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 RESTASIS Cause Incorrect product storage? 22 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Incorrect product storage have been filed in association with RESTASIS. This represents 1.9% of all adverse event reports for RESTASIS.

22
Reports of Incorrect product storage with RESTASIS
1.9%
of all RESTASIS reports
0
Deaths
0
Hospitalizations

How Dangerous Is Incorrect product storage From RESTASIS?

Of the 22 reports.

Is Incorrect product storage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RESTASIS. However, 22 reports have been filed with the FAERS database.

What Other Side Effects Does RESTASIS Cause?

Eye irritation (440) Drug ineffective (181) Eye pain (172) Vision blurred (161) Ocular hyperaemia (137) Lacrimation increased (99) Foreign body sensation in eyes (92) Eye pruritus (79) Instillation site pain (73) Dry eye (68)

What Other Drugs Cause Incorrect product storage?

ETANERCEPT (2,149) INSULIN LISPRO (1,114) ABATACEPT (583) TERIPARATIDE (573) ADALIMUMAB (476) GOLIMUMAB (392) INSULIN GLARGINE (341) INSULIN HUMAN (336) USTEKINUMAB (299) ERYTHROPOIETIN (268)

Which RESTASIS Alternatives Have Lower Incorrect product storage Risk?

RESTASIS vs RETINOL RESTASIS vs REVATIO RESTASIS vs REVEFENACIN RESTASIS vs REVLIMID RESTASIS vs REVOLADE

Related Pages

RESTASIS Full Profile All Incorrect product storage Reports All Drugs Causing Incorrect product storage RESTASIS Demographics