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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 LIFITEGRAST Cause Product complaint? 41 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 41 reports of Product complaint have been filed in association with LIFITEGRAST (Xiidra). This represents 0.3% of all adverse event reports for LIFITEGRAST.

41
Reports of Product complaint with LIFITEGRAST
0.3%
of all LIFITEGRAST reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product complaint From LIFITEGRAST?

Of the 41 reports, and 1 (2.4%) were considered life-threatening.

Is Product complaint Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LIFITEGRAST. However, 41 reports have been filed with the FAERS database.

What Other Side Effects Does LIFITEGRAST Cause?

Eye irritation (2,486) Vision blurred (2,465) Drug ineffective (1,373) Instillation site pain (1,281) Dysgeusia (1,067) Eye pain (1,032) Instillation site reaction (1,019) Dry eye (1,013) Ocular hyperaemia (570) Lacrimation increased (547)

What Other Drugs Cause Product complaint?

FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417) ALBUTEROL (2,291) FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826) FLUTICASONE\SALMETEROL (1,601) MEPOLIZUMAB (1,296) FLUTICASONE (1,112) UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108) BELIMUMAB (1,079) SUMATRIPTAN (718) NICOTINE (700)

Which LIFITEGRAST Alternatives Have Lower Product complaint Risk?

LIFITEGRAST vs LIMAPROST LIFITEGRAST vs LINACLOTIDE LIFITEGRAST vs LINAGLIPTIN LIFITEGRAST vs LINAGLIPTIN\METFORMIN LIFITEGRAST vs LINCOMYCIN

Related Pages

LIFITEGRAST Full Profile All Product complaint Reports All Drugs Causing Product complaint LIFITEGRAST Demographics