Does LIFITEGRAST Cause Condition aggravated? 195 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 195 reports of Condition aggravated have been filed in association with LIFITEGRAST (Xiidra). This represents 1.5% of all adverse event reports for LIFITEGRAST.
195
Reports of Condition aggravated with LIFITEGRAST
1.5%
of all LIFITEGRAST reports
0
Deaths
1
Hospitalizations
How Dangerous Is Condition aggravated From LIFITEGRAST?
Of the 195 reports, 1 (0.5%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LIFITEGRAST. However, 195 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 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 LIFITEGRAST Alternatives Have Lower Condition aggravated Risk?
LIFITEGRAST vs LIMAPROST
LIFITEGRAST vs LINACLOTIDE
LIFITEGRAST vs LINAGLIPTIN
LIFITEGRAST vs LINAGLIPTIN\METFORMIN
LIFITEGRAST vs LINCOMYCIN