Does LIFITEGRAST Cause Product use complaint? 326 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 326 reports of Product use complaint have been filed in association with LIFITEGRAST (Xiidra). This represents 2.4% of all adverse event reports for LIFITEGRAST.
326
Reports of Product use complaint with LIFITEGRAST
2.4%
of all LIFITEGRAST reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product use complaint From LIFITEGRAST?
Of the 326 reports, 3 (0.9%) required hospitalization.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LIFITEGRAST. However, 326 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 use complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
DIMETHICONE\LOPERAMIDE (201)
Which LIFITEGRAST Alternatives Have Lower Product use complaint Risk?
LIFITEGRAST vs LIMAPROST
LIFITEGRAST vs LINACLOTIDE
LIFITEGRAST vs LINAGLIPTIN
LIFITEGRAST vs LINAGLIPTIN\METFORMIN
LIFITEGRAST vs LINCOMYCIN