Does LIFITEGRAST Cause Product use issue? 171 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 171 reports of Product use issue have been filed in association with LIFITEGRAST (Xiidra). This represents 1.3% of all adverse event reports for LIFITEGRAST.
171
Reports of Product use issue with LIFITEGRAST
1.3%
of all LIFITEGRAST reports
1
Deaths
26
Hospitalizations
How Dangerous Is Product use issue From LIFITEGRAST?
Of the 171 reports, 1 (0.6%) resulted in death, 26 (15.2%) required hospitalization.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LIFITEGRAST. However, 171 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 issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which LIFITEGRAST Alternatives Have Lower Product use issue Risk?
LIFITEGRAST vs LIMAPROST
LIFITEGRAST vs LINACLOTIDE
LIFITEGRAST vs LINAGLIPTIN
LIFITEGRAST vs LINAGLIPTIN\METFORMIN
LIFITEGRAST vs LINCOMYCIN