Does LIFITEGRAST Cause Product container issue? 244 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 244 reports of Product container issue have been filed in association with LIFITEGRAST (Xiidra). This represents 1.8% of all adverse event reports for LIFITEGRAST.
244
Reports of Product container issue with LIFITEGRAST
1.8%
of all LIFITEGRAST reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product container issue From LIFITEGRAST?
Of the 244 reports.
Is Product container issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LIFITEGRAST. However, 244 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 container issue?
CYCLOSPORINE (910)
MINOXIDIL (556)
MOMETASONE FUROATE (450)
FORMOTEROL\MOMETASONE FUROATE (375)
ALBUTEROL (192)
LATANOPROST (158)
CARBOXYMETHYLCELLULOSE\GLYCERIN (123)
BRIMONIDINE (121)
ACETAMINOPHEN (118)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (102)
Which LIFITEGRAST Alternatives Have Lower Product container issue Risk?
LIFITEGRAST vs LIMAPROST
LIFITEGRAST vs LINACLOTIDE
LIFITEGRAST vs LINAGLIPTIN
LIFITEGRAST vs LINAGLIPTIN\METFORMIN
LIFITEGRAST vs LINCOMYCIN