Does LIFITEGRAST Cause Product quality issue? 341 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 341 reports of Product quality issue have been filed in association with LIFITEGRAST (Xiidra). This represents 2.5% of all adverse event reports for LIFITEGRAST.
341
Reports of Product quality issue with LIFITEGRAST
2.5%
of all LIFITEGRAST reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product quality issue From LIFITEGRAST?
Of the 341 reports, 3 (0.9%) required hospitalization.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LIFITEGRAST. However, 341 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which LIFITEGRAST Alternatives Have Lower Product quality issue Risk?
LIFITEGRAST vs LIMAPROST
LIFITEGRAST vs LINACLOTIDE
LIFITEGRAST vs LINAGLIPTIN
LIFITEGRAST vs LINAGLIPTIN\METFORMIN
LIFITEGRAST vs LINCOMYCIN