Does LUCENTIS Cause Product quality issue? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product quality issue have been filed in association with LUCENTIS. This represents 1.3% of all adverse event reports for LUCENTIS.
9
Reports of Product quality issue with LUCENTIS
1.3%
of all LUCENTIS reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product quality issue From LUCENTIS?
Of the 9 reports, 1 (11.1%) required hospitalization, and 1 (11.1%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LUCENTIS. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does LUCENTIS Cause?
Death (138)
Visual acuity reduced (98)
Vision blurred (64)
Cerebrovascular accident (54)
Off label use (54)
Eye pain (43)
Visual impairment (43)
Vitreous floaters (42)
Blindness (34)
Drug ineffective (33)
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 LUCENTIS Alternatives Have Lower Product quality issue Risk?
LUCENTIS vs LUCRIN DEPOT
LUCENTIS vs LUMASIRAN
LUCENTIS vs LUMATEPERONE
LUCENTIS vs LUMIGAN
LUCENTIS vs LUPRON DEPOT