Does RANIBIZUMAB Cause Device issue? 86 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 86 reports of Device issue have been filed in association with RANIBIZUMAB (CIMERLI). This represents 0.6% of all adverse event reports for RANIBIZUMAB.
86
Reports of Device issue with RANIBIZUMAB
0.6%
of all RANIBIZUMAB reports
1
Deaths
6
Hospitalizations
How Dangerous Is Device issue From RANIBIZUMAB?
Of the 86 reports, 1 (1.2%) resulted in death, 6 (7.0%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RANIBIZUMAB. However, 86 reports have been filed with the FAERS database.
What Other Side Effects Does RANIBIZUMAB Cause?
Death (2,250)
Off label use (1,467)
Visual acuity reduced (1,342)
Visual impairment (1,185)
No adverse event (1,012)
Drug ineffective (831)
Blindness (760)
Vision blurred (711)
Eye pain (632)
Cerebrovascular accident (543)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which RANIBIZUMAB Alternatives Have Lower Device issue Risk?
RANIBIZUMAB vs RANIMUSTINE
RANIBIZUMAB vs RANITIDINE
RANIBIZUMAB vs RANITIDINE\RANITIDINE
RANIBIZUMAB vs RANOLAZINE
RANIBIZUMAB vs RAPAMUNE