Does CYCLOSPORINE Cause Product quality issue? 240 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 240 reports of Product quality issue have been filed in association with CYCLOSPORINE (Verkazia). This represents 0.4% of all adverse event reports for CYCLOSPORINE.
240
Reports of Product quality issue with CYCLOSPORINE
0.4%
of all CYCLOSPORINE reports
5
Deaths
8
Hospitalizations
How Dangerous Is Product quality issue From CYCLOSPORINE?
Of the 240 reports, 5 (2.1%) resulted in death, 8 (3.3%) required hospitalization, and 6 (2.5%) 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 CYCLOSPORINE. However, 240 reports have been filed with the FAERS database.
What Other Side Effects Does CYCLOSPORINE Cause?
Drug ineffective (11,172)
Off label use (6,860)
Eye irritation (5,806)
Product use in unapproved indication (5,019)
Condition aggravated (2,310)
Eye pain (2,197)
Drug intolerance (2,176)
Pneumonia (2,022)
Pyrexia (2,020)
Treatment failure (1,961)
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 CYCLOSPORINE Alternatives Have Lower Product quality issue Risk?
CYCLOSPORINE vs CYCLOSPORINE A
CYCLOSPORINE vs CYMBALTA
CYCLOSPORINE vs CYNODON DACTYLON POLLEN
CYCLOSPORINE vs CYPROHEPTADINE
CYCLOSPORINE vs CYPROTERONE