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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does CYCLOSPORINE Cause Product container issue? 910 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 910 reports of Product container issue have been filed in association with CYCLOSPORINE (Verkazia). This represents 1.3% of all adverse event reports for CYCLOSPORINE.

910
Reports of Product container issue with CYCLOSPORINE
1.3%
of all CYCLOSPORINE reports
0
Deaths
4
Hospitalizations

How Dangerous Is Product container issue From CYCLOSPORINE?

Of the 910 reports, 4 (0.4%) required hospitalization.

Is Product container issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CYCLOSPORINE. However, 910 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 container issue?

MINOXIDIL (556) MOMETASONE FUROATE (450) FORMOTEROL\MOMETASONE FUROATE (375) LIFITEGRAST (244) ALBUTEROL (192) LATANOPROST (158) CARBOXYMETHYLCELLULOSE\GLYCERIN (123) BRIMONIDINE (121) ACETAMINOPHEN (118) CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (102)

Which CYCLOSPORINE Alternatives Have Lower Product container issue Risk?

CYCLOSPORINE vs CYCLOSPORINE A CYCLOSPORINE vs CYMBALTA CYCLOSPORINE vs CYNODON DACTYLON POLLEN CYCLOSPORINE vs CYPROHEPTADINE CYCLOSPORINE vs CYPROTERONE

Related Pages

CYCLOSPORINE Full Profile All Product container issue Reports All Drugs Causing Product container issue CYCLOSPORINE Demographics