Does ISTRADEFYLLINE Cause Product dose omission issue? 299 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 299 reports of Product dose omission issue have been filed in association with ISTRADEFYLLINE (NOURIANZ). This represents 6.0% of all adverse event reports for ISTRADEFYLLINE.
299
Reports of Product dose omission issue with ISTRADEFYLLINE
6.0%
of all ISTRADEFYLLINE reports
8
Deaths
39
Hospitalizations
How Dangerous Is Product dose omission issue From ISTRADEFYLLINE?
Of the 299 reports, 8 (2.7%) resulted in death, 39 (13.0%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ISTRADEFYLLINE. However, 299 reports have been filed with the FAERS database.
What Other Side Effects Does ISTRADEFYLLINE Cause?
Death (571)
Drug ineffective (551)
Hallucination (462)
Dyskinesia (428)
Dizziness (387)
Condition aggravated (384)
Constipation (317)
Fall (260)
Therapy non-responder (251)
Tremor (226)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which ISTRADEFYLLINE Alternatives Have Lower Product dose omission issue Risk?
ISTRADEFYLLINE vs ITACITINIB
ISTRADEFYLLINE vs ITRACONAZOLE
ISTRADEFYLLINE vs ITRACONAZOLE\SODIUM
ISTRADEFYLLINE vs IVABRADINE
ISTRADEFYLLINE vs IVACAFTOR