Does IDELALISIB Cause Product dose omission? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Product dose omission have been filed in association with IDELALISIB (Zydelig). This represents 0.3% of all adverse event reports for IDELALISIB.
18
Reports of Product dose omission with IDELALISIB
0.3%
of all IDELALISIB reports
1
Deaths
13
Hospitalizations
How Dangerous Is Product dose omission From IDELALISIB?
Of the 18 reports, 1 (5.6%) resulted in death, 13 (72.2%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IDELALISIB. However, 18 reports have been filed with the FAERS database.
What Other Side Effects Does IDELALISIB Cause?
Disease progression (1,204)
Death (779)
Diarrhoea (752)
Off label use (548)
Pneumonia (426)
Pyrexia (371)
Drug ineffective (294)
Fatigue (284)
Dehydration (242)
Dyspnoea (206)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which IDELALISIB Alternatives Have Lower Product dose omission Risk?
IDELALISIB vs IDURSULFASE
IDELALISIB vs IFOSFAMIDE
IDELALISIB vs IGURATIMOD
IDELALISIB vs ILOPERIDONE
IDELALISIB vs ILOPROST