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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 IDELALISIB Cause Product prescribing error? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product prescribing error have been filed in association with IDELALISIB (Zydelig). This represents 0.1% of all adverse event reports for IDELALISIB.

6
Reports of Product prescribing error with IDELALISIB
0.1%
of all IDELALISIB reports
4
Deaths
6
Hospitalizations

How Dangerous Is Product prescribing error From IDELALISIB?

Of the 6 reports, 4 (66.7%) resulted in death, 6 (100.0%) required hospitalization, and 6 (100.0%) were considered life-threatening.

Is Product prescribing error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for IDELALISIB. However, 6 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 prescribing error?

SOMATROPIN (1,123) SACUBITRIL\VALSARTAN (1,023) SECUKINUMAB (821) TOFACITINIB (805) DUPILUMAB (725) NIRMATRELVIR\RITONAVIR (611) PREGABALIN (476) METHOTREXATE (434) TORSEMIDE (352) METOPROLOL (325)

Which IDELALISIB Alternatives Have Lower Product prescribing error Risk?

IDELALISIB vs IDURSULFASE IDELALISIB vs IFOSFAMIDE IDELALISIB vs IGURATIMOD IDELALISIB vs ILOPERIDONE IDELALISIB vs ILOPROST

Related Pages

IDELALISIB Full Profile All Product prescribing error Reports All Drugs Causing Product prescribing error IDELALISIB Demographics