Does ELTROMBOPAG OLAMINE Cause Product prescribing error? 42 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 42 reports of Product prescribing error have been filed in association with ELTROMBOPAG OLAMINE (ELTROMBOPAG). This represents 0.3% of all adverse event reports for ELTROMBOPAG OLAMINE.
42
Reports of Product prescribing error with ELTROMBOPAG OLAMINE
0.3%
of all ELTROMBOPAG OLAMINE reports
4
Deaths
20
Hospitalizations
How Dangerous Is Product prescribing error From ELTROMBOPAG OLAMINE?
Of the 42 reports, 4 (9.5%) resulted in death, 20 (47.6%) required hospitalization, and 3 (7.1%) 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 ELTROMBOPAG OLAMINE. However, 42 reports have been filed with the FAERS database.
What Other Side Effects Does ELTROMBOPAG OLAMINE Cause?
Platelet count decreased (3,419)
Death (2,797)
Drug ineffective (1,117)
Platelet count increased (980)
Fatigue (868)
Headache (750)
Nausea (584)
Diarrhoea (558)
Product use in unapproved indication (545)
Malaise (516)
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 ELTROMBOPAG OLAMINE Alternatives Have Lower Product prescribing error Risk?
ELTROMBOPAG OLAMINE vs ELUXADOLINE
ELTROMBOPAG OLAMINE vs ELVITEGRAVIR
ELTROMBOPAG OLAMINE vs EMAPALUMAB
ELTROMBOPAG OLAMINE vs EMAPALUMAB-LZSG
ELTROMBOPAG OLAMINE vs EMEND