Does ELTROMBOPAG OLAMINE Cause Product use issue? 165 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 165 reports of Product use issue have been filed in association with ELTROMBOPAG OLAMINE (ELTROMBOPAG). This represents 1.0% of all adverse event reports for ELTROMBOPAG OLAMINE.
165
Reports of Product use issue with ELTROMBOPAG OLAMINE
1.0%
of all ELTROMBOPAG OLAMINE reports
26
Deaths
34
Hospitalizations
How Dangerous Is Product use issue From ELTROMBOPAG OLAMINE?
Of the 165 reports, 26 (15.8%) resulted in death, 34 (20.6%) required hospitalization, and 9 (5.5%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ELTROMBOPAG OLAMINE. However, 165 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 use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which ELTROMBOPAG OLAMINE Alternatives Have Lower Product use issue Risk?
ELTROMBOPAG OLAMINE vs ELUXADOLINE
ELTROMBOPAG OLAMINE vs ELVITEGRAVIR
ELTROMBOPAG OLAMINE vs EMAPALUMAB
ELTROMBOPAG OLAMINE vs EMAPALUMAB-LZSG
ELTROMBOPAG OLAMINE vs EMEND