Does ELTROMBOPAG OLAMINE Cause Intentional product use issue? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Intentional product use issue have been filed in association with ELTROMBOPAG OLAMINE (ELTROMBOPAG). This represents 0.2% of all adverse event reports for ELTROMBOPAG OLAMINE.
36
Reports of Intentional product use issue with ELTROMBOPAG OLAMINE
0.2%
of all ELTROMBOPAG OLAMINE reports
1
Deaths
17
Hospitalizations
How Dangerous Is Intentional product use issue From ELTROMBOPAG OLAMINE?
Of the 36 reports, 1 (2.8%) resulted in death, 17 (47.2%) required hospitalization, and 4 (11.1%) were considered life-threatening.
Is Intentional 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, 36 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which ELTROMBOPAG OLAMINE Alternatives Have Lower Intentional 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