Does ELTROMBOPAG OLAMINE Cause Product use complaint? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product use complaint have been filed in association with ELTROMBOPAG OLAMINE (ELTROMBOPAG). This represents 0.1% of all adverse event reports for ELTROMBOPAG OLAMINE.
10
Reports of Product use complaint with ELTROMBOPAG OLAMINE
0.1%
of all ELTROMBOPAG OLAMINE reports
1
Deaths
1
Hospitalizations
How Dangerous Is Product use complaint From ELTROMBOPAG OLAMINE?
Of the 10 reports, 1 (10.0%) resulted in death, 1 (10.0%) required hospitalization.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ELTROMBOPAG OLAMINE. However, 10 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 complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
Which ELTROMBOPAG OLAMINE Alternatives Have Lower Product use complaint Risk?
ELTROMBOPAG OLAMINE vs ELUXADOLINE
ELTROMBOPAG OLAMINE vs ELVITEGRAVIR
ELTROMBOPAG OLAMINE vs EMAPALUMAB
ELTROMBOPAG OLAMINE vs EMAPALUMAB-LZSG
ELTROMBOPAG OLAMINE vs EMEND