Does ABEMACICLIB Cause Product dose omission issue? 333 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 333 reports of Product dose omission issue have been filed in association with ABEMACICLIB (Verzenio). This represents 2.0% of all adverse event reports for ABEMACICLIB.
333
Reports of Product dose omission issue with ABEMACICLIB
2.0%
of all ABEMACICLIB reports
0
Deaths
21
Hospitalizations
How Dangerous Is Product dose omission issue From ABEMACICLIB?
Of the 333 reports, 21 (6.3%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABEMACICLIB. However, 333 reports have been filed with the FAERS database.
What Other Side Effects Does ABEMACICLIB Cause?
Diarrhoea (4,988)
Fatigue (1,878)
Nausea (1,682)
Vomiting (943)
Malignant neoplasm progression (890)
Decreased appetite (744)
Death (696)
Asthenia (678)
Drug ineffective (668)
White blood cell count decreased (566)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which ABEMACICLIB Alternatives Have Lower Product dose omission issue Risk?
ABEMACICLIB vs ABILIFY
ABEMACICLIB vs ABIRATERONE
ABEMACICLIB vs ABIRATERONE\ABIRATERONE
ABEMACICLIB vs ABOBOTULINUMTOXINA
ABEMACICLIB vs ABRAXANE