Does DOMPERIDONE Cause Product dose omission issue? 102 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 102 reports of Product dose omission issue have been filed in association with DOMPERIDONE. This represents 2.3% of all adverse event reports for DOMPERIDONE.
102
Reports of Product dose omission issue with DOMPERIDONE
2.3%
of all DOMPERIDONE reports
25
Deaths
100
Hospitalizations
How Dangerous Is Product dose omission issue From DOMPERIDONE?
Of the 102 reports, 25 (24.5%) resulted in death, 100 (98.0%) required hospitalization, and 25 (24.5%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOMPERIDONE. However, 102 reports have been filed with the FAERS database.
What Other Side Effects Does DOMPERIDONE Cause?
Off label use (1,156)
Vomiting (918)
Condition aggravated (902)
Abdominal pain upper (898)
Dyspnoea (859)
Dizziness (858)
Drug ineffective (850)
Asthenia (835)
Arthralgia (827)
Fatigue (814)
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 DOMPERIDONE Alternatives Have Lower Product dose omission issue Risk?
DOMPERIDONE vs DOMPERIDONE\PANTOPRAZOLE
DOMPERIDONE vs DONANEMAB-AZBT
DOMPERIDONE vs DONEPEZIL
DOMPERIDONE vs DONEPEZIL\DONEPEZIL
DOMPERIDONE vs DONEPEZIL\MEMANTINE