Does DOMPERIDONE Cause Intentional product use issue? 585 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 585 reports of Intentional product use issue have been filed in association with DOMPERIDONE. This represents 12.9% of all adverse event reports for DOMPERIDONE.
585
Reports of Intentional product use issue with DOMPERIDONE
12.9%
of all DOMPERIDONE reports
582
Deaths
490
Hospitalizations
How Dangerous Is Intentional product use issue From DOMPERIDONE?
Of the 585 reports, 582 (99.5%) resulted in death, 490 (83.8%) required hospitalization, and 496 (84.8%) 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 DOMPERIDONE. However, 585 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 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 DOMPERIDONE Alternatives Have Lower Intentional product use issue Risk?
DOMPERIDONE vs DOMPERIDONE\PANTOPRAZOLE
DOMPERIDONE vs DONANEMAB-AZBT
DOMPERIDONE vs DONEPEZIL
DOMPERIDONE vs DONEPEZIL\DONEPEZIL
DOMPERIDONE vs DONEPEZIL\MEMANTINE