Does DOMPERIDONE Cause Incorrect product administration duration? 64 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 64 reports of Incorrect product administration duration have been filed in association with DOMPERIDONE. This represents 1.4% of all adverse event reports for DOMPERIDONE.
64
Reports of Incorrect product administration duration with DOMPERIDONE
1.4%
of all DOMPERIDONE reports
64
Deaths
63
Hospitalizations
How Dangerous Is Incorrect product administration duration From DOMPERIDONE?
Of the 64 reports, 64 (100.0%) resulted in death, 63 (98.4%) required hospitalization, and 63 (98.4%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOMPERIDONE. However, 64 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which DOMPERIDONE Alternatives Have Lower Incorrect product administration duration Risk?
DOMPERIDONE vs DOMPERIDONE\PANTOPRAZOLE
DOMPERIDONE vs DONANEMAB-AZBT
DOMPERIDONE vs DONEPEZIL
DOMPERIDONE vs DONEPEZIL\DONEPEZIL
DOMPERIDONE vs DONEPEZIL\MEMANTINE