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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DOMPERIDONE Cause Product prescribing error? 17 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Product prescribing error have been filed in association with DOMPERIDONE. This represents 0.4% of all adverse event reports for DOMPERIDONE.

17
Reports of Product prescribing error with DOMPERIDONE
0.4%
of all DOMPERIDONE reports
0
Deaths
17
Hospitalizations

How Dangerous Is Product prescribing error From DOMPERIDONE?

Of the 17 reports, 17 (100.0%) required hospitalization.

Is Product prescribing error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DOMPERIDONE. However, 17 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 prescribing error?

SOMATROPIN (1,123) SACUBITRIL\VALSARTAN (1,023) SECUKINUMAB (821) TOFACITINIB (805) DUPILUMAB (725) NIRMATRELVIR\RITONAVIR (611) PREGABALIN (476) METHOTREXATE (434) TORSEMIDE (352) METOPROLOL (325)

Which DOMPERIDONE Alternatives Have Lower Product prescribing error Risk?

DOMPERIDONE vs DOMPERIDONE\PANTOPRAZOLE DOMPERIDONE vs DONANEMAB-AZBT DOMPERIDONE vs DONEPEZIL DOMPERIDONE vs DONEPEZIL\DONEPEZIL DOMPERIDONE vs DONEPEZIL\MEMANTINE

Related Pages

DOMPERIDONE Full Profile All Product prescribing error Reports All Drugs Causing Product prescribing error DOMPERIDONE Demographics