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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 quality issue? 437 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 437 reports of Product quality issue have been filed in association with DOMPERIDONE. This represents 9.7% of all adverse event reports for DOMPERIDONE.

437
Reports of Product quality issue with DOMPERIDONE
9.7%
of all DOMPERIDONE reports
435
Deaths
356
Hospitalizations

How Dangerous Is Product quality issue From DOMPERIDONE?

Of the 437 reports, 435 (99.5%) resulted in death, 356 (81.5%) required hospitalization, and 362 (82.8%) were considered life-threatening.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DOMPERIDONE. However, 437 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 quality issue?

ETONOGESTREL (4,651) ALBUTEROL (4,466) TIOTROPIUM (3,821) MOMETASONE FUROATE (3,406) LIDOCAINE (3,126) FLUTICASONE\SALMETEROL (2,986) FORMOTEROL\MOMETASONE FUROATE (2,458) FENTANYL (2,450) NICOTINE (1,987) EXENATIDE (1,839)

Which DOMPERIDONE Alternatives Have Lower Product quality issue 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 quality issue Reports All Drugs Causing Product quality issue DOMPERIDONE Demographics