Does DOMPERIDONE Cause Maternal exposure timing unspecified? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Maternal exposure timing unspecified have been filed in association with DOMPERIDONE. This represents 0.5% of all adverse event reports for DOMPERIDONE.
23
Reports of Maternal exposure timing unspecified with DOMPERIDONE
0.5%
of all DOMPERIDONE reports
23
Deaths
23
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From DOMPERIDONE?
Of the 23 reports, 23 (100.0%) resulted in death, 23 (100.0%) required hospitalization, and 23 (100.0%) were considered life-threatening.
Is Maternal exposure timing unspecified Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOMPERIDONE. However, 23 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 Maternal exposure timing unspecified?
RITUXIMAB (402)
METHOTREXATE (350)
ADALIMUMAB (343)
DICLOFENAC (331)
TOCILIZUMAB (327)
HYDROXYCHLOROQUINE (309)
FOLIC ACID (304)
INFLIXIMAB (303)
LEFLUNOMIDE (302)
SECUKINUMAB (301)
Which DOMPERIDONE Alternatives Have Lower Maternal exposure timing unspecified Risk?
DOMPERIDONE vs DOMPERIDONE\PANTOPRAZOLE
DOMPERIDONE vs DONANEMAB-AZBT
DOMPERIDONE vs DONEPEZIL
DOMPERIDONE vs DONEPEZIL\DONEPEZIL
DOMPERIDONE vs DONEPEZIL\MEMANTINE