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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 REMOXIPRIDE Cause Ill-defined disorder? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Ill-defined disorder have been filed in association with REMOXIPRIDE. This represents 45.5% of all adverse event reports for REMOXIPRIDE.

5
Reports of Ill-defined disorder with REMOXIPRIDE
45.5%
of all REMOXIPRIDE reports
5
Deaths
5
Hospitalizations

How Dangerous Is Ill-defined disorder From REMOXIPRIDE?

Of the 5 reports, 5 (100.0%) resulted in death, 5 (100.0%) required hospitalization, and 5 (100.0%) were considered life-threatening.

Is Ill-defined disorder Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for REMOXIPRIDE. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does REMOXIPRIDE Cause?

Dyspnoea (10) Weight increased (10) Abdominal pain upper (6) Aggression (6) Amenorrhoea (6) Dizziness (6) Hallucination (6) Hepatic pain (6) Neuroleptic malignant syndrome (6) Nightmare (6)

What Other Drugs Cause Ill-defined disorder?

ACETAMINOPHEN\OXYCODONE (9,780) ACETAMINOPHEN\HYDROCODONE (6,159) TOCILIZUMAB (4,411) RITUXIMAB (4,220) ETANERCEPT (4,202) METHOTREXATE (4,063) ABATACEPT (3,630) LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN (3,600) LEFLUNOMIDE (3,570) CERTOLIZUMAB PEGOL (3,273)

Related Pages

REMOXIPRIDE Full Profile All Ill-defined disorder Reports All Drugs Causing Ill-defined disorder REMOXIPRIDE Demographics