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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 REBAMIPIDE Cause Eosinophil count increased? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Eosinophil count increased have been filed in association with REBAMIPIDE. This represents 1.6% of all adverse event reports for REBAMIPIDE.

7
Reports of Eosinophil count increased with REBAMIPIDE
1.6%
of all REBAMIPIDE reports
1
Deaths
4
Hospitalizations

How Dangerous Is Eosinophil count increased From REBAMIPIDE?

Of the 7 reports, 1 (14.3%) resulted in death, 4 (57.1%) required hospitalization, and 1 (14.3%) were considered life-threatening.

Is Eosinophil count increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for REBAMIPIDE. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does REBAMIPIDE Cause?

Hepatic function abnormal (30) Drug eruption (28) Nausea (26) Rash (26) Vomiting (22) Pyrexia (19) Anaemia (18) Diarrhoea (18) Platelet count decreased (18) Pruritus (18)

What Other Drugs Cause Eosinophil count increased?

ALBUTEROL (1,359) PREDNISONE (846) BUDESONIDE\FORMOTEROL (719) DUPILUMAB (712) TIOTROPIUM (682) MEPOLIZUMAB (670) MONTELUKAST (504) BUDESONIDE (493) CLOZAPINE (475) FLUTICASONE\SALMETEROL (416)

Which REBAMIPIDE Alternatives Have Lower Eosinophil count increased Risk?

REBAMIPIDE vs REBETOL REBAMIPIDE vs REBIF REBAMIPIDE vs REBOXETINE REBAMIPIDE vs RECLAST REBAMIPIDE vs RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E

Related Pages

REBAMIPIDE Full Profile All Eosinophil count increased Reports All Drugs Causing Eosinophil count increased REBAMIPIDE Demographics