Does PONESIMOD Cause Product dose omission issue? 41 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 41 reports of Product dose omission issue have been filed in association with PONESIMOD (PONVORY). This represents 13.3% of all adverse event reports for PONESIMOD.
41
Reports of Product dose omission issue with PONESIMOD
13.3%
of all PONESIMOD reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product dose omission issue From PONESIMOD?
Of the 41 reports, 1 (2.4%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PONESIMOD. However, 41 reports have been filed with the FAERS database.
What Other Side Effects Does PONESIMOD Cause?
Fatigue (23)
Dizziness (16)
Dyspnoea (16)
Headache (11)
Covid-19 (10)
Drug ineffective (9)
Hypoaesthesia (9)
Multiple sclerosis relapse (9)
Nausea (9)
Pain (8)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which PONESIMOD Alternatives Have Lower Product dose omission issue Risk?
PONESIMOD vs PORACTANT ALFA
PONESIMOD vs PORFIMER
PONESIMOD vs POSACONAZOLE
PONESIMOD vs POTASSIUM
PONESIMOD vs POTASSIUM, DIBASIC