Does SONIDEGIB Cause Product dose omission issue? 66 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 66 reports of Product dose omission issue have been filed in association with SONIDEGIB (Odomzo). This represents 4.7% of all adverse event reports for SONIDEGIB.
66
Reports of Product dose omission issue with SONIDEGIB
4.7%
of all SONIDEGIB reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission issue From SONIDEGIB?
Of the 66 reports.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SONIDEGIB. However, 66 reports have been filed with the FAERS database.
What Other Side Effects Does SONIDEGIB Cause?
Muscle spasms (182)
Alopecia (107)
Off label use (100)
Fatigue (94)
Death (87)
Product use issue (70)
Nausea (69)
Therapy cessation (64)
Ageusia (59)
Asthenia (59)
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 SONIDEGIB Alternatives Have Lower Product dose omission issue Risk?
SONIDEGIB vs SORAFENIB
SONIDEGIB vs SORGHUM HALEPENSE POLLEN
SONIDEGIB vs SOTAGLIFLOZIN
SONIDEGIB vs SOTALOL
SONIDEGIB vs SOTATERCEPT