Does ONABOTULINUMTOXINA Cause Dysgeusia? 69 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 69 reports of Dysgeusia have been filed in association with ONABOTULINUMTOXINA. This represents 0.1% of all adverse event reports for ONABOTULINUMTOXINA.
69
Reports of Dysgeusia with ONABOTULINUMTOXINA
0.1%
of all ONABOTULINUMTOXINA reports
0
Deaths
9
Hospitalizations
How Dangerous Is Dysgeusia From ONABOTULINUMTOXINA?
Of the 69 reports, 9 (13.0%) required hospitalization, and 2 (2.9%) were considered life-threatening.
Is Dysgeusia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ONABOTULINUMTOXINA. However, 69 reports have been filed with the FAERS database.
What Other Side Effects Does ONABOTULINUMTOXINA Cause?
Drug ineffective (18,179)
Off label use (9,698)
Product preparation error (3,593)
Multiple use of single-use product (2,781)
Therapeutic response decreased (2,685)
Headache (2,316)
Injection site pain (2,143)
Eyelid ptosis (1,853)
Wrong technique in product usage process (1,477)
Migraine (1,232)
What Other Drugs Cause Dysgeusia?
NIRMATRELVIR\RITONAVIR (7,381)
SUNITINIB MALATE (1,226)
SODIUM (1,216)
LENALIDOMIDE (1,180)
LIFITEGRAST (1,067)
CABOZANTINIB S-MALATE (777)
CLARITHROMYCIN (717)
VISMODEGIB (706)
ADALIMUMAB (674)
PALBOCICLIB (620)
Which ONABOTULINUMTOXINA Alternatives Have Lower Dysgeusia Risk?
ONABOTULINUMTOXINA vs ONASEMNOGENE ABEPARVOVEC
ONABOTULINUMTOXINA vs ONASEMNOGENE ABEPARVOVEC-XIOI
ONABOTULINUMTOXINA vs ONBREZ
ONABOTULINUMTOXINA vs ONDANSETRON
ONABOTULINUMTOXINA vs ONFI