Does POLYSORBATE 40 Cause Product use in unapproved indication? 32 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Product use in unapproved indication have been filed in association with POLYSORBATE 40. This represents 69.6% of all adverse event reports for POLYSORBATE 40.
32
Reports of Product use in unapproved indication with POLYSORBATE 40
69.6%
of all POLYSORBATE 40 reports
0
Deaths
32
Hospitalizations
How Dangerous Is Product use in unapproved indication From POLYSORBATE 40?
Of the 32 reports, 32 (100.0%) required hospitalization, and 32 (100.0%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for POLYSORBATE 40. However, 32 reports have been filed with the FAERS database.
What Other Side Effects Does POLYSORBATE 40 Cause?
Cognitive disorder (40)
Fall (40)
Sedation complication (40)
Balance disorder (39)
Blood calcium decreased (39)
Constipation (39)
Creatinine renal clearance decreased (39)
Depressed level of consciousness (39)
Hypotension (39)
Mobility decreased (39)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)