Does METHYLCELLULOSES Cause Product use in unapproved indication? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product use in unapproved indication have been filed in association with METHYLCELLULOSES. This represents 11.5% of all adverse event reports for METHYLCELLULOSES.
7
Reports of Product use in unapproved indication with METHYLCELLULOSES
11.5%
of all METHYLCELLULOSES reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product use in unapproved indication From METHYLCELLULOSES?
Of the 7 reports, 1 (14.3%) required hospitalization.
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 METHYLCELLULOSES. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does METHYLCELLULOSES Cause?
Product use issue (34)
Flatulence (15)
Drug ineffective (14)
Off label use (14)
Expired product administered (7)
Frequent bowel movements (7)
Constipation (6)
Abdominal distension (5)
Abdominal pain upper (5)
Diarrhoea (5)
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)