Does METHYLCELLULOSE Cause Product use in unapproved indication? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product use in unapproved indication have been filed in association with METHYLCELLULOSE (CITRUCEL). This represents 13.7% of all adverse event reports for METHYLCELLULOSE.
13
Reports of Product use in unapproved indication with METHYLCELLULOSE
13.7%
of all METHYLCELLULOSE reports
5
Deaths
5
Hospitalizations
How Dangerous Is Product use in unapproved indication From METHYLCELLULOSE?
Of the 13 reports, 5 (38.5%) resulted in death, 5 (38.5%) required hospitalization, and 4 (30.8%) 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 METHYLCELLULOSE. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does METHYLCELLULOSE Cause?
Off label use (18)
Drug ineffective (16)
Incorrect product administration duration (14)
Product complaint (13)
Diabetes mellitus (11)
Dyspnoea (11)
Rectal haemorrhage (11)
Constipation (10)
Abdominal pain (9)
Choking (9)
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)