Does NOREPINEPHRINE, - Cause Product use in unapproved indication? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product use in unapproved indication have been filed in association with NOREPINEPHRINE, -. This represents 13.8% of all adverse event reports for NOREPINEPHRINE, -.
8
Reports of Product use in unapproved indication with NOREPINEPHRINE, -
13.8%
of all NOREPINEPHRINE, - reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product use in unapproved indication From NOREPINEPHRINE, -?
Of the 8 reports.
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 NOREPINEPHRINE, -. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does NOREPINEPHRINE, - Cause?
Toxic epidermal necrolysis (22)
Stevens-johnson syndrome (16)
Off label use (9)
Torsade de pointes (9)
Cardiac arrest (8)
Drug hypersensitivity (8)
Cardiogenic shock (7)
Haemorrhage (7)
Ischaemia (7)
Abdominal distension (6)
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)