Does DEXTROSE\WATER 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 DEXTROSE\WATER. This represents 27.6% of all adverse event reports for DEXTROSE\WATER.
8
Reports of Product use in unapproved indication with DEXTROSE\WATER
27.6%
of all DEXTROSE\WATER reports
7
Deaths
7
Hospitalizations
How Dangerous Is Product use in unapproved indication From DEXTROSE\WATER?
Of the 8 reports, 7 (87.5%) resulted in death, 7 (87.5%) required hospitalization, and 6 (75.0%) 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 DEXTROSE\WATER. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does DEXTROSE\WATER Cause?
Hyponatraemia (10)
Condition aggravated (9)
Off label use (9)
Drug ineffective (8)
General physical health deterioration (7)
Headache (7)
Liver disorder (7)
Multiple organ dysfunction syndrome (7)
Pyrexia (7)
Sepsis (7)
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)