Does MANNITOL Cause Intentional product misuse? 80 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 80 reports of Intentional product misuse have been filed in association with MANNITOL (Osmitrol). This represents 4.1% of all adverse event reports for MANNITOL.
80
Reports of Intentional product misuse with MANNITOL
4.1%
of all MANNITOL reports
80
Deaths
75
Hospitalizations
How Dangerous Is Intentional product misuse From MANNITOL?
Of the 80 reports, 80 (100.0%) resulted in death, 75 (93.8%) required hospitalization, and 74 (92.5%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MANNITOL. However, 80 reports have been filed with the FAERS database.
What Other Side Effects Does MANNITOL Cause?
Drug ineffective (276)
Condition aggravated (205)
Nausea (167)
Off label use (159)
Hyponatraemia (153)
Vomiting (147)
Renal impairment (144)
Pruritus (140)
Sepsis (136)
Multiple organ dysfunction syndrome (131)
What Other Drugs Cause Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which MANNITOL Alternatives Have Lower Intentional product misuse Risk?
MANNITOL vs MAPROTILINE
MANNITOL vs MARALIXIBAT
MANNITOL vs MARAVIROC
MANNITOL vs MARIBAVIR
MANNITOL vs MAVACAMTEN