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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does MANNITOL Cause Product use issue? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product use issue have been filed in association with MANNITOL (Osmitrol). This represents 0.3% of all adverse event reports for MANNITOL.

5
Reports of Product use issue with MANNITOL
0.3%
of all MANNITOL reports
1
Deaths
1
Hospitalizations

How Dangerous Is Product use issue From MANNITOL?

Of the 5 reports, 1 (20.0%) resulted in death, 1 (20.0%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MANNITOL. However, 5 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 Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which MANNITOL Alternatives Have Lower Product use issue Risk?

MANNITOL vs MAPROTILINE MANNITOL vs MARALIXIBAT MANNITOL vs MARAVIROC MANNITOL vs MARIBAVIR MANNITOL vs MAVACAMTEN

Related Pages

MANNITOL Full Profile All Product use issue Reports All Drugs Causing Product use issue MANNITOL Demographics