MANNITOL
Generic: MANNITOL
ICU Medical Inc.Manufacturer
INTRAVENOUSRoute
MANNITOLActive Substance
1987-01-08Original Approval
MANNITOL is FDA application NDA019603, sponsored by OTSUKA ICU MEDCL. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.
Top Reported Reactions
1
PAIN
615 reports
2
RENAL FAILURE
593 reports
3
ANXIETY
503 reports
4
INJURY
496 reports
5
UNEVALUABLE EVENT
471 reports
6
DRUG INEFFECTIVE
467 reports
7
STRESS
459 reports
8
FEAR
431 reports
9
DEATH
411 reports
10
RENAL IMPAIRMENT
394 reports