POTASSIUM ACETATE
Generic: POTASSIUM ACETATE
Fresenius Kabi USAManufacturer
INTRAVENOUSRoute
POTASSIUM ACETATEActive Substance
2024-11-27Original Approval
POTASSIUM ACETATE is FDA application ANDA217515, sponsored by FRESENIUS KABI USA. 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
DYSPNOEA
108 reports
2
NAUSEA
107 reports
3
DIARRHOEA
106 reports
4
FATIGUE
101 reports
5
ASTHENIA
83 reports
6
DRUG INEFFECTIVE
83 reports
7
DIZZINESS
82 reports
8
WEIGHT DECREASED
60 reports
9
HEADACHE
59 reports
10
PAIN
58 reports