LACTULOSE
Generic: LACTULOSE
Lannett CompanyManufacturer
ORALRoute
LACTULOSEActive Substance
2001-07-26Original Approval
LACTULOSE is FDA application ANDA075993, sponsored by LANNETT CO INC. 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
NAUSEA
2,500 reports
2
CONSTIPATION
2,477 reports
3
FALL
2,223 reports
4
VOMITING
2,069 reports
5
FATIGUE
1,982 reports
6
DEATH
1,913 reports
7
DYSPNOEA
1,882 reports
8
DIARRHOEA
1,877 reports
9
PNEUMONIA
1,671 reports
10
PAIN
1,669 reports