MUCUS DM
Generic: DEXTROMETHORPHAN HBR, GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, DEXTROMETHORPHAN HBR
HyVee IncManufacturer
ORALRoute
DEXTROMETHORPHAN HYDROBROMIDEActive Substance
2018-03-05Original Approval
MUCUS DM is FDA application ANDA207602, sponsored by PERRIGO R AND D. 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
DRUG INEFFECTIVE
60 reports
2
DIARRHOEA
46 reports
3
FATIGUE
35 reports
4
DIZZINESS
33 reports
5
NAUSEA
32 reports
6
DYSPNOEA
30 reports
7
PNEUMONIA
26 reports
8
COVID-19
25 reports
9
PAIN
24 reports
10
COUGH
23 reports