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
DYSPNOEA
597 reports
2
PNEUMONIA
561 reports
3
NAUSEA
516 reports
4
DRUG INEFFECTIVE
490 reports
5
FATIGUE
490 reports
6
PAIN
452 reports
7
DIARRHOEA
450 reports
8
COUGH
394 reports
9
HEADACHE
392 reports
10
OFF LABEL USE
385 reports