MUCUS RELIEF
Generic: GUAIFENESIN, GUAIFENESIN 1200 MG, GUAIFENESIN 600 MG
Grocery OutletManufacturer
ORALRoute
GUAIFENESINActive Substance
2023-08-21Original Approval
MUCUS RELIEF is FDA application ANDA217780, sponsored by PHARMAZONE. 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
568 reports
2
PNEUMONIA
530 reports
3
NAUSEA
486 reports
4
FATIGUE
457 reports
5
DRUG INEFFECTIVE
454 reports
6
PAIN
427 reports
7
DIARRHOEA
417 reports
8
COUGH
378 reports
9
HEADACHE
370 reports
10
OFF LABEL USE
367 reports