GUAIFENESIN AND DEXTROMETHORPHAN HBR
Generic: GUAIFENESIN AND DEXTROMETHORPHAN HBR, GUAIFENESIN, DEXTROMETHORPHAN HBR, GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE
OHM LABORATORIES INCManufacturer
ORALRoute
GUAIFENESINActive Substance
2021-07-01Original Approval
GUAIFENESIN AND DEXTROMETHORPHAN HBR is FDA application ANDA214781, sponsored by SUN PHARM. 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
DEHYDRATION
3 reports
2
RENAL FAILURE ACUTE
3 reports
3
ANAEMIA
2 reports
4
CARDIO-RESPIRATORY ARREST
2 reports
5
CHRONIC OBSTRUCTIVE PULMONARY DISEASE
2 reports
6
COLITIS
2 reports
7
COMPLETED SUICIDE
2 reports
8
CONVULSION
2 reports
9
DEEP VEIN THROMBOSIS
2 reports
10
DYSPNOEA
2 reports