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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN Cause Haemoptysis? 13 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Haemoptysis have been filed in association with DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN. This represents 0.2% of all adverse event reports for DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN.

13
Reports of Haemoptysis with DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN
0.2%
of all DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN reports
0
Deaths
1
Hospitalizations

How Dangerous Is Haemoptysis From DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN?

Of the 13 reports, 1 (7.7%) required hospitalization.

Is Haemoptysis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN. However, 13 reports have been filed with the FAERS database.

What Other Side Effects Does DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN Cause?

Drug ineffective (1,155) Dizziness (759) Diarrhoea (570) Accidental overdose (515) Nausea (408) Overdose (377) Product use in unapproved indication (356) Somnolence (304) Insomnia (259) 503 Service Unavailable

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