Does DEXTROMETHORPHAN HYDROBROMIDE\DOXYLAMINE Cause Product use in unapproved indication? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product use in unapproved indication have been filed in association with DEXTROMETHORPHAN HYDROBROMIDE\DOXYLAMINE. This represents 6.1% of all adverse event reports for DEXTROMETHORPHAN HYDROBROMIDE\DOXYLAMINE.
5
Reports of Product use in unapproved indication with DEXTROMETHORPHAN HYDROBROMIDE\DOXYLAMINE
6.1%
of all DEXTROMETHORPHAN HYDROBROMIDE\DOXYLAMINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product use in unapproved indication From DEXTROMETHORPHAN HYDROBROMIDE\DOXYLAMINE?
Of the 5 reports.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXTROMETHORPHAN HYDROBROMIDE\DOXYLAMINE. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does DEXTROMETHORPHAN HYDROBROMIDE\DOXYLAMINE Cause?
Drug ineffective (11)
Loss of consciousness (10)
Somnolence (8)
Cough (7)
Nausea (7)
Dizziness (6)
Dyspnoea (6)
Pain (6)
Vomiting (6)
Diarrhoea (5)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)