Does ALBUTEROL\AMBROXOL\GUAIFENESIN Cause Off label use? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Off label use have been filed in association with ALBUTEROL\AMBROXOL\GUAIFENESIN. This represents 27.5% of all adverse event reports for ALBUTEROL\AMBROXOL\GUAIFENESIN.
11
Reports of Off label use with ALBUTEROL\AMBROXOL\GUAIFENESIN
27.5%
of all ALBUTEROL\AMBROXOL\GUAIFENESIN reports
0
Deaths
11
Hospitalizations
How Dangerous Is Off label use From ALBUTEROL\AMBROXOL\GUAIFENESIN?
Of the 11 reports, 11 (100.0%) required hospitalization, and 11 (100.0%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALBUTEROL\AMBROXOL\GUAIFENESIN. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does ALBUTEROL\AMBROXOL\GUAIFENESIN Cause?
Balance disorder (28)
Blood calcium decreased (28)
Cognitive disorder (28)
Constipation (28)
Creatinine renal clearance decreased (28)
Depressed level of consciousness (28)
Fall (28)
Hypotension (28)
Mobility decreased (28)
Orthostatic hypotension (28)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)