Does AMINOPHYLLINE\BROMHEXINE\CHLORPHENIRAMINE Cause Off label use? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Off label use have been filed in association with AMINOPHYLLINE\BROMHEXINE\CHLORPHENIRAMINE. This represents 58.3% of all adverse event reports for AMINOPHYLLINE\BROMHEXINE\CHLORPHENIRAMINE.
7
Reports of Off label use with AMINOPHYLLINE\BROMHEXINE\CHLORPHENIRAMINE
58.3%
of all AMINOPHYLLINE\BROMHEXINE\CHLORPHENIRAMINE reports
0
Deaths
7
Hospitalizations
How Dangerous Is Off label use From AMINOPHYLLINE\BROMHEXINE\CHLORPHENIRAMINE?
Of the 7 reports, 7 (100.0%) required hospitalization, and 7 (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 AMINOPHYLLINE\BROMHEXINE\CHLORPHENIRAMINE. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does AMINOPHYLLINE\BROMHEXINE\CHLORPHENIRAMINE Cause?
Sedation complication (8)
Balance disorder (7)
Blood calcium decreased (7)
Cognitive disorder (7)
Constipation (7)
Creatinine renal clearance decreased (7)
Creatinine renal clearance increased (7)
Depressed level of consciousness (7)
Drug abuse (7)
Drug interaction (7)
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)