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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 COMBIVENT Cause Off label use? 311 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 311 reports of Off label use have been filed in association with COMBIVENT. This represents 24.9% of all adverse event reports for COMBIVENT.

311
Reports of Off label use with COMBIVENT
24.9%
of all COMBIVENT reports
1
Deaths
36
Hospitalizations

How Dangerous Is Off label use From COMBIVENT?

Of the 311 reports, 1 (0.3%) resulted in death, 36 (11.6%) required hospitalization, and 2 (0.6%) 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 COMBIVENT. However, 311 reports have been filed with the FAERS database.

What Other Side Effects Does COMBIVENT Cause?

Product quality issue (385) Dyspnoea (262) Drug ineffective (257) Cough (107) Overdose (103) Prescribed overdose (73) Pneumonia (47) Drug prescribing error (39) Choking (33) Wheezing (32)

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)

Which COMBIVENT Alternatives Have Lower Off label use Risk?

COMBIVENT vs COMBIVIR COMBIVENT vs COMETRIQ COMBIVENT vs CONCERTA COMBIVENT vs CONESTAT ALFA COMBIVENT vs COPANLISIB

Related Pages

COMBIVENT Full Profile All Off label use Reports All Drugs Causing Off label use COMBIVENT Demographics