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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 SEREVENT Cause Investigation? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Investigation have been filed in association with SEREVENT. This represents 17.2% of all adverse event reports for SEREVENT.

5
Reports of Investigation with SEREVENT
17.2%
of all SEREVENT reports
0
Deaths
5
Hospitalizations

How Dangerous Is Investigation From SEREVENT?

Of the 5 reports, 5 (100.0%) required hospitalization.

Is Investigation Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SEREVENT. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does SEREVENT Cause?

Dyspnoea (6)

What Other Drugs Cause Investigation?

ARANESP (403) NEULASTA (371) XGEVA (115) FLUTICASONE\SALMETEROL (96) DARBEPOETIN ALFA (86) ADVAIR (77) DENOSUMAB (65) ADVAIR HFA (51) ALBUTEROL (51) VENTOLIN (47)

Related Pages

SEREVENT Full Profile All Investigation Reports All Drugs Causing Investigation SEREVENT Demographics