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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 SYMBICORT PMDI Cause Adverse event? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Adverse event have been filed in association with SYMBICORT PMDI. This represents 5.8% of all adverse event reports for SYMBICORT PMDI.

5
Reports of Adverse event with SYMBICORT PMDI
5.8%
of all SYMBICORT PMDI reports
0
Deaths
1
Hospitalizations

How Dangerous Is Adverse event From SYMBICORT PMDI?

Of the 5 reports, 1 (20.0%) required hospitalization.

Is Adverse event Listed in the Official Label?

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

What Other Side Effects Does SYMBICORT PMDI Cause?

Drug dose omission (37) Dyspnoea (31) Off label use (23) Intentional product misuse (18) Intentional drug misuse (16) Chronic obstructive pulmonary disease (13) Gastrooesophageal reflux disease (11) Malaise (11) Feeling abnormal (10) Pneumonia (10)

What Other Drugs Cause Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Related Pages

SYMBICORT PMDI Full Profile All Adverse event Reports All Drugs Causing Adverse event SYMBICORT PMDI Demographics