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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 Cause Intentional product misuse? 69 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 69 reports of Intentional product misuse have been filed in association with SYMBICORT. This represents 18.1% of all adverse event reports for SYMBICORT.

69
Reports of Intentional product misuse with SYMBICORT
18.1%
of all SYMBICORT reports
1
Deaths
16
Hospitalizations

How Dangerous Is Intentional product misuse From SYMBICORT?

Of the 69 reports, 1 (1.4%) resulted in death, 16 (23.2%) required hospitalization, and 2 (2.9%) were considered life-threatening.

Is Intentional product misuse Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SYMBICORT. However, 69 reports have been filed with the FAERS database.

What Other Side Effects Does SYMBICORT Cause?

Dyspnoea (92) Off label use (70) Drug dose omission (60) Asthma (38) Cough (38) Circumstance or information capable of leading to medication error (35) Malaise (32) Pneumonia (31) Device misuse (27) Drug ineffective (24)

What Other Drugs Cause Intentional product misuse?

ETANERCEPT (3,992) PREGABALIN (3,731) BUDESONIDE\FORMOTEROL (3,399) ACETAMINOPHEN (2,924) ESOMEPRAZOLE (2,852) MINOXIDIL (2,418) TOFACITINIB (2,331) CINACALCET (2,092) QUETIAPINE (1,855) ALPRAZOLAM (1,709)

Which SYMBICORT Alternatives Have Lower Intentional product misuse Risk?

SYMBICORT vs SYNAGIS SYMBICORT vs SYNTHROID SYMBICORT vs TACROLIMUS SYMBICORT vs TACROLIMUS\TACROLIMUS ANHYDROUS SYMBICORT vs TADALAFIL

Related Pages

SYMBICORT Full Profile All Intentional product misuse Reports All Drugs Causing Intentional product misuse SYMBICORT Demographics