Does SYMBICORT Cause Incorrect product storage? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Incorrect product storage have been filed in association with SYMBICORT. This represents 1.6% of all adverse event reports for SYMBICORT.
6
Reports of Incorrect product storage with SYMBICORT
1.6%
of all SYMBICORT reports
0
Deaths
2
Hospitalizations
How Dangerous Is Incorrect product storage From SYMBICORT?
Of the 6 reports, 2 (33.3%) required hospitalization.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SYMBICORT. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does SYMBICORT Cause?
Dyspnoea (92)
Off label use (70)
Intentional product misuse (69)
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)
What Other Drugs Cause Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
Which SYMBICORT Alternatives Have Lower Incorrect product storage Risk?
SYMBICORT vs SYNAGIS
SYMBICORT vs SYNTHROID
SYMBICORT vs TACROLIMUS
SYMBICORT vs TACROLIMUS\TACROLIMUS ANHYDROUS
SYMBICORT vs TADALAFIL