Does BUDESONIDE\FORMOTEROL Cause Wrong product administered? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Wrong product administered have been filed in association with BUDESONIDE\FORMOTEROL. This represents 0.1% of all adverse event reports for BUDESONIDE\FORMOTEROL.
18
Reports of Wrong product administered with BUDESONIDE\FORMOTEROL
0.1%
of all BUDESONIDE\FORMOTEROL reports
1
Deaths
6
Hospitalizations
How Dangerous Is Wrong product administered From BUDESONIDE\FORMOTEROL?
Of the 18 reports, 1 (5.6%) resulted in death, 6 (33.3%) required hospitalization.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE\FORMOTEROL. However, 18 reports have been filed with the FAERS database.
What Other Side Effects Does BUDESONIDE\FORMOTEROL Cause?
Dyspnoea (11,158)
Asthma (10,045)
Wheezing (5,632)
Cough (4,466)
Therapeutic product effect incomplete (4,392)
Drug ineffective (3,469)
Intentional product misuse (3,399)
Loss of personal independence in daily activities (3,397)
Off label use (3,269)
Device malfunction (2,771)
What Other Drugs Cause Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which BUDESONIDE\FORMOTEROL Alternatives Have Lower Wrong product administered Risk?
BUDESONIDE\FORMOTEROL vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE\FORMOTEROL vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE\FORMOTEROL vs BUMETANIDE
BUDESONIDE\FORMOTEROL vs BUPIVACAINE
BUDESONIDE\FORMOTEROL vs BUPIVACAINE\BUPIVACAINE ANHYDROUS