Does DOBUTAMINE Cause Intentional product misuse? 123 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 123 reports of Intentional product misuse have been filed in association with DOBUTAMINE (Dobutamine). This represents 7.5% of all adverse event reports for DOBUTAMINE.
123
Reports of Intentional product misuse with DOBUTAMINE
7.5%
of all DOBUTAMINE reports
122
Deaths
113
Hospitalizations
How Dangerous Is Intentional product misuse From DOBUTAMINE?
Of the 123 reports, 122 (99.2%) resulted in death, 113 (91.9%) required hospitalization, and 109 (88.6%) 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 DOBUTAMINE. However, 123 reports have been filed with the FAERS database.
What Other Side Effects Does DOBUTAMINE Cause?
Drug ineffective (556)
Off label use (325)
Cardiogenic shock (316)
Multiple organ dysfunction syndrome (297)
Condition aggravated (272)
Sepsis (264)
Abdominal distension (259)
General physical health deterioration (258)
Hyponatraemia (256)
Appendicitis (252)
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 DOBUTAMINE Alternatives Have Lower Intentional product misuse Risk?
DOBUTAMINE vs DOBUTAMINE\DOBUTAMINE
DOBUTAMINE vs DOCETAXEL
DOBUTAMINE vs DOCETAXEL ANHYDROUS
DOBUTAMINE vs DOCETAXEL\DOCETAXEL ANHYDROUS
DOBUTAMINE vs DOCONEXENT