Does DOBUTAMINE Cause Condition aggravated? 272 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 272 reports of Condition aggravated have been filed in association with DOBUTAMINE (Dobutamine). This represents 16.7% of all adverse event reports for DOBUTAMINE.
272
Reports of Condition aggravated with DOBUTAMINE
16.7%
of all DOBUTAMINE reports
197
Deaths
190
Hospitalizations
How Dangerous Is Condition aggravated From DOBUTAMINE?
Of the 272 reports, 197 (72.4%) resulted in death, 190 (69.9%) required hospitalization, and 154 (56.6%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOBUTAMINE. However, 272 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)
Sepsis (264)
Abdominal distension (259)
General physical health deterioration (258)
Hyponatraemia (256)
Appendicitis (252)
Ascites (252)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which DOBUTAMINE Alternatives Have Lower Condition aggravated Risk?
DOBUTAMINE vs DOBUTAMINE\DOBUTAMINE
DOBUTAMINE vs DOCETAXEL
DOBUTAMINE vs DOCETAXEL ANHYDROUS
DOBUTAMINE vs DOCETAXEL\DOCETAXEL ANHYDROUS
DOBUTAMINE vs DOCONEXENT