Does DOBUTAMINE Cause Activated partial thromboplastin time prolonged? 72 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 72 reports of Activated partial thromboplastin time prolonged have been filed in association with DOBUTAMINE (Dobutamine). This represents 4.4% of all adverse event reports for DOBUTAMINE.
72
Reports of Activated partial thromboplastin time prolonged with DOBUTAMINE
4.4%
of all DOBUTAMINE reports
72
Deaths
68
Hospitalizations
How Dangerous Is Activated partial thromboplastin time prolonged From DOBUTAMINE?
Of the 72 reports, 72 (100.0%) resulted in death, 68 (94.4%) required hospitalization, and 68 (94.4%) were considered life-threatening.
Is Activated partial thromboplastin time prolonged Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOBUTAMINE. However, 72 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 Activated partial thromboplastin time prolonged?
DABIGATRAN ETEXILATE (264)
HEPARIN (225)
RIVAROXABAN (163)
WARFARIN (146)
ACETAMINOPHEN (119)
ALLOPURINOL (110)
AMIODARONE (99)
METRONIDAZOLE (98)
SIMVASTATIN (94)
DARBEPOETIN ALFA (93)
Which DOBUTAMINE Alternatives Have Lower Activated partial thromboplastin time prolonged Risk?
DOBUTAMINE vs DOBUTAMINE\DOBUTAMINE
DOBUTAMINE vs DOCETAXEL
DOBUTAMINE vs DOCETAXEL ANHYDROUS
DOBUTAMINE vs DOCETAXEL\DOCETAXEL ANHYDROUS
DOBUTAMINE vs DOCONEXENT