Does BUFEXAMAC\LIDOCAINE Cause Activated partial thromboplastin time prolonged? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Activated partial thromboplastin time prolonged have been filed in association with BUFEXAMAC\LIDOCAINE. This represents 24.5% of all adverse event reports for BUFEXAMAC\LIDOCAINE.
12
Reports of Activated partial thromboplastin time prolonged with BUFEXAMAC\LIDOCAINE
24.5%
of all BUFEXAMAC\LIDOCAINE reports
12
Deaths
10
Hospitalizations
How Dangerous Is Activated partial thromboplastin time prolonged From BUFEXAMAC\LIDOCAINE?
Of the 12 reports, 12 (100.0%) resulted in death, 10 (83.3%) required hospitalization, and 10 (83.3%) 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 BUFEXAMAC\LIDOCAINE. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does BUFEXAMAC\LIDOCAINE Cause?
Abdominal distension (43)
Vomiting (42)
Stress (41)
Abdominal pain (40)
Appendicitis (40)
Appendicolith (40)
Ascites (40)
Hyponatraemia (40)
Off label use (40)
Ventricular fibrillation (40)
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)