Does BUFEXAMAC Cause Condition aggravated? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Condition aggravated have been filed in association with BUFEXAMAC. This represents 53.6% of all adverse event reports for BUFEXAMAC.
30
Reports of Condition aggravated with BUFEXAMAC
53.6%
of all BUFEXAMAC reports
30
Deaths
25
Hospitalizations
How Dangerous Is Condition aggravated From BUFEXAMAC?
Of the 30 reports, 30 (100.0%) resulted in death, 25 (83.3%) required hospitalization, and 29 (96.7%) 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 BUFEXAMAC. However, 30 reports have been filed with the FAERS database.
What Other Side Effects Does BUFEXAMAC Cause?
Abdominal distension (33)
Vomiting (32)
Abdominal pain (30)
Appendicitis (30)
Appendicolith (30)
Ascites (30)
Dyspnoea (30)
Somnolence (30)
Blood phosphorus increased (29)
Dry mouth (29)
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)