Does FONDAPARINUX Cause Condition aggravated? 46 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 46 reports of Condition aggravated have been filed in association with FONDAPARINUX (Fondaparinux Sodium). This represents 2.1% of all adverse event reports for FONDAPARINUX.
46
Reports of Condition aggravated with FONDAPARINUX
2.1%
of all FONDAPARINUX reports
8
Deaths
30
Hospitalizations
How Dangerous Is Condition aggravated From FONDAPARINUX?
Of the 46 reports, 8 (17.4%) resulted in death, 30 (65.2%) required hospitalization, and 9 (19.6%) 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 FONDAPARINUX. However, 46 reports have been filed with the FAERS database.
What Other Side Effects Does FONDAPARINUX Cause?
Off label use (356)
Haematoma (168)
Anaemia (159)
Drug ineffective (117)
Pulmonary embolism (97)
Haemorrhage (89)
Cerebral haemorrhage (78)
Heparin-induced thrombocytopenia (76)
Thrombocytopenia (72)
Thrombosis (71)
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 FONDAPARINUX Alternatives Have Lower Condition aggravated Risk?
FONDAPARINUX vs FORMOTEROL
FONDAPARINUX vs FORMOTEROL\GLYCOPYRROLATE
FONDAPARINUX vs FORMOTEROL\MOMETASONE
FONDAPARINUX vs FORMOTEROL\MOMETASONE FUROATE
FONDAPARINUX vs FORTEO