Does FONDAPARINUX Cause Product use issue? 42 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 42 reports of Product use issue have been filed in association with FONDAPARINUX (Fondaparinux Sodium). This represents 1.9% of all adverse event reports for FONDAPARINUX.
42
Reports of Product use issue with FONDAPARINUX
1.9%
of all FONDAPARINUX reports
1
Deaths
30
Hospitalizations
How Dangerous Is Product use issue From FONDAPARINUX?
Of the 42 reports, 1 (2.4%) resulted in death, 30 (71.4%) required hospitalization, and 5 (11.9%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FONDAPARINUX. However, 42 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which FONDAPARINUX Alternatives Have Lower Product use issue Risk?
FONDAPARINUX vs FORMOTEROL
FONDAPARINUX vs FORMOTEROL\GLYCOPYRROLATE
FONDAPARINUX vs FORMOTEROL\MOMETASONE
FONDAPARINUX vs FORMOTEROL\MOMETASONE FUROATE
FONDAPARINUX vs FORTEO