Does FONDAPARINUX Cause Incorrect product administration duration? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Incorrect product administration duration have been filed in association with FONDAPARINUX (Fondaparinux Sodium). This represents 0.3% of all adverse event reports for FONDAPARINUX.
7
Reports of Incorrect product administration duration with FONDAPARINUX
0.3%
of all FONDAPARINUX reports
0
Deaths
7
Hospitalizations
How Dangerous Is Incorrect product administration duration From FONDAPARINUX?
Of the 7 reports, 7 (100.0%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FONDAPARINUX. However, 7 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which FONDAPARINUX Alternatives Have Lower Incorrect product administration duration Risk?
FONDAPARINUX vs FORMOTEROL
FONDAPARINUX vs FORMOTEROL\GLYCOPYRROLATE
FONDAPARINUX vs FORMOTEROL\MOMETASONE
FONDAPARINUX vs FORMOTEROL\MOMETASONE FUROATE
FONDAPARINUX vs FORTEO