Does FONDAPARINUX Cause Haemoglobin decreased? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Haemoglobin decreased have been filed in association with FONDAPARINUX (Fondaparinux Sodium). This represents 1.6% of all adverse event reports for FONDAPARINUX.
36
Reports of Haemoglobin decreased with FONDAPARINUX
1.6%
of all FONDAPARINUX reports
2
Deaths
26
Hospitalizations
How Dangerous Is Haemoglobin decreased From FONDAPARINUX?
Of the 36 reports, 2 (5.6%) resulted in death, 26 (72.2%) required hospitalization, and 8 (22.2%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FONDAPARINUX. However, 36 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 Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which FONDAPARINUX Alternatives Have Lower Haemoglobin decreased Risk?
FONDAPARINUX vs FORMOTEROL
FONDAPARINUX vs FORMOTEROL\GLYCOPYRROLATE
FONDAPARINUX vs FORMOTEROL\MOMETASONE
FONDAPARINUX vs FORMOTEROL\MOMETASONE FUROATE
FONDAPARINUX vs FORTEO