Does DALTEPARIN Cause Product dose omission issue? 60 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 60 reports of Product dose omission issue have been filed in association with DALTEPARIN (Fragmin). This represents 1.7% of all adverse event reports for DALTEPARIN.
60
Reports of Product dose omission issue with DALTEPARIN
1.7%
of all DALTEPARIN reports
24
Deaths
51
Hospitalizations
How Dangerous Is Product dose omission issue From DALTEPARIN?
Of the 60 reports, 24 (40.0%) resulted in death, 51 (85.0%) required hospitalization, and 20 (33.3%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DALTEPARIN. However, 60 reports have been filed with the FAERS database.
What Other Side Effects Does DALTEPARIN Cause?
Off label use (352)
Nausea (316)
Abdominal pain (283)
Multiple organ dysfunction syndrome (282)
Vomiting (282)
Hyponatraemia (257)
General physical health deterioration (253)
Sepsis (252)
Constipation (247)
Abdominal distension (245)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which DALTEPARIN Alternatives Have Lower Product dose omission issue Risk?
DALTEPARIN vs DAMOCTOCOG ALFA PEGOL
DALTEPARIN vs DANAPAROID
DALTEPARIN vs DANAZOL
DALTEPARIN vs DANICOPAN
DALTEPARIN vs DANTROLENE