Does ENOXAPARIN Cause Product dose omission? 61 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 61 reports of Product dose omission have been filed in association with ENOXAPARIN (Enoxaparin Sodium). This represents 0.2% of all adverse event reports for ENOXAPARIN.
61
Reports of Product dose omission with ENOXAPARIN
0.2%
of all ENOXAPARIN reports
1
Deaths
10
Hospitalizations
How Dangerous Is Product dose omission From ENOXAPARIN?
Of the 61 reports, 1 (1.6%) resulted in death, 10 (16.4%) required hospitalization, and 1 (1.6%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ENOXAPARIN. However, 61 reports have been filed with the FAERS database.
What Other Side Effects Does ENOXAPARIN Cause?
Off label use (1,707)
Exposure during pregnancy (1,215)
Haemorrhage (1,059)
Foetal exposure during pregnancy (918)
Anaemia (914)
Thrombocytopenia (834)
Dyspnoea (822)
Maternal exposure during pregnancy (818)
Drug ineffective (769)
Nausea (708)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which ENOXAPARIN Alternatives Have Lower Product dose omission Risk?
ENOXAPARIN vs ENOXAPARIN - WINTHROP
ENOXAPARIN vs ENSIFENTRINE
ENOXAPARIN vs ENTACAPONE
ENOXAPARIN vs ENTECAVIR
ENOXAPARIN vs ENTINOSTAT