Does DEXAMETHASONE Cause Product dose omission issue? 410 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 410 reports of Product dose omission issue have been filed in association with DEXAMETHASONE (Dexamethasone Sodium Phosphate). This represents 0.3% of all adverse event reports for DEXAMETHASONE.
410
Reports of Product dose omission issue with DEXAMETHASONE
0.3%
of all DEXAMETHASONE reports
56
Deaths
202
Hospitalizations
How Dangerous Is Product dose omission issue From DEXAMETHASONE?
Of the 410 reports, 56 (13.7%) resulted in death, 202 (49.3%) required hospitalization, and 36 (8.8%) 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 DEXAMETHASONE. However, 410 reports have been filed with the FAERS database.
What Other Side Effects Does DEXAMETHASONE Cause?
Off label use (13,439)
Plasma cell myeloma (9,207)
Drug ineffective (8,359)
Pneumonia (6,073)
Neutropenia (6,050)
Thrombocytopenia (5,873)
Diarrhoea (4,816)
Pyrexia (4,639)
Disease progression (4,545)
Febrile neutropenia (4,382)
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 DEXAMETHASONE Alternatives Have Lower Product dose omission issue Risk?
DEXAMETHASONE vs DEXAMETHASONE\DEXAMETHASONE
DEXAMETHASONE vs DEXAMETHASONE\NEOMYCIN
DEXAMETHASONE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEXAMETHASONE vs DEXAMETHASONE\TOBRAMYCIN
DEXAMETHASONE vs DEXCHLORPHENIRAMINE