Does PREDNISONE Cause Product dose omission issue? 755 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 755 reports of Product dose omission issue have been filed in association with PREDNISONE (prednisone). This represents 0.5% of all adverse event reports for PREDNISONE.
755
Reports of Product dose omission issue with PREDNISONE
0.5%
of all PREDNISONE reports
19
Deaths
315
Hospitalizations
How Dangerous Is Product dose omission issue From PREDNISONE?
Of the 755 reports, 19 (2.5%) resulted in death, 315 (41.7%) required hospitalization, and 23 (3.0%) 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 PREDNISONE. However, 755 reports have been filed with the FAERS database.
What Other Side Effects Does PREDNISONE Cause?
Drug ineffective (29,059)
Off label use (17,867)
Pain (14,347)
Fatigue (14,320)
Dyspnoea (12,830)
Rheumatoid arthritis (11,678)
Condition aggravated (10,751)
Asthma (10,028)
Alopecia (9,276)
Rash (9,252)
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 PREDNISONE Alternatives Have Lower Product dose omission issue Risk?
PREDNISONE vs PREGABALIN
PREDNISONE vs PREMARIN
PREDNISONE vs PREMPRO
PREDNISONE vs PRETOMANID
PREDNISONE vs PREVISCAN