Does DESOXIMETASONE Cause Incorrect product administration duration? 90 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 90 reports of Incorrect product administration duration have been filed in association with DESOXIMETASONE (Desoximetasone). This represents 0.8% of all adverse event reports for DESOXIMETASONE.
90
Reports of Incorrect product administration duration with DESOXIMETASONE
0.8%
of all DESOXIMETASONE reports
69
Deaths
68
Hospitalizations
How Dangerous Is Incorrect product administration duration From DESOXIMETASONE?
Of the 90 reports, 69 (76.7%) resulted in death, 68 (75.6%) required hospitalization, and 68 (75.6%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DESOXIMETASONE. However, 90 reports have been filed with the FAERS database.
What Other Side Effects Does DESOXIMETASONE Cause?
Systemic lupus erythematosus (7,242)
Drug ineffective (7,162)
Pain (7,080)
Alopecia (7,046)
Fatigue (7,044)
Pemphigus (7,043)
Abdominal discomfort (6,895)
Glossodynia (6,827)
Rheumatoid arthritis (6,719)
Swelling (6,250)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which DESOXIMETASONE Alternatives Have Lower Incorrect product administration duration Risk?
DESOXIMETASONE vs DESVENLAFAXINE
DESOXIMETASONE vs DETROL
DESOXIMETASONE vs DEUCRAVACITINIB
DESOXIMETASONE vs DEUTETRABENAZINE
DESOXIMETASONE vs DEUTIVACAFTOR\TEZACAFTOR\VANZACAFTOR