Does PREDNISOLONE Cause Incorrect product administration duration? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Incorrect product administration duration have been filed in association with PREDNISOLONE (Prednisolone Sodium Phosphate). This represents 0.0% of all adverse event reports for PREDNISOLONE.
35
Reports of Incorrect product administration duration with PREDNISOLONE
0.0%
of all PREDNISOLONE reports
8
Deaths
17
Hospitalizations
How Dangerous Is Incorrect product administration duration From PREDNISOLONE?
Of the 35 reports, 8 (22.9%) resulted in death, 17 (48.6%) required hospitalization, and 4 (11.4%) 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 PREDNISOLONE. However, 35 reports have been filed with the FAERS database.
What Other Side Effects Does PREDNISOLONE Cause?
Off label use (8,817)
Drug ineffective (8,459)
Product use in unapproved indication (3,414)
Pyrexia (3,159)
Condition aggravated (3,143)
Pneumonia (2,713)
Treatment failure (2,616)
Sepsis (2,281)
Dyspnoea (2,248)
Diarrhoea (2,192)
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 PREDNISOLONE Alternatives Have Lower Incorrect product administration duration Risk?
PREDNISOLONE vs PREDNISOLONE METAZOATE
PREDNISOLONE vs PREDNISOLONE\PREDNISOLONE\PREDNISOLONE
PREDNISOLONE vs PREDNISONE
PREDNISOLONE vs PREGABALIN
PREDNISOLONE vs PREMARIN