Does METHYLPREDNISOLONE Cause Product dose omission in error? 25 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Product dose omission in error have been filed in association with METHYLPREDNISOLONE (Medroloan II SUIK). This represents 0.0% of all adverse event reports for METHYLPREDNISOLONE.
25
Reports of Product dose omission in error with METHYLPREDNISOLONE
0.0%
of all METHYLPREDNISOLONE reports
1
Deaths
6
Hospitalizations
How Dangerous Is Product dose omission in error From METHYLPREDNISOLONE?
Of the 25 reports, 1 (4.0%) resulted in death, 6 (24.0%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for METHYLPREDNISOLONE. However, 25 reports have been filed with the FAERS database.
What Other Side Effects Does METHYLPREDNISOLONE Cause?
Off label use (10,364)
Drug ineffective (9,959)
Product use in unapproved indication (4,115)
Condition aggravated (3,784)
Headache (3,419)
Fatigue (3,250)
Pyrexia (3,226)
Pain (3,165)
Nausea (3,105)
Pneumonia (3,006)
What Other Drugs Cause Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which METHYLPREDNISOLONE Alternatives Have Lower Product dose omission in error Risk?
METHYLPREDNISOLONE vs METHYLPREDNISOLONE ACEPONATE
METHYLPREDNISOLONE vs METHYLPREDNISOLONE HEMISUCCINATE
METHYLPREDNISOLONE vs METILDIGOXIN
METHYLPREDNISOLONE vs METOCLOPRAMIDE
METHYLPREDNISOLONE vs METOLAZONE