Does HYDROCORTISONE PROBUTATE Cause Device dislocation? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Device dislocation have been filed in association with HYDROCORTISONE PROBUTATE. This represents 1.2% of all adverse event reports for HYDROCORTISONE PROBUTATE.
6
Reports of Device dislocation with HYDROCORTISONE PROBUTATE
1.2%
of all HYDROCORTISONE PROBUTATE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Device dislocation From HYDROCORTISONE PROBUTATE?
Of the 6 reports, 6 (100.0%) required hospitalization, and 6 (100.0%) were considered life-threatening.
Is Device dislocation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HYDROCORTISONE PROBUTATE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does HYDROCORTISONE PROBUTATE Cause?
Maternal exposure during pregnancy (239)
Hypertension (237)
Fibromyalgia (233)
Hand deformity (233)
Dry mouth (232)
Folliculitis (229)
Osteoarthritis (227)
Lower respiratory tract infection (226)
Duodenal ulcer perforation (224)
Pemphigus (224)
What Other Drugs Cause Device dislocation?
LEVONORGESTREL (13,757)
COPPER (6,955)
CARBIDOPA\LEVODOPA (2,937)
ETONOGESTREL (2,909)
TREPROSTINIL (1,626)
MIRENA (677)
BACLOFEN (492)
PARAGARD 380A (479)
ADALIMUMAB (372)
EPOPROSTENOL (358)
Which HYDROCORTISONE PROBUTATE Alternatives Have Lower Device dislocation Risk?
HYDROCORTISONE PROBUTATE vs HYDROCORTISONE\HYDROCORTISONE
HYDROCORTISONE PROBUTATE vs HYDROCORTISONE\NEOMYCIN\POLYMYXIN B
HYDROCORTISONE PROBUTATE vs HYDROCORTISONE\PRAMOXINE
HYDROCORTISONE PROBUTATE vs HYDROGEN PEROXIDE
HYDROCORTISONE PROBUTATE vs HYDROMORPHONE