Does HYDROCORTISONE\PRAMOXINE Cause Device defective? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Device defective have been filed in association with HYDROCORTISONE\PRAMOXINE. This represents 2.0% of all adverse event reports for HYDROCORTISONE\PRAMOXINE.
9
Reports of Device defective with HYDROCORTISONE\PRAMOXINE
2.0%
of all HYDROCORTISONE\PRAMOXINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device defective From HYDROCORTISONE\PRAMOXINE?
Of the 9 reports.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HYDROCORTISONE\PRAMOXINE. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does HYDROCORTISONE\PRAMOXINE Cause?
Off label use (127)
Product quality issue (104)
Drug ineffective (57)
Device delivery system issue (47)
Product leakage (43)
Device leakage (34)
Wrong technique in product usage process (32)
Device issue (31)
Incorrect dose administered (27)
Device difficult to use (24)
What Other Drugs Cause Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which HYDROCORTISONE\PRAMOXINE Alternatives Have Lower Device defective Risk?
HYDROCORTISONE\PRAMOXINE vs HYDROGEN PEROXIDE
HYDROCORTISONE\PRAMOXINE vs HYDROMORPHONE
HYDROCORTISONE\PRAMOXINE vs HYDROQUINONE
HYDROCORTISONE\PRAMOXINE vs HYDROXOCOBALAMIN
HYDROCORTISONE\PRAMOXINE vs HYDROXYCHLOROQUINE