Does HYDROCORTISONE\PRAMOXINE Cause Device issue? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Device issue have been filed in association with HYDROCORTISONE\PRAMOXINE. This represents 7.0% of all adverse event reports for HYDROCORTISONE\PRAMOXINE.
31
Reports of Device issue with HYDROCORTISONE\PRAMOXINE
7.0%
of all HYDROCORTISONE\PRAMOXINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device issue From HYDROCORTISONE\PRAMOXINE?
Of the 31 reports.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HYDROCORTISONE\PRAMOXINE. However, 31 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)
Incorrect dose administered (27)
Device difficult to use (24)
Pain (24)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which HYDROCORTISONE\PRAMOXINE Alternatives Have Lower Device issue Risk?
HYDROCORTISONE\PRAMOXINE vs HYDROGEN PEROXIDE
HYDROCORTISONE\PRAMOXINE vs HYDROMORPHONE
HYDROCORTISONE\PRAMOXINE vs HYDROQUINONE
HYDROCORTISONE\PRAMOXINE vs HYDROXOCOBALAMIN
HYDROCORTISONE\PRAMOXINE vs HYDROXYCHLOROQUINE