Does HYDROCORTISONE\PRAMOXINE Cause Device delivery system issue? 47 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 47 reports of Device delivery system issue have been filed in association with HYDROCORTISONE\PRAMOXINE. This represents 10.5% of all adverse event reports for HYDROCORTISONE\PRAMOXINE.
47
Reports of Device delivery system issue with HYDROCORTISONE\PRAMOXINE
10.5%
of all HYDROCORTISONE\PRAMOXINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device delivery system issue From HYDROCORTISONE\PRAMOXINE?
Of the 47 reports.
Is Device delivery system issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HYDROCORTISONE\PRAMOXINE. However, 47 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)
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)
Pain (24)
What Other Drugs Cause Device delivery system issue?
ALBUTEROL (9,509)
SOMATROPIN (1,848)
EXENATIDE (1,533)
BUDESONIDE\FORMOTEROL (1,260)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (1,181)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (523)
LEVALBUTEROL (459)
MOMETASONE FUROATE\OLOPATADINE (347)
ABATACEPT (342)
PEGFILGRASTIM (323)
Which HYDROCORTISONE\PRAMOXINE Alternatives Have Lower Device delivery system issue Risk?
HYDROCORTISONE\PRAMOXINE vs HYDROGEN PEROXIDE
HYDROCORTISONE\PRAMOXINE vs HYDROMORPHONE
HYDROCORTISONE\PRAMOXINE vs HYDROQUINONE
HYDROCORTISONE\PRAMOXINE vs HYDROXOCOBALAMIN
HYDROCORTISONE\PRAMOXINE vs HYDROXYCHLOROQUINE