Does HYDROCORTISONE\PRAMOXINE Cause Product container issue? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product container issue have been filed in association with HYDROCORTISONE\PRAMOXINE. This represents 1.8% of all adverse event reports for HYDROCORTISONE\PRAMOXINE.
8
Reports of Product container issue with HYDROCORTISONE\PRAMOXINE
1.8%
of all HYDROCORTISONE\PRAMOXINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product container issue From HYDROCORTISONE\PRAMOXINE?
Of the 8 reports.
Is Product container issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HYDROCORTISONE\PRAMOXINE. However, 8 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 Product container issue?
CYCLOSPORINE (910)
MINOXIDIL (556)
MOMETASONE FUROATE (450)
FORMOTEROL\MOMETASONE FUROATE (375)
LIFITEGRAST (244)
ALBUTEROL (192)
LATANOPROST (158)
CARBOXYMETHYLCELLULOSE\GLYCERIN (123)
BRIMONIDINE (121)
ACETAMINOPHEN (118)
Which HYDROCORTISONE\PRAMOXINE Alternatives Have Lower Product container issue Risk?
HYDROCORTISONE\PRAMOXINE vs HYDROGEN PEROXIDE
HYDROCORTISONE\PRAMOXINE vs HYDROMORPHONE
HYDROCORTISONE\PRAMOXINE vs HYDROQUINONE
HYDROCORTISONE\PRAMOXINE vs HYDROXOCOBALAMIN
HYDROCORTISONE\PRAMOXINE vs HYDROXYCHLOROQUINE