Does HYDROQUINONE Cause Product use in unapproved indication? 38 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 38 reports of Product use in unapproved indication have been filed in association with HYDROQUINONE (Obagi-C Rx system C-Therapy Night Skin Lightening with Vitamins C and E). This represents 13.7% of all adverse event reports for HYDROQUINONE.
38
Reports of Product use in unapproved indication with HYDROQUINONE
13.7%
of all HYDROQUINONE reports
5
Deaths
0
Hospitalizations
How Dangerous Is Product use in unapproved indication From HYDROQUINONE?
Of the 38 reports, 5 (13.2%) resulted in death.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HYDROQUINONE. However, 38 reports have been filed with the FAERS database.
What Other Side Effects Does HYDROQUINONE Cause?
Squamous cell carcinoma of skin (43)
Drug ineffective (32)
Erythema (29)
Acne (24)
Dry skin (23)
Skin atrophy (22)
Rash (19)
Pruritus (18)
Swelling face (18)
Skin exfoliation (17)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which HYDROQUINONE Alternatives Have Lower Product use in unapproved indication Risk?
HYDROQUINONE vs HYDROXOCOBALAMIN
HYDROQUINONE vs HYDROXYCHLOROQUINE
HYDROQUINONE vs HYDROXYCHLOROQUINE DIPHOSPHATE
HYDROQUINONE vs HYDROXYETHYL STARCH 130/0.4
HYDROQUINONE vs HYDROXYPROGESTERONE