Does ESTRADIOL\NORETHINDRONE Cause Application site dryness? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Application site dryness have been filed in association with ESTRADIOL\NORETHINDRONE. This represents 1.1% of all adverse event reports for ESTRADIOL\NORETHINDRONE.
49
Reports of Application site dryness with ESTRADIOL\NORETHINDRONE
1.1%
of all ESTRADIOL\NORETHINDRONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Application site dryness From ESTRADIOL\NORETHINDRONE?
Of the 49 reports.
Is Application site dryness Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ESTRADIOL\NORETHINDRONE. However, 49 reports have been filed with the FAERS database.
What Other Side Effects Does ESTRADIOL\NORETHINDRONE Cause?
Product adhesion issue (734)
Product storage error (698)
Off label use (585)
Application site erythema (533)
No adverse event (508)
Application site pruritus (463)
Wrong technique in product usage process (428)
Application site irritation (341)
Hot flush (307)
Product quality issue (263)
What Other Drugs Cause Application site dryness?
MINOXIDIL (1,027)
INGENOL MEBUTATE (365)
SUMATRIPTAN (208)
BUPRENORPHINE (100)
TESTOSTERONE (63)
ADAPALENE (60)
DICLOFENAC (55)
ESTRADIOL (52)
NICOTINE (48)
TRETINOIN (44)
Which ESTRADIOL\NORETHINDRONE Alternatives Have Lower Application site dryness Risk?
ESTRADIOL\NORETHINDRONE vs ESTRADIOL\NORETHINDRONE\RELUGOLIX
ESTRADIOL\NORETHINDRONE vs ESTRADIOL\PROGESTERONE
ESTRADIOL\NORETHINDRONE vs ESTRAMUSTINE
ESTRADIOL\NORETHINDRONE vs ESTRING
ESTRADIOL\NORETHINDRONE vs ESTRIOL