Does ESTRADIOL\NORETHINDRONE Cause Device use issue? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Device use issue have been filed in association with ESTRADIOL\NORETHINDRONE. This represents 0.4% of all adverse event reports for ESTRADIOL\NORETHINDRONE.
16
Reports of Device use issue with ESTRADIOL\NORETHINDRONE
0.4%
of all ESTRADIOL\NORETHINDRONE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device use issue From ESTRADIOL\NORETHINDRONE?
Of the 16 reports, 2 (12.5%) required hospitalization.
Is Device use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ESTRADIOL\NORETHINDRONE. However, 16 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 Device use issue?
SOMATROPIN (2,571)
LEVONORGESTREL (2,489)
COPPER (1,318)
BUDESONIDE\FORMOTEROL (1,236)
EXENATIDE (992)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976)
DUPILUMAB (528)
ALIROCUMAB (471)
INSULIN GLARGINE (469)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)
Which ESTRADIOL\NORETHINDRONE Alternatives Have Lower Device use issue Risk?
ESTRADIOL\NORETHINDRONE vs ESTRADIOL\NORETHINDRONE\RELUGOLIX
ESTRADIOL\NORETHINDRONE vs ESTRADIOL\PROGESTERONE
ESTRADIOL\NORETHINDRONE vs ESTRAMUSTINE
ESTRADIOL\NORETHINDRONE vs ESTRING
ESTRADIOL\NORETHINDRONE vs ESTRIOL