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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ESTRADIOL\NORETHINDRONE Cause Device breakage? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Device breakage have been filed in association with ESTRADIOL\NORETHINDRONE. This represents 0.3% of all adverse event reports for ESTRADIOL\NORETHINDRONE.

14
Reports of Device breakage with ESTRADIOL\NORETHINDRONE
0.3%
of all ESTRADIOL\NORETHINDRONE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device breakage From ESTRADIOL\NORETHINDRONE?

Of the 14 reports.

Is Device breakage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ESTRADIOL\NORETHINDRONE. However, 14 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 breakage?

COPPER (9,201) SOMATROPIN (7,761) ETONOGESTREL (4,140) LEVONORGESTREL (2,726) ETHINYL ESTRADIOL\ETONOGESTREL (741) CARBIDOPA\LEVODOPA (634) TREPROSTINIL (396) ADALIMUMAB (375) ALBUTEROL (256) EPOPROSTENOL (240)

Which ESTRADIOL\NORETHINDRONE Alternatives Have Lower Device breakage Risk?

ESTRADIOL\NORETHINDRONE vs ESTRADIOL\NORETHINDRONE\RELUGOLIX ESTRADIOL\NORETHINDRONE vs ESTRADIOL\PROGESTERONE ESTRADIOL\NORETHINDRONE vs ESTRAMUSTINE ESTRADIOL\NORETHINDRONE vs ESTRING ESTRADIOL\NORETHINDRONE vs ESTRIOL

Related Pages

ESTRADIOL\NORETHINDRONE Full Profile All Device breakage Reports All Drugs Causing Device breakage ESTRADIOL\NORETHINDRONE Demographics