Does ESTRADIOL\NORETHINDRONE Cause Product storage error? 698 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 698 reports of Product storage error have been filed in association with ESTRADIOL\NORETHINDRONE. This represents 16.3% of all adverse event reports for ESTRADIOL\NORETHINDRONE.
698
Reports of Product storage error with ESTRADIOL\NORETHINDRONE
16.3%
of all ESTRADIOL\NORETHINDRONE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product storage error From ESTRADIOL\NORETHINDRONE?
Of the 698 reports, 3 (0.4%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ESTRADIOL\NORETHINDRONE. However, 698 reports have been filed with the FAERS database.
What Other Side Effects Does ESTRADIOL\NORETHINDRONE Cause?
Product adhesion issue (734)
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)
Drug ineffective (247)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which ESTRADIOL\NORETHINDRONE Alternatives Have Lower Product storage error Risk?
ESTRADIOL\NORETHINDRONE vs ESTRADIOL\NORETHINDRONE\RELUGOLIX
ESTRADIOL\NORETHINDRONE vs ESTRADIOL\PROGESTERONE
ESTRADIOL\NORETHINDRONE vs ESTRAMUSTINE
ESTRADIOL\NORETHINDRONE vs ESTRING
ESTRADIOL\NORETHINDRONE vs ESTRIOL