Does ESTRADIOL\NORETHINDRONE Cause Recalled product administered? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Recalled product administered have been filed in association with ESTRADIOL\NORETHINDRONE. This represents 0.4% of all adverse event reports for ESTRADIOL\NORETHINDRONE.
15
Reports of Recalled product administered with ESTRADIOL\NORETHINDRONE
0.4%
of all ESTRADIOL\NORETHINDRONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Recalled product administered From ESTRADIOL\NORETHINDRONE?
Of the 15 reports.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ESTRADIOL\NORETHINDRONE. However, 15 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which ESTRADIOL\NORETHINDRONE Alternatives Have Lower Recalled product administered Risk?
ESTRADIOL\NORETHINDRONE vs ESTRADIOL\NORETHINDRONE\RELUGOLIX
ESTRADIOL\NORETHINDRONE vs ESTRADIOL\PROGESTERONE
ESTRADIOL\NORETHINDRONE vs ESTRAMUSTINE
ESTRADIOL\NORETHINDRONE vs ESTRING
ESTRADIOL\NORETHINDRONE vs ESTRIOL