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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 Cause Recalled product administered? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Recalled product administered have been filed in association with ESTRADIOL (Estradiol). This represents 0.0% of all adverse event reports for ESTRADIOL.

6
Reports of Recalled product administered with ESTRADIOL
0.0%
of all ESTRADIOL reports
0
Deaths
1
Hospitalizations

How Dangerous Is Recalled product administered From ESTRADIOL?

Of the 6 reports, 1 (16.7%) required hospitalization.

Is Recalled product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ESTRADIOL. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does ESTRADIOL Cause?

Product adhesion issue (4,774) Drug ineffective (4,010) Off label use (3,238) Hot flush (2,264) Wrong technique in product usage process (1,871) Product quality issue (1,671) Headache (1,504) No adverse event (1,493) Application site pruritus (1,181) Application site erythema (1,117)

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 Alternatives Have Lower Recalled product administered Risk?

ESTRADIOL vs ESTRADIOL CYPIONATE ESTRADIOL vs ESTRADIOL\LEVONORGESTREL ESTRADIOL vs ESTRADIOL\NORETHINDRONE ESTRADIOL vs ESTRADIOL\NORETHINDRONE\RELUGOLIX ESTRADIOL vs ESTRADIOL\PROGESTERONE

Related Pages

ESTRADIOL Full Profile All Recalled product administered Reports All Drugs Causing Recalled product administered ESTRADIOL Demographics