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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\PROGESTERONE Cause Product dose omission issue? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product dose omission issue have been filed in association with ESTRADIOL\PROGESTERONE. This represents 3.0% of all adverse event reports for ESTRADIOL\PROGESTERONE.

14
Reports of Product dose omission issue with ESTRADIOL\PROGESTERONE
3.0%
of all ESTRADIOL\PROGESTERONE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product dose omission issue From ESTRADIOL\PROGESTERONE?

Of the 14 reports.

Is Product dose omission issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ESTRADIOL\PROGESTERONE. However, 14 reports have been filed with the FAERS database.

What Other Side Effects Does ESTRADIOL\PROGESTERONE Cause?

Off label use (61) Drug ineffective (57) Headache (52) Vaginal haemorrhage (52) Hot flush (38) Dizziness (37) Breast tenderness (36) Nausea (30) Weight increased (23) Fatigue (18)

What Other Drugs Cause Product dose omission issue?

DUPILUMAB (18,189) USTEKINUMAB (9,405) GUSELKUMAB (9,267) LENALIDOMIDE (8,145) MEPOLIZUMAB (5,873) TOFACITINIB (5,646) VOXELOTOR (5,122) BELIMUMAB (4,671) SECUKINUMAB (4,572) APREMILAST (4,460)

Which ESTRADIOL\PROGESTERONE Alternatives Have Lower Product dose omission issue Risk?

ESTRADIOL\PROGESTERONE vs ESTRAMUSTINE ESTRADIOL\PROGESTERONE vs ESTRING ESTRADIOL\PROGESTERONE vs ESTRIOL ESTRADIOL\PROGESTERONE vs ESTROGENS ESTRADIOL\PROGESTERONE vs ESTROGENS, CONJUGATED

Related Pages

ESTRADIOL\PROGESTERONE Full Profile All Product dose omission issue Reports All Drugs Causing Product dose omission issue ESTRADIOL\PROGESTERONE Demographics