Does PROGESTERONE Cause Product formulation issue? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Product formulation issue have been filed in association with PROGESTERONE (Progesterone). This represents 0.3% of all adverse event reports for PROGESTERONE.
17
Reports of Product formulation issue with PROGESTERONE
0.3%
of all PROGESTERONE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product formulation issue From PROGESTERONE?
Of the 17 reports, 3 (17.6%) required hospitalization, and 2 (11.8%) were considered life-threatening.
Is Product formulation issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PROGESTERONE. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does PROGESTERONE Cause?
Off label use (736)
Headache (701)
Exposure during pregnancy (684)
Pain (591)
Hypersensitivity (579)
Product use issue (542)
Fatigue (535)
Hyperhidrosis (534)
Drug hypersensitivity (512)
Hepatic enzyme increased (509)
What Other Drugs Cause Product formulation issue?
MINOXIDIL (1,369)
LEVOTHYROXINE (740)
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (174)
OMEPRAZOLE (99)
METHYLPHENIDATE (78)
OXYCODONE (73)
ACETAMINOPHEN\HYDROCODONE (62)
ACETAMINOPHEN\OXYCODONE (61)
ACETAMINOPHEN (59)
BUPROPION (59)
Which PROGESTERONE Alternatives Have Lower Product formulation issue Risk?
PROGESTERONE vs PROGRAF
PROGESTERONE vs PROHANCE
PROGESTERONE vs PROLIA
PROGESTERONE vs PROMACTA
PROGESTERONE vs PROMAZINE