Does PROGESTERONE Cause Incorrect product administration duration? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Incorrect product administration duration have been filed in association with PROGESTERONE (Progesterone). This represents 0.1% of all adverse event reports for PROGESTERONE.
5
Reports of Incorrect product administration duration with PROGESTERONE
0.1%
of all PROGESTERONE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Incorrect product administration duration From PROGESTERONE?
Of the 5 reports, 1 (20.0%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PROGESTERONE. However, 5 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which PROGESTERONE Alternatives Have Lower Incorrect product administration duration Risk?
PROGESTERONE vs PROGRAF
PROGESTERONE vs PROHANCE
PROGESTERONE vs PROLIA
PROGESTERONE vs PROMACTA
PROGESTERONE vs PROMAZINE