Does PROGESTERONE Cause Poor quality product administered? 81 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 81 reports of Poor quality product administered have been filed in association with PROGESTERONE (Progesterone). This represents 1.5% of all adverse event reports for PROGESTERONE.
81
Reports of Poor quality product administered with PROGESTERONE
1.5%
of all PROGESTERONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Poor quality product administered From PROGESTERONE?
Of the 81 reports.
Is Poor quality product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PROGESTERONE. However, 81 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 Poor quality product administered?
ONABOTULINUMTOXINA (495)
ICOSAPENT ETHYL (452)
MINOXIDIL (428)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (376)
ADALIMUMAB (239)
TESTOSTERONE CYPIONATE (235)
SOMATROPIN (234)
POLYETHYLENE GLYCOL 3350 (223)
IBUPROFEN (222)
INSULIN GLARGINE (133)
Which PROGESTERONE Alternatives Have Lower Poor quality product administered Risk?
PROGESTERONE vs PROGRAF
PROGESTERONE vs PROHANCE
PROGESTERONE vs PROLIA
PROGESTERONE vs PROMACTA
PROGESTERONE vs PROMAZINE