Does PRASTERONE Cause Poor quality product administered? 40 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Poor quality product administered have been filed in association with PRASTERONE (Androbalance). This represents 2.6% of all adverse event reports for PRASTERONE.
40
Reports of Poor quality product administered with PRASTERONE
2.6%
of all PRASTERONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Poor quality product administered From PRASTERONE?
Of the 40 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 PRASTERONE. However, 40 reports have been filed with the FAERS database.
What Other Side Effects Does PRASTERONE Cause?
Off label use (653)
Application site discharge (111)
Drug ineffective (105)
Vaginal discharge (82)
Vulvovaginal burning sensation (71)
Headache (59)
Rash (57)
Alopecia (55)
Product dose omission issue (55)
Therapeutic response unexpected (52)
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 PRASTERONE Alternatives Have Lower Poor quality product administered Risk?
PRASTERONE vs PRASUGREL
PRASTERONE vs PRAVASTATIN
PRASTERONE vs PRAVASTATIN\PRAVASTATIN
PRASTERONE vs PRAZAXA
PRASTERONE vs PRAZEPAM