Does PRASTERONE Cause Product dose omission issue? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of Product dose omission issue have been filed in association with PRASTERONE (Androbalance). This represents 3.6% of all adverse event reports for PRASTERONE.
55
Reports of Product dose omission issue with PRASTERONE
3.6%
of all PRASTERONE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product dose omission issue From PRASTERONE?
Of the 55 reports, 2 (3.6%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRASTERONE. However, 55 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)
Therapeutic response unexpected (52)
Product administration error (47)
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 PRASTERONE Alternatives Have Lower Product dose omission issue Risk?
PRASTERONE vs PRASUGREL
PRASTERONE vs PRAVASTATIN
PRASTERONE vs PRAVASTATIN\PRAVASTATIN
PRASTERONE vs PRAZAXA
PRASTERONE vs PRAZEPAM