Does PRASTERONE Cause Application site discharge? 111 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 111 reports of Application site discharge have been filed in association with PRASTERONE (Androbalance). This represents 7.3% of all adverse event reports for PRASTERONE.
111
Reports of Application site discharge with PRASTERONE
7.3%
of all PRASTERONE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Application site discharge From PRASTERONE?
Of the 111 reports, 1 (0.9%) required hospitalization.
Is Application site discharge Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRASTERONE. However, 111 reports have been filed with the FAERS database.
What Other Side Effects Does PRASTERONE Cause?
Off label use (653)
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)
Product administration error (47)
What Other Drugs Cause Application site discharge?
INGENOL MEBUTATE (188)
BUPRENORPHINE (138)
ESTRADIOL (72)
BECAPLERMIN (52)
MECHLORETHAMINE (45)
MINOXIDIL (45)
PICATO (31)
NICOTINE (20)
IMIQUIMOD (14)
DICLOFENAC (12)
Which PRASTERONE Alternatives Have Lower Application site discharge Risk?
PRASTERONE vs PRASUGREL
PRASTERONE vs PRAVASTATIN
PRASTERONE vs PRAVASTATIN\PRAVASTATIN
PRASTERONE vs PRAZAXA
PRASTERONE vs PRAZEPAM