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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does PRASTERONE Cause Product dose omission? 20 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Product dose omission have been filed in association with PRASTERONE (Androbalance). This represents 1.3% of all adverse event reports for PRASTERONE.

20
Reports of Product dose omission with PRASTERONE
1.3%
of all PRASTERONE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product dose omission From PRASTERONE?

Of the 20 reports.

Is Product dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PRASTERONE. However, 20 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 Product dose omission?

APREMILAST (4,567) DUPILUMAB (2,729) ALBUTEROL (1,742) USTEKINUMAB (1,653) INSULIN GLARGINE (1,500) ETANERCEPT (1,400) LENALIDOMIDE (1,400) RUXOLITINIB (1,376) ALIROCUMAB (1,354) DIMETHYL (1,248)

Which PRASTERONE Alternatives Have Lower Product dose omission Risk?

PRASTERONE vs PRASUGREL PRASTERONE vs PRAVASTATIN PRASTERONE vs PRAVASTATIN\PRAVASTATIN PRASTERONE vs PRAZAXA PRASTERONE vs PRAZEPAM

Related Pages

PRASTERONE Full Profile All Product dose omission Reports All Drugs Causing Product dose omission PRASTERONE Demographics