Does PIRFENIDONE Cause Product dose omission? 211 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 211 reports of Product dose omission have been filed in association with PIRFENIDONE (PIRFENIDONE). This represents 0.6% of all adverse event reports for PIRFENIDONE.
211
Reports of Product dose omission with PIRFENIDONE
0.6%
of all PIRFENIDONE reports
0
Deaths
63
Hospitalizations
How Dangerous Is Product dose omission From PIRFENIDONE?
Of the 211 reports, 63 (29.9%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PIRFENIDONE. However, 211 reports have been filed with the FAERS database.
What Other Side Effects Does PIRFENIDONE Cause?
Death (7,221)
Nausea (4,944)
Fatigue (3,597)
Decreased appetite (3,126)
Diarrhoea (3,026)
Dyspnoea (2,526)
Weight decreased (2,113)
Dizziness (2,027)
Rash (1,982)
Cough (1,692)
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 PIRFENIDONE Alternatives Have Lower Product dose omission Risk?
PIRFENIDONE vs PIRIBEDIL
PIRFENIDONE vs PIRITRAMIDE
PIRFENIDONE vs PIROXICAM
PIRFENIDONE vs PIRTOBRUTINIB
PIRFENIDONE vs PIT VIPER IMMUNE GLOBULIN ANTIVENIN