Does RIOCIGUAT Cause Product dose omission? 137 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 137 reports of Product dose omission have been filed in association with RIOCIGUAT (Adempas). This represents 0.8% of all adverse event reports for RIOCIGUAT.
137
Reports of Product dose omission with RIOCIGUAT
0.8%
of all RIOCIGUAT reports
11
Deaths
109
Hospitalizations
How Dangerous Is Product dose omission From RIOCIGUAT?
Of the 137 reports, 11 (8.0%) resulted in death, 109 (79.6%) required hospitalization, and 1 (0.7%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RIOCIGUAT. However, 137 reports have been filed with the FAERS database.
What Other Side Effects Does RIOCIGUAT Cause?
Death (4,500)
Dyspnoea (2,881)
Headache (2,462)
Dizziness (2,208)
Hypotension (2,192)
Nausea (2,020)
Hospitalisation (1,864)
Diarrhoea (1,790)
Fatigue (1,638)
Vomiting (1,124)
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 RIOCIGUAT Alternatives Have Lower Product dose omission Risk?
RIOCIGUAT vs RIPRETINIB
RIOCIGUAT vs RISANKIZUMAB
RIOCIGUAT vs RISANKIZUMAB-RZAA
RIOCIGUAT vs RISDIPLAM
RIOCIGUAT vs RISEDRONATE