Does RIOCIGUAT Cause Incorrect product administration duration? 98 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 98 reports of Incorrect product administration duration have been filed in association with RIOCIGUAT (Adempas). This represents 0.5% of all adverse event reports for RIOCIGUAT.
98
Reports of Incorrect product administration duration with RIOCIGUAT
0.5%
of all RIOCIGUAT reports
10
Deaths
64
Hospitalizations
How Dangerous Is Incorrect product administration duration From RIOCIGUAT?
Of the 98 reports, 10 (10.2%) resulted in death, 64 (65.3%) required hospitalization, and 2 (2.0%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RIOCIGUAT. However, 98 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which RIOCIGUAT Alternatives Have Lower Incorrect product administration duration Risk?
RIOCIGUAT vs RIPRETINIB
RIOCIGUAT vs RISANKIZUMAB
RIOCIGUAT vs RISANKIZUMAB-RZAA
RIOCIGUAT vs RISDIPLAM
RIOCIGUAT vs RISEDRONATE