Does VERICIGUAT Cause Product dose omission issue? 48 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 48 reports of Product dose omission issue have been filed in association with VERICIGUAT (VERQUVO). This represents 5.0% of all adverse event reports for VERICIGUAT.
48
Reports of Product dose omission issue with VERICIGUAT
5.0%
of all VERICIGUAT reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission issue From VERICIGUAT?
Of the 48 reports, 3 (6.3%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VERICIGUAT. However, 48 reports have been filed with the FAERS database.
What Other Side Effects Does VERICIGUAT Cause?
Hypotension (115)
Death (94)
Cardiac failure (81)
Dizziness (67)
No adverse event (42)
Blood pressure decreased (34)
Malaise (33)
Anaemia (32)
Dyspnoea (32)
Fatigue (26)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which VERICIGUAT Alternatives Have Lower Product dose omission issue Risk?
VERICIGUAT vs VERTEPORFIN
VERICIGUAT vs VESICARE
VERICIGUAT vs VFEND
VERICIGUAT vs VIAGRA
VERICIGUAT vs VIBEGRON