Does MACITENTAN Cause Product dose omission? 908 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 908 reports of Product dose omission have been filed in association with MACITENTAN (OPSYNVI). This represents 2.0% of all adverse event reports for MACITENTAN.
908
Reports of Product dose omission with MACITENTAN
2.0%
of all MACITENTAN reports
145
Deaths
664
Hospitalizations
How Dangerous Is Product dose omission From MACITENTAN?
Of the 908 reports, 145 (16.0%) resulted in death, 664 (73.1%) required hospitalization, and 17 (1.9%) 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 MACITENTAN. However, 908 reports have been filed with the FAERS database.
What Other Side Effects Does MACITENTAN Cause?
Dyspnoea (8,315)
Death (5,864)
Headache (4,856)
Diarrhoea (3,669)
Pneumonia (3,531)
Nausea (3,463)
Hospitalisation (3,414)
Fatigue (3,172)
Fluid retention (2,861)
Dizziness (2,704)
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 MACITENTAN Alternatives Have Lower Product dose omission Risk?
MACITENTAN vs MACITENTAN\TADALAFIL
MACITENTAN vs MAGNESIUM
MACITENTAN vs MAGNESIUM ASPARTATE
MACITENTAN vs MAGNESIUM ASPARTATE\POTASSIUM ASPARTATE
MACITENTAN vs MAGNESIUM HYDROXIDE