Does MACITENTAN Cause Wrong technique in product usage process? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of Wrong technique in product usage process have been filed in association with MACITENTAN (OPSYNVI). This represents 0.1% of all adverse event reports for MACITENTAN.
55
Reports of Wrong technique in product usage process with MACITENTAN
0.1%
of all MACITENTAN reports
5
Deaths
18
Hospitalizations
How Dangerous Is Wrong technique in product usage process From MACITENTAN?
Of the 55 reports, 5 (9.1%) resulted in death, 18 (32.7%) required hospitalization, and 2 (3.6%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MACITENTAN. However, 55 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which MACITENTAN Alternatives Have Lower Wrong technique in product usage process Risk?
MACITENTAN vs MACITENTAN\TADALAFIL
MACITENTAN vs MAGNESIUM
MACITENTAN vs MAGNESIUM ASPARTATE
MACITENTAN vs MAGNESIUM ASPARTATE\POTASSIUM ASPARTATE
MACITENTAN vs MAGNESIUM HYDROXIDE