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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does MACITENTAN Cause Device issue? 119 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 119 reports of Device issue have been filed in association with MACITENTAN (OPSYNVI). This represents 0.3% of all adverse event reports for MACITENTAN.

119
Reports of Device issue with MACITENTAN
0.3%
of all MACITENTAN reports
22
Deaths
90
Hospitalizations

How Dangerous Is Device issue From MACITENTAN?

Of the 119 reports, 22 (18.5%) resulted in death, 90 (75.6%) required hospitalization, and 8 (6.7%) were considered life-threatening.

Is Device issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MACITENTAN. However, 119 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 Device issue?

ADALIMUMAB (17,630) SOMATROPIN (5,131) PEGFILGRASTIM (5,071) ETANERCEPT (4,143) INSULIN GLARGINE (3,175) EXENATIDE (2,862) LEVONORGESTREL (2,623) CARBIDOPA\LEVODOPA (2,574) GOLIMUMAB (1,827) USTEKINUMAB (1,716)

Which MACITENTAN Alternatives Have Lower Device issue Risk?

MACITENTAN vs MACITENTAN\TADALAFIL MACITENTAN vs MAGNESIUM MACITENTAN vs MAGNESIUM ASPARTATE MACITENTAN vs MAGNESIUM ASPARTATE\POTASSIUM ASPARTATE MACITENTAN vs MAGNESIUM HYDROXIDE

Related Pages

MACITENTAN Full Profile All Device issue Reports All Drugs Causing Device issue MACITENTAN Demographics