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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 SELEXIPAG Cause Product administration interrupted? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product administration interrupted have been filed in association with SELEXIPAG (Selexipag). This represents 0.1% of all adverse event reports for SELEXIPAG.

14
Reports of Product administration interrupted with SELEXIPAG
0.1%
of all SELEXIPAG reports
1
Deaths
10
Hospitalizations

How Dangerous Is Product administration interrupted From SELEXIPAG?

Of the 14 reports, 1 (7.1%) resulted in death, 10 (71.4%) required hospitalization.

Is Product administration interrupted Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SELEXIPAG. However, 14 reports have been filed with the FAERS database.

What Other Side Effects Does SELEXIPAG Cause?

Headache (5,693) Diarrhoea (4,341) Dyspnoea (3,705) Nausea (3,392) Pain in jaw (2,072) Fatigue (2,009) Death (1,893) Pain (1,870) Pain in extremity (1,797) Dizziness (1,796)

What Other Drugs Cause Product administration interrupted?

CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446) SODIUM OXYBATE (1,272) CANNABIDIOL (511) ISOTRETINOIN (503) APREMILAST (314) TREPROSTINIL (295) EPOPROSTENOL (205) LENALIDOMIDE (146) ETANERCEPT (142) INTERFERON BETA-1A (115)

Which SELEXIPAG Alternatives Have Lower Product administration interrupted Risk?

SELEXIPAG vs SELINEXOR SELEXIPAG vs SELPERCATINIB SELEXIPAG vs SELUMETINIB SELEXIPAG vs SEMAGLUTIDE SELEXIPAG vs SEMUSTINE

Related Pages

SELEXIPAG Full Profile All Product administration interrupted Reports All Drugs Causing Product administration interrupted SELEXIPAG Demographics