SELEXIPAG

N/A

Manufactured by Actelion Pharmaceuticals US, Inc.

96,284 FDA adverse event reports analyzed

Last updated: 2026-04-14

About SELEXIPAG

SELEXIPAG is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Actelion Pharmaceuticals US, Inc.. The most commonly reported adverse reactions for SELEXIPAG include HEADACHE, DIARRHOEA, DYSPNOEA, NAUSEA, FATIGUE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for SELEXIPAG.

Top Adverse Reactions

HEADACHE6,584 reports
DIARRHOEA5,062 reports
DYSPNOEA4,646 reports
NAUSEA4,014 reports
FATIGUE2,516 reports
DEATH2,488 reports
PAIN IN JAW2,375 reports
DIZZINESS2,250 reports
PAIN2,169 reports
PAIN IN EXTREMITY2,074 reports
MYALGIA1,946 reports
VOMITING1,905 reports
MALAISE1,771 reports
PNEUMONIA1,770 reports
HYPOTENSION1,680 reports
PULMONARY ARTERIAL HYPERTENSION1,656 reports
ARTHRALGIA1,586 reports
HOSPITALISATION1,396 reports
DECREASED APPETITE1,386 reports
FLUID RETENTION1,297 reports
COUGH1,204 reports
DYSPNOEA EXERTIONAL1,176 reports
CONDITION AGGRAVATED1,169 reports
ASTHENIA1,125 reports
FLUSHING1,125 reports
PERIPHERAL SWELLING1,074 reports
OXYGEN SATURATION DECREASED1,046 reports
CHEST PAIN1,025 reports
WEIGHT DECREASED1,024 reports
OEDEMA PERIPHERAL1,021 reports
ABDOMINAL DISCOMFORT968 reports
BACK PAIN890 reports
PULMONARY HYPERTENSION871 reports
FEELING ABNORMAL852 reports
SYNCOPE850 reports
FALL844 reports
ABDOMINAL PAIN UPPER832 reports
INSOMNIA803 reports
OFF LABEL USE773 reports
CARDIAC FAILURE757 reports
ANAEMIA743 reports
PYREXIA732 reports
NASOPHARYNGITIS715 reports
DRUG INEFFECTIVE682 reports
OEDEMA681 reports
WEIGHT INCREASED657 reports
PALPITATIONS648 reports
NASAL CONGESTION622 reports
ABDOMINAL PAIN589 reports
RIGHT VENTRICULAR FAILURE587 reports
PRODUCT DOSE OMISSION ISSUE579 reports
MUSCLE SPASMS571 reports
ABDOMINAL DISTENSION550 reports
CONSTIPATION542 reports
CHEST DISCOMFORT535 reports
DYSPEPSIA522 reports
UNEVALUABLE EVENT510 reports
EPISTAXIS489 reports
LOSS OF CONSCIOUSNESS488 reports
MIGRAINE476 reports
RASH461 reports
HAEMOGLOBIN DECREASED453 reports
HEART RATE INCREASED445 reports
BLOOD PRESSURE DECREASED435 reports
HYPOXIA429 reports
PULMONARY OEDEMA415 reports
DEHYDRATION411 reports
ANXIETY409 reports
THERAPY NON RESPONDER400 reports
DISEASE PROGRESSION396 reports
ATRIAL FIBRILLATION391 reports
INFLUENZA387 reports
PRURITUS385 reports
DRUG INTOLERANCE384 reports
SWELLING380 reports
NECK PAIN379 reports
GAIT DISTURBANCE375 reports
URINARY TRACT INFECTION375 reports
RESPIRATORY FAILURE373 reports
INFUSION SITE PAIN365 reports
CARDIAC FAILURE CONGESTIVE355 reports
PLEURAL EFFUSION349 reports
SOMNOLENCE345 reports
PRODUCT DOSE OMISSION343 reports
GASTROOESOPHAGEAL REFLUX DISEASE342 reports
FLUID OVERLOAD336 reports
PRODUCTIVE COUGH328 reports
TRANSFUSION328 reports
COVID 19319 reports
THERAPY CHANGE316 reports
CHILLS311 reports
GASTROINTESTINAL DISORDER310 reports
JOINT SWELLING310 reports
ERYTHEMA302 reports
ASCITES299 reports
CARDIAC DISORDER295 reports
PERICARDIAL EFFUSION290 reports
ADVERSE EVENT281 reports
ILLNESS281 reports
BRONCHITIS278 reports

Report Outcomes

Out of 24,800 classified reports for SELEXIPAG:

Serious 75.2%Non-Serious 24.8%

The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.

Demographics Breakdown

Reports by Sex

Female17,500 (73.6%)
Male6,263 (26.4%)
Unknown2 (0.0%)

Reports by Age

Age 70556 reports
Age 72505 reports
Age 65472 reports
Age 69457 reports
Age 75442 reports
Age 62441 reports
Age 71439 reports
Age 68431 reports
Age 73419 reports
Age 66415 reports
Age 74404 reports
Age 76404 reports
Age 67401 reports
Age 64392 reports
Age 61388 reports
Age 60384 reports
Age 63382 reports
Age 57367 reports
Age 56363 reports
Age 59363 reports

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

Frequently Asked Questions

How many FDA adverse event reports are associated with SELEXIPAG?

This profile reflects 96,284 FDA FAERS reports that mention SELEXIPAG. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for SELEXIPAG?

Frequently reported terms in FAERS include HEADACHE, DIARRHOEA, DYSPNOEA, NAUSEA, FATIGUE, DEATH. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures SELEXIPAG?

Labeling and FAERS entries often list Actelion Pharmaceuticals US, Inc. in connection with SELEXIPAG. Always verify the specific product and NDC with your pharmacist.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.