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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 AMBRISENTAN Cause Condition aggravated? 1,071 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,071 reports of Condition aggravated have been filed in association with AMBRISENTAN (AMBRISENTAN). This represents 1.2% of all adverse event reports for AMBRISENTAN.

1,071
Reports of Condition aggravated with AMBRISENTAN
1.2%
of all AMBRISENTAN reports
111
Deaths
491
Hospitalizations

How Dangerous Is Condition aggravated From AMBRISENTAN?

Of the 1,071 reports, 111 (10.4%) resulted in death, 491 (45.8%) required hospitalization, and 20 (1.9%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AMBRISENTAN. However, 1,071 reports have been filed with the FAERS database.

What Other Side Effects Does AMBRISENTAN Cause?

Dyspnoea (13,367) Death (7,497) Headache (7,325) Pneumonia (4,693) Dizziness (4,561) Fatigue (4,436) Diarrhoea (4,312) Nausea (3,986) Fluid retention (3,927) Malaise (3,839)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which AMBRISENTAN Alternatives Have Lower Condition aggravated Risk?

AMBRISENTAN vs AMBROSIA ARTEMISIIFOLIA POLLEN AMBRISENTAN vs AMBROXOL AMBRISENTAN vs AMDINOCILLIN PIVOXIL AMBRISENTAN vs AMG-510 AMBRISENTAN vs AMIFAMPRIDINE

Related Pages

AMBRISENTAN Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated AMBRISENTAN Demographics