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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 Investigation? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Investigation have been filed in association with AMBRISENTAN (AMBRISENTAN). This represents 0.0% of all adverse event reports for AMBRISENTAN.

8
Reports of Investigation with AMBRISENTAN
0.0%
of all AMBRISENTAN reports
1
Deaths
7
Hospitalizations

How Dangerous Is Investigation From AMBRISENTAN?

Of the 8 reports, 1 (12.5%) resulted in death, 7 (87.5%) required hospitalization.

Is Investigation Listed in the Official Label?

Yes, Investigation is listed as a known adverse reaction in the official FDA drug label for AMBRISENTAN.

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 Investigation?

ARANESP (403) NEULASTA (371) XGEVA (115) FLUTICASONE\SALMETEROL (96) DARBEPOETIN ALFA (86) ADVAIR (77) DENOSUMAB (65) ADVAIR HFA (51) ALBUTEROL (51) VENTOLIN (47)

Which AMBRISENTAN Alternatives Have Lower Investigation 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 Investigation Reports All Drugs Causing Investigation AMBRISENTAN Demographics