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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 XTANDI Cause Investigation? 31 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Investigation have been filed in association with XTANDI. This represents 2.2% of all adverse event reports for XTANDI.

31
Reports of Investigation with XTANDI
2.2%
of all XTANDI reports
6
Deaths
31
Hospitalizations

How Dangerous Is Investigation From XTANDI?

Of the 31 reports, 6 (19.4%) resulted in death, 31 (100.0%) required hospitalization.

Is Investigation Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for XTANDI. However, 31 reports have been filed with the FAERS database.

What Other Side Effects Does XTANDI Cause?

Malignant neoplasm progression (235) Death (234) Fatigue (162) Drug ineffective (158) Prostatic specific antigen increased (94) Nausea (69) Asthenia (62) Decreased appetite (56) Dizziness (52) Diarrhoea (51)

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 XTANDI Alternatives Have Lower Investigation Risk?

XTANDI vs XYLAZINE XTANDI vs XYLOMETAZOLINE XTANDI vs XYREM XTANDI vs XYREM , /ML XTANDI vs YASMIN

Related Pages

XTANDI Full Profile All Investigation Reports All Drugs Causing Investigation XTANDI Demographics