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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 ARANESP Cause Investigation? 403 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 403 reports of Investigation have been filed in association with ARANESP. This represents 13.1% of all adverse event reports for ARANESP.

403
Reports of Investigation with ARANESP
13.1%
of all ARANESP reports
28
Deaths
401
Hospitalizations

How Dangerous Is Investigation From ARANESP?

Of the 403 reports, 28 (6.9%) resulted in death, 401 (99.5%) required hospitalization.

Is Investigation Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ARANESP. However, 403 reports have been filed with the FAERS database.

What Other Side Effects Does ARANESP Cause?

Death (2,018) Hospitalisation (289) Dialysis (35) Haemoglobin decreased (32) Aplasia pure red cell (26) Transfusion (18) Dyspnoea (17) Haemoglobin abnormal (17) Anaemia (16) Fatigue (16)

What Other Drugs Cause Investigation?

NEULASTA (371) XGEVA (115) FLUTICASONE\SALMETEROL (96) DARBEPOETIN ALFA (86) ADVAIR (77) DENOSUMAB (65) ADVAIR HFA (51) ALBUTEROL (51) VENTOLIN (47) VOTRIENT (40)

Which ARANESP Alternatives Have Lower Investigation Risk?

ARANESP vs ARAVA ARANESP vs AREDIA ARANESP vs ARFORMOTEROL ARANESP vs ARGATROBAN ARANESP vs ARGININE

Related Pages

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