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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 RELUGOLIX Cause Product dose omission in error? 293 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 293 reports of Product dose omission in error have been filed in association with RELUGOLIX (Orgovyx). This represents 1.4% of all adverse event reports for RELUGOLIX.

293
Reports of Product dose omission in error with RELUGOLIX
1.4%
of all RELUGOLIX reports
1
Deaths
26
Hospitalizations

How Dangerous Is Product dose omission in error From RELUGOLIX?

Of the 293 reports, 1 (0.3%) resulted in death, 26 (8.9%) required hospitalization.

Is Product dose omission in error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RELUGOLIX. However, 293 reports have been filed with the FAERS database.

What Other Side Effects Does RELUGOLIX Cause?

Hot flush (6,845) Fatigue (5,203) Therapy interrupted (3,251) Incorrect dose administered (1,917) Asthenia (1,718) Arthralgia (1,385) Diarrhoea (1,383) Product dose omission issue (1,189) Dizziness (1,146) Constipation (902)

What Other Drugs Cause Product dose omission in error?

DUPILUMAB (7,586) TOFACITINIB (2,461) LENALIDOMIDE (618) PALBOCICLIB (592) DIROXIMEL (481) ABALOPARATIDE (457) NIRAPARIB (428) RUXOLITINIB (425) TERIFLUNOMIDE (371) DIMETHYL (308)

Which RELUGOLIX Alternatives Have Lower Product dose omission in error Risk?

RELUGOLIX vs REMDESIVIR RELUGOLIX vs REMERON RELUGOLIX vs REMICADE RELUGOLIX vs REMIFENTANIL RELUGOLIX vs REMIMAZOLAM

Related Pages

RELUGOLIX Full Profile All Product dose omission in error Reports All Drugs Causing Product dose omission in error RELUGOLIX Demographics