Does BUSERELIN Cause Product prescribing error? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product prescribing error have been filed in association with BUSERELIN. This represents 17.7% of all adverse event reports for BUSERELIN.
12
Reports of Product prescribing error with BUSERELIN
17.7%
of all BUSERELIN reports
0
Deaths
12
Hospitalizations
How Dangerous Is Product prescribing error From BUSERELIN?
Of the 12 reports, 12 (100.0%) required hospitalization.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUSERELIN. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does BUSERELIN Cause?
Ovarian hyperstimulation syndrome (14)
Alanine aminotransferase increased (12)
Aspartate aminotransferase increased (12)
Blood creatine phosphokinase increased (12)
Blood lactate dehydrogenase increased (12)
Gamma-glutamyltransferase increased (12)
Muscular weakness (12)
Pyrexia (12)
Abdominal distension (5)
Ascites (5)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)