Does GANIRELIX Cause Incorrect product storage? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Incorrect product storage have been filed in association with GANIRELIX (Ganirelix Acetate). This represents 0.7% of all adverse event reports for GANIRELIX.
14
Reports of Incorrect product storage with GANIRELIX
0.7%
of all GANIRELIX reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product storage From GANIRELIX?
Of the 14 reports.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GANIRELIX. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does GANIRELIX Cause?
Ovarian hyperstimulation syndrome (672)
Ascites (222)
Dyspnoea (91)
No adverse event (91)
Product storage error (90)
Needle issue (85)
Abdominal pain (73)
Pleural effusion (72)
Abdominal distension (71)
Nausea (71)
What Other Drugs Cause Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
Which GANIRELIX Alternatives Have Lower Incorrect product storage Risk?
GANIRELIX vs GATIFLOXACIN
GANIRELIX vs GEFITINIB
GANIRELIX vs GELATIN
GANIRELIX vs GEMCITABINE
GANIRELIX vs GEMCITABINE\GEMCITABINE