FDA label 482153ed-785f-4eb0-9e22-3a608fd0dcc4

openFDA label record#

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Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
7f0b9a4f-a561-420f-970a-69b3151dcc53
SPL ID
482153ed-785f-4eb0-9e22-3a608fd0dcc4
Version
3
Effective date
2019-11-06
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:50:07

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Ganirelix acetate injection should be prescribed by physicians who are experienced in infertility treatment. Before starting treatment with ganirelix acetate, pregnancy must be excluded. Safe use of ganirelix acetate during pregnancy has not been established (see CONTRAINDICATIONS and PRECAUTIONS ).

Adverse reactions cross-check#

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Adverse reactions sections page 1 of 1 · 2 matching rows.

adverse reactions

ADVERSE REACTIONS The safety of ganirelix acetate injection was evaluated in two randomized, parallel-group, multicenter controlled clinical studies. Treatment duration for ganirelix acetate ranged from 1 to 14 days. Table IV represents adverse events (AEs) from first day of ganirelix acetate administration until confirmation of pregnancy by ultrasound at an incidence of ≥ 1% in ganirelix acetate-treated subjects without regard to causality. TABLE IV: Incidence of common adverse events (Incidence ≥ 1% in ganirelix acetate-treated subjects). Completed controlled clinical studies (All-subjects-treated group). Adverse Events Occurring in ≥ 1% Ganirelix Acetate N=794 % (n) Abdominal Pain (gynecological) 4.8 (38) Death Fetal 3.7 (29) Headache 3 (24) Ovarian Hyperstimulation Syndrome 2.4 (19) Vaginal Bleeding 1.8 (14) Injection Site Reaction 1.1 (9) Nausea 1.1 (9) Abdominal Pain (gastrointestinal) 1 (8) During postmarketing surveillance, rare cases of hypersensitivity reactions, including anaphylactoid reactions, have been reported, as early as with the first dose (see PRECAUTIONS ). Congenital Anomalies Ongoing clinical follow-up studies of 283 newborns of women administered ganirelix acetate injection were reviewed. There were three neonates with major congenital anomalies and 18 neonates with minor congenital anomalies. The major congenital anomalies were: hydrocephalus/meningocele, omphalocele, and Beckwith-Wiedemann Syndrome. The minor congenital anomalies were: nevus, skin tags, sacral sinus, hemangioma, torticollis/asymmetric skull, talipes, supernumerary digit finger, hip subluxation, torticollis/high palate, occiput/abnormal hand crease, hernia umbilicalis, hernia inguinalis, hydrocele, undescended testis, and hydronephrosis. The causal relationship between these congenital anomalies and ganirelix acetate is unknown. Multiple factors, genetic and others (including, but not limited to ICSI, IVF, gonadotropins, progesterone) may confound ART (Assisted Reproductive Technology) procedures.

adverse reactions table

<table cellspacing="0" cellpadding="0" border="0" width="578"> <caption>TABLE IV: Incidence of common adverse events (Incidence &#x2265; 1% in ganirelix acetate-treated subjects). Completed controlled clinical studies (All-subjects-treated group). </caption> <colgroup> <col width="49.4809688581315%"/> <col width="50.5190311418685%"/> </colgroup> <tbody> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule" valign="top"> <content styleCode="bold">Adverse Events Occurring in </content>&#x2265;<content styleCode="bold"> 1% </content> </td> <td styleCode="Rrule" align="center" valign="top"> <content styleCode="bold">Ganirelix Acetate N=794</content> <content styleCode="bold">% (n)</content> </td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule" valign="middle">Abdominal Pain (gynecological) </td> <td styleCode="Rrule" align="center" valign="middle">4.8 (38) </td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule" valign="middle">Death Fetal </td> <td styleCode="Rrule" align="center" valign="middle">3.7 (29) </td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule" valign="middle">Headache </td> <td styleCode="Rrule" align="center" valign="middle">3 (24) </td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule" valign="middle">Ovarian Hyperstimulation Syndrome </td> <td styleCode="Rrule" align="center" valign="middle">2.4 (19) </td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule" valign="middle">Vaginal Bleeding </td> <td styleCode="Rrule" align="center" valign="middle">1.8 (14) </td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule" valign="middle">Injection Site Reaction </td> <td styleCode="Rrule" align="center" valign="middle">1.1 (9) </td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule" valign="middle">Nausea </td> <td styleCode="Rrule" align="center" valign="middle">1.1 (9) </td> </tr> <tr> <td styleCode="Lrule Rrule" valign="middle">Abdominal Pain (gastrointestinal) </td> <td styleCode="Rrule" align="center" valign="middle">1 (8) </td> </tr> </tbody> </table>

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.