FDA label e9129510-e2e2-4452-a1d4-705d99c4ee9b

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SPL set ID
d4e0bcb6-7c24-494b-a775-a1b23d1cdc71
SPL ID
e9129510-e2e2-4452-a1d4-705d99c4ee9b
Version
6
Effective date
2023-11-30
Source export date
2026-08-01
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/d245bd7ce31d1d8ed63276109973402ece6c44860774da30f25b731cd7418983/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:32:11

Warnings cross-check#

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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

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>