Ganirelix Acetate

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

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

Brand name
Ganirelix Acetate
Generic name
GANIRELIX ACETATE
Manufacturer
Amphastar Pharmaceuticals, Inc.
Product type
HUMAN PRESCRIPTION DRUG
SPL set ID
9c286f64-8039-44ec-8fdd-d1a2f52b4c3c
SPL ID
0e71b74d-723d-46a4-b2e5-7c7157949ad4
Version
1
Effective date
2022-04-19
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:30:53
Harmonized routes table
Harmonized routes
SUBCUTANEOUS

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 3.0 (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) 1.0 (8) During post-marketing 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 width="80%"><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="60%" align="left" valign="top"/><col width="40%" align="center" valign="top"/></colgroup><thead><tr styleCode="First Last"><th styleCode="Lrule" align="left">Adverse Events Occurring in &#x2265; 1%</th><th styleCode="Lrule Rrule" align="center">Ganirelix Acetate N=794 % (n)</th></tr></thead><tbody><tr styleCode="Botrule First"><td styleCode="Lrule" align="left">Abdominal Pain (gynecological)</td><td styleCode="Lrule Rrule" align="center">4.8 (38)</td></tr><tr styleCode="Botrule"><td styleCode="Lrule" align="left">Death Fetal</td><td styleCode="Lrule Rrule" align="center">3.7 (29)</td></tr><tr styleCode="Botrule"><td styleCode="Lrule" align="left">Headache</td><td styleCode="Lrule Rrule" align="center">3.0 (24)</td></tr><tr styleCode="Botrule"><td styleCode="Lrule" align="left">Ovarian Hyperstimulation Syndrome</td><td styleCode="Lrule Rrule" align="center">2.4 (19)</td></tr><tr styleCode="Botrule"><td styleCode="Lrule" align="left">Vaginal Bleeding</td><td styleCode="Lrule Rrule" align="center">1.8 (14)</td></tr><tr styleCode="Botrule"><td styleCode="Lrule" align="left">Injection Site Reaction</td><td styleCode="Lrule Rrule" align="center">1.1 (9)</td></tr><tr styleCode="Botrule"><td styleCode="Lrule" align="left">Nausea</td><td styleCode="Lrule Rrule" align="center">1.1 (9)</td></tr><tr><td styleCode="Lrule" align="left">Abdominal Pain (gastrointestinal)</td><td styleCode="Lrule Rrule" align="center">1.0 (8)</td></tr></tbody></table>

Reported adverse events (FAERS/openFDA)#

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