Na-enyocha...
Atụgharịrị ya na-akpaghị aka. Maka ọnụọgụ ọgwụ na ịdọ aka ná ntị: lee nke mbụ n'asụsụ Bekee. Gụọ n'asụsụ Bekee
Home / Ọgwụ A–Z / Cetrorelix

Cetrorelix

Cetrorelix acetate for injection is indicated for the inhibition of premature LH surges in women undergoing controlled ovarian stimulation.

Prescription medicine Safety alerts on record

How to use Cetrorelix

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

Cetrorelix acetate for injection is indicated for the inhibition of premature LH surges in women undergoing controlled ovarian stimulation.

How to take it and how often
  • Ovarian stimulation therapy with gonadotropins (FSH, hMG) is started on cycle Day 2 or 3
  • The dose of gonadotropins should be adjusted according to individual response
  • Cetrorelix acetate for injection 0.25 mg may be administered subcutaneously once daily during the early- to mid-follicular phase
  • Cetrorelix acetate for Injection 0.25 mg is administered on either stimulation day 5 (morning or evening) or day 6 (morning) and continued daily until the day of hCG administration
  • When assessment by ultrasound shows a sufficient number of follicles of adequate size, hCG is administered to induce ovulation and final maturation of the oocytes
  • No hCG should be administered if the ovaries show an excessive response to the treatment with gonadotropins to reduce the chance of developing ovarian hyperstimulation syndrome (OHSS)
  • Administration Cetrorelix acetate for Injection 0.25 mg can be administered by the patient herself after appropriate instructions by her doctor
  • Directions for using Cetrorelix Acetate for Injection 0.25 mg with the enclosed needles and pre-filled syringe: 1
  • Wash hands thoroughly with soap and water. 2
  • Flip off the plastic cover of the vial and wipe the aluminum ring and the rubber stopper with an alcohol swab. 3
  • Twist the injection needle with the yellow mark (20 gauge) on the pre-filled syringe. 4
  • Push the needle through the center of the rubber stopper of the vial and slowly inject the solvent into the vial. 5
  • Leaving the syringe in the vial, gently swirl the vial until the solution is clear and without residues
  • Avoid forming bubbles. 6. …
Talk to a doctor first if
  • Cetrorelix acetate for injection is contraindicated under the following conditions: 1
  • Hypersensitivity to cetrorelix acetate, extrinsic peptide hormones or mannitol. 2
  • Known hypersensitivity to GnRH or any other GnRH analogs. 3
  • Known or suspected pregnancy, and lactation (see PRECAUTIONS). 4
  • Severe renal impairment
Warnings

Cetrorelix acetate for injection should be prescribed by physicians who are experienced in fertility treatment. Before starting treatment with cetrorelix acetate for injection, pregnancy must be excluded (see CONTRAINDICATIONS and PRECAUTIONS).

Possible side effects

The safety of cetrorelix acetate for injection in 949 patients undergoing controlled ovarian stimulation in clinical studies was evaluated. Women were between 19 and 40 years of age (mean: 32). 94.0% of them were Caucasian. Cetrorelix acetate for injection was given in doses ranging from 0.1 mg to 5 mg as either a single or multiple dose. Table 3 shows systemic adverse events, reported in clinical studies without regard to causality, from the beginning of cetrorelix acetate for injection treatment until confirmation of pregnancy by ultrasound at an incidence ≥ 1% in cetrorelix acetate for injection treated subjects undergoing COS. …

If you take too much

There have been no reports of overdosage with cetrorelix acetate for injection 0.25 mg or 3 mg in humans. Single doses up to 120 mg cetrorelix acetate for injection have been well tolerated in patients treated for other indications without signs of overdosage.

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2024-08-08.

Brands around the world

Products with Cetrorelix as the active ingredient. Names differ between countries.

Registered products

United States (FDA)

Cetrorelix Powder (synthetic)CETRORELIX .45 g/.45g · Powder · Piramal Pharma Limited
NDC 41701-011Label
Cetrorelix Powder (synthetic)CETRORELIX 16.5 g/16.5g · Powder · Piramal Pharma Limited
NDC 41701-011Label
Cetrorelix Powder (synthetic)CETRORELIX 1 g/g · Powder · Piramal Pharma Limited
NDC 41701-011Label
Cetrorelix Powder (synthetic)CETRORELIX 10 g/10g · Powder · Piramal Pharma Limited
NDC 41701-011Label
Cetrorelix AcetateCETRORELIX ACETATE 25 kg/25kg · Powder · Azico Biophore India Private Limited
NDC 69575-4039Label

Nigeria (NAFDAC)

NAFDACIetrocare Injection A4-100980

Other countries: check your pack's registration number and we point you to your regulator.

Safety alerts and recalls

Cetrorelix Acetate for Injection (Kit), 0.25 mg per vial, Single-Dose Kit, Rx Only, Mfd. for: Meitheal Pharmaceuticals, Chicago, IL NDC 71288-558-90.U.S. FDA Class II
9 Feb 2026 · Meitheal Pharmaceuticals, Inc · OngoingDefective Delivery System: Missing or duplicated needles within the injection kit
Cetrorelix Acetate for Injection, 0.25 mg, , One carton contains one packaged tray which contains: 1 vial with lyophilized powder for reconstitution, 1 pre-filled syringe with diluU.S. FDA Class II
26 Apr 2023 · Akorn, Inc. · OngoingCGMP Deviations: Firm went out of business and could no longer continue stability studies.
Cetrotide (cetrorelix acetate for Injection) 0.25 mg, Sterile - for subcutaneous use only, Rx Only, Manufactured for: EMD Serono, Inc., Rockland, MD 02370, NDC: 44087-1225-1U.S. FDA Class II
29 Jun 2020 · EMD Serono, Inc. · TerminatedDefective Container: Market complaints of missing rubber stoppers from drug vial. Missing rubber stoppers could lead to lack of sterility assurance.

A recall usually affects certain batches only. Compare the lot number on your pack.

Check your pack of Cetrorelix

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

Questions about Cetrorelix

What is Cetrorelix used for?

Cetrorelix acetate for injection is indicated for the inhibition of premature LH surges in women undergoing controlled ovarian stimulation. (From the official U.S. FDA label.)

How do I take Cetrorelix?

Follow your prescription or the leaflet in your pack. The official label says: Ovarian stimulation therapy with gonadotropins (FSH, hMG) is started on cycle Day 2 or 3. The dose of gonadotropins should be adjusted according to individual response. Cetrorelix acetate for injection 0.25 mg may be administered subcutaneously once daily during the early- to mid-follicular phase. Cetrorelix acetate for Injection 0.25 mg is administered on either stimulation da…

Do I need a prescription for Cetrorelix?

Usually yes. Cetrorelix is a prescription medicine in most countries. Rules differ by country.

What brands contain Cetrorelix?

Cetrorelix is sold under names such as Cetrotide, Cetrorelix Acetate. Brand names differ between countries.

How can I check that my Cetrorelix is genuine?

Scan the registration number on your pack with PillVera (NAFDAC number in Nigeria, NDC in the United States, DIN in Canada), check the expiry date and buy only from licensed pharmacies.