lutrepulse kit
Pharmaranks rates Lutrepulse Kit 3.6/5 for recall safety — an independent score from its FDA recall history and its manufacturer's record. Lutrepulse Kit (Gonadorelin Acetate) is a medication used to treat Amenorrhea, Ovarian Cysts, Delayed Puberty, Precocious Puberty.
Gonadorelin Acetate · by Ferring Pharms Inc
Based on 1 source · Recall-safety score from FDA recall history — this product's own recalls and its manufacturer's record. Not an efficacy or quality rating. methodology →
Key facts
- Active ingredient
- Gonadorelin Acetate
- Form
- Injectable
- Strength
- Gonadorelin Acetate 0.8MG/VIAL · Gonadorelin Acetate 3.2MG/VIAL
- Type
- Prescription (Rx)
- Brand or generic
- Brand-name
- May treat
- amenorrhea, ovarian cysts, delayed puberty
- Manufacturer
- Ferring Pharms Inc
- FDA application
- NDA019687
- Availability
- Discontinued (per FDA)
May treat (source: NIH RxClass)
- amenorrhea
- ovarian cysts
- delayed puberty
- precocious puberty
Dosage forms
Injectable
The forms currently marketed in the U.S., per the FDA National Drug Code Directory.
Ways to save
Ask for the generic
Same active ingredient, far cheaper. Is there a generic? →
Request a 90-day supply
Bulk fills usually lower the per-dose price vs monthly refills.
Use copay cards
Manufacturer copay cards & patient-assistance programs — especially for brand drugs.
Compare alternatives
A same-class option may cost less. See alternatives →
Frequently asked questions
- What does Lutrepulse Kit treat?
- Lutrepulse Kit (Gonadorelin Acetate) may be used to treat amenorrhea, ovarian cysts, delayed puberty, precocious puberty, based on NIH RxClass drug-classification data (conditions a drug may treat — not a verbatim copy of the FDA-approved label). This is general reference, not medical advice.
- How is Lutrepulse Kit rated?
- pharmaranks gives Lutrepulse Kit a composite score of 3.6 out of 5, currently based on 1 weighted source (FDA regulatory recall-safety data weighted highest). See our methodology at /how-we-rate.
- Is there a coupon or discount for Lutrepulse Kit?
- pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Lutrepulse Kit. To pay less, ask your prescriber or pharmacist whether a generic equivalent exists, check the manufacturer's copay/savings card and patient-assistance program, and compare a pharmacy discount card against your insurance copay. Prices vary by pharmacy, insurance, and location, so always confirm at the counter. This is general reference, not medical or financial advice.
- Who makes Lutrepulse Kit?
- Lutrepulse Kit is marketed by Ferring Pharms Inc. You can see Ferring Pharms Inc's full profile, rating, and other products on pharmaranks.
- Is Lutrepulse Kit a brand-name or generic drug?
- Lutrepulse Kit is a brand-name product with the active ingredient Gonadorelin Acetate.
- Is Lutrepulse Kit available over the counter?
- No. Lutrepulse Kit is a prescription (Rx) medication in the US — you need a prescription from a licensed clinician (in person or via telehealth); it isn't sold over the counter. For some conditions there are OTC alternatives — ask your pharmacist.
- What forms does Lutrepulse Kit come in?
- Lutrepulse Kit is currently marketed as injectable, per the FDA's National Drug Code Directory.
- Is Lutrepulse Kit FDA-registered?
- Lutrepulse Kit is on record with the U.S. FDA under application number NDA019687. You can verify this on its official FDA label.
- Has Lutrepulse Kit been recalled by the FDA?
- Lutrepulse Kit has no FDA recalls recorded under its own application in the openFDA enforcement database. Its recall-safety score reflects its manufacturer's overall recall record. This is general reference, not medical advice — check the FDA recall database for the latest alerts.
- Is Lutrepulse Kit safe?
- There's no single safe-or-not verdict. pharmaranks gives Lutrepulse Kit a recall-safety score of 72/100, based on its FDA recall history (no recalls under its own FDA application) — not an efficacy or side-effect rating. Review its FDA-label side effects and warnings before use, and always consult a licensed professional.
Information is sourced from public FDA regulatory data. Provided for general reference only — not medical advice. Always consult a licensed professional and the current prescribing information.
What people report to the FDA about GONADORELIN ACETATE
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 32 reports naming GONADORELIN ACETATE — the active ingredient in Lutrepulse Kit, and the FDA flagged 91% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:
- recalled product administered4 reports
- injection site reaction3 reports
- nausea3 reports
- rash3 reports
- vomiting3 reports
- abdominal pain2 reports
- anaemia2 reports
- anaphylactic shock2 reports
Read these as a signal, not a rate. A report does not mean GONADORELIN ACETATE caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label.
Source: openFDA drug/event (FAERS), retrieved September 25, 2026.
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lutrepulse kit
72/100