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thypinone

Pharmaranks rates Thypinone 3.6/5 for recall safety — an independent score from its FDA recall history and its manufacturer's record. Thypinone (Protirelin) is a medication supplied as an injectable.

Protirelin · by Abbott

72/100Limited · 1 source

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 →

Rated against independent regulatory sources·Last updated October 6, 2026·How we rate
Verified againstopenFDANIH DailyMedRxClass

Key facts

Active ingredient
Protirelin
Form
Injectable
Strength
Protirelin 0.5MG/ML
Type
Prescription (Rx)
Brand or generic
Brand-name
Manufacturer
Abbott
FDA application
NDA017638
Availability
Discontinued (per FDA)

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

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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.

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Frequently asked questions

How is Thypinone rated?
pharmaranks gives Thypinone 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 Thypinone?
pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Thypinone. 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 Thypinone?
Thypinone is marketed by Abbott. You can see Abbott's full profile, rating, and other products on pharmaranks.
Is Thypinone a brand-name or generic drug?
Thypinone is a brand-name product with the active ingredient Protirelin.
Is Thypinone available over the counter?
No. Thypinone 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 Thypinone come in?
Thypinone is currently marketed as injectable, per the FDA's National Drug Code Directory.
Is Thypinone FDA-registered?
Thypinone is on record with the U.S. FDA under application number NDA017638. You can verify this on its official FDA label.
Has Thypinone been recalled by the FDA?
Thypinone 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 Thypinone safe?
There's no single safe-or-not verdict. pharmaranks gives Thypinone 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 PROTIRELIN

The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 26 reports naming PROTIRELIN — the active ingredient in Thypinone, and the FDA flagged 96% 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:

  • pituitary haemorrhage10 reports
  • nausea4 reports
  • pyrexia4 reports
  • headache3 reports
  • vision blurred3 reports
  • vomiting3 reports
  • blindness2 reports
  • blood glucose increased2 reports

Read these as a signal, not a rate. A report does not mean PROTIRELIN 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 26, 2026.

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72/100