gomekli
Gomekli (Mirdametinib) is a medication used to treat Plexiform Neurofibroma.
Mirdametinib · by Springworks
Key facts
- Active ingredient
- Mirdametinib
- Form
- Capsule, Tablet
- Strength
- Mirdametinib 1MG · Mirdametinib 2MG
- Type
- Prescription (Rx)
- Brand or generic
- Brand-name
- May treat
- plexiform neurofibroma
- Manufacturer
- Springworks
- FDA application
- NDA219389
May treat (source: NIH RxClass)
Dosage forms
Capsule and Tablet
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
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Frequently asked questions
- What does Gomekli treat?
- Gomekli (Mirdametinib) may be used to treat plexiform neurofibroma, 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.
- Is there a coupon or discount for Gomekli?
- pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Gomekli. 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 Gomekli?
- Gomekli is marketed by Springworks. You can see Springworks's full profile, rating, and other products on pharmaranks.
- Is Gomekli a brand-name or generic drug?
- Gomekli is a brand-name product with the active ingredient Mirdametinib.
- Is Gomekli available over the counter?
- No. Gomekli 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 Gomekli come in?
- Gomekli is currently marketed as capsule and tablet, per the FDA's National Drug Code Directory.
- Is Gomekli FDA-registered?
- Gomekli is on record with the U.S. FDA under application number NDA219389. You can verify this on its official FDA label.
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 MIRDAMETINIB
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 19 reports naming MIRDAMETINIB — the active ingredient in Gomekli, and the FDA flagged 95% 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:
- diarrhoea6 reports
- dehydration5 reports
- dermatitis acneiform4 reports
- fatigue4 reports
- nausea4 reports
- abdominal discomfort3 reports
- acne3 reports
- blindness unilateral3 reports
Read these as a signal, not a rate. A report does not mean MIRDAMETINIB 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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