Skip to main content
FDA ApprovedPrescription Medicine

Hot Flash Pills

A daily prescription pill (neurokinin receptor antagonist) that blocks NK3 receptors in the brain to reduce hot flashes and night sweats.

Last verified Updated Sources

Hot Flash Pills (Prescription Medicine)

Method facts

Hot Flash Pills
Measured outcome
Recommended
How long it lasts
Daily pill (ongoing)
Reversibility
Reversible
Used for
Hot flash & night sweat relief
How you get it
Telehealth Prescription
Cost
$25–$618 / monthlyInsurance coverage: Varies
Status
FDA Approved

Outcome & guideline status

Recommended

Recommended by the Menopause Society for symptom relief.

This method class covers NK3 antagonists and dual NK1/NK3 antagonists. In Phase 3 trials, fezolinetant 45 mg reduced the daily frequency of moderate to severe hot flashes and night sweats more than placebo at week 12, with a difference in least squares mean change of -2.55 (SKYLIGHT 1) and -2.53 (SKYLIGHT 2) episodes per day; for elinzanetant 120 mg the difference was -3.2 episodes per day in both OASIS 1 and OASIS 2 (all statistically significant). The trials report changes in daily episodes, not a single percentage for the class. NAMS 2023 lists fezolinetant as a Level I recommendation; elinzanetant was still in development when the statement was published and was FDA-approved in October 2025, so the statement gives it no rating.

The details

What the evidence says

How well it works, what to watch for, who should avoid it, and the studies behind it.

How it works in the body

Clinical class
Neurokinin receptor antagonist

Blocks neurokinin-3 (NK3) and/or neurokinin-1 (NK1) receptors in the hypothalamus to interrupt the temperature-regulation pathway that triggers hot flashes and night sweats.

Side effects

Special monitoring required

Hot Flash Pills requires blood tests (baseline and follow-up liver function tests) to monitor safety during use.

  • Elevated liver enzymes (requires monitoring)
  • Abdominal pain
  • Diarrhea
  • Insomnia
  • Back pain
  • Hot flush
  • Headache
  • Somnolence, dizziness, and fatigue (dual NK1/NK3 antagonists such as elinzanetant)

Who shouldn't use this

Talk to a clinician first if any of these apply

  • Known cirrhosis (NK3 antagonists such as fezolinetant)Severe liver damage or reduced liver function
  • Severe renal impairment or end-stage renal disease (NK3 antagonists such as fezolinetant)Reduced kidney function or kidney disease
  • Concomitant use of CYP1A2 inhibitors such as fluvoxamine (NK3 antagonists such as fezolinetant)Taking medicines that block the CYP1A2 enzyme, such as fluvoxamine, mexiletine, or cimetidine. They raise fezolinetant levels in the blood.
  • Pregnancy (dual NK1/NK3 antagonists such as elinzanetant)Being pregnant or possibly pregnant. Some of these treatments may harm a fetus or lead to pregnancy loss.

Clinical guidelines

Cost and insurance

Cash prices as of October 2026 (Drugs.com) are about $578 for 30 fezolinetant tablets and about $618 for 60 elinzanetant capsules, each a 30-day supply at the labeled dose. With commercial insurance, manufacturer copay cards can bring the monthly cost down to as little as $25-$30.

Insurance coverageVaries

What to know about Hot Flash Pills

How it works

Neurokinin receptor antagonists are a new class of non-hormonal prescription pills for menopause hot flashes and night sweats. They block neurokinin receptors in the hypothalamus, the part of the brain that regulates body temperature. By interrupting the pathway that triggers hot flashes, they reduce both the frequency and severity of vasomotor symptoms.

Research and approval status

Two neurokinin receptor antagonists are FDA-approved. The FDA approved fezolinetant, an NK3 antagonist, in 2023, and approved elinzanetant, a dual NK1/NK3 antagonist, in 2025. In SKYLIGHT 1 and SKYLIGHT 2, fezolinetant 45 mg reduced daily hot flash and night sweat frequency by 2.53 to 2.55 episodes per day more than placebo at week 12 (p<0.001). In the OASIS 1 and 2 trials, elinzanetant 120 mg reduced daily frequency by about 3.2 episodes per day more than placebo at week 12. The NAMS 2023 position statement lists fezolinetant as a Level I recommendation; the FDA approved elinzanetant in October 2025, after the 2023 statement was published.

Side effects and cautions

Fezolinetant carries an FDA boxed warning about the risk of hepatotoxicity (liver injury). Neurokinin antagonists can affect the liver, so you need baseline liver function blood tests before starting one. With NK3 antagonists such as fezolinetant, tests are repeated monthly for the first 3 months, then again at 6 and 9 months. With dual NK1/NK3 antagonists such as elinzanetant, a repeat test at 3 months is recommended. Do not take an NK3 antagonist if you have known cirrhosis, severe kidney impairment or end-stage kidney disease, or take CYP1A2 inhibitors such as fluvoxamine. Dual NK1/NK3 antagonists are contraindicated in pregnancy and not recommended for people with moderate or severe hepatic impairment or end-stage renal disease. Avoid strong CYP3A4 inhibitors (including grapefruit juice) and strong or moderate CYP3A4 inducers; if you take a moderate CYP3A4 inhibitor, reduce the dose to 60 mg (one capsule). Elinzanetant can cause sleepiness and affect your ability to drive or do hazardous activities the next day, and people with a history of seizures should talk to their clinician before using it.

Where to get it

You need a prescription, which you can get through telehealth or a menopause specialist. You take it as a daily pill. Check our provider directory for clinics near you.

Clinical trials behind Hot Flash Pills

The research that backs Hot Flash Pills, with links to the public trial records.

2 products in this category

Specific branded items that use this method. Compare manufacturer details, active ingredients, and regulatory status.

Frequently asked questions

Sources (14)
  1. Research source: Lederman S et al. 2023, SKYLIGHT 1 phase 3 RCT of fezolinetant 45 mg (PMID 36924778)
  2. Research source: Johnson KA et al. 2023, SKYLIGHT 2 phase 3 RCT of fezolinetant 45 mg (PMID 36734148)
  3. Research source: Pinkerton JV et al. 2024, OASIS 1 and 2 phase 3 RCTs of elinzanetant 120 mg (PMID 39172446)
  4. Clinical trial: SKYLIGHT 1 (fezolinetant)
  5. Clinical trial: SKYLIGHT 2 (fezolinetant)
  6. Clinical trial: OASIS 1 (elinzanetant)
  7. Clinical trial: OASIS 2 (elinzanetant)
  8. Research source: DailyMed — fezolinetant FDA label
  9. Research source: DailyMed — elinzanetant FDA label
  10. Clinical guideline: NAMS 2023 Nonhormone Therapy Position Statement for hot flashes and night sweats
  11. Research source: Drugs.com — Lynkuet (elinzanetant) FDA approval history
  12. Research source: Drugs.com — Veozah (fezolinetant) price guide
  13. Research source: Drugs.com — Lynkuet (elinzanetant) price guide
  14. Research source: Veozah telehealth page (Astellas)

How we verify