What are the side effects of Nurtec (rimegepant) when used for migraine in a perimenopausal woman?

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Last updated: February 28, 2026View editorial policy

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Nurtec (Rimegepant) Side Effects for Perimenopause Migraines

Nurtec ODT is generally well tolerated with nausea being the most common side effect, occurring in approximately 2-15% of patients, whether used for acute treatment or prevention of migraine. 1, 2

Most Common Side Effects

For Acute Treatment (As-Needed Dosing)

  • Nausea is the primary side effect reported in clinical trials 1, 3
  • Urinary tract infection 3
  • Dizziness 3

For Preventive Treatment (Every-Other-Day Dosing)

  • Nausea (most common) 1, 2
  • Stomach pain (abdominal pain) 1
  • Indigestion (dyspepsia) 1
  • Constipation (1.0% in long-term studies) 4
  • Upper respiratory tract infection (0.8%) 4
  • Weight increase (0.7%) 4

Serious but Rare Side Effects

Allergic Reactions

  • Allergic reactions can occur days after taking Nurtec ODT and require immediate medical attention 1
  • Symptoms include:
    • Swelling of face, mouth, tongue, or throat 1
    • Trouble breathing 1
    • Rash 1

Liver Safety Profile

  • No evidence of hepatotoxicity has been identified in clinical trials, including long-term studies up to 52 weeks 2, 4
  • In the 52-week open-label extension study, hepatic-related adverse events occurred in only 1.8% of participants 4
  • Only 0.3% discontinued due to liver enzyme-related adverse events 4
  • No participant experienced ALT or AST >3× upper limit of normal concurrent with total bilirubin >2× upper limit of normal 4

Cardiovascular Safety

  • No evidence of cardiovascular toxicity has been demonstrated in clinical trials 2
  • Rimegepant works through a nonvasoconstrictive mechanism (CGRP receptor antagonism without serotonergic activity), potentially carrying lower cardiovascular risks than triptans 5

Overall Tolerability Profile

  • Most adverse events are mild in severity; severe adverse events occurred in only 2.3% of participants in long-term studies 4
  • Serious adverse events are uncommon (2.2% in 52-week studies), with none being liver-related 4
  • Discontinuation due to adverse events is rare (2.8% over 52 weeks) 4
  • Treatment-related adverse events occurred in 15.1% of participants, with most being mild 4

Special Considerations for Perimenopausal Women

Pregnancy and Breastfeeding Concerns

  • Very small amounts of Nurtec ODT pass into breast milk 1
  • Safety during pregnancy is not fully established; women who become pregnant while taking Nurtec ODT should enroll in the MONITOR pregnancy registry by calling 1-877-366-0324 1

Dosing Limits to Prevent Side Effects

  • For acute treatment: do not take more than 1 tablet in 24 hours 1
  • It is not known if taking more than 18 doses in 30 days is safe 1
  • For preventive treatment: take 1 tablet every other day 1

Long-Term Safety Data

  • In a 52-week study, 71% of participants completed the full year of treatment, demonstrating good long-term tolerability 4
  • No diminution of effect or tolerance development was observed over 52 weeks 4
  • The safety profile remained favorable with both every-other-day scheduled dosing and as-needed dosing 4

Concomitant Use with Other CGRP Therapies

  • Rimegepant appears safe when used concomitantly with CGRP monoclonal antibodies (erenumab, fremanezumab, galcanezumab) for patients requiring both acute and preventive treatment 6
  • In a substudy of 13 patients using rimegepant with CGRP mAbs, only 38% reported any adverse events, all mild to moderate 6

Common Pitfalls to Avoid

  • Do not push the tablet through the foil packaging; peel back the foil to avoid damaging the orally disintegrating tablet 1
  • Do not store tablets outside the blister pack for future use 1
  • Patients with liver or kidney problems should inform their healthcare provider before starting Nurtec ODT 1
  • Monitor for allergic reactions, which can occur days after administration, not just immediately 1

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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