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Aquipta 60 mg tablets – patient leaflet, side effects, dosage

Last updated: · Text from the MHRA, as of · About this document

Medicine status: Prescription only (POM) ▼ Additional monitoring Details

Medicine strength:
60 mg
Contains active substance:

Patient leaflet - Aquipta 60 mg tablets

1. What AQUIPTA is and what it is used for

AQUIPTA contains the active substance atogepant.

How AQUIPTA works

AQUIPTA works by blocking the activity of the calcitonin gene- related peptide (CGRP) molecule which has been linked to migraine. This reduction in CGRP’s activity reduces migraine attacks.

Mock-Up-Package-Leaflet-Aquipta-10mg + 60mg

20098876 10 mg tablets 60 mg tablets atogepant

What AQUIPTA is used for

AQUIPTA is used in adult patien

ts to:

Pregnancy, breast-feeding and fertility

AQUIPTA is not recommended during pregnancy.

  • treat an active migraine atta

    ck

  • prevent migraine in those w

    ho have at least 4 migraine days

    per month

    If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before using this medicine.

2. What you need to know b

efore you take AQUIPTA

Do not take AQUIPTA

Driving and using machines

AQUIPTA may make you feel sleepy. Do not drive or use machines if you are affected.

  • If you are allergic to atogep

    ant or any of the other

    ingredients of this medicine

    (listed in section 6).

Warnings and precautions

Talk to your doctor, pharmacist especially if you:

or nurse before taking AQUIPTA,

AQUIPTA contains sodium

This medicine contains 31.5 mg sodium (main component of cooking/table salt) in each 60 mg tablet. This is equivalent to 1.6% of the recommended maximum daily dietary intake of sodium for an adult.

  • have liver problems
  • have kidney problems

    This medicine contains less than 1 mmol sodium (23 mg) per

    10 mg tablet, that is to say essentially ‘sodium-free’.

Allergic reactions

Stop taking AQUIPTA and tell y experience any symptoms of an • difficulty breathing

our doctor immediately if you allergic reaction such as:

  • swelling of the face

3. How to take AQUIPTA

Always take this medicine exactly as your doctor has told you. Speak to your doctor or pharmacist if you are not sure.

  • rash, itching, or hives

Some of these symptoms can o AQUIPTA.

ccur several days after you take

Children and adolescents

Do not give this medicine to chi years old) because the use of A this age group.

ldren or adolescents (under 18 QUIPTA has not been studied in

How much to take

The maximum dose per day is 60 mg.

For treatment of a migraine attack as needed, the recommended dose is 60 mg.

For prevention of migraine, the recommended dose is 60 mg once a day.

Other medicines and AQUIPT

A

Tell your doctor or pharmacist if taken or might take any other m increase the risk of getting side

you are taking, have recently edicines. Some medicines may effects.

Your doctor may tell you to take a lower dose if you are taking other medicines (listed in section 2) or if you have severe kidney problems. Speak to your doctor if you are undergoing dialysis.

The following is a list of exampl your doctor to lower the dose of • ketoconazole, itraconazole,

es of medicines that may require AQUIPTA:

voriconazole, clarithromycin, edicines used to treat fungal or

telithromycin, rifampicin (m bacterial infections)

  • atazanavir, indinavir, nelfina

    vir, ritonavir, saquinavir,

    How to take

    AQUIPTA may be taken with or without food.

    If you take more AQUIPTA than you should

    If you have used more AQUIPTA than you should, tell your doctor.

    tipranavir (medicines used • ciclosporin (medicine that a • telmisartan (medicine used

    to treat HIV)

    ffects your immune system) to treat high blood pressure)

If any of the above apply to you doctor or pharmacist before tak

or you are not sure, talk to your ing AQUIPTA.

If you forget to take AQUIPTA

If you take AQUIPTA for the prevention of migraine and forget to take it:

A missed dose should be taken straight away. If it is close to your scheduled next dose, do not take a double dose to make up for a forgotten tablet.

If you stop taking AQUIPTA

If you take AQUIPTA for the prevention of migraine, do not stop using it without talking to your doctor first. Your symptoms may return if you stop the treatment.

If you have any further questions on the use of this medicine, ask your doctor, pharmacist or nurse.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Serious side effects

Stop taking AQUIPTA and contact your doctor immediately if you have any of the following symptoms, which may be part of

a serious allergic reaction:

  • difficulty breathing
  • swelling of the face
  • rash, itching, or hives

Other side effects

Tell your doctor or nurse if you notice any of the following side effects:

Common (may affect up to 1 in 10 people)

  • feeling sick (nausea)
  • constipation
  • tiredness (fatigue) or sleepiness (somnolence) • decreased appetite
  • weight loss

Uncommon (may affect up to 1 in 100 people) • increased levels of liver enzymes

Reporting of side effects

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme.

Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.

By reporting side effects, you can help provide more information on the safety of this medicine.

Mock-Up-Package-Leaflet-Aquipta-10mg + 60mg

5. How to store AQUIPTA

Keep this medicine out of the si

ght and reach of children.

This medicinal product does no conditions.

t require any special storage

Do not use this medicine after t the carton and blister after EXP day of that month.

he expiry date which is stated on . The expiry date refers to the last

Do not throw away any medicin waste. Ask your pharmacist ho you no longer use. These meas environment.

es via wastewater or household w to throw away medicines ures will help to protect the

6. Contents of the pack and

other information

What AQUIPTA contains

The active substance is atogep

ant.

  • Each tablet contains either • The other ingredients are:

    10 mg or 60 mg of atogepant. Polyvinylpyrrolidone/Vinyl E polyethylene glycol succinate, ellulose, sodium chloride, lloidal silicon dioxide and

    acetate copolymer, vitamin mannitol, microcrystalline c croscarmellose sodium, co sodium stearyl fumarate.

What AQUIPTA looks like an

d contents of the pack

AQUIPTA 10 mg tablets AQUIPTA 10 mg tablet is a whit tablet debossed with “A” and “1

e to off-white, round biconvex 0” on one side.

AQUIPTA 60 mg tablets AQUIPTA 60 mg tablet is a whit tablet debossed with “A60” on o

e to off-white, oval biconvex ne side.

For packs of 2 tablets, each blis

ter contains 2 tablets.

For packs of 7, 28 or 98 tablets

, each blister contains 7 tablets.

Not all pack sizes may be mark

eted.

Marketing Authorisation Hol

der

AbbVie Ltd

Maidenhead

SL6 4UB

UK

Tel: +44 (0) 1628 561090

Manufacturer

AbbVie S.r.l

S.R. 148 Pontina Km 52 Snc

Campoverde di Aprilia, Latina 04011

Italy

This leaflet was last revised in November 2025.

To listen to or request a copy of this leaflet in Braille, large print or audio, please contact the Marketing Authorisation Holder.

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PLGB 41042/0089

Last revision stated in the text: November 2025 · MHRA data as of 13 October 2026

Found a mistake? Tell us on the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Facts about Aquipta 60 mg tablets

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Atogepant
Strength 60 mg
Pharmaceutical form Oral tablet
White to off-white, oval biconvex tablet debossed with “A60” on one side.
How is it taken Oral
Excipients Polyvinylpyrrolidone/Vinyl acetate copolymer, Vitamin E polyethylene glycol succinate, Mannitol, Microcrystalline cellulose, Sodium chloride, Croscarmellose sodium, Colloidal silicon dioxide, Sodium stearyl fumarate
Pack sizes 2 tablet, 7 tablet, 28 tablet
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 3 years
Storage This medicinal product does not require any special storage conditions.
Drug group (ATC) {Analgesics, antimigraine preparations}
Additional monitoring Yes ▼ – new safety information is collected quickly. Report any side effect to the Yellow Card scheme.
Marketing authorisation PLGB 41042/0089 (first authorised 30 August 2023)
Marketing authorisation holder AbbVie Ltd
Codes GTIN 8054083025643, 8054083031798, 8054083031804 · BNF 04070402

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.2.0 of 19 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.