InfoCons Consumer Protection informs you – QUVIVIQ – Package Leaflet

QUVIVIQ – Package Leaflet: InfoCons – Consumer Protection presents, in an accessible format, the official package leaflet of the medicine QUVIVIQ, as authorised in the European Union and published in the Union Register of medicinal products.

📋 QUVIVIQ – at a glance
Active substance daridorexant
ATC code N05CJ03
EU authorisation number EU/1/22/1638
Marketing Authorisation Holder Idorsia Pharmaceuticals Deutschland GmbH
Therapeutic indication Quviviq is indicated for the treatment of adult patients with insomnia characterised by symptoms present for at least 3 months and considerable impact on daytime functioning.
Last Commission decision 2026-06-19

Before anything else

Read all of this leaflet ca refully before you start taking this medicine because it contains important information for you.

  • Keep this leaflet. You may need to read it again.
  • If you have any further questions, ask your doctor or pharmacist.
  • This medicine has been prescribed for yo u only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
  • If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.

ℹ️ 1. What QUVIVIQ is and what it is used for

QUVIVIQ contains the active substance daridorexant, which belongs to the class of medicines called “orexin receptor antagonists”.

QUVIVIQ is to treat insomnia in adults.

How QUVIVIQ works

Orexin is a substance produced by the brain that helps keep you awake. By blocking the action of orexin, QUVIVIQ enables you to fall asleep faster and stay asleep longer, and improves your ability to function normally during the day .

⚠️ 2. What you need to know before you take QUVIVIQ

Do not take QUVIVIQ

  • if you are allergic to daridorexant or any of the other ingredients of this medicine (listed in section 6).
  • if you have narcolepsy, a condition that causes you to suddenly and unexpectedly fall asleep at any time.
  • if you are taking medicines which may increase the level of QUVIVIQ in your blood such as:
  • oral medicines to treat fungal infections such as ketoconazole, posaconazole, voriconazole, itraconazole .
  • certain medicines to treat bacterial infection s such as the antibiotic s clarithromycin , josamycin, telithromycin, trolean domycin.
  • certain medicines to treat HIV infection such as ritonavir , elvitegravir, indinavir, saquinavir, telaprevir, danopr evir, lopinavir, nelfinavir, boceprevir .
  • certain medicines to treat cancer such as ceritinib, idelalisib, ribociclib, tucatinib .

Ask your doctor if the medicine you are taking prevents you from taking QUVIVIQ.

Warnings and precautions

Talk to your doctor or pharmacist before taking QUVIVIQ if you:

  • have depression or have or ever had suicidal thoughts
  • have a psychiatric disorder
  • currently take medicinal products that affect your brain such as treatments for anxiety or depression
  • have regularly taken drugs (except as medicines) or been addicted to drugs or alcohol
  • have liver problems : depending on their severity, QUVIVIQ may not be recommended, or a lower dose might b e required.
  • have breathing difficulties (such as severe chronic obstructive pulmonary disease)
  • have a history of falling and are older than 65 (because there is generally a higher risk of falling in patients > 65).

Your doctor may want to monitor how the medicine affects you.

Tell your doctor if you get any of the following side effects while taking QUVIVIQ:

  • sleep paralysis : a temporary inability to mo ve or talk for up to several minutes upon awakening or falling asleep
  • hallucinations : seeing or hear ing vivid or disturbing things that are not real upon awakening or falling asleep If you have depression and you experience a worsening or have thoughts of harming yourself, call your doctor straight away.

Children and adolescents

This medicine is not for children and adolescents under 18 years of age because QUVIVIQ has not been tested in this age group.

Other medicines and QUVIVIQ

Tell your doctor or pharmacist if you are taking , have recently taken or might take any other medicines because:

  • certain antibiotics (erythromycin, ciprofloxacin, clarithromycin , rifampicin ), immuno – suppressants (cyclosporine), antifungal agents (itraconazole) , cancer tr eatments (ceritinib), or HIV treatments (ritonavir , efavirenz ) can increase or decrease the level of QUVIVIQ in the blood. Some of these medicine s may be contra -indicated with QUVIVIQ (see section “Do not take QUVIVIQ”) . Your doctor will advise you on this.
  • certain medicines that work in your brain (e.g., diazepam, alprazolam) could interact with QUVIVIQ. Your doctor will advise you on this.
  • certain medicines to treat blood coagulation disorder such as dabigatran could interact with QUVIVIQ , which would require some precaution. Your doctor will advise you on this.
  • certain medicine s to treat cardiac impairment such as digoxin could interact with QUVIVIQ , which would require some precaution. Your doctor will advise you on this.

QUVIVIQ with food, drink and alcohol

Drinking alcohol with QUVIVIQ can increase the risk of impaired balance and coordination .

Avoid grapefruit or grapefruit juice in the evening as they may increase the level of QUVIVIQ in the blood.

Pregnancy, breast -feeding and fertility 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 taking this medicine.

It is not known if QUVIVIQ can harm your unborn baby.

A small amount of QUVIVIQ passes into your breast milk. Talk to your doctor about the best way to feed your baby during treatment with QUVIVIQ.

It is not known if QUVIVIQ affects human fertility.

Driving and using machines

A period of approximately 9 hours is recommended between taking QUVIVIQ and driving or using machines. Be cautious about driving or using machines in the morning after taking QUVIVIQ. Do not engage in potentially hazardous activities if you are not sure you are fully alert , especially in the first few days of treatment .

QUVIVIQ contains sodium

This medicine contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially ‘sodium – free’.

💊 3. How to take QUVIVIQ

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

How much QUVIVIQ to take Your doctor will advise you on the dose of QUVIVIQ to take.

The recommended dose is one 50-mg tablet of QUVIVIQ per night.

If you have liver problems or take certain other medicines, your doctor may prescribe you a lower dose of one 25 -mg tablet of QUVIVIQ per night.

The treatment duration should be as short as possible. The appropriateness of c ontinued treatment will be assessed within 3 months by your doctor and periodically thereafter .

  • Take QUVIVIQ, one time per night, by mouth, in the half hour before going to bed at night.
  • You can take QUVIVIQ with or without food, however it may take lon ger to work if you take it with or right after a large meal.

If you take more Q UVIVIQ than you should

If you take more QUVIVIQ than you should, you may experience excessive sleepiness and muscle weakness. Contact your doctor straight away.

If you forget to take QUVIVIQ

If you forget to take QUVIVIQ at bedtime, then you should not take it later during the night , otherwise you may feel drowsy in the morning . Do not take a double dose to make up for a forgotten tablet.

If you stop taking QUVIVIQ

Treatment with QUVIVIQ can be stopped without a need to gradually reduce the dose , and without harmful effects.

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

❗ 4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them. The following side effects may happen with this medicine:

Common (may affect up to 1 in 10 people)

  • headache
  • excessive sleepiness
  • dizziness
  • tiredness
  • feeling sick (nausea)

Uncommon (may affect up to 1 in 100 people )

  • temporary inability to move or talk (sleep paralysis) for up to several minutes while you are going to sleep or waking up (see section 2) .
  • seeing or hearing vivid or disturbing things that are not real (hallucinations ; see section 2 )
  • allergic reactions (including rash, urticaria)
  • abnormal dreams, nightmares
  • sleepwalking Please talk to your doctor if any of these happen to you.

Reporting of side effects

If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system listed in Appendix V . By reporting side effects , you can help provide more information on the safety of this medicine.

🌡️ 5. How to store QUVIVIQ

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiry date which is stated on the carton and blister after EXP.

The expiry date refers to the last day of that month.

This medicine does not require any special storage conditions.

Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer require. These measures will help to protect the environment.

📦 6. Contents of the pack and other information

What QUVIVIQ contains

The active subs tance is daridorexant.

QUVIVIQ 25 mg film -coated tablets Each tablet contains daridorexant hydrochloride, equivalent to 25 mg of daridorexant.

QUVIVIQ 50 mg film -coated tablets Each tablet contains daridorexant hydrochloride, equivalent to 50 mg of daridorexant.

The other ingredients are:

31 Tablet cores: Mannitol (E421), microcrystalline cellulose (E460), povidone, croscarmellose sodium (see section 2 “QUVIVIQ contains sodium”), silicon dioxide, magnesium stearate.

Film coating: Hypromellose (E464), microcrystalline cellulose (E460), glycerol, talc (E553), titanium dioxide (E171), iron oxide red (E172), iron oxide black (E172), iron oxide yellow (E172; 50 mg tablets only).

What QUVIVIQ looks like and contents of the pack

Film-coated tablet (tablet) QUVIVIQ 25 mg film-coated tablets Light purple, triangular tablet with 25 on one side, and ‘i’ (Idorsia logo) on the other side.

QUVIVIQ 50 mg film-coated tablets Light orange, triangular tablet with 50 on one side, and ‘i’ (Idorsia logo) on the other side.

QUVIVIQ is available in blister packs of 10, 20 or 30 film-coated tablets.

Not all pack sizes may be marketed.

Marketing Authorisation Holder

Idorsia Pharmaceuticals Deutschland GmbH Marie-Curie-Strasse 8 79539 Lörrach Germany

Manufacturer

Idorsia Pharmaceuticals Deutschland GmbH Marie-Curie-Strasse 8 79539 Lörrach Germany

This leaflet was last revised in

Detailed information on this medicine is available on the European Medicines Agency web site: https://www.ema.europa.eu .

📄 Package Leaflet – official source

This article reproduces the information in the official package leaflet, as authorised in the European Union. You can consult the original document here: Product information QUVIVIQ (PDF, ec.europa.eu).

You can check this medicine at any time in the Union Register of medicinal products (EU number EU/1/22/1638).

⚠️ Important: This article is for information purposes only and does not replace medical advice or the package leaflet inside the medicine box. Read the leaflet carefully before use. For any questions about your treatment, talk to your doctor or pharmacist. If you experience side effects, tell your doctor or pharmacist and report them through your national reporting system.

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