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Pharmacy Guide

Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.

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Migard 2.5 mg film-coated tablets

⚠ This medicine appears to have been discontinued

The electronic medicines compendium (emc) no longer publishes a Summary of Product Characteristics for this product, which usually means it is no longer marketed in the UK. The patient leaflet below is kept for reference, but the product may not be available.

If you were prescribed this medicine, other products containing Frovatriptan succinate monohydrate may still be available. Do not stop your treatment — ask your pharmacist or GP what to use instead.

Active substance: Frovatriptan succinate monohydrate

Equivalent medicines (same active substance, strength and form)

Source: electronic medicines compendium (emc)
Official leaflet: Read the PIL on emc

What it is and what it is used for

for

MIGARD 2.5 mg tablets contain frovatriptan, an anti-migraine treatment belonging to the class of triptans (5-hydroxytryptamine (5HT1) selective receptor agonists). MIGARD 2.5 mg tablets is a medicine for the treatment of the headache phase of a migraine attack with or without aura (a temporary strange feeling before a migraine, which varies from person to person but can affect, for example, vision, smell, hearing). MIGARD 2.5 mg tablets should not be used to prevent a migraine attack. MIGARD is used to treat migraine attacks in adults. 2.

What you need to know before you take it

e MIGARD

The diagnosis of migraine must have been clearly established by your doctor Do not take MIGARD

  • If you are allergic to frovatriptan or any of the other ingredients of this medicine (listed in section 6.1).
  • if you have had a heart attack, or suffer or have suffered from certain cardiovascular diseases such as angina pectoris (characterised by crushing pain in the chest which can extend into the left arm), or circulation disorders of the legs or arms (especially in the fingers and toes),
  • if you have had a stroke or a transient ischaemic attack (TIA),
  • if you have severely or moderately high blood pressure, or if your blood pressure is not adequately controlled,
  • if you have severe liver disease,
  • in combination with certain other medicines also used in the treatment of migraine (ergotamine and ergotamine derivatives (including methysergide) or other triptans (5-hydroxytryptamine (5HT1) agonists). Warning and precautions Talk to your doctor before taking MIGARD: if you are a patient at risk of coronary artery disease, including if: 1

> you are a heavy smoker or a user of nicotine substitution therapy > you are a post-menopausal female or a male aged over 40 years Stop taking MIGARD and talk to your doctor right away if you: >

>

experience a feeling of tightness or pain in the chest, shortness of breath and/or pain or discomfort in one or both arms, your back, shoulders, neck, jaw, or upper part of the stomach; these might be symptoms of a heart attack, which can occur when taking triptans, even in patients with no history of cardio-vascular disease (see also section 4). have generalized skin rash and itching, rapid-onset swelling (especially around the lips, eyes, or of the tongue), with possible sudden difficulty in breathing and a fast heartbeat and thumping heart. These are all symptoms and signs of allergy and whole-body hypersensitivity reaction (see also section 4).

Children and adolescents Do not give this medicine to children and adolescents (under 18 years of age) because the safety and efficacy of MIGARD have not been established in these groups. Other medicines and MIGARD Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines, including medicines obtained without a prescription. You should not take this medicine at the same time as certain other medicines used for the treatment of migraine:

  • especially ergotamine, ergotamine derivatives (including methysergide); you should allow at least 24 hours to elapse between the discontinuation of these medicines and the administration of MIGARD 2.5 mg tablets. Similarly, you should not take these medicines within 24 hours following a dose of MIGARD 2.5 mg tablets.
  • especially other triptans (5-HT1 agonists, such as sumatriptan, almotriptan, eletriptan, naratriptan, rizatriptan or zolmitriptan). Unless otherwise directed by your doctor, you should not take this medicine at the same time as monoamine oxidase inhibitor (MAOI) medicines used in the treatment of depression (phenelzine, isocarboxazid, tranylcypromine, moclobemide).
  • you should also tell your doctor or pharmacist if you are taking oral contraceptives or selective serotoninreuptake inhibitors (citalopram, fluoxetine, fluvoxamine, paroxetine, sertraline). It is recommended that you do not take MIGARD 2.5 mg tablets at the same time as taking St. John's Wort (hypericum perforatum). Concomitant use of MIGARD with the medicines listed above (especially monoamine oxidase inhibitors, selective serotonin-reuptake inhibitors and hypericum perforatum) may also increase the risk of serotonin syndrome (the symptoms of serotonin syndrome include: shivering, sweating, agitation, trembling and abrubt contraction of muscles, nausea, fever, confusion). If you have any doubt about taking other medicines with MIGARD 2.5 mg tablets, consult your doctor or pharmacist. MIGARD with food and drink MIGARD 2.5 mg tablets can be taken with food or on an empty stomach, always with an adequate amount of water. Pregnancy and breast-feeding If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine. MIGARD 2.5 mg tablets should not be used during pregnancy or when breast feeding, unless you are told so by your doctor. In any case, you should not breastfeed for 24 hours after taking MIGARD and during this time any breast milk expressed should be discarded. Driving and using machines 2

MIGARD 2.5 mg tablets and the migraine itself can cause drowsiness. If affected, driving or operating machinery can be dangerous and should be avoided. MIGARD contains lactose This product contains lactose. If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine. MIGARD contains sodium This medicine contains less than 1 mmol sodium (23 mg) per dosage unit, that is to say essentially 'sodiumfree'. 3.

How to take it

MIGARD

Always take this medicine exactly as your doctor has told you. Check with your doctor if you are not sure. Take MIGARD 2.5 mg tablets as early as possible after the onset of the migraine headache. Swallow one tablet whole with water. If the first dose does not give you any relief, do not take a second dose during the same attack. You can use MIGARD 2.5 mg tablet for any following attacks. If you obtain relief after the first dose, but later on suffer from the re-appearance of a headache within 24 hours, you can take a second dose provided that at least 2 hours have elapsed between the 2 doses. Do not exceed the maximum dose of 5 mg (two tablets) in 24 hours. Excessive use (repeated use over several consecutive days) of MIGARD 2.5 mg tablets constitutes incorrect use of this medicine and may cause an increase in side effects and lead to chronic daily headaches requiring the temporary discontinuation of treatment. Consult your doctor if you start having too frequent or daily headaches as you may be suffering from medication overuse headache. Use in children and adolescents MIGARD should not be used in patients under 18 years of age. Elderly As there is little experience in patients over 65 years, the use of MIGARD is not recommended in patients in this age group. If you take more MIGARD than you should If you accidentally take an overdose of this medicine, tell your doctor or pharmacist immediately or go to the emergency department of your nearest hospital. Please remember to take the remaining tablets or this leaflet with you. If you stop taking MIGARD No special precautions are necessary when stopping the drug. If you have any further questions on the use of thismedicine, ask your doctor or pharmacist. 4.

Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them. Stop taking MIGARD and tell your doctor right away if you experience any of the following symptoms: > a feeling of tightness or pain in the chest, shortness of breath and/or pain or discomfort in one or both arms, your back, shoulders, neck, jaw, or upper part of the stomach; these might be symptoms of a heart attack (myocardial infarction), which can occur when taking triptans, even in patients with no history of cardio-vascular disease;

3

> have generalized skin rash and itching, rapid-onset swelling (especially around the lips, eyes, or of the tongue and mucosa), with possible sudden difficulty in breathing and a fast heartbeat and thumping heart. These are all symptoms and signs of allergy and whole-body hypersensitivity reaction (hypersensitivity reactions, angioedema, anaphylaxis). The side-effects reported with MIGARD 2.5 mg tablets were temporary, generally mild to moderate and disappeared spontaneously. Some symptoms reported may be caused by the migraine itself. The following side-effects were commonly observed (estimated frequency is more than 1 person out of 100 and less than 1 person out of 10):

  • nausea (feeling sick), dry mouth, digestion problems, stomach pain,
  • fatigue, chest discomfort (sensation of slight heaviness, pressure or tightness in the chest),
  • headache, dizziness, sensation of pins and needles, most frequently in the arms and legs, reduction or disturbance of the sensations of touch, extreme sleepiness,
  • hot flushes,
  • tightness in the throat,
  • sight disturbances,
  • increased sweating. The following were uncommonly observed (estimated frequency is more than 1 person out of 1000 and less than 1 person out of 100):
  • altered sense of taste, trembling, poor concentration, lethargy, increased sensation of touch, drowsiness, involuntary muscle contractions,
  • diarrhoea, difficulty in swallowing, gas in stomach or bowel, stomach discomfort, bloated stomach,
  • awareness of heart beat (palpitations), fast heart beat, high blood pressure, chest pain (intense tightness or feeling of pressure in the chest),
  • feeling hot, reduced tolerance of heat and cold, pain, weakness, thirst, sluggishness, increased energy, generally feeling unwell, sensation of spinning,
  • anxiety, inability to sleep, confusion, nervousness, agitation, depression, loss of sense of personal identity,
  • coldness in the hands and feet,
  • irritation of the nose, inflamed sinus, sore throat and/or voice box,
  • muscle stiffness, muscle and bone pain, pain in the hands and feet, back pain, painful joints,
  • eye pain, eye irritation, painful oversensitivity to light,
  • itchiness,
  • ringing in the ears, earache,
  • dehydration,
  • passing urine frequently, production of large amounts of urine. The following were rare (estimated frequency is more than 1 person out of 10,000 and less than 1 person out of 1000):
  • muscle spasm, floppy muscles, diminution of reflexes (hyporeflexia), movement problems,
  • constipation, burping, heartburn, irritable bowel syndrome, lip blisters, lip pain, spasm of the gullet, blisters in the mouth, ulcer in the stomach or upper part of the small intestine, pain in the salivary gland, inflammation of the mouth, toothache,
  • fever,
  • loss of memory, abnormal dreams, personality disorder,
  • nosebleed, hiccups, overbreathing, breathing disorder, irritation in the throat,
  • night blindness,
  • skin reddening, sensation of hairs standing on end, purplish spots or patches on skin and mucous surfaces of the body, hives,
  • slow heart beat,
  • ear discomfort, eardisorder, ear itchiness, sensitive hearing,
  • increase in bilirubin (a substance produced by the liver) in the blood, decrease of calcium in the blood, abnormal urine analysis,
  • low sugar in the blood,
  • passing urine frequently at night, pain in the kidneys, 4
  • self-inflicted injury (eg bite or bruising),
  • swollen lymph nodes,
  • breast pain or discomfort. Although the frequency cannot be estimated from the available data, the following events were also reported:
  • allergic reactions (hypersensitivity) including generalized skin rash and itching, rapid-onset swelling (especially around the lips, eyes, or of the tongue), with possible sudden difficulty in breathing, that can be associated with fast heartbeat and thumping heart (anaphylaxis),
  • heart attack (myocardial infarction),
  • chest discomfort or pain that is caused by a temporary spasm (constriction) in your coronary arteries (the blood vessels that bring oxygen and nutrients to your heart, i.e. coronary artery spasm). 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 Yellow Card Scheme at 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. 5.

How to store it

MIGARD

Do not use this medicine after the expiry date which is stated on the carton. The expiry date refers to the last day of that month. Do not store above 30°C. Store in the original package in order to protect from moisture. Keep this medicine out of the sight and reach of children. Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help to protect the environment. 6.

Contents of the pack and other information

What MIGARD contains The active substance is frovatriptan as succinate monohydrate. Each tablet contains 2.5 mg of frovatriptan. The other ingredients are: Tablet core: anhydrous lactose, microcrystalline cellulose, magnesium stearate, sodium starch glycollate (type A), silica colloidal anhydrous. Tablet coat: OPADRY white: titanium dioxide (E171), anhydrous lactose, hypromellose (E464), macrogol 3000, triacetin. What MIGARD looks like and contents of the pack MIGARD 2.5 mg film-coated tablets are available in the form of round film-coated tablets, debossed with "m" on one side and "2.5" on the other. MIGARD is packed in: PVC/PE/PVDC/Aluminium blister: 1, 2, 3, 4, 6 or 12 tablets per each blister Not all pack sizes may be marketed.

5

Marketing Authorisation Holder and Manufacturer Marketing Authorisation Holder: Menarini International Operations Luxembourg S.A. 1, Avenue de la Gare L-1611, Luxembourg Manufacturer: Berlin-Chemie AG Glienicker Weg 125 – D-12489 Berlin, Germany or A.Menarini Manufacturing Logistics and services s.r.l. Via Campo di Pile – L'Aquila (AQ), Italy or Laboratorios Menarini S.A. Alfonso XII, 587, 08918 – Badalona (Barcelona), Spain Marketed by: A. Menarini Farmaceutica Internazionale SRL This medicinal product is authorised in the Member States of the EEA under the following names: France (RMS): Isimig Austria: Eumitan Belgium, Estonia, Finland, Hungary, Latvia, Lithuania, Luxembourg, Portugal, The Netherlands, United Kingdom (Northern Ireland): Migard Greece: Pitunal Italy: Rilamig Spain: Forvey This leaflet was last revised in May 2021. Frovatriptan developed by Vernalis Ltd

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Frequently asked questions about Migard 2.5 mg film-coated tablets

How do I take Migard 2.5 mg film-coated tablets?

Migard 2.5 mg film-coated tablets comes as tablet containing 2.5mg. Always follow the dose your doctor or pharmacist has given you, and read the leaflet that comes with the medicine.

What is the active substance in Migard 2.5 mg film-coated tablets?

The active substance in Migard 2.5 mg film-coated tablets is frovatriptan succinate monohydrate.

Are there equivalent medicines to Migard 2.5 mg film-coated tablets?

Medicines with the same active substance, strength and form include: Frovatriptan 2.5 mg Film-coated Tablets, Frovatriptan 2.5 mg film coated tablets. They are interchangeable only if your prescriber or pharmacist says so.

Where does this information come from?

This leaflet reproduces the patient information leaflet approved for Migard 2.5 mg film-coated tablets, as published on the electronic medicines compendium (emc). The version printed inside your medicine’s packaging is the one that applies to you.

Can I get Migard 2.5 mg film-coated tablets without a prescription?

Whether a medicine is available over the counter or on prescription only depends on its licence. Check the leaflet, or ask your pharmacist — they can tell you straight away.

About this leaflet

The text above reproduces the patient information leaflet approved for this medicine, restructured for easier reading.

Medical disclaimer: This page is for information only and does not replace advice from your doctor or pharmacist. Always read the leaflet supplied with your medicine. If you are unwell, call NHS 111; in an emergency, call 999.

Medicines with the same active substance: Frovatriptan succinate monohydrate (3 medicines)
See every medicine containing this substance, or browse the full A–Z of active substances.
⚕For healthcare professionals — Summary of Product Characteristics (SmPC)Full SmPC: dosage, interactions, contraindications, warnings+
Technical information intended for healthcare professionals (doctors and pharmacists). The Summary of Product Characteristics (SmPC) is the official document approved by the MHRA/EMA. It does not replace the patient leaflet or a doctor’s advice.

4.1. Therapeutic indications

Acute treatment of the headache phase of migraine attacks with or without aura.

MIGARD is indicated in adults.

4.2. Posology and method of administration

Posology

Frovatriptan should be taken as early as possible after the onset of a migraine attack but it is also effective when taken at a later stage. Frovatriptan should not be used prophylactically.

If a patient does not respond to the first dose of frovatriptan, a second dose should not be taken for the same attack, since no benefit has been shown.

Frovatriptan may be used for subsequent migraine attacks.

Adults (18 to 65 years of age)

The recommended dose of frovatriptan is 2.5 mg.

If the migraine recurs after initial relief, a second dose may be taken, providing there is an interval of at least 2 hours between the two doses.

The total daily dose should not exceed 5 mg per day.

Paediatric population (under 18 years)

The safety and efficacy of MIGARD in children and adolescents aged below the age of 18 years have not been established. Therefore, its use in this age group is not recommended. No data are available.

Elderly (over 65 years)

Frovatriptan data in patients over 65 years remain limited. Therefore, its use in this category of patients is not recommended.

Renal impairment

No dosage adjustment is required in patients with renal impairment (see section 5.2).

Hepatic impairment

No dosage adjustment is required in patients with mild to moderate hepatic impairment (see section 5.2). Frovatriptan is contraindicated in patients with severe hepatic impairment (see section 4.3).

Method of administration

Oral use.

The tablets should be swallowed whole with water.

4.3. Contraindications

- hypersensitivity to the active substance or to any of the excipients listed in section 6.1.

- patients with a history of myocardial infarction, ischaemic heart disease, coronary vasospasm (e.g. Prinzmetal's angina), peripheral vascular disease, patients presenting with symptoms or signs compatible with ischaemic heart disease.

- Moderately severe or severe hypertension, uncontrolled mild hypertension.

- previous cerebrovascular accident (CVA) or transient ischaemic attack (TIA).

- severe hepatic impairment (Child-Pugh C).

- Concomitant administration of frovatriptan with ergotamine or ergotamine derivatives (including méthysergide) or other 5-hydroxytryptamine (5-HT1) receptor agonists.

4.4. Special warnings and precautions for use

Frovatriptan should only be used where a clear diagnosis of migraine has been established.

Frovatriptan is not indicated for the management of hemiplegic, basilar or ophthalmoplegic migraine.

As with other treatments of migraine attack, it is necessary to exclude other, potentially serious, neurological conditions before treating the headache of patients without a previous diagnosis of migraine, or migraine patients presenting with atypical symptoms. It should be noted that migraineurs present an increased risk of certain cerebral vascular events (eg CVA or TIA).

The safety and efficacy of frovatriptan administered during the aura phase, before the headache phase of migraine, has not been established.

As for other 5-HT1 receptor agonists, frovatriptan must not be administered to patients at risk of coronary artery disease (CAD), including heavy smokers or users of nicotine substitution therapy without a prior cardiovascular evaluation (see section 4.3). Specific attention should be given to post- menopausal women and men over 40 years of age presenting with these risk factors.

However, cardiac evaluations may not identify every patient who has cardiac disease. In very rare cases serious cardiac events have occurred in patients with no underlying cardio-vascular disease when taking 5-HT1 receptor agonists.

Frovatriptan administration can be associated with transient symptoms including chest pain or tightness which may be intense and involve the throat. (see section 4.8).

Where such symptoms are thought to indicate ischaemic heart disease no further doses of frovatriptan should be taken and additional investigations should be carried out.

Patients should be informed of the early signs and symptoms of hypersensitivity reactions including cutaneous disorders, angioedema and anaphylaxis (see section 4.8). In case of serious allergic/hypersensitivity reactions, frovatriptan treatment should be discontinued immediately and it should not be administered again.

It is advised to wait 24 hours following the use of frovatriptan before administering an ergotamine- type medication. At least 24 hours should be elapse after administration of an ergotamine-containing preparation before frovatriptan is given (see sections 4.3 and 4.5).

In case of too frequent use (repeated administration several days in a row corresponding to a misuse of the product), the active substance can accumulate leading to an increase of the side-effects.

Prolonged use of any type of painkiller for headaches can make them worse. If this situation is experienced or suspected, medical advice should be obtained and treatment should be discontinued. The possibility of MOH should be taken into consideration in patients who have frequent or daily headaches despite (or because of) the regular use of headache medications.

Do not exceed the recommended dose of frovatriptan.

Undesirable effects may be more common during concomitant use of triptans (5HT agonists) and herbal preparations containing St John's Wort (Hypericum perforatum).

This medicinal product contains lactose, therefore patients with rare hereditary problems of galactose intolerance, total lactase deficiency or glucose-galactose malabsorption should not take this medicine.

This medicine contains less than 1 mmol sodium (23 mg) per dosage unit, that is to say essentially 'sodium-free'.

4.5. Interaction with other medicinal products and other forms of interaction

CONTRAINDICATIONS OF CONCOMITANT USE

Ergotamine and ergotamine derivatives (including méthysergide) and other 5 HT1 agonists

Risks of hypertension and coronary artery constriction due to additive vasospastic effects when used concomitantly for the same migraine attack (see section 4.3).

Effects can be additive. It is recommended to wait at least 24 hours after administration of ergotamine-type medication before administering frovatriptan. Conversely it is recommended to wait 24 hours after frovatriptan administration before administering an ergotamine-type medication (see section 4.4 ).

CONCOMITANT USE NOT RECOMMENDED

Monoamine Oxidase Inhibitors

Frovatriptan is not a substrate for MAO-A, however a potential risk of serotonin syndrome or hypertension cannot be excluded (see section 5.2).

CONCOMITANT USE REQUIRING CAUTION

Selective serotonin-reuptake inhibitors (citalopram, fluoxetine, fluvoxamine, paroxetine, sertraline)

Potential risk of hypertension, coronary vasoconstriction or serotonin syndrome.

Strict adherence to the recommended dose is an essential factor to prevent this syndrome.

Methylergometrine

Risks of hypertension, coronary artery constriction.

Fluvoxamine

Fluvoxamine is a potent inhibitor of cytochrome CYP1A2 and has been shown to increase the blood levels of frovatriptan by 27-49%.

Oral contraceptives

In female subjects taking oral contraceptives, concentrations of frovatriptan were 30% higher than in females not taking oral contraceptives. No increased incidence in the adverse event profile was reported.

Hypericum perforatum (St. John wort) (oral route)

As with other triptans the risk of the occurence of serotonin syndrome may be increased.

4.6. Fertility, pregnancy and lactation

Pregnancy

There are no or limited amount of data from the use of frovatriptan in pregnant women.

Studies in animals have shown reproductive toxicity (see section 5.3). The potential risk for humans is unknown. MIGARD is not recommended during pregnancy and in women of childbearing potential not using contraception, unless clearly necessary.

Breast-feeding

It is unknown whether Frovatriptan/metabolites are excreted in human milk.

Frovatriptan and/or its metabolites are excreted in the milk of lactating rats with the maximum concentration in milk being four-fold higher than maximum blood levels.

A risk to the breastfeeding newborns/infants cannot be excluded.

MIGARD is not recommended during breast-feeding, unless is clearly needed. In this case, a 24 hours interval must be observed.

4.7. Effects on ability to drive and use machines

No studies on the effects on the ability to drive and use machines have been performed.

Migraine or treatment with frovatriptan may cause somnolence. Patients should be advised to evaluate their ability to perform complex tasks such as driving during migraine attacks and following administration of frovatriptan.

4.8. Undesirable effects

Frovatriptan has been administered to over 2700 patients at the recommended dose of 2.5 mg and the most common side effects (<10%) include dizziness, fatigue, paraesthesia, headache and vascular flushing. The undesirable effects reported in clinical trials with frovatriptan were transient, generally mild to moderate and resolved spontaneously. Some of the symptoms reported as undesirable effects may be associated symptoms of migraine.

The table below shows all the adverse reactions that are considered to be related to treatment with 2.5 mg frovatriptan and showed a greater incidence than with placebo in the 4 placebo controlled trials. They are listed in decreasing incidence by body-system. Adverse reactions collected in the post-marketing experience are noted with an asterisk *

System organ class

Common

≥1/100 <1/10

Uncommon

≥1/1000 <1/100

Rare

≥1/10,000 <1/1000

Not known (cannot be estimated from the available data)

Blood and the lymphatic system disorders

Lymphadenopathy

Immune system disorders

hypersensitivity reactions* (including cutaneous disorders, angioedema and anaphylaxis)

Metabolism and nutrition disorders

Dehydration,

Hypoglycaemia

Psychiatric disorders

Anxiety, insomnia, confusional state, nervousness, agitation, depression, depersonalisation

Abnormal dreams, personality disorder

Nervous system disorders

Dizziness, paraesthesia, headache, somnolence, dysaesthesia, hypoaesthesia

Dysgeusia, tremor, disturbance in attention, lethargy, hyperaesthesia, sedation

vertigo, involuntary muscle contractions

Amnesia, Hypertonia, Hypotonia, hyporeflexia, movement disorder

Eye disorders

Visual disturbance

Eye pain, eye irritation, photophobia

Night blindness

Ear and labyrinth disorders

Tinnitus, ear pain

Ear discomfort, ear disorder, ear pruritus, hyperacusis

Cardiac disorders

Palpitations, tachycardia

Bradycardia

Myocardial infarction*, Arteriospasm coronary*

Vascular disorders

Flushing

Peripheral coldness, Hypertension

Respiratory, thoracic and mediastinal disorders

Throat tightness

Rhinitis, sinusitis, pharingolaringeal pain

Epistaxis, hiccups, hyperventilation, respiratory disorder, throat irritation

Gastrointestinal disorders

Nausea, dry-mouth, dyspepsia, abdominal pain

Diarrhoea, dysphagia, flatulence, stomach discomfort, abdominal distension

Constipation, eructation, gastroesophageal reflux disease, irritable bowel syndrome, lip blister, lip pain, oesophageal spasm, oral mucosal blistering, peptic ulcer, salivary gland pain, stomatitis, toothache

Skin and subcutaneous tissue disorders

Hyperhidrosis

Pruritus

Erithema, piloerection, purpura, urticaria

Musculoskeletaland connective tissue disorders

Musculoskeletal stiffness, musculoskeletal pain, pain in extremity, back pain, arthralgia

Renal and urinary disorders

Pollakiuria, polyuria

Nocturia, renal pain

Reproductive system and breast disorders

Breast tenderness

General disorders and administration site conditions

Fatigue, chest discomfort

Chest pain, feeling hot, temperature intolerance, pain, asthaenia, thirst, sluggishness, energy increased, malaise

Pyrexia

Investigations

Blood bilirubin increased, blood calcium decreased, urine analysis abnormal

Injury, poisoning and procedural complications

Bite

In two open long-term clinical studies the observed effects were not different from those listed above.

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions 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.

4.9. Overdose

There is limited data on overdose with frovatriptan tablets. The maximum single oral dose of frovatriptan given to male and female patients with migraine was 40 mg (16 times the recommended clinical dose of 2.5 mg) and the maximum single dose given to healthy male subjects was 100 mg (40 times the recommended clinical dose). Both were not associated with side effects other than those mentioned in section 4.8. However, one post-marketing serious case of coronary vasospasm has been reported, following intake of 4 times the recommended dose of frovatriptan on three consecutive days, in a patient taking migraine prophylactic treatment with a tricyclic antidepressant. The patient recovered.

There is no specific antidote for frovatriptan. The elimination half-life of frovatriptan is approximately 26 hours (see section 5.2.).

The effects of haemodialysis or peritoneal dialysis on serum concentrations of frovatriptan are unknown.

Treatment

In case of overdose with frovatriptan, the patient should be monitored closely for at least 48 hours and be given any necessary supportive therapy.

💬 Ask about this leaflet

Ask anything about Migard 2.5 mg film-coated tablets. The assistant answers only from this leaflet — if the leaflet does not cover it, it will say so. It does not give medical advice.

Answers come from the patient leaflet published on the electronic medicines compendium (emc). They are not medical advice. Ask a pharmacist or your GP if you are unsure. For urgent help call NHS 111, or 999 in an emergency.

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