4.1. Therapeutic indications

Suvexx is indicated for the acute treatment of the headache phase of migraine attacks with or without aura in adults where treatment with a mono-entity product has been insufficient.

4.2. Posology and method of administration

Posology

Adults

Suvexx is indicated for the acute treatment of migraine and it should not be used prophylactically. The recommended dose of sumatriptan/naproxen should not be exceeded.

It is advisable that sumatriptan/naproxen be given as early as possible after the onset of migraine headache, but it is effective when administered at any stage of the headache phase.

The recommended dosage for adults is one tablet of sumatriptan/naproxen 85 mg/457 mg.

If the patient does not respond to the first dose of sumatriptan/naproxen, a second dose should not be taken for the same attack.

If the patient has responded to the first dose but the symptoms recur a second dose may be given provided that there is a minimum interval of two hours between the two doses.

The maximum recommended dosage in a 24-hour period is 2 tablets, taken at least 2 hours apart.

The safety of treating an average of more than 5 migraine attacks in a 30-day period has not been established.

Paediatric population

The efficacy and safety of sumatriptan/naproxen in children aged less than 18 years have not been established.

Elderly (Over 65 years of age)

Sumatriptan/naproxen has not been studied in geriatric patients and its use in this population is not recommended. Elderly patients are more likely to have age-associated decreased hepatic and renal function.

Hepatic Impairment

The effect of hepatic impairment on the pharmacokinetics of sumatriptan/naproxen has not been studied. Sumatriptan/naproxen is contraindicated in patients with moderate and severe (Child Pugh B and C) hepatic impairment (see section 4.3). Sumatriptan/naproxen is not recommended in patients with mild hepatic impairment (Child Pugh A). If there is a need to use sumatriptan/naproxen in patients with mild hepatic impairment, only one dose should be used within a 24-hour period and patient should be monitored during treatment.

Renal Impairment

The effect of renal impairment on the pharmacokinetics of sumatriptan/naproxen has not been studied. Sumatriptan/naproxen is contraindicated for use in patients with GFR less than 30 mL/min/1.73m2 (see section 4.3). In patients with mild or moderate renal impairment, only one dose should be administered within a 24-hour period and renal function should be monitored during treatment.

Method of administration

Oral use.

Suvexx tablets should be swallowed whole with water. Tablets should not be split, crushed, or chewed as this can affect the optimised rate of drug absorption.

Suvexx tablets may be administered with or without food.

4.3. Contraindications

• Hypersensitivity to the active substances or to any of the excipients listed in section 6.1

Sumatriptan/naproxen is contraindicated in patients with

• severe cardiac failure, history of myocardial infarction or ischaemic heart disease, coronary vasospasm (Prinzmetal's angina), peripheral vascular disease or symptoms or signs consistent with ischaemic heart disease

• history of ischaemic stroke or transient ischemic attack (TIA), because these patients are at a higher risk of ischaemic stroke.

• previously shown hypersensitivity reactions (e.g. nasal polyps, asthma, rhinitis, angioedema or urticaria) in response to ibuprofen, aspirin or other non-steroidal anti-inflammatory/analgesic drugs (NSAIDs). These reactions have the potential of being fatal. Severe anaphylactic-like reactions to naproxen have been reported in such patients.

• history of upper gastrointestinal bleeding or perforation, related to previous NSAIDs therapy

• active acute peptic ulcer or gastrointestinal bleeding or recurring previous episodes (two or more distinct episodes of proven ulceration or bleeding)

• moderate and severe hypertension and mild uncontrolled hypertension

• severe renal impairment (glomerular filtration rate, GFR <30 mL/min/1.73m2)

• moderate and severe hepatic impairment.

Sumatriptan/naproxen must not be used

• concomitantly with ergotamine, or derivatives of ergotamine (including methysergide) or any triptan/5-hydroxytryptamine1 (5-HT1) receptor agonist

• concomitantly with reversible (e.g. moclobemide) or irreversible (e.g. selegiline) monoamine oxidase inhibitors (MAOIs) (see section 4.5).

• within 2 weeks of discontinuation of therapy with MAOIs (see section 4.5).

• during the last trimester of pregnancy (see section 4.6).

4.4. Special warnings and precautions for use

Sumatriptan/naproxen should only be used where there is a clear diagnosis of migraine.

Sumatriptan/naproxen is not indicated for use in the management of hemiplegic, basilar or ophthalmoplegic migraine.

Before treating with sumatriptan/naproxen, care should be taken to exclude potentially serious neurological conditions (e.g. stroke, TIA) if the patient presents with atypical symptoms or if they have not received an appropriate diagnosis for sumatriptan use.

Undesirable effects may be minimised by using the lowest effective dose for the shortest duration necessary to control symptoms (see section 4.2, and gastrointestinal and cardiovascular risks below). Patients treated with NSAIDs long-term should undergo regular medical supervision to monitor for adverse events. According to International Headache Society (IHS), regular intake of acute or symptomatic migraine medication for more than 9 days a month and more than 3 months may predispose to medication overuse headache (MOH). It usually, but not invariably, resolves after the overuse is stopped.

Cardiovascular and cerebrovascular effects

Sumatriptan

Sumatriptan, a component of Suvexx, can cause coronary artery vasospasm. Sumatriptan/naproxen is contraindicated in patients with uncontrolled hypertension, ischemic coronary artery disease, cardiac arrhythmias, and those with history of myocardial infarction (see section 4.3). Sumatriptan/naproxen is not recommended in patients with family history or risk factors predictive of coronary artery disease.

Sumatriptan can be associated with transient symptoms including chest pain and 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 sumatriptan should be given and an appropriate evaluation should be carried out.

Sumatriptan should not be given to patients with risk factors for ischaemic heart disease, including those patients who are heavy smokers or users of nicotine substitution therapies, without prior cardiovascular evaluation (see section 4.3). Special consideration should be given to postmenopausal women and males over 40 with these risk factors. These evaluations however, may not identify every patient who has cardiac disease and, in very rare cases, serious cardiac events have occurred in patients without underlying cardiovascular disease.

Sumatriptan should be administered with caution to patients with mild controlled hypertension, since transient increases in blood pressure and increased peripheral vascular resistance have been observed in a small proportion of patients (see section 4.3).

Naproxen

Naproxen sodium, a component of Suvexx, is a non-steroidal anti-inflammatory drug (NSAID). Use of some NSAIDs is associated with an increased incidence of cardiovascular adverse events (such as myocardial infarction, stroke or thrombotic events) which can be fatal. The risk may increase with duration of use. Patients with cardiovascular disease or risk factors for cardiovascular disease may be at greater risk.

Use of NSAIDs, such as naproxen sodium, which is a component of Suvexx, can promote sodium retention in a dose-dependent manner, through a renal mechanism, which can result in increased blood pressure and/or exacerbation of congestive heart failure.

Information from clinical studies and epidemiological data suggest that the use of some NSAIDs (especially in high doses and with long-term use) can be associated with a slightly increased risk of thrombosis in the arteries (for instance myocardial infarction or stroke). Epidemiological studies suggest that naproxen in low doses (1 000 mg per day) can be associated with a lower risk, some risk cannot be ruled out.

Patients with uncontrolled hypertension, congestive heart failure, established ischaemic cardiac disease, peripheral arterial disease, and/or cerebrovascular disease should only be treated with naproxen after careful consideration. The same consideration should be made before a long-term treatment is started in patients with risk factors for cardiovascular disease (for instance hypertension, hyperlipidaemia, diabetes mellitus and smoking).

Gastrointestinal bleeding, ulceration and perforation

Naproxen

Gastro-intestinal bleeding, ulceration and perforation, which can be fatal, have been reported with the use of all NSAIDs at any time during the treatment, with or without warning symptoms or the prior occurrence of severe gastro-intestinal side effects.

The risk of gastro-intestinal bleeding, ulceration and perforation is greater with higher doses, the prior occurrence of ulceration, in particular if complicated by bleeding and perforation (see section 4.3) and in elderly patients. These patients should start the treatment with the lowest available dosage. Combination treatment with protective products (for example misoprostol or protonpump inhibitors) should be considered in these patients as well as in patients who concomitantly need low doses of acetyl salicylic acid or other medicinal products that probably increase the gastro-intestinal risk (see section 4.5).

Patients, who previously had a problem with gastro-intestinal toxicity, in particular elderly patients, should report any unusual abdominal symptoms (especially bleeding), in particular at the beginning of the treatment. Caution is needed in patients who are concomitantly treated with medicinal products, which may increase the risk of ulceration or bleeding, such as oral corticosteroids, anticoagulants such as warfarin, selective serotonin reuptake inhibitors and products that counteract the platelet aggregation, such as acetyl salicylic acid (see section 4.5).

When gastro-intestinal bleeding or ulceration occurs in patients who are receiving naproxen, the treatment should be stopped (see section 4.3). NSAIDs should be used with caution in patients with a history of gastro-intestinal diseases (ulcerative colitis, Crohn's disease) as these conditions can worsen (see section 4.8).

Serotonin syndrome

Sumatriptan

There have been rare post-marketing reports describing patients with serotonin syndrome (including altered mental status, autonomic instability and neuromuscular abnormalities) following use of a selective serotonin reuptake inhibitor (SSRI) and sumatriptan. Serotonin syndrome has been reported following concomitant treatment with triptans and serotonin noradrenaline reuptake inhibitors (SNRIs). If concomitant treatment with sumatriptan and a SSRI or a SNRI is clinically warranted, appropriate observation of the patient is advised (see section 4.5).

Severe cutaneous adverse reactions (SCARs)

Naproxen

Exfoliative dermatitis, Stevens-Johnson's syndrome (SJS), toxic epidermal necrolysis (TEN) and drug reaction with eosinophilia and systemic symptoms (DRESS) which can be life-threatening or fatal, have been reported post-marketing in association with naproxen treatment (see section 4.8). Patients appear to have the greatest risk of these reactions at the beginning of the treatment: in the majority of the cases the reaction started in the first month of the treatment. If signs and symptoms suggestive of these reactions appear, Suvexx should be withdrawn immediately. If the patient has developed SJS, or TEN or DRESS with the use of Suvexx, treatment with Suvexx must not be restarted and should be permanently discontinued.

Haematological reactions

Naproxen

Naproxen reduces the platelet aggregation and prolongs the bleeding time. Patients who have coagulation disorders or are receiving drug therapy that interferes with haemostasis should be carefully observed if naproxen-containing products are administered (see section 4.5).

Seizures

Sumatriptan

Sumatriptan should be used with caution in patients with a history of seizures or other risk factors which lower the seizure threshold, as seizures have been reported in association with sumatriptan (see section 4.8).

Hypersensitivity reactions

Sumatriptan

Patients with known hypersensitivity to sulphonamides may exhibit an allergic reaction following administration of sumatriptan. Reactions may range from cutaneous hypersensitivity to anaphylaxis. Evidence of cross sensitivity is limited, however, caution should be exercised before using sumatriptan in these patients.

Naproxen

Hypersensitivity reactions may occur in susceptible individuals. Anaphylactic (anaphylactoid) reactions may occur both in patients with and without a history of hypersensitivity or exposure to acetyl salicylic acid, other NSAIDs or naproxen-containing products. They may also occur in individuals with a history of angio-oedema, bronchospastic reactivity (e.g. asthma), rhinitis and nasal polyps. Anaphylactoid reactions, like anaphylaxis, may have a fatal outcome.

Renal effects

Naproxen

Dehydration during the use of an anti-inflammatory analgesic (i.e. NSAID) increases the risk of acute renal failure, so the patient's possible dehydration should be corrected before naproxen treatment is initiated. The naproxen treatment should be started with caution in patients with a history of considerable dehydration. Like other anti-inflammatory analgesics, long-term treatment with naproxen has caused renal papillary necrosis and other pathological renal alterations.

The administration of an NSAID may cause a dose dependent reduction in prostaglandin formation and precipitate renal failure. Patients at greatest risk of this reaction are those with impaired renal function, cardiac impairment, liver dysfunction, those taking diuretics, angiotensin converting enzyme inhibitors, angiotensin II receptor antagonists and the elderly. Renal function should also be monitored in these patients (see also section 4.2).

There have been reports of impaired renal function, renal failure, acute interstitial nephritis, haematuria, proteinuria, renal papillary necrosis and occasionally nephrotic syndrome associated with naproxen.

Respiratory disorders

Naproxen

Caution is required if administered to patients suffering from or with a previous history of, bronchial asthma or allergic disease since NSAIDs have been reported to precipitate bronchospasm in such patients.

Elderly

Naproxen

The elderly and/or debilitated patients have an increased frequency of adverse reactions to NSAIDs especially gastrointestinal bleeding and perforation which may be fatal (see section 4.2). Prolonged use of NSAIDs in these patients is not recommended. Where prolonged therapy is required, patients should be reviewed regularly.

Use in patients with impaired liver or renal function

Naproxen

As with other NSAIDs, elevations of one or more liver function tests may occur. Hepatic abnormalities may be the result of hypersensitivity rather than direct toxicity. Severe hepatic reactions, including jaundice and hepatitis (some cases of hepatitis have been fatal) have been reported with this drug as with other NSAIDs. Cross reactivity has been reported.

In patients with renal insufficiency naproxen must be administered with extreme caution, especially if it concerns a long-term treatment. Also sufficient diuresis must be taken care of.

In case of a reduced renal perfusion, it is recommended to monitor the renal function before and during the treatment with naproxen.

Sumatriptan

Sumatriptan should be administered with caution to patients with conditions that may affect significantly the absorption, metabolism or excretion of the drugs, e.g. impaired hepatic (Child Pugh grade A or B; see sections 4.2 and 5.2) or renal function.

Combination with other NSAIDs

Naproxen

The combination of naproxen-containing products and other NSAIDs, including cyclooxygenase-2 selective inhibitors, is not recommended, because of the cumulative risks of inducing serious NSAID-related adverse events.

Ocular effects

Naproxen

Studies have not shown changes in the eye attributable to naproxen administration. In rare cases, adverse ocular disorders including papillitis, retrobulbar optic neuritis and papilloedema, (see section 4.8) have been reported in users of NSAIDs, including naproxen, although a cause-and-effect relationship cannot be established; accordingly, patients who develop visual disorders during the treatment with naproxen-containing products should have an ophthalmological examination.

Other warnings

Sumatriptan

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

Naproxen

The antipyretic and anti-inflammatory activities of naproxen may reduce fever and inflammation, thereby diminishing their utility as diagnostic signs.

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 diagnosis of medication overuse headache (MOH) should be suspected in patients who have frequent or daily headaches despite (or because of) the regular use of headache medication.

In patients with systemic lupus erythematosus (SLE) and mixed connective tissue disorders there may be an increased risk of aseptic meningitis (see section 4.8).

In a few patients a mild peripheral oedema has been reported.

No sodium retention has been observed with metabolic studies, but it cannot be ruled out that certain patients with (presumably) abnormal cardiac functions are at a greater risk of showing this side effect symptom.

If the skin becomes delicate, if blisters or other symptoms occur indicating pseudoporphyria, the treatment must be discontinued and the patient should be carefully monitored.

In exceptional cases varicella can cause severe infectious complications of the skin and soft tissues. To this day the contributing role of NSAIDs in the potentiation of these infections cannot be ruled out. It is therefore recommended to avoid the use of naproxen in case of varicella.

Elderly patients

Caution is recommended when high doses of naproxen are administered to elderly patients, as there are indications that the quantity of non-protein bound naproxen increases in these patients.

Elderly patients more frequently experience side effects of NSAIDs, in particular gastro-intestinal bleeding and perforation, which can be fatal (see section 4.2).

Excipients

This medicinal product contains 60 mg sodium per tablet, equivalent to 3% of the WHO recommended maximum daily intake of 2 g sodium for an adult.

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

Interaction studies have not been conducted with Suvexx and other drugs. Interactions with Suvexx would be expected to reflect those of the individual components.

Ergotamine and triptan/5-HT1 receptor agonists

Sumatriptan

Ergot-containing drugs have been reported to cause prolonged vasospastic reactions. Because there is a theoretical basis for these effects being additive, ergot-containing or ergot-type medications (like dihydroergotamine or methysergide) are contraindicated within 24 hours of sumatriptan/naproxen administration (see section 4.3).

The administration of sumatriptan/naproxen with other 5-HT1 agonists has not been evaluated in migraine patients. As an increased risk of coronary vasospasm is a theoretical possibility with coadministration of 5-HT1 agonists, use of these drugs within 24 hours of each other is contraindicated (see section 4.3).

Monoamine oxidase inhibitors

Sumatriptan

In studies conducted in a limited number of patients, MAO inhibitors reduce sumatriptan succinate clearance, significantly increasing systemic exposure. Therefore, treatment with sumatriptan/naproxen is contraindicated in patients receiving MAOIs and within 2 weeks of discontinuation of therapy with MAOIs (see section 4.3).

Selective serotonin reuptake inhibitors

Sumatriptan

There have been rare post-marketing reports describing patients with serotonin syndrome (including altered mental status, autonomic instability and neuromuscular abnormalities) following the use of SSRIs and sumatriptan. Serotonin syndrome has also been reported following concomitant treatment with triptans and SNRIs (see section 4.4).

Naproxen

There is an increased risk of gastrointestinal bleeding (see section 4.4) when SSRIs are combined with NSAIDs.

Anticoagulants

Naproxen

It is considered unsafe to take NSAIDs in combination with anticoagulants such as warfarin or heparin unless under direct medical supervision, as NSAIDs may enhance the effects of anticoagulants (see section 4.4).

Methotrexate

Naproxen

Caution is advised where methotrexate is given concurrently because of possible enhancement of its toxicity, since naproxen, among other NSAIDs, has been reported to reduce the tubular secretion of methotrexate in an animal model.

Cardiac glycosides

Naproxen

NSAIDs may increase cardiac glycoside plasma levels when co-administered with cardiac glycosides such as digoxin. Increased monitoring and dosage adjustments of digitalis glycosides may be necessary during and following concurrent NSAID therapy.

Lithium

Sumatriptan

Concomitant use of sumatriptan and lithium can increase the risk of serotonin syndrome.

Naproxen

Monitoring of plasma lithium concentrations is advised when stopping or starting a NSAID, as increased lithium concentrations can occur.

Ciclosporin

Naproxen

As with all NSAIDs caution is advised when ciclosporin is coadministered because of the increased risk of nephrotoxicity.

Tacrolimus

Naproxen

There is a possible risk of nephrotoxicity when NSAIDs are given with tacrolimus.

Acetylsalicylic acid

Naproxen

Clinical pharmacodynamic data suggest that concomitant naproxen usage for more than one day consecutively may inhibit the effect of low-dose acetylsalicylic acid on platelet activity and this inhibition may persist for up to several days after stopping naproxen therapy. The clinical relevance of this interaction is not known.

Anti-platelet agents

Naproxen

There is an increased risk of gastrointestinal bleeding (see section 4.4) when antiplatelet agents are combined with NSAIDs.

Experimental studies have found that clopidrogrel increases naproxen-induced gastrointestinal blood loss. This is likely to apply to all NSAIDs.

NSAIDs should not be combined with ticlopidine due to the additional inhibition of thrombocyte function.

Laboratory tests

The ability of sumatriptan/naproxen to interfere with commonly employed clinical laboratory tests has not been investigated.

Sumatriptan

Sumatriptan succinate is not known to interfere with commonly employed clinical laboratory tests.

Naproxen

It is suggested that naproxen therapy be temporarily discontinued 48 hours before adrenal function tests are performed, because naproxen may artifactually interfere with some tests for 17-ketogenic steroids. Similarly, naproxen may interfere with some assays of urinary 5-hydroxyindoleacetic acid.

Naproxen may decrease platelet aggregation and prolong bleeding time. This effect should be kept in mind when bleeding times are determined.

4.6. Fertility, pregnancy and lactation

Pregnancy

Naproxen

Inhibition of the prostaglandin synthesis may negatively affect the pregnancy and/or the embryonal/foetal development. Data from epidemiological studies suggest an increased risk of miscarriage and of cardiac malformations and gastroschisis after the use of prostaglandin synthesis inhibitors in the early stages of the pregnancy. The absolute risk of cardiovascular malformation was increased from less than 1% to approximately 1.5%. It is accepted that the risk increases with the dose and the duration of the treatment.

From the 20th week of pregnancy onward, naproxen use may cause oligohydramnios resulting from foetal renal dysfunction. This may occur shortly after treatment initiation and is usually reversible upon discontinuation. In addition, there have been reports of ductus arteriosus constriction following treatment in the second trimester, most of which resolved after treatment cessation.

During the third trimester of the pregnancy all prostaglandin synthesis inhibitors can expose the foetus to:

• cardiopulmonary toxicity (premature constriction / closure of the ductus arteriosus and pulmonary hypertension)

• renal dysfunction, which may develop into renal failure with oligohydroamnios (see above and below).

At the end of the pregnancy the mother and neonate are exposed to:

• possible prolongation of the bleeding time, an anti-aggregation effect, which may occur even at very low doses

• inhibition of the contraction of the uterus resulting in a delayed or prolonged delivery.

Sumatriptan

Post-marketing data on the use of sumatriptan during the first trimester of pregnancy in over 1 000 women are available. Although the data contain insufficient information to draw definitive conclusions, they do not point to an increased risk of congenital defects. Experience with the use of sumatriptan in the second and third trimester is limited.

Sumatriptan/naproxen

Suvexx should not be used during the first and second trimester of the pregnancy unless this is absolutely necessary. If Suvexx is used by a woman who is trying to become pregnant, or in the first or second trimester of the pregnancy, the dose should be kept as low as possible and the treatment should be as short as possible. Antenatal monitoring for oligohydramnios and ductus arteriosus constriction should be considered after exposure to naproxen for several days from gestational week 20 onward. Suvexx should be discontinued if oligohydramnios or ductus arteriosus constriction are found.

Suvexx is contra-indicated during the third trimester of the pregnancy (see section 4.3).

Breastfeeding

Both active components of Suvexx, sumatriptan and naproxen sodium have been reported to be excreted in human breast milk. Sumatriptan is excreted into breast milk with average relative infant doses of < 4% following administration of a single dose of sumatriptan. Because of the possible adverse effects of these drugs on neonates, use of Suvexx in nursing mothers should be avoided. Any breast milk expressed for at least 12 hours after treatment should be discarded.

Fertility

The use of naproxen, as with any drug known to inhibit cyclooxygenase/prostaglandin synthesis, may impair fertility and is not recommended in women attempting to conceive. In women who have difficulty conceiving or are undergoing investigation of infertility, withdrawal of naproxen should be considered.

4.7. Effects on ability to drive and use machines

No studies on the effect on the ability to drive and use machines have been performed. Suvexx can cause drowsiness and dizziness which can influence the ability to drive and use machines.

4.8. Undesirable effects

Summary of safety profile

Since Suvexx contains both sumatriptan succinate and naproxen sodium, the same pattern of adverse reactions reported for these individual components may occur with the combination product.

Serious cardiac events, including some that have been fatal, have occurred following the use of 5-HT1 agonists, such as sumatriptan. These events are very rare and most have been reported in patients with risk factors predictive of coronary artery disease (CAD). Events reported have included coronary artery vasospasm, transient myocardial ischemia, myocardial infarction, ventricular tachycardia, and ventricular fibrillation (see sections 4.3 and 4.4).

The most common adverse reactions encountered with NSAIDs, such as naproxen, are gastrointestinal, of which peptic ulcer, with or without bleeding, is the most severe. Fatalities have occurred particularly in the elderly.

Most commonly reported adverse reactions in adults with sumatriptan/naproxen in clinical trials (incidence ≥ 2%) were: dizziness, somnolence, paresthesia, nausea, dry mouth, dyspepsia, chest discomfort. No new safety findings were identified during sumatriptan/naproxen treatment compared to the established safety profile for the individual substances.

Tabulated list of adverse reactions

Frequencies have been defined as: very common (≥ 1/10); common (≥ 1/100 to < 1/10); uncommon (≥ 1/1 000 to < 1/100); rare (≥ 1/10 000 to < 1/1 000); very rare (< 1/10 000); not known (cannot be estimated from the available data).

Sumatriptan

Organ system

Common

Rare

Very rare

Not known

Immune system disorders

Hypersensitivity reactions ranging from cutaneous hypersensitivity (such as urticaria) to anaphylaxis

Psychiatric disorders

Anxiety

Nervous system disorders

Dizziness, tingling, drowsiness, sensory disturbance including paraesthesia and hypoaesthesia

Seizures*, tremor, dystonia, nystagmus, scotoma

Eye disorders

Flickering, diplopia, reduced vision. Loss of vision including permanent defects**

Cardiac disorders

Bradycardia, tachycardia, palpitations, cardiac arrhythmias, transient ischaemic ECG changes, coronary artery vasospasm, angina, myocardial infarction (see sections 4.3 and 4.4)

Vascular disorders

Transient increases in blood pressure arising soon after treatment. flushing

Hypotension, Raynaud's syndrome

Respiratory, thoracic and mediastinal disorders

Dyspnoea

Gastrointestinal disorders

Nausea and vomiting***

Ischaemic colitis, diarrhoea, dysphagia

Skin and subcutaneous tissue disorders

Hyperhidrosis

Musculoskeletal and connective tissue disorders

Myalgia

Neck stiffness, arthralgia

Reproductive system and breast disorders

Breast pain

General disorders and administration site conditions

Pain, sensations of heat or cold, pressure or tightness (these events are usually transient and may be intense and affect any part of the body including the chest and throat). Feelings of weakness, fatigue (both events are mostly mild to moderate in intensity and transient)

Pain trauma activated, pain inflammation activated

Investigations

Minor disturbances in liver function tests have occasionally been observed

*Some have occurred in patients with either a history of seizures or concurrent conditions predisposing to seizures. There are also reports in patients where no such predisposing factors are apparent.

**Visual disorders may also occur during a migraine attack itself.

***Occurred in some patients but it is unclear if this is related to sumatriptan or the underlying condition.

Naproxen

Organ system

Very common

Common

Uncommon

Rare

Very rare

Not known

Blood and lymphatic system disorders

eosinophilia, thrombocytopenia, leucopenia, pancytopenia, haemolytic anaemia, aplastic anaemia, agranulocytosis

Immune system disorders

Hypersitivity reactions, anaphylactic reaction, angioneurotic oedema

Metabolism and nutrition disorders

Hyperkalemia, fluid retention

Psychiatric disorders

Mood changes, depression, impaired ability to concentrate, cognitive disorder, insomnia, sleep disorder

Nervous system disorders

Headache, dizziness, lightheadedness

Convulsions, retrobulbar optic neuritis

Aseptic meningitis, worsening of Parkinson's disease

Eye disorders

Visual disturbances

Corneal opacity, papillitis or papilloedema

Ear and labyrinth disorders

Tinnitus, hearing disorders

Hearing loss

Cardiac disorders*)

Worsening of heart failure (oedema, dyspnoea)

Palpitations

Vascular disorders*)

Vasculitis

Respiratory, thoracic and mediastinal disorders

Pulmonary oedema, worsening of asthma

Eosinophilic pneumonitis

Gastro-intestinal disorders **)

Upper abdominal pain, heartburn, nausea, constipation

Stomatitis, diarrhoea, vomiting, dyspepsia,

Gastrointestinal ulcers, haemorrhages and/or perforations, haematemesis, melaena, exacerbation of ulcerative colitis and Crohn's disease

Sialadenitis, pancreatitis

Hepatobiliary disorders

Elevated liver enzyme levels, jaundice

Toxic hepatitis

Skin and subcutaneous tissue disorders

Pruritus, skin rashes, urticaria, increased sweating, purpura, ecchymosis

Hair loss, photosensitivity, pseudoporphyria

Exacerbation of lichen planus, exacerbation of erythema nodosum, exacerbation of lupus erythematosus disseminatus (SLE), toxic epidermal necrolysis, erythema multiforme, Stevens-Johnson syndrome

Drug reaction with eosinophilia and systemic symptoms (DRESS) (see section 4.4), fixed drug eruption

Musculoskeletal and connective tissue disorders

Myalgia, muscle weakness

Renal and urinary disorders

Haematuria, renal failure, glomerulonephritis, interstitial nephritis, nephrotic syndrome, papillary necrosis

Reproductive system and breast disorders

Menstrual disorder

General disorders and administration site disorders

Tiredness

Thirst

Pyrexia

Description of selected adverse reactions

*)Oedema formation, hypertension and heart failure have been reported in association with treatment with an NSAID.

Information from clinical studies as well as epidemiological data suggest that the use of naproxen, especially in high doses and with long-term use, can be associated with a slightly increased risk of thrombosis in the arteries (for instance myocardial infarction or stroke).

**)Gastrointestinal tract: Most frequently observed adverse effects are related to the gastrointestinal tract. Ulcers, perforations and gastrointestinal bleedings can appear. These can sometimes be life-threatening, especially for elderly people. Nausea, vomiting, diarrhoea, flatulence, constipation, heartburn, abdominal pain, melaena, haematemesis, ulcerative stomatitis and exacerbation of colitis or Crohn's disease has been reported after use of naproxen. Gastritis has been observed more rarely.

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

4.9. Overdose

Symptoms

Symptoms related to naproxen overdose

Symptoms of overdose can consist of nausea, vomiting, pain in the gastric region, drowsiness, dizziness, disorientation, diarrhoea, gastric bleeding, convulsions (rarely), transient changes in hepatic functions, hypothrombinemia, renal failure, apnoea and metabolic acidosis.

Symptoms related to sumatriptan overdose

Doses in excess of 400 mg orally and 16 mg subcutaneously were not associated with side effects other than those mentioned in the SPC section 4.8.

Treatment

Treatment related to naproxen overdose

Patients should be treated symptomatically as required. Activated charcoal should be administered to the patient within one hour to inhibit absorption and to interrupt the enterohepatic circulation.

Haemodialysis does not decrease the plasma concentration of naproxen because of the high degree of protein binding. However, haemodialysis may still be appropriate in a patient with renal failure who has taken naproxen. Haemodialysis can accelerate elimination of the main metabolite of naproxen, 6-O-demethylnaproxen.

Administration of a H2 blocker or proton-pump inhibitor should be considered to prevent gastrointestinal complications. Good urine output should be ensured. Renal and liver function should be closely monitored. Other measures may be indicated by the patient's clinical condition.

Treatment related to sumatriptan overdose

If overdosage occurs, the patient should be monitored for at least 10 hours and standard supportive treatment applied as required. It is unknown what effect haemodialysis or peritoneal dialysis has on the plasma concentrations of sumatriptan.