Epilepsy is a serious neurological condition that can cause recurrent seizures. If you or someone you love has epilepsy, Keppra Oral Solution can help manage this condition. Keppra Oral Solution contains the active ingredient levetiracetam, which is an antiepileptic medicine. This medicine works by reducing the number and severity of seizures in people with epilepsy. It is available in a convenient oral solution form, making it easy to take. Keppra Oral Solution is a safe and effective way to manage seizures in people with epilepsy. Give Keppra Oral Solution a try today and see how it can help you or your loved one live a seizure-free life.
Keppra oral solution is used:
Can be used to treat seizures in dogs and cats when prescribed by vet
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The price of Keppra Oral Solution is £47.60
You can buy Keppra Oral Solution at Dock Pharmacy Essex UK, UK Online Pharmacy.
Keppra Oral Solution is not available to buy over the counter. You need a prescription to buy Keppra Oral Solution
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How to take Keppra oral solution
Always take this medicine exactly as your doctor or pharmacist has told you.
Check with your doctor or pharmacist if you are not sure.
Keppra must be taken twice a day, once in the morning and once in the evening, at about the same time each day. Take the oral solution following your doctor’s instructions.
What you need to know before you take Keppra oral solution
Do not take Keppra • If you are allergic to levetiracetam, pyrrolidone derivatives or any of the other ingredients of this medicine (listed in Section 6). Warnings and precautions Talk to your doctor before taking Keppra • If you suffer from kidney problems, follow your doctor’s instructions. He/she may decide if your dose should be adjusted. • If you notice any slowdown in the growth or unexpected puberty development of your child, please contact your doctor. • A small number of people being treated with anti-epileptics such as Keppra have had thoughts of harming or killing themselves. If you have any symptoms of depression and/or suicidal ideation, please contact your doctor. • If you have a family or medical history of irregular heart rhythm (visible on an electrocardiogram), or if you have a disease and/or take a treatment that make(s) you prone to heartbeat irregularities or salt imbalances. Tell your doctor or pharmacist if any of the following side effects gets serious or last longer than a few days: • Abnormal thoughts, feeling irritable or reacting more aggressively than usually, or if you or your family and friends notice important changes in mood or behaviour. • Aggravation of epilepsy Your seizures may rarely become worse or happen more often, mainly during the first month after the start of the treatment or increase of the dose. If you experience any of these new symptoms while taking Keppra, see a doctor as soon as possible. Children and adolescents • Keppra is not indicated in children and adolescents below 16 years on its own (monotherapy) Other medicines and Keppra Tell your doctor or pharmacist if you are taking or have recently taken or might take any other medicines. Do not take macrogol (a drug used as laxative) for one hour before and one hour after taking levetiracetam as this may results in a reduction of its effect. Pregnancy and breast-feeding If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor for advice before taking this medicine. Levetiracetam can be used during pregnancy, only if after careful assessment it is considered necessary by your doctor. You should not stop your treatment without discussing this with your doctor. A risk of birth defects for your unborn child cannot be completely excluded. Breast-feeding is not recommended during treatment. Driving and using machines Keppra may impair your ability to drive or operate any tools or machinery, as it may make you feel sleepy. This is more likely at the beginning of treatment or after an increase in the dose. You should not drive or use machines until it is established that your ability to perform such activities is not affected. Keppra contains methyl parahydroxybenzoate, propyl parahydroxybenzoate and maltitol Keppra oral solution includes methyl parahydroxybenzoate (E218) and propyl parahydroxybenzoate (E216) which may cause allergic reactions (possibly delayed). Keppra oral solution also contains maltitol. If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.
Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them. Tell your doctor immediately, or go to your nearest emergency department, if you experience: • weakness, feel light-headed or dizzy or have difficulty breathing, as these may be signs of a serious allergic (anaphylactic) reaction • swelling of the face, lips, tongue and throat (Quincke’s oedema) • flu-like symptoms and a rash on the face followed by an extended rash with a high temperature, increased levels of liver enzymes seen in blood tests and an increase in a type of white blood cell (eosinophilia) and enlarged lymph nodes (Drug Reaction with Eosinophilia and Systemic Symptoms [DRESS]),. • symptoms such as low urine volume, tiredness, nausea, vomiting, confusion and swelling in the legs, ankles or feet, as this may be a sign of sudden decrease of kidney function • a skin rash which may form blisters and look like small targets (central dark spots surrounded by a paler area, with a dark ring around the edge) (erythema multiforme) • a widespread rash with blisters and peeling skin, particularly around the mouth, nose, eyes and genitals (Stevens-Johnson syndrome) • a more severe form of rash causing skin peeling in more than 30% of the body surface (toxic epidermal necrolysis) • signs of serious mental changes or if someone around you notices signs of confusion, somnolence (sleepiness), amnesia (loss of memory), memory impairment (forgetfulness), abnormal behaviour or other neurological signs including involuntary or uncontrolled movements. These could be symptoms of an encephalopathy. The most frequently reported adverse reactions were nasopharyngitis, somnolence (sleepiness), headache, fatigue and dizziness. At the beginning of the treatment or at dose increase side effects like sleepiness, tiredness and dizziness may be more common. These effects should however decrease over time. Very common: may affect more than 1 in 10 people • nasopharyngitis; • somnolence (sleepiness), headache. Common: may affect up to 1 in 10 people • anorexia (loss of appetite); • depression, hostility or aggression, anxiety, insomnia, nervousness or irritability; • convulsion, balance disorder (equilibrium disorder), dizziness (sensation of unsteadiness), lethargy (lack of energy and enthusiasm), tremor (involuntary trembling); • vertigo (sensation of rotation); • cough; • abdominal pain, diarrhoea, dyspepsia (indigestion), vomiting, nausea; • rash; • asthenia/fatigue (tiredness). Uncommon: may affect up to 1 in 100 people • decreased number of blood platelets, decreased number of white blood cells; • weight decrease, weight increase; • suicide attempt and suicidal ideation, mental disorder, abnormal behaviour, hallucination, anger, confusion, panic attack, emotional instability/mood swings, agitation; • amnesia (loss of memory), memory impairment (forgetfulness), abnormal coordination/ataxia (impaired coordinated movements), paraesthesia (tingling), disturbance in attention (loss of concentration); • diplopia (double vision), vision blurred; • elevated/abnormal values in a liver function test; • hair loss, eczema, pruritus; • muscle weakness, myalgia (muscle pain); • injury. Rare: may affect up to 1 in 1,000 people • infection; • decreased number of all blood cell types; • severe allergic reactions (DRESS, anaphylactic reaction [severe and important allergic reaction], Quincke’s oedema [swelling of the face, lips, tongue and throat]); • decreased blood sodium concentration; • suicide, personality disorders (behavioural problems), thinking abnormal (slow thinking, unable to concentrate); • delirium; • encephalopathy (see sub-section “Tell your doctor immediately” for a detailed description of symptoms); • seizures may become worse or happen more often; • uncontrollable muscle spasms affecting the head, torso and limbs, difficulty in controlling movements, hyperkinesia (hyperactivity); • change of the heart rhythm (Electrocardiogram); • pancreatitis; • liver failure, hepatitis; • sudden decrease in kidney function; • skin rash, which may form blisters and looks like small targets (central dark spots surrounded by a paler area, with a dark ring around the edge) (erythema multiforme), a widespread rash with blisters and peeling skin, particularly around the mouth, nose, eyes and genitals (Stevens-Johnson syndrome), and a more severe form causing skin peeling in more than 30% of the body surface (toxic epidermal necrolysis); • rhabdomyolysis (breakdown of muscle tissue) and associated blood creatine phosphokinase increase. Prevalence is significantly higher in Japanese patients when compared to non-Japanese patients. • limp or difficulty walking. Evidence also suggests a possible predisposition of the Japanese population to neuroleptic malignant syndrome (NMS). 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 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
What Keppra oral solution contains
The active substance is called levetiracetam. Each ml contains 100 mg of levetiracetam.
The other ingredients are: sodium citrate, citric acid monohydrate, methyl parahydroxybenzoate (E218), propyl parahydroxybenzoate (E216), ammonium glycyrrhizate, glycerol (E422), maltitol liquid (E965), acesulfame potassium (E950), grape flavour, purified water
How to store Keppra
Keep this medicine out of the sight and reach of children. Do not use this medicine after the expiry date stated on the cardboard box and bottle after EXP: The expiry date refers to the last day of the month. Do not use after 7 months of first opening the bottle. Store in the original bottle, in order to protect from light. 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 protect the environment.
Click here for the Patient Information leaflet
Please read before using the product
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