MELATONIN TEVA XL is a brand name for Melatonin. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: Melatonin Teva XL is indicated as monotherapy for the short-term treatment of primary insomnia characterised by poor quality of sleep in patients who are aged 55 or over.
Verbatim from this product's MHRA label. Tap a section to expand.
Posology The recommended dose is 2 mg once daily, 1-2 hours before bedtime and after food. This dosage may be continued for up to thirteen weeks. Paediatric population The safety and efficacy of Melatonin Teva XL in children aged 0 to 18 years has not yet been established.
Other pharmaceutical forms/strengths may be more appropriate for administration to this population. 1. Renal impairment The effect of any stage of renal impairment on melatonin pharmacokinetics has not been studied. Caution should be used when melatonin is administered to such patients.
Hepatic impairment There is no experience of the use of melatonin in patients with liver impairment. Published data demonstrates markedly elevated endogenous melatonin levels during daytime hours due to decreased clearance in patients with hepatic impairment.
Therefore, Melatonin Teva XL is not recommended for use in patients with hepatic impairment. Method of administration Oral use. Tablets should be swallowed whole to maintain prolonged release properties. Crushing or chewing should not be used to facilitate swallowing.
8% taking placebo. 743– placebo vs. 013– melatonin). The most common adverse reactions were headache, nasopharyngitis, back pain, and arthralgia , which were common, by MedDRA definition, in both the melatonin and placebo treated groups.
Tabulated list of adverse reactions The following adverse reactions were reported in clinical trials and from post- marketing spontaneous reporting. 4% of patients taking placebo. Only those adverse reactions reported during clinical trials occurring in patients at an equivalent or greater rate than placebo have been included below.
Within each frequency grouping, undesirable effects are presented in order of decreasing seriousness. 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 established from the available data).
System Organ Class Very Common Common Uncommo n Rare Not known Infections and infestations Herpes zoster Blood and lymphatic system disorders Leukopeni a, thrombocy topenia Immune system disorders Hyper- sensitivity reaction Metabolis m and nutrition disorders Hypertrigl yceridaem ia, hypocalca emia, hyponatra emia Psychiatric disorders Irritability, nervousnes s, restlessness , insomnia, abnormal dreams, nightmares, anxiety Mood altered, aggression , agitation, crying, stress symptoms , disorientat ion, early morning awakening , libido increased, depressed mood, depression Nervous system disorders Migraine, headache, lethargy, psychomot or hyperactivi ty, dizziness, somnolenc e Syncope, memory impairmen t, disturbanc e in attention, dreamy state, restless legs syndrome, poor quality sleep, paraesthes ia Eye disorders Visual acuity reduced, vision blurred, lacrimatio n increased Ear and labyrinth disorders Vertigo positional, vertigo Cardiac disorders Angina pectoris, palpitation s Vascular disorders Hypertensi on Hot flush Gastrointes tinal disorders Abdominal pain, abdominal pain upper, dyspepsia, mouth ulceration, dry mouth, nausea Gastro- oesophage al reflux disease, gastrointes tinal disorder, oral mucosal blistering, tongue ulceration, gastrointes tinal upset, vomiting, bowel sounds abnormal, flatulence, salivary hypersecre tion, halitosis, abdominal discomfort , gastric disorder, gastritis Hepatobilia ry disorders Hyperbiliru binaemia Skin and subcutaneo us tissue disorders Dermatitis, night sweats, pruritus, rash, pruritus generalised , dry skin Eczema, erythema, hand dermatitis, psoriasis, rash generalise d, rash pruritic, nail disorder Angioedem a, oedema of mouth, tongue oedema Musculosk eletal and connective tissue disorders Pain in extremity Arthritis, muscle spasms, neck pain, night cramps Renal and urinary disorders Glycosuria, proteinuria Polyuria, haematuri a, nocturia Reproducti ve system and breast disorders Menopausa l symptoms Priapism, prostatitis Galactorrh oea General disorders and administrat Asthenia, chest pain Fatigue, pain, thirst ion site conditions Investigatio ns Liver function test abnormal, weight increased Hepatic enzyme increased, blood electrolyes abnormal, laboratory test abnormal Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important.
Melatonin may cause drowsiness. Therefore Melatonin Teva XL should be used with caution if the effects of drowsiness are likely to be associated with a risk to safety. No clinical data exist concerning the use of melatonin in individuals with autoimmune diseases.
Therefore, Melatonin Teva XL is not recommended for use in patients with autoimmune diseases. Excipients Lactose Patients with rare hereditary problems of galactose intolerance, total lactase deficiency or glucose-galactose malabsorption should not take this medicinal product.
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Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
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