Patient Leaflet Updated 09-Sep-2024 | Neuraxpharm UK Ltd
Melatonin Neuraxpharm 2 mg Prolonged-release Tablets
Melatonin Neuraxpharm 2 mg
Prolonged-release Tablets
melatonin
1. What Melatonin Neuraxpharm 2 mg Prolonged-release Tablets are and what they are used for
2. What you need to know before you take Melatonin Neuraxpharm 2 mg Prolonged-release Tablets
3. How to take Melatonin Neuraxpharm 2 mg Prolonged-release Tablets
4. Possible side effects
5. How to store Melatonin Neuraxpharm 2 mg Prolonged-release Tablets
6. Contents of the pack and other information
The name of your medicine is Melatonin Neuraxpharm 2 mg Prolonged-release Tablets.
The active substance of, melatonin, belongs to a natural group of hormones produced by the body.
Melatonin Neuraxpharm 2 mg Prolonged-release Tablets are used on its own for the short-term treatment of primary insomnia (persistent difficulty in getting to sleep or staying asleep, or poor quality of sleep) in patients aged 55 years and older. ‘Primary’ means that the insomnia does not have any identified cause, including any medical, mental or environmental cause.
2. What you need to know before you take Melatonin Neuraxpharm 2 mg Prolonged-release Tablets
Talk to your doctor before taking Melatonin Neuraxpharm 2 mg Prolonged-release Tablets :
Do not give this medicine to children between the ages of 0 to 18 years as it has not been tested and its effects are unknown. Another medicine containing melatonin may be more appropriate for administration to children between the ages of 2 to 18 - please ask your doctor or pharmacist for advice.
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
These medicines include:
Take Melatonin Neuraxpharm 2 mg Prolonged-release Tablets after you have eaten. Do not drink alcohol before, during or after taking Neuraxpharm 2 mg Prolonged-release Tablets , because it reduces the effectiveness of the medicine.
Do not take Melatonin Neuraxpharm 2 mg Prolonged-release Tablets if you are pregnant, think you may be pregnant, trying to become pregnant or breast-feeding. Ask your doctor or pharmacist for advice before taking this medicine.
This medicine may cause drowsiness. If you are affected, you should not drive or operate machinery. If you suffer from continued drowsiness, then you should consult your doctor.
If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.
Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.
The recommended dose is one tablet (2 mg) taken daily by mouth, after food, 1 - 2 hours before bedtime. This dosage may be continued for up to thirteen weeks.
You should swallow the tablet whole. The tablets should not be crushed or cut in half.
If you have accidentally taken too much of your medicine, contact your doctor or pharmacist as soon as possible.
Taking more than the recommended daily dose may make you feel drowsy.
If you forget to take your tablet, take it as soon as you remember, before going to sleep, or wait until it is time to take your next dose, then go on as before.
Do not take a double dose to make up for a forgotten dose.
There are no known harmful effects if treatment is interrupted or ended early. The use of this medicine is not known to cause any withdrawal effects after treatment completion.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
If you experience any of the following serious side effects, stop taking this medicine and contact your doctor immediately:
Uncommon: (may affect up to 1 in 100 people)
Rare: (may affect up to 1 in 1000 people)
If you experience any of the following non-serious side effects contact your doctor and/or seek medical advice:
Uncommon: (may affect up to 1 in 100 people)
Irritability, nervousness, restlessness, insomnia, abnormal dreams, nightmares, anxiety, migraine, headache, lethargy (tiredness, lack of energy), restlessness associated with increased activity, dizziness, tiredness, high blood pressure, upper abdominal pain, indigestion, mouth ulceration, dry mouth, nausea, changes in the composition of your blood which could cause yellowing of the skin or eyes, inflammation of the skin, night sweats, itching, rash, dry skin, pain in extremities, menopausal symptoms, feeling of weakness, excretion of glucose in the urine, excess proteins in the urine, abnormal liver function and weight increase.
Rare: (may affect up to 1 in 1000 people)
Shingles, high level of fatty molecules in the blood, low serum calcium levels in the blood, low sodium levels in the blood, altered mood, aggression, agitation, crying, stress symptoms, early morning awakening, increased sex drive, depressed mood, memory impairment, disturbance in attention, dreamy state, restless legs syndrome, poor quality sleep, ‘pins and needles’ feeling, watery eyes, dizziness when standing or sitting, hot flushes, acid reflux, stomach disorder, blistering in the mouth, tongue ulceration, stomach upset, vomiting, abnormal bowel sounds, wind, excess saliva production, bad breath, abdominal discomfort, gastric disorder, inflammation of the stomach lining, eczema, skin rash, hand dermatitis, itchy rash, nail disorder, arthritis, muscle spasms, neck pain, night cramps, prolonged erection that might be painful, inflammation of the prostate gland, tiredness, pain, thirst, passing large volumes of urine, urinating during the night, increased liver enzymes, abnormal blood electrolytes and abnormal laboratory tests.
Frequency not known: (cannot be established from the available data)
Hypersensitivity reaction, swelling of mouth or tongue, swelling of the skin and abnormal milk secretion.
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 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.
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 after ‘EXP’. The expiry date refers to the last day of that month.
Do not store above 25°C. Store in the original package 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.
a. The active substance is melatonin. Each prolonged-release tablet contains 2 mg melatonin.
b. The other ingredients are ammonio methacrylate copolymer type B, calcium hydrogen phosphate dihydrate, lactose monohydrate (see section 2 “Melatonin Neuraxpharm 2 mg Prolonged-release Tablets contains lactose monohydrate”), silica (colloidal anhydrous), talc and magnesium stearate.
Melatonin Neuraxpharm 2 mg Prolonged-release Tablets are white to off-white, biconvex, oval tablets, 5.2 x 10 mm, with ‘A6’ debossed on one side.
Melatonin Neuraxpharm 2 mg Prolonged-release Tablets are available in blister packs of 30 prolonged-release tablets.
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This leaflet was last revised in July 2024.
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Neuraxpharm UK Ltd, Suite 2, Arlington Flex, Third Floor, Building 1420, Arlington Business Park, Theale, Reading, Berkshire, RG7 4SA, UK