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Top Quality Discount Medications

Nitrazepam 10 MG

Regular price £ 32

Nitrazepam 10 MG

Qty Price per pills Our Price
10MG 30 (pills) £ 1.07 £ 32
10MG 60 (pills) £ 0.83 £ 50
10MG 90 (pills) £ 0.87 £ 78
10MG 120 (pills) £ 0.82 £ 98
10MG 150 (pills) £ 0.77 £ 115
10MG 180 (pills) £ 0.75 £ 135

Product Details

Nitrosun (Nitrazepam) tablets 10mg

What Nitrosun (nitrazepam) tablets are and what they are used for?

Nitrosun (nitrazepam) belongs to a class of drugs called benzodiazepines that are known for their sedative properties. Nitrosun (nitrazepam) is a powerful hypnotic drug that causes sedation, relieve anxiety, amnesia and convulsions and also relax skeletal muscles. It shortens the time required to fall asleep and lengthens the duration of sleep. This medicine is only recommended in adults and elderly for short term treatment of severe sleeplessness (insomnia) that also causes distress.

What you need to know before you take Nitrosun (Nitrazepam) Tablets

Do not take Nitrazepam tablets if you:

·         are allergic to nitrazepam

·         are allergic to any drug belongs to benzodiazepines class

·         have severe breathing problem or chest problem

·         suffering from acute porphyria

·         suffering from myasthenia gravis

·         suffering from sleep apnoea syndrome (difficulty in breathing during sleep)

·         suffering from any mental illness or personality disorder (phobia or obsession)

How it works?

Nitrazepam is a benzodiazepine compound having sedative properties. It shortens the time required to fall asleep and lengthens the duration of sleep. It acts in 30 to 60 minutes to produce sleep lasting up to 6 to 8 hours.

How to take Nitrazepam tablet?

Always take this medicine following the instructions of your doctor or pharmacist.

Treatment should be for a short duration of time and must be started with the lowest effective dose. The maximum dose should not be exceeded. Generally, the duration of treatment varies from a few days to two weeks, with a maximum of four weeks; including the tapering off process (gradually reducing the dose before ending the treatment). Dosage should be adjusted on an individual basis. If possible, the treatment should be on an intermittent basis. Long-term chronic use of this medicine is not recommended.

Dose:

Adults: 5 mg before rsleep. This dose may be increased for up to 10 mg. Do not give this medicine to the children under 12 years of age.

Method of administration: For oral administration only.

Take the medicine just before going to bed and making sure you can sleep for 7-8 hours without being disturbed after taking the tablets.

Swallow the whole tablet with water or with some other non-alcoholic drink, without crushing or chewing the tablet.


If you take more Nitrosun (nitrazepam) tablets than you should

If you take too many tablets or someone else accidentally takes your medicine, contact your doctor, pharmacist immediately or go to the nearest hospital straight away.

If you forget to take Nitrosun (nitrazepam) tablets

If you forget to take your scheduled dose, you should never make up for the missing dose by doubling the dose next time. Instead, simply continue with the single next dose at the right time.

If you stop taking Nitrosun (nitrazepam) tablets

If you abruptly stop taking Nitrazepam tablet withdrawal symptoms like headache, depression, confusion, mood changes, nervousness, irritability, extreme anxiety, restlessness etc. may occur as this medicine causes dependence. Therefore, stop using medicine as per instructions of your doctor who will advise to discontinue the medicine by following dose tapering technique.

Please remember that nitrazepam is not suitable for long-term use. The beneficial effects of nitrazepam decrease as tolerance develops with its long-term use and it can also cause dependency. Therefore, you should always follow the dosing instructions advised by your doctor to ensure that long-term use is avoided.

Special warning and precaution for use

Nitrosun (nitrazepam) tablets should not be used alone to treat depression or anxiety, since this medicine exaggerate suicidal thoughts in patients suffering with depression.

In patients with chronic pulmonary insufficiency and in patients with chronic kidney or liver disease, a dose reduction is required usually half of the usual adult dose. Benzodiazepines are contraindicated in patients with severe hepatic insufficiency.

Pregnancy, Fertility and Lactation

If you are breast feeding mother do not take this medicine as this medicine excrete in breast milk.

If you are planning pregnancy then you must consider withdrawal effects of this medicine as it causes dependency.

Effects on ability to drive and use machines

The use Nitrosun (nitrazepam) causes sedation, amnesia, impaired concentration and impaired muscular function that can adversely affect the ability to drive or to use machinery. This medicine can also impair your cognitive function and thus caution is required while drive or avoid driving.

Possible side effects

·         Allergic reaction/ hypersensitivity: swelling of face, lips, tongue or throat or difficulty in breathing or swallowing may also be experienced.

·         Skin rash, itching, red colored irregular raised patches on skin are also observed.

·         Dizziness, drowsiness, feeling numb, feeling tired etc.

If you experience any of the above symptoms, stop using the medicine and immediately seek advice of your doctor.

How to store Nitrosun (Nitrazepam) tablets?

Store this medicine at room temperature below 25oC and protect from light. Keep this medicine out of reach and sight of children.

Do not use this medicine after the expiry date mentioned on the pack and blister strip.

Reference links:

1 ) https://www.medicines.org.uk/emc/product/5893/smpc#gref

2 ) https://www.medicines.org.uk/emc/files/pil.5893.pdf

Product Information

Food Interaction

Alcohol Interaction

Patients should be advised that, like all medicines of this type, Nitrazepam tablets may modify patients' performance at skilled tasks. Sedation, amnesia, impaired concentration and impaired muscular function may adversely affect the ability to drive or to use machinery. If insufficient sleep duration occurs, the likelihood of impaired alertness may be increased (see Section 4.5). Patients should further be advised that alcohol may intensify any impairment, and should, therefore, be avoided during treatment. This medicine can impair cognitive function and can affect a patient's ability to drive safely. This class of medicine is in the list of drugs included in regulations under 5a of the Road Traffic Act 1988. When prescribing this medicine, patients should be told: • This medicine is likely to affect how you drive • Do not drive until you know how the medicine affects you • It is an offence to drive while under the influence of this medicine • However, you would not be committing an offence (called 'statutory defence') if: o The medicine has been prescribed to treat a medical or dental problem and o You have taken it according to the instructions given by the prescriber and in the information provided with the medicine and o It was not affecting your ability to drive safely

Pragnancy Interaction

Fertility, pregnancy and lactation An increased risk of congenital malformations in humans has been associated with its use, particularly in the first and second trimesters. If the product is prescribed to a woman of childbearing potential, she should be warned to contact her physician regarding discontinuance of the product if she intends to become or suspects that she is pregnant. If, for compelling medical reasons, the product is administered during the late phase of pregnancy, or during labour at high doses, effects on the neonate, such as hypothermia, hypotonia and moderate respiratory depression, can be expected, due to the pharmacological action of the compound. Irregularities to foetal heart and poor sucking in the neonate have also been reported. Moreover, infants born to mothers who took benzodiazepines chronically during the latter stages of pregnancy may have developed physical dependence and may be at some risk for developing withdrawal symptoms in the postnatal period. Since benzodiazepines are found in the breast milk, benzodiazepines should not be given to breast feeding mothers.

Lactation Interaction

Medicine Interaction

Not recommended: Concomitant intake with alcohol. The sedative effects may be enhanced when the product is used in combination with alcohol. This adversely affects the ability to drive or use machines. Antipsychotics (neuroleptics), tranquillisers, hypnotics, analgesics, anxiolytics/sedatives, antidepressant agents, narcotic analgesics, anti-epileptic products, anaesthetics, sedative antihistamines, lofexidine, and nabilone: Concomitant use may lead to enhancement of the central depressive effect. The elderly require special supervision. Narcotic analgesics: Enhancement of the euphoric effect may also occur, leading to an increase in psychological dependence. Anti-epileptic drugs: When used in conjunction with nitrazepam, side effects and toxicity may be more evident, particularly with hydantoins or barbiturates or combinations which include them. This requires extra care in adjusting dosage in the initial stages of treatment. Dopaminergics: Concurrent use with benzodiazepines may decrease the therapeutic effects of levodopa. Caffeine and theophylline: Concurrent use may result in reduced sedative and anxiolytic effects of nitrazepam. Cimetidine, oestrogen-containing contraceptives, disulfiram: These medicines may inhibit hepatic metabolism of nitrazepam. Antibacterials: Rifampicin may increase the metabolism of nitrazepam. Isoniazid may inhibit the metabolism of benzodiazepines. Antivirals: Retonavir may inhibit benzodiazepine hepatic metabolism. Antihypertensives: Enhanced hypotensive effects. Enhances sedative effect with alpha blockers or moxonidine. Baclofen and tizanidine: Enhanced sedative effect. Probenecid: May increase effects and possibility of excessive sedation.

Faq for Medicine

Treatment should be as short as possible and should be started with the lowest effective dose. The maximum dose should not be exceeded. Generally the duration of treatment varies from a few days to two weeks, with a maximum of four weeks; including the tapering off process. Dosage should be adjusted on an individual basis. If possible, the treatment should be on an intermittent basis. Long-term chronic use is not recommended. Adults: 5 mg before retiring. This dose may be increased, if necessary, to 10 mg. Children below the age of 12 years: Do not use. Elderly and debilitated patients: 2.5 – 5 mg before retiring, doses should not exceed half those normally recommended for adults. In patients with chronic pulmonary insufficiency, and in patients with chronic renal or hepatic disease, dosage may need to be reduced. Further details are given in Section 4.4 Special warnings and precautions for use, Duration of treatment. Method of administration: For oral administration.

Expert Advice

Treatment should be as short as possible and should be started with the lowest effective dose. The maximum dose should not be exceeded. Generally the duration of treatment varies from a few days to two weeks, with a maximum of four weeks; including the tapering off process. Dosage should be adjusted on an individual basis. If possible, the treatment should be on an intermittent basis. Long-term chronic use is not recommended. Adults: 5 mg before retiring. This dose may be increased, if necessary, to 10 mg. Children below the age of 12 years: Do not use. Elderly and debilitated patients: 2.5 – 5 mg before retiring, doses should not exceed half those normally recommended for adults. In patients with chronic pulmonary insufficiency, and in patients with chronic renal or hepatic disease, dosage may need to be reduced. Further details are given in Section 4.4 Special warnings and precautions for use, Duration of treatment. Method of administration: For oral administration.

Dosage

Treatment should be as short as possible and should be started with the lowest effective dose. The maximum dose should not be exceeded. Generally the duration of treatment varies from a few days to two weeks, with a maximum of four weeks; including the tapering off process. Dosage should be adjusted on an individual basis. If possible, the treatment should be on an intermittent basis. Long-term chronic use is not recommended. Adults: 5 mg before retiring. This dose may be increased, if necess

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2)From the date of written confirmation of refund to the customer, the amount will be refunded within the next 7-10 business days. The amount will be refunded in the customer's mode of payment.

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