Noctamid 1 mg comprimidos

PROSPECTO: INFORMATION FOR THE USER

Noctamid 1 mg tablets

Lormetazepam

Noctamid is a medication from the group of hypnotics that promotes sleep: normalizes the time needed to fall asleep and its total duration, while reducing the number of interruptions of it.

• Short-term treatment of insomnia.

• Induction of sleep in pre and postoperative periods.

Noctamid belongs to a group of hypnotic medications called benzodiazepines. Benzodiazepines are only indicated for the treatment of an intense disorder, which limits the patient's activity or subjects them to an important stress situation.

Do not take Noctamid 1 mg tablets:

• If you are allergic (hypersensitive) to lormetazepam, benzodiazepines, or any of the other components of this medication (listed in section 6).
• If you have myasthenia gravis (a disease characterized by the appearance of an abnormal degree of muscle weakness).
• If you have severe respiratory insufficiency.
• If you have sleep apnea syndrome (interruption of breathing during sleep).
• In case of acute intoxication with alcohol, hypnotics, analgesics, or medications that act on the central nervous system (neuroleptics, antidepressants, lithium).

Warnings and precautions:

• If you have chronic respiratory insufficiency, as you should receive a lower dose than usual.
• If you have liver insufficiency.
• If you have severe renal insufficiency.
• Noctamid should not be used as a first-line treatment for psychiatric disease or as a single treatment for anxiety or sleep disorders associated with depression.
• Noctamid should be administered with caution to patients with medullary or cerebellar ataxia.

Consult your doctor or pharmacist before starting to take this medication.

Tolerance

• After continuous use for several weeks, a certain degree of loss of efficacy with respect to hypnotic effects may be detected.

Dependence

• Noctamid may induce the appearance of physical and psychological dependence. The risk of dependence increases with the dose and duration of treatment and is also higher in patients with a history of substance abuse or alcohol consumption. Abrupt termination of treatment may be accompanied by withdrawal symptoms, such as severe anxiety, tension, restlessness, confusion, irritability, headaches, and muscle pain. In more severe cases, derealization, depersonalization, hallucinations, paresthesia in the extremities, intolerance to light, sound, and physical contact, hyperacusis, and epileptic seizures may occur. Follow exactly the administration instructions for Noctamid indicated by your doctor to avoid these symptoms as much as possible.

Rebound insomnia and anxiety

• You may experience a rebound episode (transient reappearance of symptoms that led to the initiation of treatment). The probability of appearance of a withdrawal/rebound phenomenon is higher after abrupt termination of treatment, so it is recommended to gradually reduce the dose until its definitive suppression.

Follow exactly the recommended use and administration instructions for Noctamid indicated by your doctor to avoid these symptoms as much as possible.

Amnesia

• Noctamid may induce anterograde amnesia, i.e., difficulty remembering recent events; this occurs more frequently in the first hours after taking the medication, so to reduce this risk, ensure that you can sleep without interruption for 7-8 hours (see section 4).

Psychiatric and paradoxical reactions

• Noctamid may produce restlessness, agitation, irritability, aggression, delirium, anger attacks, nightmares, hallucinations, psychosis, abnormal and inadequate behavior, and other adverse effects on behavior. These reactions occur more frequently in children, the elderly, and patients with organic brain syndrome (physical disorders that produce a decrease in mental functions). Your doctor will suspend your treatment with Noctamid if these reactions appear.
• Inform your doctor if you have depression. Noctamid should not be used as a single treatment for sleep disorders associated with depression.
• • Noctamid should not be used as a first-line treatment for psychiatric disease (see section 4).

Children and adolescents

Noctamid should not be administered to patients under 18 years of age for the treatment of insomnia without a careful evaluation of the need for it by your doctor. Additionally, the duration of treatment should be the minimum possible (see section 3).

Use in the elderly

Elderly patients should receive a lower dose than usual as they are more susceptible to the effects of the medication. Your doctor will recommend the most suitable dosage (see section 3).

Use of Noctamid 1 mg tablets with other medications

Inform your doctor or pharmacist if you are using or have recently used other medications, even those purchased without a prescription.

A potentiation of the effect of Noctamid may occur when administered concomitantly with the following medications:

Interactions have also been reported with some medications used to treat hypertension (beta-blockers) and with central nervous system stimulants (methylxanthines).

The concomitant use of lormetazepam and opioids (potent analgesics, substitution therapy medications, and some cough medications) increases the risk of drowsiness, difficulty breathing (respiratory depression), coma, and may be potentially fatal. Therefore, concomitant use should only be considered when other treatment options are not possible.

However, if your doctor prescribes lormetazepam along with opioids, your doctor should limit the dose and duration of concomitant treatment.

Inform your doctor about all the opioid medications you are taking and follow your doctor's recommendation exactly regarding the dose. It may be helpful to inform friends or family members who are aware of the signs and symptoms mentioned above. Contact your doctor when you experience these symptoms.

Consult your doctor if you are taking other medications.

Taking Noctamid 1 mg tablets with food, drinks, and alcohol

During treatment with Noctamid, avoid alcoholic beverages.

Benzodiazepines should be used with extreme caution in patients with a history of substance abuse or alcohol consumption. The sedative effect may be potentiated when this medication is administered in combination with alcohol, so it is recommended to avoid the consumption of alcoholic beverages. This should be taken into account especially since it affects the ability to drive or operate machinery (see section "Driving and operating machinery").

Pregnancy and breastfeeding

Consult your doctor or pharmacist before using any medication.

Pregnancy

If you are pregnant or breastfeeding, or if you think you may be pregnant, consult your doctor before using this medication.

If, for strict medical reasons, the medication is administered during the third trimester of pregnancy or during delivery, it is predictable that there may be effects on the newborn, such as hypothermia, hypotonia, and moderate respiratory depression, and difficulties with breastfeeding.

Children born to mothers who take benzodiazepines chronically during the last trimester of pregnancy may develop physical dependence, which may trigger a withdrawal syndrome in the postnatal period.

Breastfeeding

Due to the fact that benzodiazepines pass into breast milk, their use is contraindicated in lactating mothers.

Driving and operating machinery

Noctamid is a medication that induces sleep, so it significantly affects the ability to drive or operate machinery. Do not drive or operate machinery if you feel drowsy or if you notice that your attention and reaction time are reduced. Pay special attention to the start of treatment or if the dose is increased.

Important information about some of the components of Noctamid 1 mg tablets

This medication contains lactose. If your doctor has indicated that you have an intolerance to certain sugars, consult with him before taking this medication.

Follow exactly the administration instructions for Noctamid indicated by your doctor. Consult your doctor or pharmacist if you have any doubts. Remember to take your medication.

Short-term treatment of insomnia

The treatment duration should be as short as possible. Generally, it varies between a few days and two weeks, with a maximum period, including a gradual dose reduction, of four weeks.

The tablets should be taken with a small amount of liquid a little before going to bed.

Adults

It is recommended to administer 1 mg of lormetazepam (one Noctamid 1 mg tablet or ½ of the alternative presentation Noctamid 2 mg tablet) in a single dose.

In cases of severe or persistent insomnia and always according to strict medical criteria, the dose can be increased to 2 mg of lormetazepam (two Noctamid 1 mg tablets or one Noctamid 2 mg tablet).

Older adults

It is recommended to administer ½ Noctamid 1 mg tablet per day (0.5 mg of lormetazepam) as a single dose.

In older adults, benzodiazepines may be associated with a higher risk of falls due to muscle weakness, dizziness, drowsiness, and fatigue. Therefore, your doctor will indicate the dose that best suits your condition.

If you estimate that the action of Noctamid is too strong or too weak, consult your doctor or pharmacist.

Induction of sleep in pre- and postoperative periods

The doses will depend on the patient's age, weight, and general condition.

Adults

It is recommended to administer a medium dose of 2 mg of lormetazepam per day. The dose range is 0.5 to 3 mg of lormetazepam per day.

Children

It is recommended to administer a dose of 0.5 to 1 mg of lormetazepam per day.

Older adults and patients at risk

It is generally recommended to administer a dose of 1 mg of lormetazepam per day. One hour before the operation, it is recommended to administer half of these doses.

Consider reducing the dose in patients with mild or moderate breathing difficulties or in patients with liver insufficiency.

Children and adolescents

Noctamid should not be used in children and adolescents under 18 years of age without a careful evaluation of the need for treatment.

If you take more Noctamid 1 mg tablets than you should

Overdose does not represent a vital threat unless its administration is combined with other central nervous system depressants (including alcohol).In case of overdose, it is essential to consider the possibility that the patient has ingested multiple products.

Overdosing with benzodiazepines generally manifests itself by different degrees of central nervous system depression, ranging from drowsiness to coma. In moderate cases, symptoms include drowsiness, confusion, and lethargy (drowsiness); in more serious cases, ataxia (alteration of movement coordination), visual disturbances, hypotonia (muscle tone decrease), hypotension (low blood pressure), respiratory depression, rarely coma, and very rarely death may occur.

In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone: 91 562 04 20, indicating the medication and the amount ingested.

If you forget to take Noctamid 1 mg tablets

Do not take a double dose to compensate for the missed doses.

If you interrupt treatment with Noctamid 1 mg tablets

Your doctor will indicate the duration of treatment with Noctamid. Do not suspend treatment prematurely, as the desired effect may not be achieved.

If you have any other doubts about the use of this product, ask your doctor or pharmacist.

Like all medicines, this medicine can cause side effects, although not everyone will experience them.

If the dosage is not adapted to the individual conditions of each patient, side effects may appear due to excessive sedation and muscle relaxation.

At the beginning of treatment, daytime drowsiness, emotional alteration, fainting, confusion, fatigue, headache, dizziness, muscle weakness, ataxia (alteration of movement coordination) or double vision may appear. All these side effects predominantly appear at the beginning of treatment and usually disappear with repeated administration.

The most serious adverse reactions observed in patients treated with Noctamid are angioedema (swelling), completed or attempted suicide, usually associated with the masking of a pre-existing depression.

The most frequently observed adverse reactions in patients treated with Noctamid are headache, sedation, and anxiety.

Very common side effects

(may affect more than 1 in 10 patients)

Common side effects

(may affect up to 1 in 10 patients)

• • Angioedema (swelling of the face, lips, mouth, tongue, or throat that may cause difficulty swallowing or breathing).
  • Anxiety, decreased libido (sexual desire).
  • Dizziness, sedation, somnolence (drowsiness), attention disorder, amnesia, visual disorder, speech disorder, dysgeusia, mental slowing.
  • Tachycardia (acceleration of heartbeats).
  • Vomiting, nausea, upper abdominal pain, constipation, dry mouth.
  • Pruritus (itching).
• Urination disorder.
• • Asthenia (lack of strength), excessive sweating.

Side effects of unknown frequency

(cannot be estimated from available data)

For more information on the following points, see the "Warnings and precautions" section.

Dependence:

The administration of Noctamid and other benzodiazepines may induce the development of physical and psychological dependence (see "Warnings and precautions" section).

Mental disorders:

Insomnia rebound may appear when the medication is discontinued (see "Warnings and precautions" section).

- Psychiatric and paradoxical reactions: When using Noctamid, reactions such as restlessness, agitation, irritability, aggression, delirium (false ideas that are believed to be true and cannot be proven), anger attacks, nightmares, hallucinations (false perceptions of the senses), psychosis (a type of mental disorder), abnormal and inappropriate behavior, and other conduct alterations may appear.

- Depression: The use of benzodiazepines may mask a pre-existing depression. In these patients, suicides may be triggered. Noctamid should be used with caution in patients with depression.

Nervous system disorders

- Amnesia::Noctamid may cause anterograde amnesia (difficulty remembering recent events). (See "Warnings and precautions" section).

Reporting of side effects

If you experience any type of side effect, consult your doctor or pharmacist, even if it is a side effect that does not appear in this prospectus. You can also report them directly through the Spanish System for the Vigilance of Medicines for Human Use:www.notificaRAM.es.By reporting side effects, you can contribute to providing more information on the safety of this medicine.

Keep out of the reach and sight of children.

Noctamid does not require special conditions for conservation.

Do not use Noctamid after the expiration date that appears on the packaging after CAD. The expiration date is the last day of the month indicated.

Medicines should not be thrown down the drains or in the trash. Dispose of the packaging and the

medicines that you do not need at the SIGRE point of the pharmacy.In case of doubt, ask your pharmacist how to dispose of the packaging and the medicines that you do not need.By doing so, you will help protect the environment.

Composition of Noctamid 1 mg tablets

The active ingredient is lormetazepam. Each tablet contains 1 mg of lormetazepam. The other components are lactose monohydrate, cornstarch, povidone 25000, and magnesium stearate.

Appearance of the product and contents of the packaging

Noctamid 1 mg tablets: round white tablets, scored on one side and with the anagram “CF” inscribed in a hexagon on the other. The tablet can be divided into equal doses. It is presented in blisters, in packs of 30 tablets.

Other presentations:

Noctamid 2 mg tablets, 20 tablets.

Noctamid 2.5 mg/ml oral drops in solution, containing 20 ml of solution.

Holder of the marketing authorization and responsible for manufacturing

Holder of the marketing authorization:

Teofarma, S.R.L.

Via F. Lli Cervi, 8

I-27010- Valle Salimbene (Pavia). Italy

Responsible for manufacturing:

TEOFARMA, S.R.L.

Viale Certosa 8 /a, Pavia I-27100 Italy

or

DOPPEL FARMACEUTICI S.r.l.

Via Volturno, 48

20089 Quinto de’ Stampi – Rozzano, Italy

This leaflet was approved in February 2022

The detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es