Prospect: information for the user
Diazepam Qualigen 10 mg tablets EFG
Read this prospect carefully before starting to take this medicine, as it contains important information for you.
1 What is Diazepam Qualigen and what is it used for
2. What you need to knowbefore starting to takeDiazepam Qualigen
3. How to take Diazepam Qualigen
4. Possible adverse effects
5. Storage of Diazepam Qualigen
6. Contents of the package and additional informationl
Diazepam Qualigen contains as active ingredient diazepam, which belongs to a group of medicines called benzodiazepines.
Diazepam has tranquilizing, sedative, muscle relaxant and anticonvulsant effects.
Doctors prescribe diazepam to people who experience symptoms of anxiety, agitation and mental tension caused by psychoneurotic states and transient situational disorders. Benzodiazepines are only indicated for the treatment of an intense disorder that limits their activity or subjects them to a significant stressful situation.
It may also be useful for relieving symptoms of acute agitation, tremors and hallucinations in patients with alcohol withdrawal syndrome.
Diazepam contributes to the relief of muscle pain caused by spasms or inflammation of muscles or joints, trauma, etc. It can also be used to combat spasms originating from diseases such as cerebral palsy (a group of disorders that affect a person's ability to move, maintain balance and posture) and paraplegia (paralysis of the lower half of the body, affecting both legs), as well as in atetosis (continuous, involuntary, slow and extravagant movements of fingers and hands) and in generalized rigidity syndrome.
Diazepam may be used as an adjunctive treatment (treatment administered after the primary treatment to increase the chances of a cure) for convulsive disorders (such as epilepsy, seizures), but it has not been proven useful as a single treatment. In these cases, your doctor will periodically evaluate the usefulness of the medication for your case.
This medication is not recommended for the primary treatment of psychotic disorders (serious mental disorders that cause abnormal ideas and perceptions), nor should it be used as the sole treatment for patients with depression, alone or associated with anxiety. Your doctor has probably prescribed another medication for these cases.
Do not use this medication in children under 6 months of age.
Warnings and Precautions
Consult your doctor or pharmacist before starting to take Diazepam Qualigen.
Your doctor will decide whether you should take a lower dose of Diazepam Qualigen or not take it at all.
In patients with depression, Diazepam Qualigen acts on the anxious component, so it is not a treatment for depression itself and may eventually unmask some of its symptoms.
If you are epilepticand are following a long-term treatment with Diazepam Qualigen, do not use the benzodiazepine antagonist Anexate (flumazenil) to reverse the effect of Diazepam Qualigen, as this may cause seizures.
Your doctor will pay special attention to the high risk associated with you being an elderly patient or severely debilitated.
Children
The duration of treatment should be as short as possible.
Elderly patients
Elderly patients may need lower doses of Diazepam Qualigen than younger patients. The pharmacological effects of benzodiazepines in elderly patients appear to be greater than in the younger population.
If you are an elderly patient, your doctor may prescribe a lower dose and check your response to treatment. Please follow your doctor's instructions carefully.
Patients with liver disorders
The sedative effect of diazepam is increased in patients with cirrhosis.
Other medications and Diazepam Qualigen
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication. This is extremely important because the simultaneous use of multiple medications can increase or decrease their effect.
For example, tranquilizers, sleep inducers, and similar medications act on the brain and nerves and can enhance the effect of Diazepam Qualigen.
Cisapride, cimetidine, ketoconazole, fluconazole, voriconazole, fluvoxamine, fluoxetine, hormonal contraceptives, disulfiram, isoniazid, diltiazem, idelasib, modafinil, armodafinil, esomeprazole, and omeprazole temporarily increase the sedative effect of Diazepam Qualigen, increasing the risk of drowsiness. The same occurs with grapefruit juice.
On the other hand, medications such as rifampicin and carbamazepine reduce the effects of diazepam.
Furthermore, the metabolism of phenytoin may be affected if you are taking Diazepam Qualigen, so if you are taking this medication, your doctor will adjust the doses accordingly.
The sedative effect and respiratory depression may be increased when combining Diazepam Qualigen with other central nervous system depressants, potentially causing coma or death.
Xanthines such as theophylline and caffeine counteract the sedative effects of Diazepam Qualigen.
Therefore, do not use Diazepam Qualigen with any other medication unless your doctor has allowed it.
If you need more information about this, consult your doctor or pharmacist.
Taking Diazepam Qualigen with food, drinks, and alcohol
Alcoholic beverages increase the sedative effects of Diazepam Qualigen, so avoid using alcoholic beverages during treatment. If you need additional information, consult your doctor.
Do not take diazepam in combination with grapefruit juice, as this can increase diazepam levels in your body.
Food and antacids may slow down the absorption of diazepam from the tablet, but will not decrease it; this may lead to milder effects after a single dose, but does not affect treatment with multiple doses.
Prokinetic medications (medications to improve intestinal transit) increase the absorption of diazepam.
Risk of dependence
The use of benzodiazepines and benzodiazepine-like drugs can lead to physical and psychological dependence. This occurs mainly after taking the medication continuously for a long time. To minimize the risk of dependence, the following precautions should be taken:
•Take benzodiazepines only under medical prescription (never because they have worked for other patients), and never advise others to take them.
•Do not increase the prescribed doses or prolong treatment beyond the recommended duration.
• Consult your doctor regularly to decide whether to continue treatment.
Pregnancy and breastfeeding
Consult your doctor or pharmacist before using any medication.
If you are pregnant or breastfeeding, or think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
If, by strict medical necessity, you take Diazepam Qualigen before or during delivery, hypothermia (abnormally low body temperature), weakness, hypotension, and respiratory difficulties may appear in the newborn. Additionally, cases of withdrawal syndrome in newborns have been reported.
Benzodiazepines pass into breast milk, so you should consult your doctor about taking or not taking Diazepam Qualigen while breastfeeding.
Driving and operating machinery
Do not drive or operate machinery because this medication can cause drowsiness, amnesia, difficulty concentrating, and muscle weakness, which can negatively affect your ability to drive vehicles or operate machinery. Your doctor will decide when you can resume these activities. This effect is increased if you have also consumed alcohol.
Diazepam Qualigen contains lactose
This medication contains lactose. If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.
Follow exactly the administration instructions of this medication as indicated by your doctor. In case of doubt, consult your doctor or pharmacist again.
Depending on the nature of your illness, your age and weight, your doctor will prescribe the most suitable dose and indicate the duration of your treatment with diazepam.
Remember to take your medication.
Follow these instructions unless your doctor has given you different instructions:
Adults:
Anxiety symptoms:2 to 10 mg, 2 to 4 times a day, depending on the severity of the symptoms.
Acute alcohol withdrawal relief:10 mg, 3 or 4 times during the first 24 hours, reducing to 5 mg 3 or 4 times a day, as needed.
Muscle skeletal spasm relief:
Coadjuvant:2 to 10 mg, 3 or 4 times a day.
Anticonvulsant therapy coadjuvant:2 to 10 mg, 2 or 4 times a day.
Special populations dosage:
Use in children:2 to 2.5 mg, 1 or 2 times a day, increasing gradually as needed and tolerated; as a general rule, 0.1-0.3 mg/kg per day. Due to the variety of responses of children to medications acting on the CNS, treatment should begin with the lowest dose and increase as needed. Do not use in children under 6 months of age.
In elderly patients or in the presence of debilitating diseases:2 to 2.5 mg, 1 or 2 times a day, increasing gradually as needed and tolerated.
Treatment should begin with the lowest dose. Do not exceed the maximum dose.
If you estimate that the action of diazepam is too strong or too weak, inform your doctor or pharmacist.
In patients with liver or kidney disease, muscle weakness, children, debilitated patients, or those with low serum albumin levels, the doctor will prescribe a lower dose.
Guidelines for correct administration
Do not increase the doses prescribed by your doctor at all.
Each individual dose should not exceed the indicated limits, and the total daily dose should not either, unless your doctor prescribes a higher dose.
Diazepam tablets should be taken without chewing, with a little water or a non-alcoholic beverage.
Diazepam tablets should be taken at the hours when they are most needed, usually in the afternoon or evening. Never change the dose that has been prescribed for you.
Treatment duration
The duration of treatment should be as short as possible and never exceed 2-3 months. Consult your doctor regularly to decide if treatment should be continued.
Do not prolong treatment beyond the recommended time.
To avoid withdrawal symptoms, do not stop taking diazepam abruptly, especially if you have been taking it for a long time.
If you take more Diazepam Qualigen than you should
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological Information Service. Phone: 91 562 04 20 indicating the medication and the amount ingested.
If you forget to take Diazepam Qualigen
Do not take a double dose to compensate for the missed doses. Instead, continue with the normal dose.
If you interrupt treatment with Diazepam Qualigen
Stopping administration may cause restlessness, anxiety, insomnia, lack of concentration, headaches, and hot flashes. It is not generally recommended to stop medication abruptly, but rather to gradually reduce the dose, according to the doctor's instructions.
If you have any other doubts about the use of this medication, ask your doctor or pharmacist.
If you consider that any of the side effects you experience are severe or if you notice any side effect not mentioned in this leaflet, inform your doctor or pharmacist.
Most patients tolerate Diazepam Qualigen well, but the most common side effects, which occur especially at the beginning of treatment, are fatigue, muscle weakness, and drowsiness.
Occasionally, other side effects of the type of confusion, decreased alertness, loss of sensitivity, dizziness, emotional disturbances, mood changes, constipation, depression, double vision, ataxia (inability to coordinate voluntary muscle movements), difficulty articulating words, digestive changes, heart rhythm alterations, headache, hypotension, circulatory changes, changes in libido (sexual desire), nausea, dry mouth or hypersalivation (excessive salivation), incontinence or urinary retention, skin eruptions, stuttering, tremor, vertigo, and blurred vision have been described. The most common skin reactions are inflammation (skin inflammation), urticaria (red itchy patches), and pruritus (uncomfortable itching that causes the desire to scratch the affected area).
Very rarely, an increase in transaminases and alkaline phosphatase, jaundice (yellowish discoloration of the skin and eyes), and cardiac arrest have been reported.
An increased risk of falls and fractures has been observed in elderly patients and in patients taking other sedatives (including alcoholic beverages) at the same time.
Heart failure, respiratory depression, including respiratory insufficiency, may occur.
It is known that when benzodiazepines are used, side effects on behavior such as restlessness, disorientation, agitation, irritability, delirium (incoherent ideas), outbursts of anger, aggression, nervousness, hostility, anxiety, nightmares, abnormal dreams, hallucinations, psychosis (loss of contact with reality), hyperactivity, or inappropriate behavior may occur. These reactions are more frequent in the elderly and in children. If you experience these side effects, you should discontinue treatment and contact your doctor immediately.
On the other hand, the use of benzodiazepines can lead to dependence, mainly when the medication is taken continuously for a long time. It is generally not recommended to stop treatment abruptly, always following the doctor's instructions.
Amnesia (difficulty remembering recent events) may appear at normal doses, and the risk increases with increased doses. Amnesic effects may be associated with behavioral changes.
If any other reaction not described in this leaflet is observed, consult your doctor or pharmacist.
Reporting of side effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this leaflet.You can also report them directly through the Spanish System for Pharmacovigilance 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 this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the packaging after CAD. The expiration date is the last day of the month indicated.
Medications should not be disposed of through drains or in the trash. Dispose of the packaging and medications you no longer need at the SIGRE collection point of the pharmacy. Ask your pharmacist how to dispose of the packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition of Diazepam Qualigen
• The active ingredient is diazepam. Each tablet contains 10 mg of diazepam.
•The other components are lactose monohydrate, cornstarch, and magnesium stearate (E-572).
Appearance of the product and content of the packaging
Diazepam Qualigen 10 mg tablets: round, flat, and bisected tablets, white or almost white in color, with the inscription E1 on one face.
Diazepam Qualigen 10 mg tablets are available in packs of 25 and 30 tablets.
Holder of the marketing authorization and responsible for manufacturing
Holder of the marketing authorization:
Neuraxpharm Spain, S.L.U.
Avda. Barcelona 69
08970 Sant Joan Despí
Barcelona – Spain
Responsible for manufacturing:
Neuraxpharm Pharmaceuticals, S.L.
Avda. Barcelona, 69
08970 Sant Joan Despí (Barcelona) - Spain
Last review date of this leaflet:February 2024
The detailed information of this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/
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