
Ask a doctor about a prescription for Lorafen
Lorazepam
Lorafen contains the active substance lorazepam, which belongs to a group of medicines called benzodiazepines. Lorafen has anxiolytic, sedative, and weaker anticonvulsant and muscle relaxant effects. Lorafen is used for the short-term treatment of:
If you have:
General information about the effects observed after treatment with benzodiazepines and other medicines with similar effects to benzodiazepines that should be taken into account when taking Lorafen.
Tolerance: After taking Lorafen for several weeks, its effectiveness may decrease.
Dependence: Long-term use of lorazepam can lead to psychological and physical dependence. The risk of dependence increases with the dose and duration of treatment and is higher in patients who are addicted to alcohol or drugs, as well as in patients with personality disorders.
Withdrawal symptoms: In case of sudden discontinuation of the medicine, the patient may experience withdrawal symptoms, such as headaches, muscle pain, increased anxiety, tension, excitement, restlessness, disorientation, sleep disturbances, irritability. In more severe cases, the following may occur: loss of sense of reality, personality disorders, hypersensitivity to sound, touch, light, noise, feeling of tingling and numbness of limbs, hallucinations, and delusions, epileptic seizures.
Rebound phenomenon and anxiety: When discontinuing Lorafen, a transient recurrence of intensified symptoms that were the reason for taking the medicine (so-called rebound phenomenon) may occur. These symptoms are often accompanied by mood changes, anxiety, sleep disturbances, and insomnia. To minimize the risk of these symptoms, it is recommended to gradually reduce the dose of the medicine.
Anterograde amnesia (inability to remember events after taking the medicine): Lorafen may cause anterograde amnesia (difficulty learning and remembering new information - new data is not permanently stored). This condition usually occurs within a few hours of taking the medicine, especially in high doses. If the doctor has prescribed taking Lorafen once a day, to reduce the risk of anterograde amnesia, it is recommended to take the medicine half an hour before going to bed and ensuring adequate conditions for continuous, uninterrupted sleep lasting 7-8 hours.
Psychotic and paradoxical reactions: In children and the elderly, the risk of abnormal psychotic and paradoxical reactions (opposite to expected) increases, such as anxiety, excitement, irritability, aggression, anger, rage, delusions, nightmares, hallucinations, psychoses, behavioral disorders. If such symptoms occur, you should contact your doctor immediately.
Specific patient groups:
Patient with impaired liver or kidney function or with chronic respiratory failure should inform their doctor about their condition before taking Lorafen.
Patients with depression: Before taking Lorafen, you should inform your doctor about any mental illnesses. Patients with symptoms of depression or anxiety associated with depression should take several medicines at the same time. Administering only Lorafen to patients with depression may exacerbate symptoms of depression, including suicidal thoughts.
During treatment with benzodiazepines, masked depression may be revealed.
Patients addicted to alcohol, drugs, or medicines should inform their doctor about these addictions before taking Lorafen, as they are at high risk of developing psychological and physical dependence. This group of patients should take Lorafen under close medical supervision.
Lorafen in patients with porphyria may exacerbate symptoms of this disease. Patients with porphyria should inform their doctor about this disease before starting treatment with Lorafen.
Patients with glaucoma (an eye disease characterized by increased pressure in the eyes) should inform their doctor about this disease before starting treatment with Lorafen.
During prolonged treatment with lorazepam, the doctor usually orders periodic blood tests (morphology with smear) and urine analysis.
Tell your doctor about all medicines you are currently taking or have recently taken, as well as medicines you plan to take.
This is especially important if you are taking any of the following medicines or drinking alcohol:
If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a child, ask your doctor or pharmacist for advice before taking this medicine.
Lorafen should not be taken during pregnancy.
Lorafen passes into breast milk. If treatment is necessary, breastfeeding should be discontinued.
Do not drive or operate machinery while taking Lorafen.
Your ability to drive or operate machinery may be impaired due to the possibility of somnolence, decreased concentration, or other adverse effects that reduce concentration (see section 4, Possible side effects).
Always take Lorafen exactly as your doctor has told you.
If you are not sure, ask your doctor.
For anxiety disorders, usually 2 mg to 3 mg of lorazepam per day is administered in 2 or 3 divided doses, and then, if necessary, the doctor will increase the dose of the medicine to 6 mg per day, in 2 or 3 divided doses.
The dose of lorazepam will be increased gradually, starting with an increase in the dose taken in the evening. A maximum of 10 mg/day can be administered.
For sleep disorders caused by anxiety, usually 2 mg to 4 mg of lorazepam is administered once a day before sleep.
The safety and efficacy of lorazepam in children under 12 years have not been established.
Usually, half of the dose recommended for adult patients is sufficient (see section 2, Warnings and precautions).
The duration of treatment is determined by the doctor.
Lorafen tablets should be swallowed with a small amount of water.
The doctor will start treatment with the lowest effective dose and, if necessary, will gradually increase it.
Symptoms of overdose are impaired consciousness, somnolence, slurred speech. In severe cases of poisoning, the following may occur: ataxia, hypotension, muscle weakness, respiratory disorders, coma, and even death.
In case of taking a higher dose of Lorafen than recommended, you should immediately contact your doctor or go to the nearest emergency department in a hospital. You should take the medicine in its original packaging so that the medical staff can accurately check which medicine was taken.
If you forget to take a dose of Lorafen, you should take the next dose as soon as you remember. However, if it is almost time for the next dose, you should skip the missed dose and take the next dose as recommended. If you forget to take two or more doses, you should contact your doctor.
Do not take a double dose to make up for a missed dose.
Do not stop taking Lorafen unless it is in agreement with your doctor. It is possible that the symptoms of the disease will recur. If the doctor decides to discontinue the medicine, the dose of the medicine should be gradually reduced over several days.
In case of doubts related to the use of the medicine, you should consult your doctor.
Like all medicines, Lorafen can cause side effects, although not everybody gets them.
The frequency of side effects occurring after taking the medicine is defined as follows:
Very common- occurs in more than 1 in 10 people;
Common- occurs in less than 1 in 10 people;
Uncommon- occurs in less than 1 in 100 people;
Rare- occurs in less than 1 in 1,000 people;
Very rare- occurs in less than 1 in 10,000 people;
Frequency not known- cannot be estimated from the available data.
If any of the above side effects occur, you should immediatelyinform your doctor or go to the nearest emergency department in a hospital.
The following side effects occur very commonly:
The following side effects occur commonly:
The following side effects occur rarely:
The following side effects occur very rarely:
The following side effects occur with unknown frequency:
If you experience any side effects, including any not listed in this leaflet, you should tell your doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181C, 02-222 Warsaw
Tel.: +48 22 49 21 301
Fax: +48 22 49 21 309
Website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder.
By reporting side effects, you can help provide more information on the safety of this medicine.
Keep out of the sight and reach of children.
Store in a temperature below 25°C. Store in the original packaging to protect from light and moisture.
Do not use the medicine after the expiry date (EXP) stated on the packaging. The expiry date refers to the last day of the month.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
The active substance of the medicine is lorazepam.
Lorafen 1 mg: One scored tablet contains 1 mg of lorazepam.
Other ingredients are: potato starch, sodium carboxymethyl starch (type A), gelatin, talc, magnesium stearate, lactose monohydrate, polyvinyl alcohol, maltodextrin, sucrose, titanium dioxide, Opaglos 6000
Lorafen 2.5 mg: One scored tablet contains 2.5 mg of lorazepam.
Other ingredients are: potato starch, sodium carboxymethyl starch (type A), gelatin, talc, cochineal red (E-124), magnesium stearate, lactose monohydrate, polyvinyl alcohol, maltodextrin, sucrose, cochineal red lake (E-124), titanium dioxide, Opaglos 6000
Lorafen, 1 mg: White, round, biconvex, smooth scored tablets.
Lorafen, 2.5 mg: Pink, round, biconvex, smooth scored tablets.
Package:25 scored tablets
Tarchomińskie Zakłady Farmaceutyczne "Polfa" Spółka Akcyjna
ul. A. Fleminga 2
03-176 Warsaw
Phone number: 22 811-18-14
To obtain more detailed information, you should contact the representative of the marketing authorization holder.
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Discuss dosage, side effects, interactions, contraindications, and prescription renewal for Lorafen – subject to medical assessment and local rules.