IBUPROFEN Abbey 200 mg film -coated tablets, 20 pcs

Instructions for use for IBUPROFEN Abbey 200 mg film -coated tablets, 20 pcs

Field of use

Ibuprofen Abz 200mg (pack size: 20 pc) is an anti -inflammatory and pain relieving drug (non -steroidal anti -inflammatory/analgesic). It contains the active ingredient ibuprofen. The medicine is used for light to moderately severe pain such as headache, toothache, regulation pain; fever.

Active ingredients / ingredients / ingredients

Ibuprofen ABF 200MG (pack size: 20 pcs) contains: Active ingredient: 200 mg ibuprofen. Other ingredients: Pre-pasted corn starch, hypromellosis, croscarmellosis sodium, stearic acid, high-disperse silicon dioxide, macrogol 8000, titanium dioxide.

Contradictions

In the case of known hypersensitivity to one of the ingredients, the product should not be taken.

dosage

Application recommendation of ibuprofen Abz 200mg (pack size: 20 pc): For adults: If this medicine is taken for more than 3 days with a fever or for more than 4 days in pain or if the symptoms worsen, medical advice should be obtained. For children and young people: If this drug is required for children and adolescents for more than 3 days or if the symptoms worsen, medical advice should be obtained. The recommended dose is: Body weight (old) single dose max. Daily dose 20 - 29 kg (children: 6 - 9 years) 1 film -coated tablet (corresponding to 200 mg ibuprofen) 3 film -coated tablets (corresponding to 600 mg ibuprofen) 30 - 39 kg (children: 10 - 11 years) 1 film tablet (corresponding to 200 mg ibuprofen) 4 Film-coated tablets (corresponding to 800 mg ibuprofen) ≥ 40 kg (adolescents from 12 years and adults) 1-2 film-coated tablets (corresponding to 200-400 mg ibuprofen) 6 film tablets (corresponding to 1,200 mg ibuprofen). If you have taken the maximum single dose, wait at least 6 hours until the next income. The lowest effective dose should be used for the shortest time required to relieve the symptoms. If you have an infection, consult a doctor immediately if the symptoms (e.g. fever and pain) stop or worsen (see section 2). Dosage in older people: No special dose adjustment is required.

Taking

• Please take the covered tablets with plenty of liquid (e.g. a glass of water) during or after a meal.
• For patients who have a sensitive stomach, it is advisable to take the tablets during meals.
• Side effects can be minimized by using the lowest effective effective dose required for symptom control over the shortest possible period.

Patient information

• Warnings and Precautions
  • Please speak to your pharmacist before taking the preparation.
  • Side effects can be minimized by using the lowest effective effective dose required for symptom control over the shortest period.
  • Security in the gastrointestinal tract
    • Simultaneous use with other non-steroidal inflammatory inhibitors, including so-called COX-2 inhibitors (cyclooxygenase-2 inhibitors), should be avoided.
    • Older patients:
      • In older patients, side effects occur more frequently after using NSAR, in particular bleeding and breakthroughs in the stomach and intestinal area, which may be life-threatening. Therefore, particularly careful medical monitoring is required in older patients.
    • Bleeding of the gastrointestinal tract, ulcers and breakthroughs (perforations):
      • Bleeding of the gastrointestinal tract, ulcers and perforations, even with a fatal outcome, were carried out during treatment with all NSAR bedirected. They occurred with or without prior warning symptoms or serious events in the gastrointestinal tract in the prehistory at any time of therapy.
      • The risk of the occurrence of gastrointestinal bleeding, ulcers and breakthroughs is higher with increasing NSAR dose, in patients with ulcers in the history, especially with the complications bleeding or breakthrough, and in older patients. These patients should begin treatment with the lowest available dose.
      • For these patients as well as for patients who need accompanying therapy with low-dose acetylsalicylic acid (ASA) or other medicines that can increase the risk of gastrointestinal diseases, a combination therapy with gastric mucosa should protect drugs (e.g. misoprostol or Proton pump inhibitors).
      • If you have a history of side effects on the gastrointestinal tract, especially at older age, you should report any unusual symptoms in the abdomen (especially gastrointestinal bleeding), especially at the beginning of therapy.
      • Caution is advisable if you get medicines that can increase the risk of ulcers or bleeding, such as: B. Oral corticosteroids, anti-blood clotting drugs such as warfarin, selective serotonin reuptake inhibitors that are used, among other things, to treat depressive moods, or thrombocyte aggregation inhibitors such as ASA.
      • If you have gastrointestinal bleeding or ulcers during treatment with this preparation, the treatment must be discontinued.
      • In patients with a gastrointestinal disease in the prehistory (ulcerative colitis, Crohn's disease), caution should be used because their condition can deteriorate.
  • Effects on the cardiovascular system
    • Anti -inflammatory agents/painkillers such as ibuprofen can go hand in hand with a slightly increased risk of heart attack or stroke, especially when using in high doses. Do not exceed the recommended dose or duration of treatment.
    • You should discuss your treatment with your doctor or pharmacist before taking the preparation
      • having heart disease, including heart failure (heart failure) and angina pectoris (chest pain), or a heart attack, a bypass surgery, peripheral arterial disease (circulatory disorders in the legs or feet due to narrowed or closed arteries) or any kind of stroke (including mini -Stroke or transitory ischemic attack, "tia").
      • Heavy prints, diabetes or high cholesterol levels or heart diseases or strokes occur in their family history or when they are smokers.
  • Skin reactions
    • Under NSAR therapy, serious skin reactions with redness and bladder formation, some with a fatal outcome, were reported (exfediative dermatitis, Stevens-Johnson syndrome and toxic epidermal necrolysis/lyell syndrome). The highest risk of such reactions seems to exist at the beginning of therapy, since these reactions occurred in the majority of cases in the first month of treatment. At the first sign of rashes, mucosal defects or other signs of a hypersensitivity reaction, the medicine should be discontinued and the doctor should be consulted immediately.
    • An application should be avoided during a chickenpox infection (varicella infection).
  • Other information
    • The medicine should only be used with the strict weighing of the benefit-risk ratio:
      • for certain innate blood formation disorders (e.g. B. acute intermittent porphyria);
      • for certain autoimmune diseases (systemic lupus erythematosus and mixed collagenosis), since these patients have an increased risk of aseptic meningitis.
    • A particularly careful medical monitoring is required:
      • with restricted kidney function, since it can continue to deteriorate;
      • for liver dysfunction; Liver dysfunction increases the risk of the occurrence of kidney harmfulness and damage, as well as for severe, possibly fatal livesreactions;
      • directly after larger surgical interventions;
      • in allergies (e.g. skin reactions to other medicines, asthma, hay fever), chronic nasal mucosal swelling or chronic, respiratory respiratory diseases.
    • Severe acute hypersensitivity reactions (e.g. anaphylactic shock) are very rarely observed. At the first sign of a severe hypersensitivity reaction after taking the drug, the therapy must be canceled. The symptoms corresponding, medically required measures must be initiated by expert persons.
    • Ibuprofen, the active ingredient of the preparation, can temporarily inhibit the platelet function (thrombocyte aggregation). Patients with blood clotting disorders should therefore be carefully monitored.
    • When the use of ibuprofen-containing medicinal products at the same time, the anticoagulant effect of low-dose acetylsalicylic acid (prevention of the development of blood clots) can be impaired. In this case, you should therefore not use ibuprofen-containing medicines without the express instruction of your doctor.
    • If you are taking on medicinal products at the same time to inhibit blood clotting or to reduce the blood sugar, the blood clotting or blood sugar levels should take place as a precaution.
    • If the preparation is permanently increasing, regular control of the liver values, the kidney function and the blood count is required.
    • When taking surgical interventions, the doctor or dentist must be questioned or informed.
    • The longer use of all kinds of painkillers against headaches can make them worse. If this is the case or if this is suspected, medical advice should be obtained and the treatment can be canceled. The diagnosis of headache in the use of medication (Medication Overuse Headache, MOH) should be assumed in patients who suffer from frequent or daily headaches, although (or precisely because) they regularly take medicines for headaches.
    • In general, the habitual intake of pain relievers, especially when combining several pain relieving active ingredients, can lead to permanent kidney damage with the risk of kidney failure (analgesic nephropathy).
    • When using NSAIDs, the simultaneous enjoyment of alcohol, active ingredient side effects, in particular Soche, which affect the gastrointestinal tract or the central nervous system, can be reinforced.
  • Children and adolescents
    • There is a risk of kidney dysfunction in dehydrated children and adolescents.
    • Please note the information in category "contraindications".

• Wateriness and operating machines
  • Since when using the drug in higher dosage, central nervous side effects such as tiredness and dizziness can occur, the reaction capacity can be changed in individual cases and the ability to actively participate in road traffic and to operate machines can be impaired. This applies even more in combination with alcohol. You can then no longer react quickly and specifically to unexpected and sudden events. Do not drive a car or other vehicles in this case! Do not operate any tools or machines! Do not work without a safe grip!

Pregnancy

If you are pregnant or breastfeed, or if you suspect that you are pregnant or intend to become pregnant, ask your doctor or pharmacist for advice before taking this drug. If a pregnancy is determined during the application of ibuprofen ABF, the doctor must be notified. You can only use ibuprofen in the first and second thirds of pregnancy after consultation with your doctor. In the last third of the pregnancy, ibuprofen is not allowed to be used due to an increased risk of complications for mother and child.

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