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 EXPRESS CAPSULES 200MG - 8 tablets



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- headache and toothache;

- migraine;

- Algomenorrhea;

- neuralgia;

- backache;

- myalgia;

- rheumatic pains;

- Fever with flu and ARVI.

Dosage and administration

For adults and children over 12 years old appoint inside 200 mg 3-4 times / day.

To achieve a rapid therapeutic effect, the dose can be increased to 400 mg (2 capsules) 3 times / day.

Do not take more than 6 caps / day. Maximum Daily Dose for adultsis 1.2 g. The maximum daily dose for children and adolescents aged 12 to 17 years is 1 year

Capsules should be washed down with water.

The patient should be warned that if the symptoms of the disease persist when taking the drug for 2-3 days, it is necessary to stop treatment and consult a doctor.

Adverse effects

Gastrointestinal: NPVS-gastropathy (abdominal pain, nausea, vomiting, heartburn, loss of appetite, diarrhea, flatulence, constipation; possibly increased activity of hepatic transaminases; rarely - erosive and ulcerative lesions of the gastrointestinal mucosa, which in some cases are complicated by perforation and bleeding); irritation or dryness of the oral mucosa, pain in the mouth, ulceration of the mucous membrane of the gums, aphthous stomatitis, pancreatitis, hepatitis.

From the side of the central nervous system: headache, dizziness, insomnia, anxiety, nervousness, irritability, agitation, drowsiness, depression, confusion, hallucinations; rarely, aseptic meningitis (more often in patients with autoimmune diseases).

Cardiovascular: heart failure, tachycardia, increased blood pressure.

Urogenital: acute renal failure, allergic nephritis, nephrotic syndrome (edema), polyuria, cystitis; perhaps - a decrease in QA, an increase in serum concentration of creatinine.

Special senses: hearing loss, ringing or tinnitus, toxic damage to the optic nerve, blurred vision or diplopia, dryness and irritation of the eyes, conjunctival edema and eyelids (allergic origin), scotoma.

Respiratory: shortness of breath, bronchospasm.

Hemic and lymphatic: anemia (incl.hemolytic and aplastic), thrombocytopenia, thrombocytopenic purpura, agranulocytosis, leukopenia; possibly an increase in bleeding time, a decrease in hematocrit or hemoglobin.

Allergic reactions: skin rash (usually erythematous or urticaria), pruritus, angioedema, anaphylactopiama reactions, anaphylactic shock, bronchospasm or dyspnea, fever, erythema multiforme exudative (including Stevens-Johnson syndrome), toxicity epidermus erythema, including toxic erythema, including toxic erythema, including toxic erythema, including toxic erythema, including toxic erythema and erythema;, eosinophilia, allergic rhinitis.

Other: increased sweating; may decrease the concentration of glucose in the blood.

When using the drug for 2-3 days, side effects are very rare.


- erosive and ulcerative lesions of the gastrointestinal tract in the acute phase (including gastric ulcer and duodenal ulcer, Crohn's disease, UC);

- hemophilia, hypocoagulation state, hemorrhagic diathesis;

- the period after coronary artery bypass surgery;

- Gastrointestinal bleeding and intracranial hemorrhage;

- severe liver failure or active liver disease;

- renal failure severe, confirmed hyperkalemia;

- pregnancy;

- children's age up to 12 years;

- hypersensitivity to the drug;

- Hypersensitivity to Acetylsalicylic acid or other NSAIDs in history: including indications of attacks of bronchial obstruction, rhinitis, urticaria after taking acetylsalicylic acid or another NSAID; complete or incomplete intolerance syndrome acetylsalicylic acid (rhinosinusitis, urticaria, polyps of the nasal mucosa, bronchial asthma).

WITH caution prescribe the drug to elderly patients, patients with heart failure, arterial hypertension, coronary artery disease, cerebrovascular diseases, dyslipidemia / hyperlipidemia, diabetes, peripheral artery disease, smokers, with frequent use of alcohol, with cirrhosis of the liver with portal hypertension, with QC <60 ml / min, hepatic and / or renal failure, patients with nephrotic syndrome, hyperbilirubinemia, with indications of a history of peptic ulcer and duodenal ulcer, patient there with gastritis, enteritis, colitis,in the presence of Helicobacter pylori infection, with blood diseases of unknown etiology (leukopenia and anemia), during lactation, with prolonged use of NSAIDs, patients with severe somatic diseases, simultaneously with oral GCS (including prednisone), with anticoagulants (including with warfarin), with antiplatelet agents (including with acetylsalicylic acid, with clopidogrel), selective serotonin reuptake inhibitors (including with citalopram, Fluoxetine, paroxetine, sertraline).

Use during pregnancy and lactation

Nurofen® UltraCap is contraindicated for use in the third trimester of pregnancy.

The use of the drug in the I and II trimesters of pregnancy and lactation is possible only in the case when the intended benefit to the mother outweighs the potential risk to the fetus or baby.

If necessary, the appointment of the drug during lactation should decide on the termination of breastfeeding.

Application for violations of the liver

The drug is contraindicated in marked disorders of the liver.

WITH caution should be prescribed in the presence of concomitant liver diseases.

Application for violations of kidney function

The drug is contraindicated in severe renal impairment.

WITH caution should be prescribed in the presence of concomitant kidney disease.

Use in children

Contraindicated in children under 12 years.

Maximum Daily Dose for children and adolescents aged 12 to 17 years is 1 year

Use in elderly patients

Be wary appoint patients older. 

Special notes

Treatment with the drug should be carried out in the minimum effective dose, the shortest possible course.

The patient should be informed that if side effects occur, the drug should be stopped and the doctor should be consulted. During the period of treatment is not recommended to use ethanol.

Control of laboratory parameters

During long-term treatment, it is necessary to control the picture of peripheral blood and the functional state of the liver and kidneys. When symptoms of gastropathy appear, a careful monitoring is shown, including esophagogastroduodenoscopy, complete blood count (hemoglobin determination), fecal occult blood test.

If necessary, determine the 17-ketosteroids drug should be canceled 48 hours before the study.

Influence on ability to drive motor transport and control mechanisms

Patients should refrain from all activities that require increased attention and high-speed psychomotor reactions.


Symptoms: abdominal pain, nausea, vomiting, lethargy, drowsiness, depression, headache, tinnitus, metabolic acidosis, coma, acute renal failure, lowering blood pressure, bradycardia, tachycardia, atrial fibrillation, respiratory arrest.

Treatment: gastric lavage (only one hour after ingestion), Activated carbon, alkaline drink, forced diuresis; if necessary, conduct symptomatic therapy.

Drug interaction

The simultaneous use of Nurofen UltraCap with acetylsalicylic acid and other NSAIDs is not recommended.

With the simultaneous appointment of Ibuprofen reduces the anti-inflammatory and antiplatelet effect of acetylsalicylic acid (it is possible to increase the incidence of acute coronary insufficiency after starting ibuprofen in patients receiving small doses of acetylsalicylic acid as an antiplatelet agent).

With simultaneous use with anticoagulants and thrombolytic drugs (including alteplazy, streptokinase, urokinase) increases the risk of bleeding.

Simultaneous administration with serotonin reuptake inhibitors (including citalopram, fluoxetine, paroxetine, sertraline) increases the risk of serious bleeding from the gastrointestinal tract.

When combined with ibuprofen, cefamundol, cefoperazone, cefotetan, valproic acid, plicamycin increase the incidence of hypoprothrombinemia.

With the combined use of cyclosporine and gold preparations enhance the effect of ibuprofen on the synthesis of prostaglandin in the kidneys, which leads to increased nephrotoxicity. Ibuprofen increases the plasma concentration of cyclosporine and the likelihood of its hepatotoxic effects.

Drugs that block tubular secretion, with simultaneous use, reduce excretion and increase the plasma concentration of ibuprofen.

When used together, inducers of microsomal oxidation (includingPhenytoin, ethanol, barbiturates, rifampicin, phenylbutazone, tricyclic antidepressants) increase the production of hydroxylated active metabolites, increasing the risk of severe intoxication.

Inhibitors of microsomal oxidation reduce the risk of the development of the hepatotoxic effect of ibuprofen.

With the combined use of ibuprofen reduces the hypotensive activity of vasodilators, the natriuretic effect of Furosemide and hydrochlorothiazide.

Ibuprofen reduces the effectiveness of uricosuric drugs, enhances the effect of indirect anticoagulants, antiplatelet agents, fibrinolytics.

Enhances the side effects of mineralocorticoids, GCS, estrogen, ethanol. 

When used together, it enhances the effect of oral hypoglycemic drugs (sulfonylurea derivatives) and insulin .

While taking antacids and Kolestiramin reduce the absorption of ibuprofen. 

With the combined use of ibuprofen increases the concentration in the blood of Digoxin, lithium preparations, Methotrexate .

Drugs with myelotoxic effects enhance the manifestations of Nurofen UltraCap hematotoxicity.

Caffeine enhances the analgesic effect of ibuprofen.

Terms and conditions of storage

The drug should be stored in a dry place inaccessible to children at a temperature not higher than 25 ° C. 

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