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Flamotal 400 mg 30 tablets

  • Symptomatic treatment of pain and inflammation;
  • Acute arthritis (including exacerbation of gout);
  • Chronic arthritis (rheumatoid arthritis);
  • Ankylosing spondylitis and other inflammatory diseases of the spine;
  • Arthroses and spondyloarthroses;
  • Post-traumatic pain;
  • Moderate to moderate pain syndrome;
  • Fever.

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Product quantities

• Sharm El Sheikh: In stock
• Hurghada: In stock
• El-Alamein: In stock
• Cairo: Out of stock
• El-Tor: Out of stock

Form of Release: Tablets

Flamotal 400 mg 30 tablets

Composition:

Active Ingredient: Each tablet contains Ibuprofen 400 mg.
Excipients: Microcrystalline cellulose, sodium starch glycolate, colloidal silicon dioxide, magnesium stearate.

Product Description:

Flamotal belongs to the group of nonsteroidal anti-inflammatory drugs (NSAIDs).
The medication provides analgesic, antipyretic, and anti-inflammatory effects.
The mechanism of action of ibuprofen is due to the inhibition of prostaglandin synthesis, which serve as mediators of pain, inflammation, and hyperthermic reactions.

Indications for Use:

  • Symptomatic treatment of pain and inflammation.
  • Acute arthritis (including acute gout attacks).
  • Chronic arthritis (rheumatoid arthritis).
  • Ankylosing spondylitis and other inflammatory spinal diseases.
  • Arthrosis and spondyloarthrosis.
  • Post-traumatic pain.
  • Mild to moderate pain syndrome.
  • Fever.

Method of Administration and Dosage:

  • Administered orally.
  • Dosage: 
    For adults and children aged 12 years and older with a body weight greater than 40 kg, it is recommended to take 1 tablet (400 mg) every 6 hours, but not more than 3 tablets per day.
    Elderly patients and patients with impaired liver function do not require a dose reduction.
  • The product is intended for short-term use.
  • If symptoms such as fever or pain persist for 3 days, a doctor must be consulted.

Contraindications:

  • Hypersensitivity to the components of the product.
  • History of bronchospasm, rhinitis, or urticaria after taking acetylsalicylic acid or another NSAID.
  • Erosive and ulcerative gastrointestinal diseases.
  • Age under 15 years.
  • Severe hepatic and renal impairment.
  • Pregnancy.
  • Gastrointestinal bleeding and intracranial hemorrhage.
  • Hemophilia and other blood clotting disorders.

Precautions:

  • It is recommended to use the shortest possible course and the lowest effective dose necessary to relieve symptoms.
  • In case of necessary systemic use for more than 10 days, a physician must be consulted.
  • During long-term treatment, monitoring of peripheral blood, liver, and kidney function is required.
  • Due to severe purulent complications, it is recommended to avoid using ibuprofen during chickenpox.
  • Ibuprofen affects ovulation, disrupting female reproductive function (reversible after discontinuing treatment).
  • Keep out of reach of children.

Adverse Reactions / Side Effects:

  • Abdominal pain, nausea, vomiting, heartburn, decreased appetite.
  • Bronchospasm, hearing loss, tinnitus, visual disturbances.
  • Headache, insomnia, dizziness.
  • Increased blood pressure, heart failure.
  • Nephrotic syndrome, cystitis.
  • Allergic reactions, anemia, thrombocytopenia.

Pregnancy and Lactation:

The use of the product is contraindicated during pregnancy.
A mandatory medical consultation is required before use during lactation.

Storage Conditions:

Store at a temperature not exceeding 30 °C.
Keep out of reach of children.

Packaging:

A cardboard box containing 3 blisters of 10 tablets each, along with a paper package leaflet.

Active Ingredients:

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