Ponstan Tablet Forte 500mg

Indications

• Ponstan Forte is primarily indicated in conditions like Dysmenorrhoea, Fever, fever, Inflammation, Juvenile chronic arthritis, Menorrhagia, Migraine, Musculoskeletal disorders, Osteoarthritis, Pain, Post-operative pain, Post-partum pain, Rheumatoid arthritis. Symptomatic relief of GI disorders. Toothache. Traumatic pain.

Side Effects

• The severe or irreversible adverse effects of Ponstan Forte, which give rise to further complications include Diarrhoea, Peripheral edema, Urticaria, Gi bleeding, I bleeding. Proteinuria, Aplastic anemia Aplastic anemia, Epidermal necrolysis, Jaundice, Jaundice Nephrotic syndrome, Interstitial nephritis, Papillary necrosis, Hemolysis Proctocolitis, Enteritis, Large bowel perforation, Epidermal necrolysis, Platelet dysfunction, Aplastic anemia, Gl perforation, Proteinuria, proteinuria, Haemolytic anemia. Ponstan Forte produces potentially life-threatening effects which include Agranulocytosis, Thrombocytopenia, Pancytopenia, Leucopenia, Heart failure, Bone marrow hypoplasia, Reversible autoimmune hemolysis, which are responsible for the discontinuation of Ponstan Forte therapy. The signs and symptoms that are produced after the acute overdosage of Ponstan Forte include Grand Mal Secures (epilepsy). Excitation, Depression, Incoordination. The symptomatic adverse reactions produced by Ponstan Forte are more or less tolerable and if they become severe, they can be treated symptomatically, these include Dizziness, Headache, Drowsiness, Skin rashes, Maculopapular rash, Hematuria, Elevation of liver enzymes, Anemia, Azotemia, Bullous rash, Skin rashes, dizziness.

Warnings

• Ponstan Forte should be used with caution in patients with intrinsic coagulation defects and those on anticoagulant therapy. It should be used with caution in patients with compromised cardiac function, hypertension and other conditions predisposing to fluid retention. It should be used with extra care in the presence of existing uncontrolled infection Perform periodic auditory function test during chronic therapy Discontinue drug if skin reaction occurs