Article Contents ::
- 1 The Brand Name PURON Has Generic Salt :: DEXKetoprofen
- 2 PURON Is From Company Zuventus Priced :: Rs. 33.9
- 3 PURON have DEXKetoprofen is comes under Sub class #N/A of Main Class #N/A
- 4 Main Medicine Class:: #N/A Sub Medicine Class :: #N/A
- 5 Disclaimer ::
- 6 The Information available on this site is for only Informational Purpose , before any use of this information please consult your Doctor .Price of the drugs indicated above may not match to real price due to many possible reasons may , including local taxes etc.. These are only approximate indicative prices of the drug.
The Brand Name PURON Has Generic Salt :: DEXKetoprofen
PURON Is From Company Zuventus Priced :: Rs. 33.9
PURON have DEXKetoprofen is comes under Sub class #N/A of Main Class #N/A
Main Medicine Class:: #N/A Sub Medicine Class :: #N/A
|Salt Name : OR Generic Name||Form||Price : MRP /Probable||Packing|
Indications for Drugs ::
Pain, Dysmenorrhea, Rheumatic disorders
Drug Dose ::
Adult: PO Rheumatic disorders 100-200 mg/day in 2-4 divided doses. Max: 300 mg/day in divided doses. Pain and inflammation 25-50 mg 6-8 hrly. Max: 300 mg/day. IM Pain and inflammation associated w/ musculoskeletal and joint disorders; Pain following orthopaedic surgery 50-100 mg by deep inj into the gluteal muscle 4 hrly. Max: 200 mg/24 hr for up to 3 days.
Dexketoprofen tablets are not recommended to use in patients who are: – Allergic to this product or any of its components, aspirin or other non-steroidal anti-inflammatory medicines. – Have suffered attacks of asthma, bronchospasm, acute rhinitis, nasal polyps, urticaria, angioedema (swollen face, eyes, lips, or tongue, or difficulty in breathing), after taking aspirin or other non-steroidal anti-inflammatory medicines. – Have or have previously suffered from a peptic ulcer or chronic gastro-intestinal disorders. – Have had previously gastro-intestinal haemorrhage (bleeding). – Have suffered from bronchial asthma. – Have severe heart failure, moderate to severe renal dysfunction or severely impaired hepatic function. – Have a bleeding disorder, a blood clotting disorder or taking an anticoagulant. – Pregnant or breast-feeding.
Drug Precautions ::
The medicine should be used with caution in conditions mentioned below: – Allergic to any other medicines. – Kidney disease, liver disease, heart disease or fluid retention conditions. – Blood disorder, systemic lupus erythematosus or mixed connective tissue disease.
Drug Side Effects ::
As with all medicines, Dexketoprofen may cause some unwanted effects in some patients. These are described below and are characteristic of non steroidal anti-inflammatory drugs: – Common (1 – 10%): nausea, vomiting, diarrhoea, stomach pain or heartburn. – Uncommon (0.1 – 1%): sleep disorders, nervousness, headache, dizziness,vertigo, palpitations, constipation, dry mouth, flatulence, skin rash, fatigue, hot flushes, shivering, general malaise. – Rare (0.01-0.1%): stomach ulceration, gastric haemorrhage or perforation, pins and needles, high blood pressure, water retention, slowed breathing rate, increased hepatic enzymes, increased sweating. – Very rare / isolated cases (<0.01%): blurred vision, ringing in the ear, low blood pressure, haematological reactions, hepatic or renal damage, dermatological and photosensitivity reactions, bronchospasm or anaphylaxis. - In patients with systemic lupus erythematosus or mixed connective tissue disease, anti-inflammatory medicines may rarely cause isolated cases of fever, headache and rigidity of the nape (back of the neck).
Pregnancy category ::
Drug Mode of Action ::
Dexketoprofen exhibits anti-inflammatory, analgesic and antipyretic properties. It potently inhibits the enzyme cyclooxygenase resulting in prostaglandin synthesis inhibition.
Drug Interactions ::
Increased risk of GI ulcers & bleeding (synergistic effect) w/ other NSAIDs. Increased risk of haemorrhagic effect of oral anticoagulants. Increased risk of haemorrhage w/ heparin. Increased blood lithium levels, which may reach toxic values, w/ lithium. Increased haematological toxicity of methotrexate at high dose of ?15 mg/wk. Increased toxic effects of hydantoins & sulphonamides. Increase risk of bleeding & damage of GI mucosal w/ anticoagulant. Increase hypoglycemic effect of sulfonylurea agents.