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- NEODOL-50 TABLET 50 MG [SIN09392P]
NEODOL-50 TABLET 50 MG [SIN09392P]
Active ingredients: NEODOL-50 TABLET 50 MG
Product Info
NEODOL-50 TABLET 50 MG
[SIN09392P]
Product information
Active Ingredient and Strength | DICLOFENAC SODIUM - 50 MG |
Dosage Form | ENTERIC COATED TABLET |
Manufacturer and Country | MICRO LABS LTD - INDIA |
Registration Number | SIN09392P |
Licence Holder | NAINA MOHAMED & SONS PRIVATE LIMITED |
Forensic Classification | PRESCRIPTION ONLY MEDICINES |
Anatomical Therapeutic Chemical (ATC) code | M01AB05 |
INDICATIONS AND USES:
Acute and chronic treatment of the signs and symptoms of rheumatoid arthritis, osteoarthritis, and ankylosing spondylitis.
DOSAGE AND ADMINISTRATION:
Administration as 25 mg and 75mg, patients should be generally maintained on the lowest dosage, consistent with achieving satisfactory and therapeutic response. Encourage to take with food or just after food.
Osteoarthritis : 100 – 150 mg/day in divided doses, 50 mg b.i.d or t.i.d. or 75 mg b.i.d.
Rheumatoid arthritis: 150–200 mg/day, in divided doses, 50 mg t.i.d or q.i.d or 75 mg b.i.d.
Ankylosing spondylitis: 100–125 mg/day, or 25 mg q.i.d with an extra 25 mg extra dose at bed time if necessary.
Special populations
Established cardiovascular disease or significant cardiovascular risk factors
The use of high dose diclofenac (150mg/day) for more than 4 weeks is contraindicated in patients with established cardiovascular disease (congestive heart failure, established ischemic heart disease, peripheral arterial disease) or uncontrolled hypertension. If diclofenac treatment is needed, patients with established cardiovascular disease, uncontrolled hypertension or significant cardiovascular risk factors (e.g. hypertension, hyperlipidaemia, diabetes mellitus and smoking) should be treated only after careful consideration and at doses ≤ 100 mg daily if the treatment is for more than 4 weeks. As the cardiovascular risks of diclofenac may increase with dose and duration of exposure, diclofenac should always be prescribed at the lowest effective daily dose and for the shortest duration possible.
CONTRAINDICATIONS:
Diclofenac is contraindicated in patients with history of Hypersensitivity, or active or suspected peptic ulcer or GI bleeding, and in those who are known to develop asthma, urticarial or other allergic reactions with aspirin or other NSAIDs. Acute porphyria is a contraindication for diclofenac. Hepatic and Renal insufficiency. Not recommended in pregnancy.
The use of high dose diclofenac (150mg/day) for more than 4 weeks is contraindicated in patients with established cardiovascular disease (congestive heart failure, established ischemic heart disease, peripheral arterial disease) or uncontrolled hypertension.
