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LOFNAC - 50 / 100 Delayed Release Tablets
Composition
Lofnac 100 Suppository Lofnac 50 Suppository
Each Suppository contains: Each Suppository contains:
Diclofenac Sodium B.P. 100mg Diclofenac Sodium B.P. 50mg
Soluble Base: q.s Soluble Base: q.s
Colour: Titanium Dioxide. Colour: Titanium Dioxide.
Indications
Diclofenac belongs to the group of non-steroidal agents with marked analgesic and anti-inflammatory properties. It is indicated in case of severe, acute pain including :
acute joint inflammations (arthritis), gout attacks. chronic joint inflammations, especially when several joints are affected (chronic polyarthritis/rheumatoid arthritis) Bechterew's disease (ankylosing spondylitis) and other inflammatory rheumatoid disorders of the spine. Acute inflammatory condition of degenerative joint or spinal disorders (arthroses and spondylarthroses) Soft tissue rheumatisms. Painful swelling or inflammation after injuries or minor surgeries.
Contraindications, Warnings

LOFNAC is contraindicated for :
Hypersensitivity to Diclofenac Sodium.
Unclarified impairement of the blood cell formation.
Gastric and/or duodenal ulcers.
Children and adolescents.

the final three months of pregnancy
Diclofenac may inhibit labour pains and increase the tendency to bleeding. LOFNAC Rectal may only be used after careful consideration by the Physician of the benefits and risks, for: induceable porphyrias, the first six months of pregnancy (agreement by the Physician is absolutely necessary) Sometimes local reactions can occur including irritations, bloody mucous secretion or painful stools.
Interactions with other Pharmaceuticals
LOFNAC may increase plasma concentrations of Lithium and Digoxin if these substances are administered simultaneously. It may diminish the effect of dehydrating and blood pressure reducing agents (diuretics and antihypertonics). Concomitant treatment with Potassium-saving diuretics may be associated with increased Potassium levels in the serum. Concomitant administration of glucocorticoids or other anti-inflammatory agents increase the risk of gastro-intestinal bleeding. If LOFNAC is given within 24 hours before or after the administration of Methotrexate, the concentration of Methotrexate and its toxic effect may increase. The simultaneous intake of Acetyl-salicylic Acid reduces the serum concentration of Diclofenac.
Dosage and administration
Adults : If not otherwise prescribed by the physician, insert one LOFNAC 100mg. suppository daily deep into the anus, preferably after stool. The duration of administration should be determined by the physician.
Children and adolescents : LOFNAC 50mg. As directed by the Physician.
Packing
LOFNAC 50 Suppositories : Strip of 10 Suppositories per pack
LOFNAC 100 Suppositories : Strip of 10 Suppositories per pack
Storage
Preserve in well-closed, light resistant containers. Store in a cool place.
Validity
3 years.
 
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