ACE PROXYVON 30 g
Aceclofenac 1.5 %w/w, Camphor 3.1 %w/w, Capsaicin 0.01 %w/w, Linseed oil 3 %w/w, Menthol 5 %w/w, Methyl salicylate 10 %w/w
Wockhardt Ltd (Tridoss Laboratories Pvt. Ltd.)
It comes as a tablet to take by mouth, with food.
Store it in an airtight container in a cool dry place. Protect from light
In patients with severe ulcer Gastrointestinal bleeding Hypersensitivity
Spasticity : Spasticity is a feature of altered skeletal muscle performance in muscle tone involving hypertonia; it is also referred to as an unusual "tightness", stiffness, or "pull" of muscles. The cause of spasticity is not really known, but there are several theories. In general, spasticity develops when an imbalance occurs in the excitatory and inhibitory input to a motor neurons caused by damage to the spinal cord and/or central nervous system. The damage causes a change in the balance of signals between the nervous system and the muscles, leading to increased excitability in the muscles. Spasticity is found in conditions where the brain and/or spinal cord are damaged or fail to develop normally; these include cerebral palsy, multiple sclerosis, spinal cord injury and acquired brain injury including stroke. Damage to the CNS as a result of stroke or spinal cord injury, alter of peripheral nerves in the affected region. Spasticity : Spasticity is a feature of altered skeletal muscle performance in muscle tone involving hypertonia; it is also referred to as an unusual "tightness", stiffness, or "pull" of muscles. The cause of spasticity is not really known, but there are several theories. In general, spasticity develops when an imbalance occurs in the excitatory and inhibitory input to a motor neurons caused by damage to the spinal cord and/or central nervous system. The damage causes a change in the balance of signals between the nervous system and the muscles, leading to increased excitability in the muscles. Spasticity is found in conditions where the brain and/or spinal cord are damaged or fail to develop normally; these include cerebral palsy, multiple sclerosis, spinal cord injury and acquired brain injury including stroke. Damage to the CNS as a result of stroke or spinal cord injury, alter of peripheral nerves in the affected region.
Increased risk of renal impairment when Aceclofenac given with ACE inhibitors (perindopril ,captopril, enalapril, lisinopril and ramipril ), Angiotensin - II receptor antagonists ( Losartan, candesartan , telmisartan and Valsartan ), Ciclosporin,Tacrolimus and Diuretics. Antagonise hypotensive effect with ACE inhibitors, Adrenergic neurone blockers,Alphablockers, Angiotensin -II receptor antagonists, Betablockers, Calcium channel blockers, clonidine, Diazoxide, Hydralazine, Methyl dopa, Minoxidine, Moxonidine, Nitrates and Nitroprusside. Increased risk of bleeding with Antidepressants, Clopidrogel, Erlotinib, Iloprost, Pentoxifylline Sibutramine and Venlafaxine. Aceclofenac probably reduce excretion of lithium (increased risk of toxicity). Possible increased risk of convulsions when Aceclofenac given with quinolones.
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It is any effect of a drug, chemical, or other medicine that is in addition to its intended effect, especially an effect that is harmful or unpleasant.