CYCLOFEN
-Paracetamol is a para-aminophenol derivative salicylate, it is
 a non-Opioid . It has analgesic, antipyretic properties and 
 weak anti-inflammatory Activity.
-Paracetamol produces  central  and peripheral analgesia by
 elevation of the pain threshold and inhibition of prostaglandin
 biosynthesis, and antipyretic action through the effect on the
 hypothalamic heat-regulating center, resulting in peripheral  
 vasodilatation, increased blood flow through the skin, 
 sweating and heat loss. 
-Paracetamol is readily absorbed from the gastro-intestinal
 tract with peak plasma concentertion occurring about 10 to 60
 minutes after oral administration.
-Paracetamol is distributed into most body tissues. It crosses
 the placenta and  it presents in breast milk.
-Paracetamol is metabolised predominantly in the liver and
 excreted in the urine mainly as the glucuronide and sulphate
 conjugates. Less than 5% is excreted as unchanged
 Paracetamol.
-The elemination half-life of Paracetamol varies from about   
 1 to 3 hours.
-Caffeine is absorbed readily after oral dose and is widely
 distributed in the body. It is also absorbed through the skin.
-Caffeine passes readily in to the CNS. Low concentrations are
 also present in breast milk.
-Caffeine is metabolised almost Completely in the liver and 
 excreted in urine.
-The elimination half- life of Caffeine are about 3 to 7 hours.
-Pyrilamine is a first generation antihistamine targeting the H1
 receptor however, it rapidly permeates the brain often causing
 drowsiness ,these agents also have varying degrees of 
 anticholinergic and CNS activity (sedation).
-It is used in over-the-counter combination products to treat
 the common cold and menstrual symptoms.
 
                                 
                    