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NOOTROPIL is indicated for patients suffering from myoclonus of cortical origin, inspite of aetiology, and should be used in conjunction with other anti-myoclonic therapies.
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The dosage regime shows important interindividual variability, requiring an individualised dose finding approach. A reasonable protocol would be to introduce piracetam in a dosage of 7.2 g/day, increasing by 4.8 g/day every three or four days up to maximum of 20g/day, succumbed either 2 or 3 divided doses and keep other antimyoclonic drugs unchanged at their optimal dosage. If possible, determined by clinical benefit, an endeavor needs to be created to subsequently slow up the dosage of other antimyoclonic drugs.
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Take the medicine as prescribed because of your doctor.
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Store this medicine at room temperature in a very tightly-closed container, faraway from heat and light.
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The negative effects reported in association with Nootropil include nervousness, agitation, irritability, anxiety and sleep disturbances. The incidence of such during numerous studies was 5% or less and they also were more frequently noted in the older patients taking more than 2.4 g daily. In the most of cases a dose reduction sufficed to create these symptoms disappeared. Some patients may complain of fatigue or drowsiness. Gastro-intestinal problems for example nausea, vomiting, diarrhoea and stomachache seemed to be reported, on the other hand Incidence during many studies was 2% or less. Other symptoms, including vertigo, headaches, trembling and sexual stimulation have occasionally been reported.
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NOOTROPIL (Piracetam) is contra-indicated in patients with severe renal impairment (renal creatinine clearance of below 20 ml each and every minute), hepatic impairment and to those under 16 years old. It is also contraindicated in patients with cerebral haemorrhage, Huntington's Chorea plus individuals with hypersensitivity to piracetam, other pyrrolidone derivatives or one of the excipients .
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Nootropil should not be prescribed during pregnancy or when breastfeeding.
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