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Souгсe NDC Code(s): provigil prescription online 63459-201 " href="#">NDC Code(s): 63629-1611-1, 63629-1611-2, 63629-1611-3, 63629-1611-4 Packager: Bryant Ranch Prepack This is a repackaged label. Label: PROVIGIL- modafinil tablet NDC (National Drug Code) - Each drug product is assigned this unique number which can be found on the drug's outer packaging. Patients should be advised to contact their doctor if they are unsure as to whether they should discontinue modafinil treatment. Although there is no need to stop treatment immediately, patients who wish to stop can do so at any time.
such patients should be monitored closely and advised to report any suspected adverse behaviours or thoughts - patients should be assessed immediately and treatment stopped if appropriate Advice on treatment cessation Modafinil is no longer indicated for shift-worker sleep disorder and obstructive sleep apnoea. Further information Article citation: Drug Safety Update March 2011, vol 4 issue 8: A1. Reporting of suspected adverse reactions Suspected adverse reactions to modafinil should be reported promptly via the Yellow Card Scheme .
It is indicated for the treatment of excessive sleepiness in adults with narcolepsy, with or without cataplexy. New information and advice for healthcare professionals: Product information advises against use in the following groups: those with uncontrolled hypertension or cardiac arrhythmias children up to 18 years old women who are pregnant or breastfeeding Modafinil (Provigil): now restricted to narcolepsy Article date: March 2011 Modafinil (Provigil) is a wakefulness-promoting agent that acts on the CNS.
A recent European review of the benefits and risks of modafinil has recently been completed, and information about the restricted use of this drug as a result of this review was published in the August 2010 issue of Drug Safety Update . The recommended starting dose is 200mg a day. Also as a result of the review, further information and advice is available to support safer use of modafinil. Patients with abnormal findings should be further evaluated by specialists before modafinil treatment can be initiated cardiovascular function—especially blood pressure and heart rate—should be monitored regularly; modafinil should be discontinued in patients who develop arrhythmia or moderate to severe hypertension, and should not be restarted until the condition has been adequately evaluated and treated Cautions for use: modafinil should be used with caution in patients with a history of: psychosis, depression, or mania abuse of alcohol, drugs, or illicit substances Monitoring during treatment: a baseline electrocardiogram should be done before treatment initiation.
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