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Reference ID: 3733145 armodafinil Rare cases of serious or life-threatening rash, including SJS, Toxic Epidermal Necrolysis (TEN), and Drug Rash with Eosinophilia and Systemic Symptoms (DRESS) have been reported in adults and children in worldwide post-marketing experience .
The reporting rate of TEN and SJS associated with modafinil use, which is generally accepted to be an underestimate due armodafinil to underreporting, exceeds the background incidence rate .
Estimates of the background incidence rate for nuvigil rash nuvigil generic cost nuvigil patent artvigil armodafinil review armodafinil bluelight these serious skin reactions in the general population range between 1 to 2 cases per million-person years .
armodafinil Cases of serious rash similar to those observed with modafinil including skin and mouth blistering have been reported in adults in postmarketing experience with NUVIGIL .
There are no factors that are known to predict the risk of occurrence or the severity of rash associated with modafinil or armodafinil armodafinil .
Nearly all cases of serious rash associated with these drugs occurred within 1 to waklert study armodafinil vs dexamphetamine armodafinil for ms armodafinil max dose modup waklert 5 weeks after treatment initiation .
However, isolated cases have waklert price nuvigil schedule dea nuvigil glaucoma waklert does it work armodafinil nursing been reported after prolonged treatment (e . , armodafinil 3 months) .
Accordingly, duration of therapy cannot be relied upon as nuvigil narcotic nuvigil overdose amount nuvigil warnings nuvigil vs adrafinil nuvigil low dose a means to predict the potential risk heralded by the first appearance of a rash .
Although benign rashes also occur with NUVIGIL, it is not possible armodafinil to reliably predict which rashes will prove to be serious .
Accordingly, NUVIGIL should be discontinued at the first sign of rash, unless the armodafinil rash is clearly not drug-related .

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