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Scopoder FDA adverse reports: 1. View All Scopoder FDA Adverse Reports

Scopoder FDA safety alerts: No

Reported deaths: 3

Reported hospitalizations: 20

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Scopoder Side Effects Report: 5608549-0,Application Site Erythema, Application Site Irritation, Condition Aggravated, Convulsion, Off Label Use, Purulence, Skin Reaction
on Jan 14, 2008 Male patient from UNITED KINGDOM, , 22 years of age, was diagnosed with salivary hypersecretion and was treated with Scopoder. After Scopoder was administered, patient had the following side effects: Scopoder and application site erythema, Scopoder and application site irritation, Scopoder and condition aggravated, Scopoder and convulsion, Scopoder and off label use, Scopoder and purulence, Scopoder and skin reaction. Scopoder dosage: 1 Patch Every 3 Days As Required, Transdermal. During the same period patient was treated with GLUTAMINE, ASCORBIC ACID, PYRIDOXINE, ACIDIPHILUS, CLONAZEPAM, PHENYTOIN, ZONEGRAN, GLYCERIN SUPPOSITORIES.


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Scopoder Side Effects
Scopoder and Application site erythema
Scopoder and Application site irritation
Scopoder and Condition aggravated
Scopoder and Convulsion
Scopoder and Erythema
Scopoder and Off label use
Scopoder and Purulence
Scopoder and Skin reaction

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