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Index of reports
> Cases resulting in disability (7)
> Cases with Speech Disorder (3)
Below is the selection of adverse event reports related to Provigil (Modafinil) that includes cases resulting in disability where reactions include speech disorder.
Adverse event in 56 year old female receiving Provigil (Modafinil)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-29
Patient: 56 year old female, weighing 81.6 kg (179.6 pounds)
Adverse reactions / side effects: Oral Mucosal Blistering, Dysphagia, Dystonia, Impaired Work Ability, Swollen Tongue, Throat Tightness, Speech Disorder, Oral Pain, Uterine Dilation and Curettage, Oedema Mouth, Gastrooesophageal Reflux Disease
Adverse event resulted in: disablity
Suspect drug(s):
Provigil
Dosage: 50 mg qd oral
Administration route: Oral
Indication: Sleep Apnoea Syndrome
Start date: 2006-01-01
End date: 2006-09-01
Provigil
Dosage: 100 mg qd oral
Administration route: Oral
Indication: Sleep Apnoea Syndrome
Start date: 2006-09-01
End date: 2007-09-29
Other drugs received by patient: Lyrica; Nefazodone HCL; Crestor; Evista; Metoclopramide; Lisinopril; Nexium
Adverse event in 56 year old female receiving Provigil (Modafinil)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-29
Patient: 56 year old female, weighing 81.6 kg (179.6 pounds)
Adverse reactions / side effects: Oral Mucosal Blistering, Dysphagia, Dystonia, Impaired Work Ability, Swollen Tongue, Throat Tightness, Speech Disorder, Impaired Driving Ability, Oral Pain, Oedema Mouth, Gastrooesophageal Reflux Disease
Adverse event resulted in: disablity
Suspect drug(s):
Provigil
Dosage: 50 mg qd oral
Administration route: Oral
Indication: Sleep Apnoea Syndrome
Start date: 2006-01-01
End date: 2006-09-01
Provigil
Dosage: 100 mg qd oral
Administration route: Oral
Indication: Sleep Apnoea Syndrome
Start date: 2006-09-01
End date: 2007-09-29
Other drugs received by patient: Lyrica; Nefazodone HCL; Crestor; Evista; Metoclopramide; Lisinopril; Nexium
Adverse event in 38 year old female receiving Provigil (Modafinil)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-15
Patient: 38 year old female, weighing 81.8 kg (180.0 pounds)
Adverse reactions / side effects: Speech Disorder, TIC, Dyskinesia, Impaired Work Ability
Adverse event resulted in: disablity
Suspect drug(s):
Provigil
Dosage: unk oral
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Provigil
Dosage: 50 mg qd oral
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Start date: 2007-03-30
End date: 2007-04-03
Other drugs received by patient: Baclofen; Gabapentin; Synthroid; Zyrtec; Benadryl; Advil / 00109201 /; Amoxicillin; Guaifenesin; Sudafed / 00076302 /
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