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Provigil (Modafinil) - Adverse Event Reports - Disability

 



Index of reports > Cases resulting in disability (7)

     Impaired Work Ability (3)Speech Disorder (3)Oral Pain (3)Oedema Mouth (3)Oral Mucosal Blistering (2)Dysphagia (2)Dystonia (2)Dyskinesia (2)Swollen Tongue (2)Gastrooesophageal Reflux Disease (2)

Below is the selection of adverse event reports related to Provigil (Modafinil) that includes cases resulting in disability.

Adverse event in male receiving Provigil (Modafinil)

Reported by a physician from United States on 2007-10-31

Patient: male, weighing 52.6 kg (115.8 pounds)

Adverse reactions / side effects: Palpitations, Dizziness, Vision Blurred, Urinary Retention

Adverse event resulted in: disablity

Suspect drug(s):
Provigil
    Dosage: 200 mg qd oral
    Administration route: Oral
    Indication: Depression
    Start date: 2007-05-04
    End date: 2007-05-08

Provigil
    Dosage: 200 mg qd oral
    Administration route: Oral
    Indication: Somnolence
    Start date: 2007-05-04
    End date: 2007-05-08

Other drugs received by patient: Bupropion HCL; Lamictal; Restoril / 00393701 /; Percocet



Adverse event in male receiving Provigil (Modafinil)

Reported by a consumer/non-health professional from United States on 2007-10-31

Patient: male, weighing 87.1 kg (191.6 pounds)

Adverse reactions / side effects: Asthma, Dyspnoea, Drug Ineffective, Tachycardia, Chest Pain, Oedema, Vasodilatation, Hypertension

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Provigil
    Dosage: 400 mg tid oral
    Administration route: Oral
    Indication: Narcolepsy
    End date: 2007-07-01

Provigil
    Dosage: 200 mg tid oral
    Administration route: Oral
    Indication: Narcolepsy
    Start date: 2007-07-01
    End date: 2007-07-01

Provigil
    Dosage: 400 mg tid oral
    Administration route: Oral
    Indication: Narcolepsy
    Start date: 2007-07-01

Other drugs received by patient: Adderall 10



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 /



Adverse event in 56 year old male receiving Provigil (Modafinil)

Reported by a pharmacist from United States on 2007-02-28

Patient: 56 year old male, weighing 57.0 kg (125.4 pounds)

Adverse reactions / side effects: Tardive Dyskinesia

Adverse event resulted in: disablity

Suspect drug(s):
Provigil (Modafinil)



Adverse event in 53 year old female receiving Provigil (Modafinil)

Reported by a physician from United Kingdom on 2007-02-20

Patient: 53 year old female

Adverse reactions / side effects: Oral Pain, Dyskinesia, Condition Aggravated, Oedema Mouth

Adverse event resulted in: disablity

Suspect drug(s):
Provigil (Modafinil)

Other drugs received by patient: Quetiapine Fumarate; Priadel / 00033702 /; Venlafaxine HCL; Levothyroxine Sodium; Procyclidine Hydrochloride 2MG TAB; Zopiclone; Inhalers

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