|
Index of reports
> Cases resulting in a serious event (112)
> Cases with Vomiting (9)
Below is the selection of adverse event reports related to Provigil (Modafinil) that includes cases resulting in a serious event where reactions include vomiting.
Adverse event in 48 year old female receiving Provigil (Modafinil)
Reported by a consumer/non-health professional from United States on 2007-10-23
Patient: 48 year old female, weighing 190.5 kg (419.1 pounds)
Adverse reactions / side effects: Choking Sensation, Pruritus, Dyskinesia, Pain, Photopsia, Oral Discomfort, Hypoaesthesia Oral, Laboratory Test Abnormal, Oral Candidiasis, Eye Disorder, LIP Exfoliation, Respiratory Rate Increased, Migraine, Dysphagia, Vomiting, Stomatitis, Nausea, Paraesthesia Oral, LIP DRY, Anaemia, Ill-Defined Disorder, Muscle Twitching, Eye Pain, Tremor, Mucosal Inflammation, Oral Pain, Visual Disturbance, Oral Disorder, Impaired Gastric Emptying, Tardive Dyskinesia, Inflammation
Adverse event resulted in: hospitalization
Suspect drug(s):
Provigil
Dosage: qd oral
Administration route: Oral
Indication: Fatigue
Start date: 2006-09-01
End date: 2006-09-15
Risperdal
Dosage: 3 mg qd oral
Administration route: Oral
Indication: Depression
Start date: 2002-01-01
End date: 2006-09-15
Other drugs received by patient: Effexor XR; Lithium; Prilosec / 00661201 /; Enablex; Lipitor; Triamterene; Mirapex; Potassium Chloride; Coumadin
Adverse event in 54 year old male receiving Provigil (Modafinil)
Reported by a consumer/non-health professional from United States on 2007-10-02
Patient: 54 year old male, weighing 113.6 kg (249.9 pounds)
Adverse reactions / side effects: Agitation, Confusional State, Ischaemic Cardiomyopathy, Narcolepsy, Pulmonary Hypertension, Pain, Coma, Fall, Cardiac Disorder, Speech Disorder, Dizziness, Myocardial Infarction, Cardiac Failure Congestive, Pain in JAW, Blood Pressure Increased, Vomiting, Hypotension, Encephalopathy, Coronary Artery Disease, Cardiogenic Shock, Aggression, Renal Failure, Respiratory Failure, Heart Rate Increased, Ejection Fraction Decreased, Influenza Like Illness
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Dexedrine
Dosage: 70mg per day
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Start date: 1992-01-01
Provigil
Dosage: 400mg per day
Administration route: Oral
Start date: 2006-10-01
End date: 2007-07-01
Other drugs received by patient: Cymbalta; Gabapentin; Vytorin; Minocycline HCL
Adverse event in 30 year old female receiving Provigil (Modafinil)
Reported by a consumer/non-health professional from United States on 2007-10-01
Patient: 30 year old female
Adverse reactions / side effects: Vomiting, Cognitive Disorder, Delusion, Anxiety, Poor Quality Sleep, Injection Site Erythema, Eye Rolling, Multiple Sclerosis, Crying
Suspect drug(s):
Betaseron
Dosage: 2 miu, every 2d
Indication: Relapsing-Remitting Multiple Sclerosis
Start date: 2007-08-21
End date: 2007-09-01
Betaseron
Dosage: 4 miu, every 2d
Start date: 2007-09-01
Provigil
Indication: Fatigue
Adverse event in 15 year old male receiving Provigil (Modafinil)
Reported by a physician from United States on 2007-05-31
Patient: 15 year old male
Adverse reactions / side effects: Agitation, Oral Intake Reduced, Pruritus, Blood Creatine Abnormal, Blood Urea Abnormal, Coagulopathy, Urticaria, Headache, Pyrexia, Oedema Peripheral, Acute Respiratory Distress Syndrome, Pulmonary Oedema, Cough, White Blood Cell Count Increased, Cardiac Murmur, Hypotension, Drug Rash With Eosinophilia and Systemic Symptoms, Antinuclear Antibody Positive, Pancreatitis, Neutropenia, Dermatitis Exfoliative, Petechiae, Hepatitis, Myalgia, Capillary Leak Syndrome, Weight Increased, Fatigue, Vomiting, Swelling Face, Drug Hypersensitivity, Rhinorrhoea, Heart Rate Increased, Bradycardia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Provigil
Dosage: 100 mg qd oral
Administration route: Oral
Indication: Anxiety
Start date: 2006-04-13
End date: 2006-04-16
Provigil
Dosage: 100 mg qd oral
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Start date: 2006-04-13
End date: 2006-04-16
Provigil
Dosage: 200 mg qd oral
Administration route: Oral
Indication: Anxiety
Start date: 2006-04-17
End date: 2006-04-21
Provigil
Dosage: 200 mg qd oral
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Start date: 2006-04-17
End date: 2006-04-21
Provigil
Dosage: 300 mg qd oral
Administration route: Oral
Indication: Anxiety
Start date: 2006-04-22
End date: 2006-05-01
Provigil
Dosage: 300 mg qd oral
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Start date: 2006-04-22
End date: 2006-05-01
Provigil
Dosage: 400 mg qd oral
Administration route: Oral
Indication: Anxiety
Start date: 2006-05-02
End date: 2006-05-22
Provigil
Dosage: 400 mg qd oral
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Start date: 2006-05-02
End date: 2006-05-22
Other drugs received by patient: Zyprexa; Luvox; Abilify
Adverse event in 56 year old female receiving Provigil (Modafinil)
Reported by a individual with unspecified qualification from United States on 2007-05-30
Patient: 56 year old female
Adverse reactions / side effects: Speech Disorder, Vomiting, Dizziness, Vertigo, Hypertension
Adverse event resulted in: hospitalization
Suspect drug(s):
Provigil
End date: 2007-04-01
Rebif
Dosage: 44 mcg, 3 in 1 weeks, subcutaneous
Indication: Multiple Sclerosis
Start date: 2006-12-11
Other drugs received by patient: Steroids (Corticosteroid Nos); Prednisone; Accupril
Adverse event in 56 year old female receiving Provigil (Modafinil)
Reported by a individual with unspecified qualification from United States on 2007-04-17
Patient: 56 year old female
Adverse reactions / side effects: Speech Disorder, Vomiting, Vertigo, Hypertension
Adverse event resulted in: hospitalization
Suspect drug(s):
Provigil
Start date: 2004-01-01
End date: 2007-01-01
Rebif
Dosage: 44 mcg, 3 in 1 weeks, subcutaneous
Indication: Multiple Sclerosis
Start date: 2006-12-11
Other drugs received by patient: Steroids (Corticosteroid Nos); Prednisone; Accupril
Adverse event in 15 year old male receiving Provigil (Modafinil)
Reported by a physician from United States on 2007-04-04
Patient: 15 year old male
Adverse reactions / side effects: Agitation, Pruritus, Coagulopathy, Petechiae, Headache, Pyrexia, Hepatitis, Sinus Bradycardia, Capillary Leak Syndrome, Myalgia, Weight Increased, Activated Partial Thromboplastin Time Prolonged, Fatigue, Liver Function Test Abnormal, Measles, Tachypnoea, Pulmonary Oedema, Acute Respiratory Distress Syndrome, Cough, Acute Prerenal Failure, White Blood Cell Count Increased, Vomiting, Swelling Face, Cardiac Murmur, International Normalised Ratio Increased, Hypotension, Rhinorrhoea, Blood Fibrinogen Increased, Drug Rash With Eosinophilia and Systemic Symptoms, Lung Disorder, Heart Rate Increased, Pancreatitis, Feeding Disorder, Feeling Abnormal
Adverse event resulted in: hospitalization
Suspect drug(s):
Provigil
Dosage: 100 mg qd oral
Administration route: Oral
Indication: Anxiety
Start date: 2006-04-13
End date: 2006-04-16
Provigil
Dosage: 100 mg qd oral
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Start date: 2006-04-13
End date: 2006-04-16
Provigil
Dosage: 200 mg qd oral
Administration route: Oral
Indication: Anxiety
Start date: 2006-04-17
End date: 2006-04-21
Provigil
Dosage: 200 mg qd oral
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Start date: 2006-04-17
End date: 2006-04-21
Provigil
Dosage: 300 mg qd oral
Administration route: Oral
Indication: Anxiety
Start date: 2006-04-22
End date: 2006-05-01
Provigil
Dosage: 300 mg qd oral
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Start date: 2006-04-22
End date: 2006-05-01
Provigil
Dosage: 400 mg qd oral
Administration route: Oral
Indication: Anxiety
Start date: 2006-05-02
End date: 2006-05-22
Provigil
Dosage: 400 mg qd oral
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Start date: 2006-05-02
End date: 2006-05-22
Other drugs received by patient: Zyprexa; Luvox; Abilify
Adverse event in 71 year old female receiving Provigil (Modafinil)
Reported by a physician from United States on 2007-04-03
Patient: 71 year old female, weighing 72.7 kg (159.9 pounds)
Adverse reactions / side effects: Vomiting, Malaise, Blood Electrolytes Abnormal, Blood Sodium Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Provigil (Modafinil)
Other drugs received by patient: Lexapro
Adverse event in 54 year old male receiving Provigil (Modafinil)
Reported by a consumer/non-health professional from United States on 2007-03-16
Patient: 54 year old male, weighing 113.6 kg (249.9 pounds)
Adverse reactions / side effects: Vomiting, Pain, Coma, Cardiogenic Shock, Speech Disorder, Renal Failure, Dizziness, Myocardial Infarction, Pain in JAW, Influenza Like Illness
Adverse event resulted in: hospitalization
Suspect drug(s):
Dexedrine
Dosage: 40mg per day
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Start date: 1992-01-01
Provigil
Dosage: 200mg per day
Administration route: Oral
Start date: 2006-10-01
Other drugs received by patient: Cymbalta; Gabapentin
|
