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Index of reports
> Cases resulting in hospitalization (47)
Below is the selection of adverse event reports related to Provigil (Modafinil) that includes cases resulting in hospitalization.
Reports 1 - 25 of 47 Next >>
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 37 year old female receiving Provigil (Modafinil)
Reported by a consumer/non-health professional from United States on 2007-10-29
Patient: 37 year old female, weighing 79.8 kg (175.6 pounds)
Adverse reactions / side effects: Neutrophil Count Increased, Neutrophil Count Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Provigil (Modafinil)
Other drugs received by patient: Zoloft; Prednisone; Procardia; Altace; Oscal; Aspirin
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: Pruritus, Drug Ineffective, Dyskinesia, Oral Discomfort, Hypoaesthesia Oral, Dyspepsia, LIP Exfoliation, Candidiasis, Migraine, Respiratory Rate Increased, Stomatitis, Dysphagia, LIP DRY, Nausea, Paraesthesia Oral, Malnutrition, Anaemia, Muscle Twitching, Tremor, Visual Disturbance, Choking, Impaired Gastric Emptying, Tardive Dyskinesia
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 Carbonate; Prilosec; Enablex; Lipitor; Triamterene; Mirapex; Potassium Chloride; Coumadin
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 62 year old female receiving Provigil (Modafinil)
Reported by a pharmacist from United States on 2007-10-17
Patient: 62 year old female, weighing 88.9 kg (195.6 pounds)
Adverse reactions / side effects: Drug Interaction, Hypertensive Crisis
Adverse event resulted in: hospitalization
Suspect drug(s):
Emsam
Dosage: 6mg daily transdermal
Indication: Depression
Start date: 2007-10-03
End date: 2007-10-12
Provigil
Dosage: 400mg daily po
Administration route: Oral
Indication: Depression
Start date: 2007-09-18
End date: 2007-10-12
Adverse event in 38 year old female receiving Provigil (Modafinil)
Reported by a physician from United States on 2007-10-17
Patient: 38 year old female
Adverse reactions / side effects: Myalgia, Staphylococcal Infection, Skin Bacterial Infection, Nausea, Hyperhidrosis, Residual Urine, Streptococcal Infection, Muscle Spasms
Adverse event resulted in: hospitalization
Suspect drug(s):
Provigil
Dosage: 200 mg qd oral
Administration route: Oral
Indication: Fatigue
Start date: 2006-11-01
End date: 2007-08-01
Provigil
Dosage: 200 mg qd oral
Administration route: Oral
Indication: Multiple Sclerosis
Start date: 2006-11-01
End date: 2007-08-01
Other drugs received by patient: Adderall 10; Copaxone; Lunesta; Xanax; Vitamin E
Adverse event in 38 year old female receiving Provigil (Modafinil)
Reported by a physician from United States on 2007-10-17
Patient: 38 year old female
Adverse reactions / side effects: Pyoderma Gangrenosum, Folliculitis, Pyrexia, Hyperhidrosis, Treatment Noncompliance, Myalgia, Skin Lesion, Blister, Muscle Spasms, Staphylococcal Skin Infection, Nausea, Rash, Residual Urine, Streptococcal Infection, Rash Erythematous, Purulence, Pollakiuria
Adverse event resulted in: hospitalization
Suspect drug(s):
Provigil
Dosage: 200 mg qd oral
Administration route: Oral
Indication: Fatigue
Start date: 2006-11-01
End date: 2007-08-01
Provigil
Dosage: 200 mg qd oral
Administration route: Oral
Indication: Multiple Sclerosis
Start date: 2006-11-01
End date: 2007-08-01
Other drugs received by patient: Adderall 10; Copaxone; Lunesta; Xanax; Vitamin E
Adverse event in 37 year old female receiving Provigil (Modafinil)
Reported by a pharmacist from United States on 2007-10-12
Patient: 37 year old female, weighing 76.2 kg (167.6 pounds)
Adverse reactions / side effects: Agranulocytosis, Hypomagnesaemia, Febrile Neutropenia, Neutropenia, Thrombocytopenia, Normochromic Normocytic Anaemia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Provigil (Modafinil)
Other drugs received by patient: Prednisone; Procardia; Zoloft; Altace; CAL with Vitd; Aspirin
Adverse event in 69 year old female receiving Provigil (Modafinil)
Reported by a physician from United States on 2007-10-09
Patient: 69 year old female
Adverse reactions / side effects: Confusional State, Head Injury, Headache, Amnesia, Joint Injury, Loss of Consciousness, Cerebral Haemorrhage, Subdural Haematoma, Multiple Injuries, Dizziness, Feeling Abnormal
Adverse event resulted in: hospitalization
Suspect drug(s):
Provigil (Modafinil)
Other drugs received by patient: Cymbalta; Diovan; Actonel; Prempro; Darvocet
Adverse event in female receiving Provigil (Modafinil)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-04
Patient: female
Adverse reactions / side effects: Adverse Event
Adverse event resulted in: hospitalization
Suspect drug(s):
Provigil (Modafinil)
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 38 year old female receiving Provigil (Modafinil)
Reported by a physician from United States on 2007-10-01
Patient: 38 year old female, weighing 54.0 kg (118.8 pounds)
Adverse reactions / side effects: Drug Effect Decreased, Chest Discomfort, Blood Magnesium Decreased, Drug Exposure Before Pregnancy, Fall, Loss of Consciousness, Convulsion, Syncope, Heart Rate Decreased, Blood Potassium Decreased, Cataplexy, Asthenia, Pregnancy
Adverse event resulted in: hospitalization
Suspect drug(s):
Provigil
Dosage: 200 mg bid oral
Administration route: Oral
Indication: Narcolepsy
Start date: 2005-09-01
End date: 2006-02-01
Provigil
Dosage: 200 mg in am and 200mg/300 mg in pm oral
Administration route: Oral
Indication: Narcolepsy
Start date: 2006-10-01
End date: 2007-07-10
Provigil
Dosage: 300 mg bid oral
Administration route: Oral
Indication: Narcolepsy
Start date: 2007-07-19
Xyrem
Dosage: 2.25 g twice a day in evening hours
Xyrem
Dosage: 2.25 g twice a day in evening hours
Start date: 2007-07-19
Adverse event in 38 year old female receiving Provigil (Modafinil)
Reported by a consumer/non-health professional from United States on 2007-07-30
Patient: 38 year old female, weighing 54.9 kg (120.7 pounds)
Adverse reactions / side effects: Drug Effect Decreased, Syncope, Blood Potassium Decreased, Blood Magnesium Decreased, Feeling Abnormal, Convulsion
Adverse event resulted in: hospitalization
Suspect drug(s):
Provigil
Dosage: 200 mg bid oral
Administration route: Oral
Indication: Narcolepsy
Start date: 2005-09-01
End date: 2006-02-01
Provigil
Dosage: 200 mg in am and 200mg/300 mg in pm na oral
Administration route: Oral
Indication: Narcolepsy
Start date: 2006-10-01
End date: 2007-07-10
Adverse event in 22 year old male receiving Provigil (Modafinil)
Reported by a physician from United States on 2007-07-26
Patient: 22 year old male
Adverse reactions / side effects: Pneumonia Aspiration, Rhabdomyolysis, Hepatic Failure, Cardiac Disorder, Resuscitation, Ileus, Acute Respiratory Distress Syndrome, Pneumothorax, Bacterial Infection, Multiple Drug Overdose Intentional, Hypovolaemia, Mechanical Ventilation, Metabolic Acidosis, Encephalopathy, Status Epilepticus, Convulsive Threshold Lowered, Convulsion, Bronchopleural Fistula, Grand MAL Convulsion, Renal Failure, Mechanical Ventilation Complication, Respiratory Failure, Nervous System Disorder, Blood Pressure Decreased, Sinus Tachycardia
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Adderall 10
Dosage: 50 mg once oral
Administration route: Oral
Start date: 2007-05-19
End date: 2007-05-19
Provigil
Dosage: 6000 mg once oral
Administration route: Oral
Start date: 2007-05-19
End date: 2007-05-19
Other drugs received by patient: Zonegran
Adverse event in 57 year old male receiving Provigil (Modafinil)
Reported by a individual with unspecified qualification from United States on 2007-07-25
Patient: 57 year old male
Adverse reactions / side effects: Agitation, Confusional State, Drug Interaction, Memory Impairment, Fall
Adverse event resulted in: hospitalization
Suspect drug(s):
Antibiotics
Cipro
Daptomycin
Keflex
Provigil
Ritalin-SR
Administration route: Oral
Vicodin
Zosyn
Adverse event in 22 year old male receiving Provigil (Modafinil)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-29
Patient: 22 year old male
Adverse reactions / side effects: Rhabdomyolysis, Hepatic Failure, Cardiac Disorder, Aspiration, Pneumothorax, Multiple Drug Overdose Intentional, Acute Respiratory Distress Syndrome, Hypovolaemia, Medical Device Complication, Metabolic Acidosis, Encephalopathy, Status Epilepticus, Convulsive Threshold Lowered, Convulsion, Bronchopleural Fistula, Renal Failure, Lung Disorder, Pneumonia Bacterial, Respiratory Failure, Lung Infiltration, Blood Pressure Decreased, Sinus Tachycardia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Adderall 10
Dosage: 50 mg once oral
Administration route: Oral
Start date: 2007-05-19
End date: 2007-05-19
Provigil
Dosage: 6000 mg once oral
Administration route: Oral
Start date: 2007-05-19
End date: 2007-05-19
Other drugs received by patient: Zonegran
Adverse event in 17 year old female receiving Provigil (Modafinil)
Reported by a physician from United States on 2007-06-11
Patient: 17 year old female, weighing 54.4 kg (119.7 pounds)
Adverse reactions / side effects: Headache, Facial Pain, Streptococcal Infection, White Blood Cells Urine Positive, Dysuria, RED Blood Cells Urine Positive, Rash Maculo-Papular, Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Lamictal
Dosage: 150 mg qd oral
Administration route: Oral
Indication: Bipolar Disorder
Start date: 2005-10-18
Lamictal
Dosage: 300 mg bid oral
Administration route: Oral
Indication: Bipolar Disorder
Start date: 2005-11-30
End date: 2005-12-03
Provigil
Dosage: 300 mg qam oral
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Start date: 2005-10-18
End date: 2005-12-02
Provigil
Dosage: 100 mg qd oral
Administration route: Oral
Indication: Attention Deficit / Hyperactivity Disorder
Start date: 2006-01-13
End date: 2006-01-13
Other drugs received by patient: Abilify. Mfr: Otusaka Pharmaceutical Co., Ltd.; Spironolactone
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 female receiving Provigil (Modafinil)
Reported by a consumer/non-health professional from United States on 2007-05-25
Patient: female
Adverse reactions / side effects: Weight Decreased, Blood Potassium Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Provigil
Indication: Narcolepsy
Topamax
Indication: Drug Therapy
Other drugs received by patient: Synthroid; Lipitor; Relpax; Klor-CON; Magoxide; Multi-Vitamin
Adverse event in 32 year old female receiving Provigil (Modafinil)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-17
Patient: 32 year old female
Adverse reactions / side effects: Tachycardia, Restless Legs Syndrome, Serotonin Syndrome, Hallucination, Hyperhidrosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Anticonvulsant
Indication: Drug USE FOR Unknown Indication
Benzo
Indication: Drug USE FOR Unknown Indication
Duloxetine
Indication: Drug USE FOR Unknown Indication
Gastrointestinal Preparation
Indication: Drug USE FOR Unknown Indication
Levorphanol Tartrate
Indication: Drug USE FOR Unknown Indication
Muscle Relaxant
Indication: Drug USE FOR Unknown Indication
Provigil
Indication: Drug USE FOR Unknown Indication
Ssri
Indication: Drug USE FOR Unknown Indication
Tramadol ER
Indication: Drug USE FOR Unknown Indication
Adverse event in 59 year old male receiving Provigil (Modafinil)
Reported by a physician from United States on 2007-05-02
Patient: 59 year old male
Adverse reactions / side effects: Drug Dose Omission, Drug Interaction, Inadequate Analgesia, Drug Withdrawal Syndrome, Treatment Noncompliance, Delirium
Adverse event resulted in: hospitalization
Suspect drug(s):
Methadone HCL
Dosage: 20 mg tid oral
Administration route: Oral
Indication: Back Pain
Start date: 2007-01-01
Methadone HCL
Dosage: 30 mg tid oral
Administration route: Oral
Indication: Back Pain
Start date: 2007-01-19
Provigil
Dosage: 200 mg qhs oral
Administration route: Oral
Indication: Sleep Apnoea Syndrome
Start date: 2006-12-01
End date: 2007-01-01
Other drugs received by patient: Cymbalta; Cyanocobalamin; Klonopin; Remeron; Promethazine; Mucinex; Lipitor; Coreg; Androgel; Nitroglycerin; Lasix
Adverse event in 53 year old male receiving Provigil (Modafinil)
Reported by a physician from United States on 2007-04-30
Patient: 53 year old male
Adverse reactions / side effects: Blood Glucose Decreased, Convulsion
Adverse event resulted in: hospitalization
Suspect drug(s):
Aminopyridine
Indication: Gait Disturbance
Start date: 2006-12-01
End date: 2007-02-02
Provigil
Indication: Fatigue
Start date: 2007-01-19
End date: 2007-02-02
Rebif
Dosage: 44 ug three times weekly subcutaneous
Indication: Multiple Sclerosis
Start date: 2005-06-16
Other drugs received by patient: Ibuprofen; Fluoxetine; Aspirin; Clonazepam; Lipitor
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 58 year old male receiving Provigil (Modafinil)
Reported by a consumer/non-health professional from United States on 2007-04-09
Patient: 58 year old male, weighing 72.6 kg (159.7 pounds)
Adverse reactions / side effects: Drug Ineffective, Tonic Clonic Movements, Drug Interaction, Drug Withdrawal Syndrome, Disorientation, Muscle Rigidity, Mental Disorder, Hypervigilance, Drug Level Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Methadone HCL
Dosage: 30 mg, tid, oral
Administration route: Oral
Indication: Back Pain
Start date: 2007-01-01
End date: 2007-01-22
Methadone HCL
Dosage: 30 mg, tid, oral
Administration route: Oral
Indication: Pain
Start date: 2006-01-01
End date: 2007-01-01
Provigil
Dosage: 200 mg, qd at bedtime, oral
Administration route: Oral
Indication: Sleep Apnoea Syndrome
Start date: 2006-12-01
End date: 2007-01-22
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