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Provigil (Modafinil) - Adverse Event Reports - Death - Cardiac Disorder

 



Index of reports > Cases resulting in death (7) > Cases with Cardiac Disorder (4)

Below is the selection of adverse event reports related to Provigil (Modafinil) that includes cases resulting in death where reactions include cardiac disorder.

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):
Provigil
    Dosage: 6000 mg once oral
    Administration route: Oral
    Start date: 2007-05-19
    End date: 2007-05-19

Adderall 10
    Dosage: 50 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 receiving Provigil (Modafinil)

Reported by a physician from United States on 2007-04-24

Patient:

Adverse reactions / side effects: Cardiac Disorder

Adverse event resulted in: death

Suspect drug(s):
Provigil (Modafinil)



Adverse event in 39 year old female receiving Provigil (Modafinil)

Reported by a physician from United States on 2007-04-11

Patient: 39 year old female, weighing 80.7 kg (177.6 pounds)

Adverse reactions / side effects: Drug Toxicity, Subcutaneous Abscess, Alcoholism, Gastrointestinal Disorder, Cardiac Disorder, Gastroenteritis Viral, Influenza

Adverse event resulted in: death

Suspect drug(s):
Actiq
    End date: 2007-02-08

Provigil
    End date: 2007-02-08

Chloral Hydrate



Adverse event in 39 year old female receiving Provigil (Modafinil)

Reported by a consumer/non-health professional from United States on 2007-02-27

Patient: 39 year old female

Adverse reactions / side effects: Alcohol USE, Gastrointestinal Disorder, Cardiac Disorder, Influenza

Adverse event resulted in: death

Suspect drug(s):
Actiq
    End date: 2007-02-08

Provigil
    End date: 2007-02-08

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