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Provigil (Modafinil) - Adverse Event Reports - Hospitalization - Drug Ineffective

 



Index of reports > Cases resulting in hospitalization (47) > Cases with Drug Ineffective (7)

Below is the selection of adverse event reports related to Provigil (Modafinil) that includes cases resulting in hospitalization where reactions include drug ineffective.

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 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 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



Adverse event in male receiving Provigil (Modafinil)

Reported by a lawyer from United States on 2007-03-23

Patient: male

Adverse reactions / side effects: Anoxic Encephalopathy, Drug Ineffective, Intentional Overdose, Hypotension, Pain, Coma, Anxiety, Completed Suicide, Narcotic Intoxication, Respiratory Arrest, Suicide Attempt, Depression, Cardiac Arrest

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Dextrothyroxine

Neurontin
    Administration route: Oral
    Indication: Neuralgia

Oxycontin
    Administration route: Oral
    Indication: Pain

Provigil

Other drugs received by patient: Keppra; Mirtazapine; Elavil; Gabitril; Nsaid's; Zanaflex; Cymbalta; Duragesic-100; Morphine



Adverse event in male receiving Provigil (Modafinil)

Reported by a consumer/non-health professional from United States on 2007-03-08

Patient: male

Adverse reactions / side effects: Drug Ineffective, Intentional Overdose, Pain, Coma, Completed Suicide, Narcotic Intoxication, Pupil Fixed, Depression, Anoxic Encephalopathy, Pain in Extremity, Hypotension, Inadequate Analgesia, Anxiety, NO Therapeutic Response, Suicide Attempt, Respiratory Arrest, Cardiac Arrest, Cardiovascular Disorder

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Dextrothyroxine

Neurontin
    Administration route: Oral
    Indication: Neuralgia

Oxycontin
    Administration route: Oral
    Indication: Pain

Provigil

Other drugs received by patient: Keppra; Mirtazapine



Adverse event in 58 year old male receiving Provigil (Modafinil)

Reported by a consumer/non-health professional from United States on 2007-03-06

Patient: 58 year old male, weighing 72.6 kg (159.7 pounds)

Adverse reactions / side effects: Drug Ineffective, Drug Interaction, Tonic Clonic Movements, Drug Withdrawal Syndrome, 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

Provigil
    Dosage: qd,oral
    Administration route: Oral
    Indication: Sleep Apnoea Syndrome
    Start date: 2006-12-01
    End date: 2007-01-22

Other drugs received by patient: Methadone HCL



Adverse event in 58 year old male receiving Provigil (Modafinil)

Reported by a consumer/non-health professional from United States on 2007-03-06

Patient: 58 year old male, weighing 72.6 kg (159.7 pounds)

Adverse reactions / side effects: Drug Ineffective, Drug Interaction, Tonic Clonic Movements, Drug Withdrawal Syndrome

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

Provigil
    Dosage: qd, oral
    Administration route: Oral
    Indication: Sleep Apnoea Syndrome
    Start date: 2006-12-01
    End date: 2007-01-22

Other drugs received by patient: Methadose

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