DrugLib.com — Drug Information Portal

Rx drug information, pharmaceutical research, clinical trials, news, and more

Strattera (Atomoxetine) - Reports of Side Effects & Adverse Reactions

 



This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Strattera (Atomoxetine). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.

Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.

All cases (425)
     Suicidal Ideation (37)Aggression (31)Loss of Consciousness (27)more >>

Cases resulting in a serious event (410)
     Suicidal Ideation (37)Aggression (31)Loss of Consciousness (27)more >>

Cases resulting in death (21)
     Completed Suicide (8)Drug Toxicity (3)Gallbladder Disorder (3)more >>

Cases resulting in life threatening events (20)
     Suicidal Ideation (7)Suicide Attempt (5)Abnormal Behaviour (3)more >>

Cases resulting in hospitalization (134)
     Suicide Attempt (17)Intentional Overdose (11)Suicidal Ideation (11)more >>

Cases resulting in disability (12)
     Hemiplegia (4)TIC (3)Optic Nerve Disorder (2)more >>

Cases resulting in other serious reactions (283)
     Suicidal Ideation (27)Aggression (25)Loss of Consciousness (25)more >>

Below is a sample of reports where side effects / adverse reactions may be related to Strattera (Atomoxetine). For a complete list and/or a specific selection of reports, please use the links in the index above.

Adverse event in male receiving Strattera (Atomoxetine)

Reported by a health professional (non-physician/pharmacist) from Netherlands on 2007-10-31

Patient: male, weighing 52.0 kg (114.4 pounds)

Adverse reactions / side effects: Drug Toxicity, Mydriasis, Intentional Overdose, Heart Rate Increased, Loss of Consciousness

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Strattera
    Dosage: 180mg in the morning
    Indication: Attention Deficit / Hyperactivity Disorder
    Start date: 2007-01-17

Strattera
    Dosage: 5 d/f, 300mg
    Start date: 2007-01-17

Strattera
    Dosage: 20 d/f, 1200mg
    Start date: 2007-01-17



Adverse event in 12 year old male receiving Strattera (Atomoxetine)

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

Patient: 12 year old male, weighing 63.5 kg (139.7 pounds)

Adverse reactions / side effects: Anxiety, Autism Spectrum Disorder, Obsessive-Compulsive Disorder, Paranoia, Delusion

Adverse event resulted in: hospitalization

Suspect drug(s):
Strattera
    Dosage: 58 mg, unk
    Indication: Attention Deficit / Hyperactivity Disorder

Strattera
    Dosage: 40 mg, unk

Strattera
    Dosage: 60 mg, unk



Adverse event in 12 year old male receiving Strattera (Atomoxetine)

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

Patient: 12 year old male

Adverse reactions / side effects: Homicidal Ideation

Suspect drug(s):
Strattera (Atomoxetine)



Adverse event in 23 year old female receiving Strattera (Atomoxetine)

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

Patient: 23 year old female

Adverse reactions / side effects: Overdose, Suicide Attempt, Fall, Loss of Consciousness, Aggression

Adverse event resulted in: hospitalization

Suspect drug(s):
Strattera (Atomoxetine)

Other drugs received by patient: Klonopin; Topamax



Adverse event in 11 year old female receiving Strattera (Atomoxetine)

Reported by a physician from United States on 2007-10-30

Patient: 11 year old female, weighing 31.8 kg (70.0 pounds)

Adverse reactions / side effects: Spleen Palpable, Weight Decreased, Autoimmune Hepatitis, Prothrombin Time Prolonged, Pyrexia, Blood Immunoglobulin G Increased, Fatigue, Liver Palpable Subcostal, Diarrhoea, Arthralgia

Suspect drug(s):
Strattera
    Dosage: 30 mg, daily (1/d)
    Administration route: Oral
    Indication: Attention Deficit / Hyperactivity Disorder
    Start date: 2004-06-15

Strattera
    Dosage: 10 mg, daily (1/d)
    Administration route: Oral

Strattera
    Dosage: 20 mg, daily (1/d)
    Administration route: Oral

Strattera
    Dosage: 30 mg, daily (1/d)
    Administration route: Oral



Adverse event in 7 year old male receiving Strattera (Atomoxetine)

Reported by a consumer/non-health professional from United States on 2007-10-30

Patient: 7 year old male, weighing 31.8 kg (69.9 pounds)

Adverse reactions / side effects: Overweight, Enuresis, Gynaecomastia

Suspect drug(s):
Strattera
    Dosage: 60mg 2 times per day
    Indication: Attention Deficit / Hyperactivity Disorder
    Start date: 2002-02-22
    End date: 2002-04-26

Strattera
    Dosage: 40mg 2 times per day



Adverse event in 12 year old female receiving Strattera (Atomoxetine)

Reported by a physician from United States on 2007-10-30

Patient: 12 year old female, weighing 40.2 kg (88.4 pounds)

Adverse reactions / side effects: Weight Decreased, Liver Injury, Abdominal Pain, Jaundice, Vomiting, Hepatitis Acute, Diarrhoea

Adverse event resulted in: hospitalization

Suspect drug(s):
Strattera (Atomoxetine)



Adverse event in male receiving Strattera (Atomoxetine)

Reported by a physician from United States on 2007-10-29

Patient: male

Adverse reactions / side effects: Blood Bilirubin Increased

Suspect drug(s):
Strattera (Atomoxetine)



Adverse event in female receiving Strattera (Atomoxetine)

Reported by a physician from Germany on 2007-10-26

Patient: female, weighing 100.0 kg (220.0 pounds)

Adverse reactions / side effects: Alanine Aminotransferase Increased

Suspect drug(s):
Strattera
    Dosage: 10 mg, daily (1/d)
    Administration route: Oral
    Indication: Attention Deficit / Hyperactivity Disorder
    Start date: 2007-07-24
    End date: 2007-08-21

Strattera
    Dosage: 18 mg, daily (1/d)
    Administration route: Oral
    Start date: 2007-07-31
    End date: 2007-08-21

Strattera
    Dosage: 25 mg, daily (1/d)
    Administration route: Oral
    Start date: 2007-08-08
    End date: 2007-08-21

Strattera
    Dosage: 40 mg, daily (1/d)
    Start date: 2007-08-14
    End date: 2007-08-21

Strattera
    Dosage: 60 mg, daily (1/d)
    Administration route: Oral
    Start date: 2007-08-18
    End date: 2007-08-21



Adverse event in female receiving Strattera (Atomoxetine)

Reported by a consumer/non-health professional from United States on 2007-10-26

Patient: female

Adverse reactions / side effects: Palpitations, Supraventricular Tachycardia

Suspect drug(s):
Strattera (Atomoxetine)



Adverse event in female receiving Strattera (Atomoxetine)

Reported by a physician from Norway on 2007-10-26

Patient: female

Adverse reactions / side effects: Electrocardiogram QT Prolonged, Heart Rate Increased, Dizziness, Heart Rate Irregular

Suspect drug(s):
Strattera (Atomoxetine)



Adverse event in 14 year old female receiving Strattera (Atomoxetine)

Reported by a consumer/non-health professional from United States on 2007-10-24

Patient: 14 year old female, weighing 48.5 kg (106.8 pounds)

Adverse reactions / side effects: Catecholamines Urine, Overdose, Metanephrine Urine Increased

Suspect drug(s):
Strattera
    Dosage: 80 mg, unk
    Indication: Attention Deficit / Hyperactivity Disorder
    Start date: 2002-01-01

Strattera
    Dosage: 100 mg, unk
    Start date: 2007-01-01



Adverse event in 11 year old female receiving Strattera (Atomoxetine)

Reported by a physician from United States on 2007-10-24

Patient: 11 year old female, weighing 31.8 kg (70.0 pounds)

Adverse reactions / side effects: Liver Injury, Spleen Palpable, Weight Decreased, Autoimmune Hepatitis, Hepatic Fibrosis, Coagulopathy, Condition Aggravated, Pyrexia, Blood Immunoglobulin G Increased, Liver Palpable Subcostal, Arthralgia

Suspect drug(s):
Strattera
    Dosage: see image
    Administration route: Oral
    Indication: Attention Deficit / Hyperactivity Disorder
    Start date: 2004-06-15
    End date: 2004-09-30

Strattera
    Dosage: see image
    Administration route: Oral
    Indication: Attention Deficit / Hyperactivity Disorder

Strattera
    Dosage: see image
    Administration route: Oral
    Indication: Attention Deficit / Hyperactivity Disorder

Strattera
    Dosage: see image
    Administration route: Oral
    Indication: Attention Deficit / Hyperactivity Disorder



Adverse event in female receiving Strattera (Atomoxetine)

Reported by a physician from United States on 2007-10-23

Patient: female

Adverse reactions / side effects: Emotional Distress, Road Traffic Accident, Gallbladder Disorder, Hypertension, Appendicitis Perforated, Liver Disorder

Adverse event resulted in: hospitalization

Suspect drug(s):
Strattera
    Dosage: 25 mg, unk
    Indication: Attention Deficit / Hyperactivity Disorder
    Start date: 2002-01-01

Strattera
    Dosage: 40 mg, daily (1/d)
    Start date: 2005-01-01

Strattera
    Start date: 2007-10-01



Adverse event in female receiving Strattera (Atomoxetine)

Reported by a physician from Germany on 2007-10-23

Patient: female

Adverse reactions / side effects: Electrocardiogram QT Prolonged, Fall, Loss of Consciousness

Suspect drug(s):
Strattera
    Dosage: 50 mg, each morning
    Administration route: Oral
    Indication: Attention Deficit / Hyperactivity Disorder
    Start date: 2007-05-14

Strattera
    Dosage: 25 mg, each morning
    Administration route: Oral



Adverse event in 12 year old receiving Strattera (Atomoxetine)

Reported by a physician from United States on 2007-10-23

Patient: 12 year old

Adverse reactions / side effects: Death

Adverse event resulted in: death

Suspect drug(s):
Strattera (Atomoxetine)



Adverse event in 9 year old male receiving Strattera (Atomoxetine)

Reported by a consumer/non-health professional from United States on 2007-10-23

Patient: 9 year old male

Adverse reactions / side effects: Panic Attack, Anorexia, Anger, Homicidal Ideation, Mood Swings, Logorrhoea, Aggression

Suspect drug(s):
Strattera (Atomoxetine)



Adverse event in male receiving Strattera (Atomoxetine)

Reported by a physician from United States on 2007-10-23

Patient: male

Adverse reactions / side effects: Pain in Extremity, Nausea, Abasia, Headache, Pyrexia, Chest Pain, Circulatory Collapse, Vertigo, Hallucination

Suspect drug(s):
Strattera (Atomoxetine)

Other drugs received by patient: Nasonex; Claritin



Adverse event in male receiving Strattera (Atomoxetine)

Reported by a physician from Czech Republic on 2007-10-23

Patient: male

Adverse reactions / side effects: Palpitations, Tachycardia, Headache, Lacrimation Increased, Amnesia, Convulsion

Adverse event resulted in: hospitalization

Suspect drug(s):
Strattera
    Dosage: 10 mg, daily (1/d)
    Administration route: Oral
    Indication: Attention Deficit / Hyperactivity Disorder
    Start date: 2007-09-24
    End date: 2007-10-07

Strattera
    Dosage: 18 mg, daily (1/d)
    Administration route: Oral
    Start date: 2007-10-01
    End date: 2007-10-07



Adverse event in female receiving Strattera (Atomoxetine)

Reported by a physician from United States on 2007-10-23

Patient: female

Adverse reactions / side effects: Homicidal Ideation, Suicidal Ideation

Adverse event resulted in: hospitalization

Suspect drug(s):
Strattera (Atomoxetine)



Adverse event in 30 year old female receiving Strattera (Atomoxetine)

Reported by a physician from United States on 2007-10-23

Patient: 30 year old female

Adverse reactions / side effects: Vomiting, Loss of Consciousness

Suspect drug(s):
Strattera (Atomoxetine)



Adverse event in female receiving Strattera (Atomoxetine)

Reported by a physician from Australia on 2007-10-23

Patient: female

Adverse reactions / side effects: Weight Decreased, Abdominal Pain, Urinary Incontinence, Pain, Headache, Strabismus, Educational Problem, Dizziness, Intracranial Pressure Increased, Maculopathy, Visual Acuity Tests Abnormal, Vomiting, Nausea, Motor Dysfunction, Abnormal Behaviour, Faecal Incontinence, Visual Disturbance, Anorexia, Insomnia

Suspect drug(s):
Strattera
    Dosage: 10 mg, daily (1/d)
    Indication: Attention Deficit / Hyperactivity Disorder
    Start date: 2006-01-01

Strattera
    Dosage: 40 mg, daily (1/d)
    Start date: 2006-09-01

Strattera
    Dosage: 25 mg, daily (1/d)
    Start date: 2007-09-01

Other drugs received by patient: Serenace; Serenace



Adverse event in 15 year old male receiving Strattera (Atomoxetine)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-23

Patient: 15 year old male, weighing 65.6 kg (144.3 pounds)

Adverse reactions / side effects: Tachycardia, Arrhythmia, Tremor

Suspect drug(s):
Strattera
    Dosage: 60 mg, unknown
    Administration route: Oral
    End date: 2007-08-01

Strattera
    Dosage: 40 mg, unknown
    End date: 2007-08-01

Other drugs received by patient: Sertraline



Adverse event in 16 year old female receiving Strattera (Atomoxetine)

Reported by a physician from Norway on 2007-10-23

Patient: 16 year old female

Adverse reactions / side effects: Consciousness Fluctuating, Drug Level Increased, Intentional Overdose, Dyskinesia, Heart Rate Increased, Dizziness, Hypertension, Tremor

Suspect drug(s):
Strattera (Atomoxetine)

Other drugs received by patient: Concerta; Ritalin



Adverse event in 14 year old male receiving Strattera (Atomoxetine)

Reported by a physician from United Kingdom on 2007-10-19

Patient: 14 year old male, weighing 37.4 kg (82.3 pounds)

Adverse reactions / side effects: Palpitations, Tachycardia, Eczema Nummular

Suspect drug(s):
Strattera (Atomoxetine)

-- advertisement -- The American Red Cross
We comply with
HONcode standard.
Verify here.
Home | About Us | Contact Us | Site usage policy | Privacy policy

All Rights reserved - Copyright DrugLib.com, 2006-2009