ATOMOXETINE Side Effects

5574770-3 | Agitation, Nightmare, Suicidal Ideation
on Dec 26, 2007 Male patient from UNITED STATES , 32 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with Atomoxetine (View Usage). Patient experienced the following unwanted or unexpected effects: agitation, nightmare, suicidal ideation. Atomoxetine dosage: 80mg Every Day Po. Patient was hospitalized.

5218323-5 | Refusal Of Treatment By Patient, Treatment Noncompliance
Patient was taking Atomoxetine (View Usage). Patient had the following side effects: refusal of treatment by patient, treatment noncompliance on Jan 22, 2007 from UNITED STATES Additional patient health information: Male patient , 44 years of age, weighting 200.0 lb, was diagnosed with attention deficit/hyperactivity disorder and. Atomoxetine dosage: 80mg Qd Oral Was Not Taking Meds At Time Of Incident.

5210455-0 | Treatment Noncompliance
Adverse event was reported on Jan 16, 2007 by a Male patient taking Atomoxetine (View Usage) (Dosage: 80 Mg Qd Oral) was diagnosed with attention deficit/hyperactivity disorder and. Location: UNITED STATES , 44 years of age, weighting 200.0 lb, After Atomoxetine was administered, patient had the following side effects: treatment noncompliance.

5145383-2 | Abnormal Behaviour, Social Avoidant Behaviour, Speech Disorder
on Oct 11, 2006 Male patient from UNITED KINGDOM , 13 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with Atomoxetine (View Usage). Patient experienced the following unwanted or unexpected effects: abnormal behaviour, social avoidant behaviour, speech disorder. Atomoxetine dosage: . Patient was hospitalized.


4975112-4 | Blood Pressure Increased, Tachycardia
on Apr 14, 2006 Male patient from UNITED STATES , 43 years of age, weighting 192.0 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with Atomoxetine (View Usage). Patient had the following side effects: blood pressure increased, tachycardia. Atomoxetine dosage: 40mg Po Qd. During the same period patient was treated with LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), ETODOLAC (View Etodolac Review and Etodolac Label ), GLYBURIDE (View Glyburide Review and Glyburide Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ), QUETIAPINE FUMARATE (View Quetiapine Fumarate Review and Quetiapine Fumarate Label ). Patient was hospitalized.

4673160-5 | Autoimmune Hepatitis, Chronic Hepatitis, Hepatic Fibrosis, Hepatitis Acute
Patient was taking Atomoxetine (View Usage). After Atomoxetine was administered, patient had the following side effects: autoimmune hepatitis, chronic hepatitis, hepatic fibrosis, hepatitis acute on May 24, 2005 from Additional patient health information: Female patient , child 11 years of age, . Atomoxetine dosage: . During the same period patient was treated with MULTIVITAMIN WITH IRON (View Multivitamin With Iron Review and Multivitamin With Iron Label ). Patient was hospitalized.

4598280-5 | Chromaturia
Adverse event was reported on Mar 01, 2005 by a Male patient taking Atomoxetine (View Usage) (Dosage: 60mg Qnoon Oral ; 40mg Qhs Oral) was diagnosed with attention deficit/hyperactivity disorder and. Location: , weighting 170.0 lb, Patient experienced the following unwanted or unexpected effects: chromaturia.