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Rozerem (Ramelteon) - Adverse Event Reports - Hospitalization - Suicidal Ideation

 



Index of reports > Cases resulting in hospitalization (20) > Cases with Suicidal Ideation (2)

Below is the selection of adverse event reports related to Rozerem (Ramelteon) that includes cases resulting in hospitalization where reactions include suicidal ideation.

Adverse event in 48 year old female receiving Rozerem (Ramelteon)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-02

Patient: 48 year old female, weighing 77.1 kg (169.6 pounds)

Adverse reactions / side effects: Economic Problem, Drug Ineffective, Drug Screen Positive, Family Stress, Hallucination, Auditory, General Physical Health Deterioration, Condition Aggravated, Laceration, Intentional Self-Injury, Suicidal Ideation, Anger, Depression

Adverse event resulted in: hospitalization

Suspect drug(s):
Rozerem
    Dosage: 8 mg, 1 in 1 d, per oral
    Administration route: Oral
    Indication: Affective Disorder
    Start date: 2006-09-29
    End date: 2006-11-29

Rozerem
    Dosage: 8 mg, 1 in 1 d, per oral
    Administration route: Oral
    Indication: Insomnia
    Start date: 2006-09-29
    End date: 2006-11-29

Rozerem
    Dosage: 8 mg, 1 in 1 d, per oral
    Administration route: Oral
    Indication: Seasonal Affective Disorder
    Start date: 2006-09-29
    End date: 2006-11-29

Other drugs received by patient: Lamictal; Wellbutrin; Effexor XR; Klonopin



Adverse event in 48 year old female receiving Rozerem (Ramelteon)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-01-26

Patient: 48 year old female, weighing 77.1 kg (169.6 pounds)

Adverse reactions / side effects: Economic Problem, Drug Screen Positive, Hallucination, Auditory, Self Injurious Behaviour, Suicidal Ideation, Cardiac Disorder, Skin Laceration, Anger, Depression

Adverse event resulted in: hospitalization

Suspect drug(s):
Rozerem
    Dosage: 8 mg, 1 in 1 d, per oral
    Administration route: Oral
    Indication: Affective Disorder
    Start date: 2006-09-29
    End date: 2006-11-29

Rozerem
    Dosage: 8 mg, 1 in 1 d, per oral
    Administration route: Oral
    Indication: Insomnia
    Start date: 2006-09-29
    End date: 2006-11-29

Rozerem
    Dosage: 8 mg, 1 in 1 d, per oral
    Administration route: Oral
    Indication: Seasonal Affective Disorder
    Start date: 2006-09-29
    End date: 2006-11-29

Other drugs received by patient: Lamictal; Wellbutrin; Effexor XR; Klonopin

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