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Rozerem (Ramelteon) - Adverse Event Reports - Other Serious Reactions - Somnolence

 



Index of reports > Cases resulting in other serious reactions (33) > Cases with Somnolence (4)

Below is the selection of adverse event reports related to Rozerem (Ramelteon) that includes cases resulting in other serious reactions where reactions include somnolence.

Adverse event in 67 year old female receiving Rozerem (Ramelteon)

Reported by a physician from United States on 2007-07-26

Patient: 67 year old female, weighing 72.6 kg (159.7 pounds)

Adverse reactions / side effects: Impaired Driving Ability, Pollakiuria, Polyuria, Somnolence, Feeling Abnormal

Suspect drug(s):
Rozerem (Ramelteon)

Other drugs received by patient: Prevacid; Aspirin; Ultram ER (Tramadol Hydrochloride); Folic Acid / B12 / B6 (Vitamin B12 and Folic Acid); Hydrochlorothiazide; Lipitor (Atorastatin Calcium); Lisinopril; Protonix



Adverse event in female receiving Rozerem (Ramelteon)

Reported by a consumer/non-health professional from United States on 2007-06-15

Patient: female

Adverse reactions / side effects: Blood Pressure Decreased, Somnolence, Suicidal Ideation

Suspect drug(s):
Rozerem (Ramelteon)



Adverse event in female receiving Rozerem (Ramelteon)

Reported by a physician from United States on 2007-06-12

Patient: female

Adverse reactions / side effects: Irritability, Road Traffic Accident, Carbon Monoxide Poisoning, Disturbance in Attention, Drug Interaction, Memory Impairment, Morbid Thoughts, Somnolence, Suicidal Ideation

Suspect drug(s):
Rozerem
    Dosage: per oral
    Administration route: Oral

Seroquel



Adverse event in 55 year old female receiving Rozerem (Ramelteon)

Reported by a physician from United States on 2007-03-21

Patient: 55 year old female

Adverse reactions / side effects: Tongue Biting, Vision Blurred, Amnesia, Somnolence, Treatment Noncompliance

Suspect drug(s):
Rozerem
    Dosage: 8 mg, hs, per oral, 16 mg, qhs, per oral
    Administration route: Oral
    Indication: Sleep Disorder
    End date: 2006-08-01

Rozerem
    Dosage: 8 mg, hs, per oral, 16 mg, qhs, per oral
    Administration route: Oral
    Indication: Sleep Disorder
    Start date: 2006-08-01

Other drugs received by patient: Tenormin; Oramorph SR; Mirapex; Effexor XR

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