|
Index of reports
> Cases resulting in other serious reactions (33)
Below is the selection of adverse event reports related to Rozerem (Ramelteon) that includes cases resulting in other serious reactions.
Reports 1 - 25 of 33 Next >>
Adverse event in receiving Rozerem (Ramelteon)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-05
Patient:
Adverse reactions / side effects: Aggression
Suspect drug(s):
Rozerem (Ramelteon)
Adverse event in 54 year old male receiving Rozerem (Ramelteon)
Reported by a physician from United States on 2007-10-02
Patient: 54 year old male, weighing 104.3 kg (229.5 pounds)
Adverse reactions / side effects: Impaired Driving Ability, Legal Problem, Drug Interaction, Imprisonment, Amnesia, Feeling Abnormal
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Cymbalta
Dosage: 30 mg, qhs
Indication: Pain
Hydrocodone Bitartrate
Lortab
Dosage: 10/500, q12-24 hrs
Indication: Pain
Methadone HCL
Dosage: 10 mg, 2 in 1 d, per oral
Administration route: Oral
Rozerem
Dosage: per oral
Administration route: Oral
Indication: Insomnia
Start date: 2007-07-18
End date: 2007-07-24
Other drugs received by patient: Aleve; Omega 3 Fish OIL (Fish Oil); Decadron
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 51 year old male receiving Rozerem (Ramelteon)
Reported by a physician from United States on 2007-07-17
Patient: 51 year old male
Adverse reactions / side effects: Hypokinesia, Fear, Lack of Spontaneous Speech, Catatonia
Suspect drug(s):
Rozerem
Dosage: 8 mg, once, per oral
Administration route: Oral
Indication: Circadian Rhythm Sleep Disorder
Rozerem
Dosage: 8 mg, once, per oral
Administration route: Oral
Indication: Insomnia
Other drugs received by patient: Vitamin (Vitamins)
Adverse event in female receiving Rozerem (Ramelteon)
Reported by a physician from United States on 2007-07-06
Patient: female, weighing 47.6 kg (104.8 pounds)
Adverse reactions / side effects: Blood Corticotrophin Increased, Adrenal Insufficiency, Adrenal Neoplasm
Suspect drug(s):
Rozerem (Ramelteon)
Other drugs received by patient: Antihypertensive (Antihypertensives)
Adverse event in 36 year old female receiving Rozerem (Ramelteon)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-06
Patient: 36 year old female
Adverse reactions / side effects: Drug Eruption, Asthma, Condition Aggravated
Suspect drug(s):
Rozerem (Ramelteon)
Other drugs received by patient: Topamax; Paroxetine
Adverse event in 56 year old female receiving Rozerem (Ramelteon)
Reported by a physician from United States on 2007-06-26
Patient: 56 year old female
Adverse reactions / side effects: Palpitations
Suspect drug(s):
Rozerem (Ramelteon)
Adverse event in male receiving Rozerem (Ramelteon)
Reported by a physician from United States on 2007-06-20
Patient: male
Adverse reactions / side effects: NO Adverse Drug Effect, Drug Dispensing Error
Suspect drug(s):
Razadyne ER
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Rozerem
Indication: Insomnia
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 51 year old male receiving Rozerem (Ramelteon)
Reported by a physician from United States on 2007-05-30
Patient: 51 year old male
Adverse reactions / side effects: Speech Disorder, Movement Disorder, Fear, Catatonia
Suspect drug(s):
Rozerem (Ramelteon)
Other drugs received by patient: Vitamin (Vitamins) (Unknown)
Adverse event in 66 year old female receiving Rozerem (Ramelteon)
Reported by a physician from United States on 2007-05-29
Patient: 66 year old female, weighing 59.0 kg (129.7 pounds)
Adverse reactions / side effects: Drug Ineffective, Insomnia, Axillary Pain, Chest Pain, Heart Rate Irregular
Suspect drug(s):
Rozerem (Ramelteon)
Other drugs received by patient: Tylenol PM (Diphenydramine, Paracetamol); Aleve PM (Naproxen Sodium)
Adverse event in female receiving Rozerem (Ramelteon)
Reported by a physician from United States on 2007-05-24
Patient: female
Adverse reactions / side effects: Convulsion
Suspect drug(s):
Rozerem (Ramelteon)
Other drugs received by patient: Multiple Unknown Medication (All Other NON-Therapeutic Products)
Adverse event in 67 year old male receiving Rozerem (Ramelteon)
Reported by a consumer/non-health professional from United States on 2007-05-22
Patient: 67 year old male
Adverse reactions / side effects: Homicide, Suicide Attempt
Adverse event resulted in: life threatening event
Suspect drug(s):
Ambien
Cymbalta
Indication: Depression
Rozerem
Dosage: per oral
Administration route: Oral
Other drugs received by patient: Lunesta
Adverse event in 50 year old female receiving Rozerem (Ramelteon)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-21
Patient: 50 year old female
Adverse reactions / side effects: Abnormal Behaviour, Sleep Walking
Suspect drug(s):
Rozerem (Ramelteon)
Other drugs received by patient: UNK Medications (All Other Therapeutic Products)
Adverse event in male receiving Rozerem (Ramelteon)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-16
Patient: male
Adverse reactions / side effects: Medication Error, NO Adverse Drug Effect
Suspect drug(s):
Razadyne
Indication: Drug USE FOR Unknown Indication
Rozerem
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Seroquel; Depakote; Zyprexa; Lamictal
Adverse event in receiving Rozerem (Ramelteon)
Reported by a physician from United States on 2007-05-11
Patient:
Adverse reactions / side effects: Feeling Abnormal, Suicidal Ideation
Suspect drug(s):
Rozerem (Ramelteon)
Adverse event in female receiving Rozerem (Ramelteon)
Reported by a physician from United States on 2007-05-09
Patient: female
Adverse reactions / side effects: Blood Corticotrophin Increased, Skin Discolouration
Suspect drug(s):
Rozerem (Ramelteon)
Adverse event in 30 year old female receiving Rozerem (Ramelteon)
Reported by a physician from United States on 2007-05-03
Patient: 30 year old female, weighing 87.5 kg (192.6 pounds)
Adverse reactions / side effects: Completed Suicide
Adverse event resulted in: death
Suspect drug(s):
Rozerem (Ramelteon)
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 female receiving Rozerem (Ramelteon)
Reported by a physician from United States on 2007-05-01
Patient: female
Adverse reactions / side effects: Completed Suicide
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Rozerem
Dosage: per oral
Administration route: Oral
Indication: Anxiety
Start date: 2007-04-01
End date: 2007-04-01
Rozerem
Dosage: per oral
Administration route: Oral
Indication: Divorced
Start date: 2007-04-01
End date: 2007-04-01
Rozerem
Dosage: per oral
Administration route: Oral
Indication: Insomnia
Start date: 2007-04-01
End date: 2007-04-01
Rozerem
Dosage: per oral
Administration route: Oral
Indication: Mental Disorder
Start date: 2007-04-01
End date: 2007-04-01
Rozerem
Dosage: per oral
Administration route: Oral
Indication: Stress
Start date: 2007-04-01
End date: 2007-04-01
Adverse event in female receiving Rozerem (Ramelteon)
Reported by a individual with unspecified qualification from United States on 2007-04-30
Patient: female
Adverse reactions / side effects: Myalgia, Arthralgia, Insomnia, Depression, Headache, Suicidal Ideation
Suspect drug(s):
Rozerem (Ramelteon)
Other drugs received by patient: Unknown Bipolar Medication (All Other Therapeutic Products); Unknown Depression Medications (All Other Therapeutic Products)
Adverse event in female receiving Rozerem (Ramelteon)
Reported by a physician from United States on 2007-04-26
Patient: female
Adverse reactions / side effects: Completed Suicide
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Rozerem
Dosage: per oral
Administration route: Oral
Indication: Anxiety
Start date: 2007-04-01
End date: 2007-04-01
Rozerem
Dosage: per oral
Administration route: Oral
Indication: Insomnia
Start date: 2007-04-01
End date: 2007-04-01
Rozerem
Dosage: per oral
Administration route: Oral
Indication: Stress
Start date: 2007-04-01
End date: 2007-04-01
Adverse event in 76 year old female receiving Rozerem (Ramelteon)
Reported by a physician from United States on 2007-04-02
Patient: 76 year old female
Adverse reactions / side effects: Cerebral Haemorrhage
Suspect drug(s):
Rozerem (Ramelteon)
Other drugs received by patient: Coumadin
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
Page 1 Next >>
|
