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Index of reports
> Cases resulting in life threatening events (7)
Below is the selection of adverse event reports related to Ativan (Lorazepam) that includes cases resulting in life threatening events.
Adverse event in male receiving Ativan (Lorazepam)
Reported by a consumer/non-health professional from United States on 2007-10-17
Patient: male
Adverse reactions / side effects: Personality Change, Psychotic Disorder, Paranoia, Hypothyroidism, Depression, Multiple Sclerosis, Aggression, Suicidal Ideation
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Ativan
Dosage: (2 mg bid oral)
Administration route: Oral
Indication: Anxiety
Start date: 2006-01-01
End date: 2007-06-01
Benzodiazepine (Unspecified)
Dosage: (df oral)
Administration route: Oral
Indication: Anxiety
Start date: 2006-01-01
End date: 2007-06-01
Rebif
Dosage: (44 ug 3x/week subcutaneous)
Indication: Multiple Sclerosis
Start date: 2006-07-01
Xanax
Dosage: (df as needed oral)
Administration route: Oral
Indication: Anxiety
Start date: 2006-01-01
End date: 2007-06-01
Other drugs received by patient: Copaxone; Synthroid; Cholesterol; Omacor; Celebrex; Tramadol HCL; Lyrica; Toprol-XL; Cytomel; Baclofen; Detrol; Ambien; Restoril; Nexium
Adverse event in 35 year old female receiving Ativan (Lorazepam)
Reported by a consumer/non-health professional from United States on 2007-10-04
Patient: 35 year old female
Adverse reactions / side effects: Overdose, Blood Creatine Phosphokinase Increased, Respiratory Depression, Suicidal Ideation
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Ativan
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Cymbalta
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Lamictal
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Adverse event in female receiving Ativan (Lorazepam)
Reported by a consumer/non-health professional from United States on 2007-05-22
Patient: female, weighing 70.3 kg (154.7 pounds)
Adverse reactions / side effects: Hypersensitivity, Pruritus, Drug Ineffective, Impaired Work Ability, Pain, Thirst, Constipation, Hyperhidrosis, Fatigue, DRY Mouth, Hallucination, Muscle Spasms, Chest Discomfort, Dyspnoea, Rash, Drug Withdrawal Syndrome, Panic Attack, Insomnia, Heart Rate Increased, Memory Impairment, Bladder Disorder, Asthenia, Pharmaceutical Product Complaint
Adverse event resulted in: life threatening event, disablity
Suspect drug(s):
Ativan
Dosage: 1 mg tid oral
Administration route: Oral
Indication: Anxiety
Start date: 2007-01-01
End date: 2007-03-18
Ativan
Dosage: 1 mg tid oral
Administration route: Oral
Indication: Anxiety
Extra Strength Tylenol
Dosage: 2 df
Start date: 2007-03-30
Lorazepam
Start date: 2007-01-01
End date: 2007-01-01
Other drugs received by patient: Toprol-XL
Adverse event in female receiving Ativan (Lorazepam)
Reported by a physician from Germany on 2007-05-02
Patient: female
Adverse reactions / side effects: Confusional State, Victim of Crime, Multiple Drug Overdose Intentional, Suicide Attempt, Pupils Unequal
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Ativan
Dosage: 10 mg 1 x oral
Administration route: Oral
Start date: 2007-04-14
End date: 2007-04-14
Ethanol
Dosage: oral
Administration route: Oral
Start date: 2007-04-14
End date: 2007-04-14
Adverse event in 61 year old female receiving Ativan (Lorazepam)
Reported by a consumer/non-health professional from United States on 2007-04-04
Patient: 61 year old female, weighing 70.3 kg (154.7 pounds)
Adverse reactions / side effects: Pruritus, Drug Ineffective, Pain, Thirst, Constipation, Hyperhidrosis, Fatigue, DRY Mouth, Hallucination, Muscle Spasms, Chest Discomfort, Dyspnoea, Drug Hypersensitivity, Rash, Heart Rate Increased, Insomnia, Memory Impairment, Pharmaceutical Product Complaint, Asthenia
Adverse event resulted in: life threatening event, disablity
Suspect drug(s):
Ativan
Dosage: 1 mg tid po
Administration route: Oral
Indication: Anxiety
End date: 2007-03-18
Ativan
Dosage: 1 mg tid po
Administration route: Oral
Indication: Cardiac Disorder
End date: 2007-03-18
Ativan
Dosage: 1 mg tid po
Administration route: Oral
Indication: Anxiety
Ativan
Dosage: 1 mg tid po
Administration route: Oral
Indication: Cardiac Disorder
Other drugs received by patient: Toprol-XL
Adverse event in female receiving Ativan (Lorazepam)
Reported by a consumer/non-health professional from United States on 2007-03-26
Patient: female, weighing 24.9 kg (54.9 pounds)
Adverse reactions / side effects: Agitation, Abnormal Behaviour, Condition Aggravated, Faecal Incontinence, Aggression, Screaming, Gait Disturbance, Crying, Nervousness
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Ativan
Dosage: 4 doses in 5 hrs
Indication: Agitation
Start date: 2007-03-20
End date: 2007-03-21
Ativan
Dosage: 4 doses in 5 hrs
Indication: Anxiety
Start date: 2007-03-20
End date: 2007-03-21
Ativan
Dosage: 4 doses in 5 hrs
Indication: Post-Traumatic Stress Disorder
Start date: 2007-03-20
End date: 2007-03-21
Adverse event in female receiving Ativan (Lorazepam)
Reported by a individual with unspecified qualification from United States on 2007-01-11
Patient: female, weighing 70.3 kg (154.7 pounds)
Adverse reactions / side effects: Emotional Distress
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Ativan
Dosage: .5 mg as needed po
Administration route: Oral
Indication: Anxiety
Start date: 2004-01-04
End date: 2005-12-22
Ativan
Dosage: .5 mg as needed po
Administration route: Oral
Indication: Overdose
Start date: 2004-01-04
End date: 2005-12-22
Ativan
Dosage: .5 mg as needed po
Administration route: Oral
Indication: Panic Reaction
Start date: 2004-01-04
End date: 2005-12-22
Other drugs received by patient: Ativan
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