|
Index of reports
> Cases resulting in disability (6)
> Cases with Pharmaceutical Product Complaint (3)
Below is the selection of adverse event reports related to Ativan (Lorazepam) that includes cases resulting in disability where reactions include pharmaceutical product complaint.
Adverse event in female receiving Ativan (Lorazepam)
Reported by a individual with unspecified qualification from United States on 2007-10-05
Patient: female, weighing 59.9 kg (131.7 pounds)
Adverse reactions / side effects: Pharmaceutical Product Complaint, Drug Dependence
Adverse event resulted in: disablity
Suspect drug(s):
Xanax
Indication: Stress
Start date: 1993-01-01
End date: 2007-01-01
Klonopin
Indication: Anxiety
Start date: 1993-01-01
End date: 2007-01-01
Ativan
Indication: Anxiety
Start date: 1993-01-01
End date: 2007-01-01
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
Lorazepam
Start date: 2007-01-01
End date: 2007-01-01
Extra Strength Tylenol
Dosage: 2 df
Start date: 2007-03-30
Other drugs received by patient: Toprol-XL
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
|
