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Ativan (Lorazepam) - Adverse Event Reports - Serious Event - Drug Ineffective

 



Index of reports > Cases resulting in a serious event (65) > Cases with Drug Ineffective (8)

Below is the selection of adverse event reports related to Ativan (Lorazepam) that includes cases resulting in a serious event where reactions include drug ineffective.

Adverse event in male receiving Ativan (Lorazepam)

Reported by a physician from United States on 2007-10-16

Patient: male

Adverse reactions / side effects: Drug Ineffective, Pharmaceutical Product Complaint

Suspect drug(s):
Ativan
    Dosage: 1 tab qhs
    Indication: Myofascial Pain Syndrome
    Start date: 2007-10-11

Ativan
    Dosage: 1 tab qhs
    Indication: Temporomandibular Joint Syndrome
    Start date: 2007-10-11



Adverse event in 48 year old female receiving Ativan (Lorazepam)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-10

Patient: 48 year old female

Adverse reactions / side effects: Drug Ineffective, Adverse Drug Reaction, Drug Intolerance, Dizziness, Fall, Brain Neoplasm

Suspect drug(s):
Ativan
    Indication: Drug USE FOR Unknown Indication

Cymbalta
    Indication: Drug USE FOR Unknown Indication

Diazepam
    Indication: Drug USE FOR Unknown Indication

Geodon
    Indication: Drug USE FOR Unknown Indication

Klonopin
    Indication: Drug USE FOR Unknown Indication

Lexapro
    Indication: Drug USE FOR Unknown Indication

Valium
    Indication: Drug USE FOR Unknown Indication
    Start date: 1995-01-01

Xanax
    Indication: Drug USE FOR Unknown Indication

Zoloft
    Indication: Drug USE FOR Unknown Indication

Zonisamide
    Indication: Migraine

Zonisamide
    Dosage: dose adjusted

Other drugs received by patient: Lipitor; Prozac; Unspecified Drug; Lopressor



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 lawyer from United States on 2007-05-18

Patient: female

Adverse reactions / side effects: Drug Ineffective, Respiratory Failure, Unresponsive TO Stimuli, Suicide Attempt, Depression, Multiple Drug Overdose, Alcohol Poisoning

Adverse event resulted in: hospitalization

Suspect drug(s):
Alcohol

Ativan

Cyclobenzaprine HCL
    Indication: Muscle Spasms

Medroxyprogesterone
    Administration route: Oral

Neurontin
    Indication: Bipolar Disorder

Neurontin
    Indication: Pain

Propoxyphene Hydrochloride

Skelaxin



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 physician from United States on 2007-03-06

Patient: female, weighing 62.1 kg (136.6 pounds)

Adverse reactions / side effects: Drug Ineffective, Cognitive Disorder, Drug Withdrawal Syndrome, Heart Valve Insufficiency

Suspect drug(s):
Ativan

Doxepin HCL
    Indication: Sleep Disorder

Doxepin HCL
    Indication: Chronic Fatigue Syndrome

Sinequan
    Administration route: Oral
    Indication: Sleep Disorder
    Start date: 1993-01-01
    End date: 2006-11-01

Sinequan
    Indication: Chronic Fatigue Syndrome

Other drugs received by patient: Nexium; Zyrtec; Nabumetone; Corgard



Adverse event in female receiving Ativan (Lorazepam)

Reported by a lawyer from United States on 2007-02-16

Patient: female

Adverse reactions / side effects: Overdose, Drug Ineffective, Respiratory Failure, Suicide Attempt

Adverse event resulted in: hospitalization

Suspect drug(s):
Alcohol

Ativan

Cyclobenzaprine HCL

Neurontin
    Indication: Bipolar Disorder

Neurontin
    Indication: Pain

Propoxyphene Hydrochloride

Skelaxin



Adverse event in male receiving Ativan (Lorazepam)

Reported by a lawyer from United States on 2007-01-12

Patient: male

Adverse reactions / side effects: Overdose, Drug Ineffective, Suicide Attempt, Intentional Self-Injury

Adverse event resulted in: hospitalization

Suspect drug(s):
Ativan

Neurontin
    Indication: Bipolar Disorder

Other drugs received by patient: Depakote; Depakote; Lithium Carbonate; Paxil; Propranolol; Zarontin; Geodon; Perphenazine

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