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Clonazepam (Clonazepam) - Adverse Event Reports - All Cases - Anxiety

 



Index of reports > All cases (238) > Cases with Anxiety (15)

Below is the selection of adverse event reports related to Clonazepam that includes all cases where reactions include anxiety.

Adverse event in 47 year old female receiving Clonazepam

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

Patient: 47 year old female

Adverse reactions / side effects: Anxiety, Condition Aggravated, Pharmaceutical Product Complaint

Suspect drug(s):
Clonazepam



Adverse event in female receiving Clonazepam

Reported by a consumer/non-health professional from Brazil on 2007-07-27

Patient: female, weighing 52.0 kg (114.4 pounds)

Adverse reactions / side effects: Agitation, Abdominal Pain, Weight Decreased, Seborrhoeic Dermatitis, Tachycardia, Headache, Menstrual Disorder, Amenorrhoea, Eyelid Ptosis, Tendonitis, Crying, Breast Pain, Pain in Extremity, Rhinitis, Hypoaesthesia, Stress, Tremor, Galactorrhoea, Irritability, Euphoric Mood, Blood Prolactin Increased, Insomnia, Suicide Attempt, Vaginal Infection, Phobia, Confusional State, Hypersensitivity, Drug Ineffective, Haemorrhage, Pain, Dyskinesia, Constipation, Somnolence, Weight Increased, Neck Pain, Alcoholism, Skin Lesion, Dizziness, Formication, Depression, Sinusitis, Decreased Appetite, Nausea, Abortion, Musculoskeletal Pain, Premenstrual Syndrome, Anxiety, Bipolar Disorder, Grip Strength Decreased, Hypothyroidism, Blood Pressure Decreased, Shock, Influenza Like Illness

Suspect drug(s):
Zoloft
    Administration route: Oral
    Indication: Depression

Zoloft
    Indication: Bipolar Disorder

Zoloft
    Indication: Panic Reaction

Zoloft

Provera
    Administration route: Oral
    Indication: Uterine Haemorrhage

Tinidazole / Tioconazole
    Indication: Vaginitis Bacterial

Clonazepam

Diane
    Dosage: freq:daily
    Administration route: Oral
    Indication: Oral Contraception

Paroxetine
    Administration route: Oral
    Indication: Bipolar Disorder
    Start date: 2004-01-01
    End date: 2006-12-14

Other drugs received by patient: Rivotril; Piroxicam; Rohypnol; L-Lysine; Amplictil; Herbal Preparation; Betagan; ALL Other Therapeutic Products; Midazolam HCL; Multivitamin; Fenergan; Loratadine; Synthroid; Primolut-NOR; Venlafaxiine HCL



Adverse event in 53 year old female receiving Clonazepam

Reported by a consumer/non-health professional from United States on 2007-07-03

Patient: 53 year old female, weighing 58.0 kg (127.7 pounds)

Adverse reactions / side effects: Disorientation, Loss of Consciousness, Overdose, Fatigue, Dizziness, Hypersomnia, Claustrophobia, Dyspnoea, Dental Caries, Abnormal Behaviour, Hypoaesthesia, Stress, Amnesia, Aggression, Convulsion, Dysarthria, Anxiety, Dental Necrosis, Feeling Abnormal

Adverse event resulted in: hospitalization

Suspect drug(s):
Betaseron
    Dosage: 8 miu, every 2d
    Indication: Multiple Sclerosis
    Start date: 2007-04-23

Clonazepam
    Dosage: 2 mg, 4x/day
    Administration route: Oral
    End date: 2007-04-01

Clonazepam
    Dosage: 1 mg, 2x/day
    Administration route: Oral
    Start date: 2007-04-28

Other drugs received by patient: Anxiolytics; Thyroid Preparations; Cardiovascular System Drugs; Antidepressants; Lexapro; Plavix; Ibuprofen; Simvastatin; Levothyroxine Sodium; Kavain; Fosamax



Adverse event in 37 year old male receiving Clonazepam

Reported by a health professional (non-physician/pharmacist) from Canada on 2007-06-15

Patient: 37 year old male

Adverse reactions / side effects: Hypoaesthesia, Serotonin Syndrome, Hyperhidrosis, Tremor, Anxiety, Hot Flush, Palpitations, Hypertension, Panic Reaction

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

Citalopram Hydrobromide
    Indication: Drug USE FOR Unknown Indication

Linezolid
    Dosage: trade name reported as zyvoxam
    Indication: Drug USE FOR Unknown Indication

Trazodone HCL
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient: Hydromorphone HCL; Olanzapine



Adverse event in female receiving Clonazepam

Reported by a consumer/non-health professional from Brazil on 2007-06-11

Patient: female, weighing 52.0 kg (114.4 pounds)

Adverse reactions / side effects: Abdominal Pain, Weight Decreased, Seborrhoeic Dermatitis, Tachycardia, Headache, Menstrual Disorder, Amenorrhoea, Eyelid Ptosis, Tendonitis, Crying, Breast Pain, Pain in Extremity, Rhinitis, Hypoaesthesia, Stress, Tremor, Irritability, Galactorrhoea, Euphoric Mood, Blood Prolactin Increased, Insomnia, Suicide Attempt, Vaginal Infection, Phobia, Confusional State, Hypersensitivity, Haemorrhage, Drug Ineffective, Pain, Dyskinesia, Somnolence, Constipation, Weight Increased, Neck Pain, Alcoholism, Skin Lesion, Dizziness, Formication, Depression, Sinusitis, Decreased Appetite, Nausea, Abortion, Musculoskeletal Pain, Premenstrual Syndrome, Anxiety, Bipolar Disorder, Grip Strength Decreased, Hypothyroidism, Blood Pressure Decreased, Shock, Influenza Like Illness

Suspect drug(s):
Zoloft
    Administration route: Oral
    Indication: Depression

Zoloft
    Indication: Bipolar Disorder

Zoloft
    Indication: Panic Reaction

Provera
    Administration route: Oral
    Indication: Uterine Haemorrhage

Tinidazole / Tioconazole
    Indication: Vaginitis Bacterial

Clonazepam

Diane
    Dosage: freq:daily
    Administration route: Oral
    Indication: Oral Contraception

Paroxetine
    Administration route: Oral
    Indication: Bipolar Disorder
    Start date: 2004-01-01
    End date: 2006-12-14

Other drugs received by patient: Rivotril; Piroxicam; Rohypnol; L-Lysine; Amplictil; Herbal Preparation; Betagan; ALL Other Therapeutic Products; Midazolam HCL; Multivitamin; Fenergan; Loratadine; Synthroid; Venlafaxiine HCL



Adverse event in 53 year old female receiving Clonazepam

Reported by a consumer/non-health professional from United States on 2007-06-07

Patient: 53 year old female

Adverse reactions / side effects: Claustrophobia, Prescribed Overdose, Dental Caries, Abnormal Behaviour, Disorientation, Hypoaesthesia, Convulsion, Aggression, Anxiety, Dysarthria, Dental Necrosis, Dizziness, Hypersomnia

Adverse event resulted in: hospitalization

Suspect drug(s):
Betaseron
    Dosage: 2 miu, every 2d
    Indication: Multiple Sclerosis
    Start date: 2007-04-23
    End date: 2007-01-01

Betaseron
    Dosage: 6 miu, every 2d
    Start date: 2007-01-01

Clonazepam
    End date: 2007-04-01

Other drugs received by patient: Anxiolytics; Thyroid Preparations; Cardiovascular System Drugs; Antidepressants



Adverse event in 57 year old female receiving Clonazepam

Reported by a consumer/non-health professional from United States on 2007-05-21

Patient: 57 year old female, weighing 115.7 kg (254.5 pounds)

Adverse reactions / side effects: Dyspnoea, Nausea, Fear, Somnolence, Burning Sensation, Anxiety, Flushing, Hyperventilation, Fatigue, Panic Attack, Sleep Disorder, Palpitations, Balance Disorder, Vision Blurred, Dizziness

Suspect drug(s):
Clonazepam



Adverse event in male receiving Clonazepam

Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-24

Patient: male

Adverse reactions / side effects: Anxiety, Cardiac Disorder

Adverse event resulted in: hospitalization

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

Clonazepam
    Dosage: 0.25 mg, per oral
    Administration route: Oral
    Indication: Anxiety

Other drugs received by patient: Trazodone HCL



Adverse event in female receiving Clonazepam

Reported by a consumer/non-health professional from Brazil on 2007-04-06

Patient: female, weighing 52.0 kg (114.4 pounds)

Adverse reactions / side effects: Abdominal Pain, Weight Decreased, Seborrhoeic Dermatitis, Tachycardia, Headache, Menstrual Disorder, Amenorrhoea, Eyelid Ptosis, Tendonitis, Crying, Breast Pain, Pain in Extremity, Rhinitis, Hypoaesthesia, Stress, Tremor, Irritability, Galactorrhoea, Euphoric Mood, Blood Prolactin Increased, Insomnia, Suicide Attempt, Vaginal Infection, Phobia, Confusional State, Hypersensitivity, Haemorrhage, Drug Ineffective, Dyskinesia, Pain, Somnolence, Weight Increased, Alcoholism, Neck Pain, Skin Lesion, Formication, Dizziness, Depression, Sinusitis, Decreased Appetite, Nausea, Abortion, Musculoskeletal Pain, Anxiety, Bipolar Disorder, Grip Strength Decreased, Hypothyroidism, Blood Pressure Decreased, Shock, Influenza Like Illness

Suspect drug(s):
Zoloft
    Administration route: Oral
    Indication: Depression

Zoloft
    Indication: Bipolar Disorder

Zoloft
    Indication: Panic Reaction

Provera
    Administration route: Oral
    Indication: Uterine Haemorrhage

Tinidazole / Tioconazole
    Indication: Vaginitis Bacterial

Clonazepam

Diane
    Dosage: freq:daily
    Administration route: Oral
    Indication: Oral Contraception

Paroxetine HCL
    Administration route: Oral
    Indication: Bipolar Disorder
    Start date: 2004-01-01
    End date: 2006-12-14

Other drugs received by patient: Rivotril; Piroxicam; Rohypnol; L-Lysine; Amplictil; Herbal Preparation; Betagan; ALL Other Therapeutic Products; Midazolam HCL; Vitamins; Fenergan; Loratadine; Synthroid



Adverse event in female receiving Clonazepam

Reported by a consumer/non-health professional from Brazil on 2007-03-28

Patient: female, weighing 52.0 kg (114.4 pounds)

Adverse reactions / side effects: Abdominal Pain, Weight Decreased, Seborrhoeic Dermatitis, Tachycardia, Headache, Menstrual Disorder, Amenorrhoea, Eyelid Ptosis, Tendonitis, Crying, Breast Pain, Pain in Extremity, Rhinitis, Hypoaesthesia, Stress, Tremor, Irritability, Galactorrhoea, Euphoric Mood, Blood Prolactin Increased, Insomnia, Suicide Attempt, Vaginal Infection, Phobia, Confusional State, Hypersensitivity, Haemorrhage, Drug Ineffective, Dyskinesia, Pain, Somnolence, Weight Increased, Alcoholism, Neck Pain, Skin Lesion, Formication, Dizziness, Depression, Sinusitis, Decreased Appetite, Nausea, Abortion, Musculoskeletal Pain, Anxiety, Bipolar Disorder, Grip Strength Decreased, Hypothyroidism, Blood Pressure Decreased, Shock, Influenza Like Illness

Suspect drug(s):
Zoloft
    Administration route: Oral
    Indication: Depression

Zoloft
    Indication: Bipolar Disorder

Zoloft
    Indication: Panic Reaction

Provera
    Administration route: Oral
    Indication: Uterine Haemorrhage

Tinidazole / Tioconazole
    Indication: Vaginitis Bacterial

Clonazepam

Diane
    Dosage: freq:daily
    Administration route: Oral
    Indication: Oral Contraception

Paroxetine HCL
    Administration route: Oral
    Indication: Bipolar Disorder
    Start date: 2004-01-01
    End date: 2006-12-14

Other drugs received by patient: Rivotril; Piroxicam; Rohypnol; L-Lysine; Amplictil; Herbal Preparation; Betagan; ALL Other Therapeutic Products; Midazolam HCL; Vitamins; Fenergan; Loratadine; Synthroid



Adverse event in 48 year old female receiving Clonazepam

Reported by a individual with unspecified qualification from United States on 2007-03-27

Patient: 48 year old female, weighing 52.2 kg (114.8 pounds)

Adverse reactions / side effects: Weight Decreased, Tinnitus, Trigeminal Neuralgia, Impaired Work Ability, Suicidal Ideation, Sedation, Hypoaesthesia Facial, Depression, Muscle Spasms, Intervertebral Disc Protrusion, Drug Withdrawal Syndrome, Tremor, Paraesthesia, Anxiety, Burning Sensation, Myoclonus, Activities of Daily Living Impaired, Insomnia, Anorexia, Disturbance in Attention, Vision Blurred, Feeling Abnormal, Drug Dependence, Neurological Symptom

Suspect drug(s):
Clonazepam
    Dosage: 2 mg qhs po
    Administration route: Oral
    Indication: Somnolence
    Start date: 2005-05-01
    End date: 2005-09-01

Clonazepam
    Dosage: 1 mg qhs po
    Administration route: Oral
    Indication: Somnolence
    Start date: 2005-09-01

Clonazepam
    Dosage: 0.5 mg qhs po
    Administration route: Oral
    Indication: Somnolence
    Start date: 2006-08-01
    End date: 2006-09-01

Diazepam
    Dosage: 10 mg qhs po
    Administration route: Oral
    Indication: Drug Dependence
    Start date: 2006-08-01
    End date: 2006-09-01

Diazepam
    Dosage: 10 mg qhs po
    Administration route: Oral
    Indication: Somnolence
    Start date: 2006-08-01
    End date: 2006-09-01

Diazepam
    Dosage: 6 mg qhs po
    Administration route: Oral
    Indication: Drug Dependence
    Start date: 2006-04-01
    End date: 2006-05-01

Diazepam
    Dosage: 6 mg qhs po
    Administration route: Oral
    Indication: Somnolence
    Start date: 2006-04-01
    End date: 2006-05-01

Diazepam
    Dosage: 6.5 mg qhs po
    Administration route: Oral
    Indication: Drug Dependence
    End date: 2006-04-01

Diazepam
    Dosage: 6.5 mg qhs po
    Administration route: Oral
    Indication: Somnolence
    End date: 2006-04-01

Diazepam
    Dosage: 10 mg qhs po
    Administration route: Oral
    Indication: Drug Dependence

Diazepam
    Dosage: 10 mg qhs po
    Administration route: Oral
    Indication: Somnolence



Adverse event in 49 year old female receiving Clonazepam

Reported by a individual with unspecified qualification from United States on 2007-03-22

Patient: 49 year old female, weighing 52.2 kg (114.8 pounds)

Adverse reactions / side effects: Weight Decreased, Tinnitus, Head Discomfort, Trigeminal Neuralgia, Impaired Work Ability, Skin Burning Sensation, Suicidal Ideation, Sedation, Hypoaesthesia Facial, Depression, Muscle Spasms, Intervertebral Disc Protrusion, Drug Withdrawal Syndrome, Tremor, Eating Disorder, Paraesthesia, Anxiety, Burning Sensation, Myoclonus, Sensory Disturbance, Insomnia, Anorexia, Nervous System Disorder, Disturbance in Attention, Vision Blurred, Drug Dependence

Adverse event resulted in: hospitalization

Suspect drug(s):
Clonazepam
    Dosage: see image
    Administration route: Oral
    Indication: Insomnia
    Start date: 2005-05-01
    End date: 2005-09-01

Clonazepam
    Dosage: see image
    Administration route: Oral
    Indication: Insomnia
    Start date: 2006-08-01
    End date: 2006-09-01

Clonazepam
    Dosage: see image
    Administration route: Oral
    Indication: Insomnia
    Start date: 2005-09-01

Diazepam
    Dosage: see imge
    Administration route: Oral
    Indication: Sleep Disorder
    End date: 2006-04-01

Diazepam
    Dosage: see imge
    Administration route: Oral
    Indication: Sleep Disorder
    Start date: 2006-04-01
    End date: 2006-05-01



Adverse event in 49 year old female receiving Clonazepam

Reported by a individual with unspecified qualification from United States on 2007-03-09

Patient: 49 year old female, weighing 52.2 kg (114.8 pounds)

Adverse reactions / side effects: Weight Decreased, Head Discomfort, Tinnitus, Drug Ineffective, Trigeminal Neuralgia, Skin Burning Sensation, Suicidal Ideation, Sedation, Hypoaesthesia Facial, Depression, Muscle Spasms, Intervertebral Disc Protrusion, Drug Withdrawal Syndrome, Tremor, Eating Disorder, Paraesthesia, Myoclonus, Anxiety, Insomnia, Sensory Disturbance, Disturbance in Attention, Vision Blurred, Drug Dependence, Feeling Abnormal

Adverse event resulted in: hospitalization

Suspect drug(s):
Clonazepam
    Dosage: 0.5 mg, qhs, oral; 1 mg, qhs, oral, 2 mg, qhs, oral
    Administration route: Oral
    Indication: Somnolence
    Start date: 2005-05-01
    End date: 2005-09-01

Clonazepam
    Dosage: 0.5 mg, qhs, oral; 1 mg, qhs, oral, 2 mg, qhs, oral
    Administration route: Oral
    Indication: Somnolence
    Start date: 2006-08-01
    End date: 2006-09-01

Clonazepam
    Dosage: 0.5 mg, qhs, oral; 1 mg, qhs, oral, 2 mg, qhs, oral
    Administration route: Oral
    Indication: Somnolence
    Start date: 2005-09-01

Diazepam
    Dosage: 10 mg, qhs, oral, 6 mg, qhs, oral
    Administration route: Oral
    Indication: Somnolence
    Start date: 2006-04-01
    End date: 2006-05-01

Diazepam
    Dosage: 10 mg, qhs, oral, 6 mg, qhs, oral
    Administration route: Oral
    Indication: Somnolence
    Start date: 2006-08-01
    End date: 2006-09-01

Clonazepam
    Dosage: 0.5 mg, qhs,oral, 1 mg, qhs, oral, 2 mg, qhs, oral
    Administration route: Oral
    Indication: Somnolence
    Start date: 2005-05-01
    End date: 2005-09-01

Clonazepam
    Dosage: 0.5 mg, qhs,oral, 1 mg, qhs, oral, 2 mg, qhs, oral
    Administration route: Oral
    Indication: Somnolence
    Start date: 2006-08-01
    End date: 2006-09-01

Clonazepam
    Dosage: 0.5 mg, qhs,oral, 1 mg, qhs, oral, 2 mg, qhs, oral
    Administration route: Oral
    Indication: Somnolence
    Start date: 2005-09-01



Adverse event in 43 year old male receiving Clonazepam

Reported by a consumer/non-health professional from United States on 2007-02-13

Patient: 43 year old male, weighing 84.4 kg (185.6 pounds)

Adverse reactions / side effects: Anxiety, Depression, Poor Quality Drug Administered, Pharmaceutical Product Complaint

Suspect drug(s):
Clonazepam



Adverse event in male receiving Clonazepam

Reported by a consumer/non-health professional from United States on 2007-01-19

Patient: male

Adverse reactions / side effects: Agitation, Obsessive-Compulsive Disorder, Intentional Overdose, Somnolence, Suicidal Ideation, Anxiety, Bipolar Disorder, Alcoholism, Suicide Attempt, Anger, Sexual Dysfunction, Depression, Injury

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Neurontin
    Administration route: Oral
    Indication: Bipolar Disorder
    Start date: 1999-10-02
    End date: 2004-01-01

Neurontin
    Indication: Obsessive-Compulsive Disorder

Neurontin
    Indication: Anxiety

Neurontin
    Indication: Depression

Clonazepam
    Administration route: Oral
    Indication: Ill-Defined Disorder

Other drugs received by patient: Prozac; Eskalith

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