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Index of reports
> All cases (84)
> Cases with Drug Withdrawal Syndrome (12)
Below is the selection of adverse event reports related to Baclofen that includes all cases where reactions include drug withdrawal syndrome.
Adverse event in 49 year old male receiving Baclofen
Reported by a physician from United States on 2007-07-31
Patient: 49 year old male, weighing 73.9 kg (162.6 pounds)
Adverse reactions / side effects: Muscle Rigidity, Abdominal Tenderness, Abdominal Discomfort, Lymphocyte Count Decreased, Back Pain, Restlessness, Drug Withdrawal Syndrome, Respiratory Distress, Delirium, Tremor, Aggression, Respiratory Rate Decreased, Mental Disorder, Neutrophil Count Decreased, Drug Ineffective, Rectal Haemorrhage, Therapeutic Agent Toxicity, Drug Interaction, Mental Status Changes, Hepatomegaly, Frequent Bowel Movements, Fatigue, Overdose, Neck Pain, RED Blood Cell Count Decreased, Thrombocytopenia, Blood Pressure Increased, Haemoglobin Decreased, Anxiety, Haematochezia, Heart Rate Increased, Sinus Tachycardia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Start date: 2007-04-17
Celexa
Indication: Depression
Effexor
End date: 2007-04-15
Opiate (Nos)
Pegasys
Dosage: 90 mcg sc
Indication: Hepatitis C
Start date: 2006-06-15
End date: 2007-03-01
Pegasys
Dosage: 45 mcg qd sc
Indication: Hepatitis C
Start date: 2007-03-01
Voltaren
Indication: Pain
Wellbutrin
Dosage: 150 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Other drugs received by patient: Azithromycin; Hydrochlorothiazide; Toprol-XL
Adverse event in 49 year old male receiving Baclofen
Reported by a physician from United States on 2007-07-27
Patient: 49 year old male, weighing 74.0 kg (162.8 pounds)
Adverse reactions / side effects: Movement Disorder, Agitation, Blood Pressure Increased, Back Pain, Restlessness, Mental Status Changes, Drug Withdrawal Syndrome, Muscle Rigidity, Respiratory Distress, Delirium, Aggression, Tremor, Anxiety, Neck Pain, Mental Disorder, Sinus Tachycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Dosage: unknown
Start date: 2007-04-17
Caffeine
Dosage: about 10 cups
Start date: 2007-04-17
End date: 2007-04-17
Celexa
Dosage: unknown
Indication: Depression
Effexor
Dosage: unknown
End date: 2007-04-15
Nicotine
Dosage: tried to smoke 2 packs in one day
Pegasys
Dosage: 90 mcg, frequency unknown
Indication: Hepatitis C
Start date: 2006-06-15
End date: 2007-03-01
Pegasys
Dosage: 45 mcg, frequency unknown
Start date: 2007-03-01
End date: 2007-05-11
Voltaren
Dosage: unknown
Indication: Pain
Wellbutrin
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Other drugs received by patient: Azithromycin; Hydrochlorothiazide; Parafon; Toprol-XL
Adverse event in 49 year old male receiving Baclofen
Reported by a physician from United States on 2007-07-12
Patient: 49 year old male
Adverse reactions / side effects: Rectal Haemorrhage, Drug Interaction, Mental Status Changes, Muscle Rigidity, Drug Toxicity, Frequent Bowel Movements, Fatigue, Overdose, RED Blood Cell Count Decreased, Thrombocytopenia, Incorrect Dose Administered, Drug Withdrawal Syndrome, Respiratory Distress, Delirium, Blood Pressure Diastolic Increased, Aggression, Sinus Tachycardia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Dosage: oral
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-17
Celexa
Dosage: oral
Administration route: Oral
Indication: Depression
Effexor
Dosage: oral
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
End date: 2007-04-15
Opiate Nos()
Indication: Drug USE FOR Unknown Indication
Pegasys
Dosage: 45 mcg, subcutaneous
Indication: Hepatitis C
Start date: 2006-10-15
End date: 2007-05-11
Wellbutrin
Dosage: oral
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Other drugs received by patient: Zithromax Z-Pack (Azthromycin); Hydrochlorothiazide; Toprol-XL; Ativan; Benadryl; Cogentin (Benzatorpine Mesilate)
Adverse event in 49 year old male receiving Baclofen
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-26
Patient: 49 year old male
Adverse reactions / side effects: Agitation, Drug Ineffective, Dyskinesia, Rectal Haemorrhage, Drug Interaction, Mental Status Changes, Prothrombin Time Prolonged, Muscle Rigidity, Frequent Bowel Movements, Overdose, Fatigue, RED Blood Cell Count Decreased, Depression, Thrombocytopenia, White Blood Cell Count Decreased, Blood Pressure Increased, Blood Urea Increased, Restlessness, International Normalised Ratio Increased, Drug Withdrawal Syndrome, Blood Bicarbonate Decreased, Delirium, Respiratory Distress, Aggression, Tremor, Haematochezia, Anxiety, Heart Rate Increased, Mental Disorder, Sinus Tachycardia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Start date: 2007-04-17
Celexa
Indication: Depression
Opiate (Nos)
Pegasys
Dosage: 45 mcg sc
Indication: Hepatitis C
Start date: 2006-10-15
End date: 2007-05-11
Wellbutrin
Dosage: 150 mg qd po
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Other drugs received by patient: Effexor; Azithromycin; Hydrochlorothiazide; Toprol-XL
Adverse event in 48 year old female receiving Baclofen
Reported by a individual with unspecified qualification from United States on 2007-06-22
Patient: 48 year old female
Adverse reactions / side effects: Grand MAL Convulsion, Drug Dose Omission, Pneumonia, Unresponsive TO Stimuli, Drug Withdrawal Syndrome, Cerebrovascular Accident, Cerebellar Atrophy
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Adverse event in 49 year old male receiving Baclofen
Reported by a physician from United States on 2007-06-20
Patient: 49 year old male
Adverse reactions / side effects: Blood Pressure Increased, Agitation, Movement Disorder, Restlessness, Mental Status Changes, Drug Withdrawal Syndrome, Muscle Rigidity, Delirium, Respiratory Distress, Tremor, Aggression, Anxiety, Mental Disorder, Sinus Tachycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Dosage: unknown
Start date: 2007-04-17
Bupropion Hydrochloride
Administration route: Oral
Indication: Depression
Start date: 2007-04-17
Caffeine
Dosage: about 10 cups
Start date: 2007-04-17
End date: 2007-04-17
Celexa
Dosage: unknown
Indication: Depression
Effexor
Dosage: unknown
End date: 2007-04-15
Nicotine
Dosage: tried to smoke 2 packs in one day
Pegasys
Dosage: 45 mcg, frequency unknown
Indication: Hepatitis C
Start date: 2006-10-15
End date: 2007-05-11
Other drugs received by patient: Azithromycin; Toprol-XL; Hydrochlorothiazide
Adverse event in 48 year old female receiving Baclofen
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-20
Patient: 48 year old female
Adverse reactions / side effects: Pneumonia, Unresponsive TO Stimuli, Intubation, Moaning, Drug Withdrawal Syndrome, Cerebrovascular Accident, Cerebellar Atrophy, Grand MAL Convulsion
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Baclofen
Other drugs received by patient: Oxybuton; Gabapentin; Montelukast Sodium; Hydrochlorothiazide W / Irbesartan; Aspirin; Omeprazole; Atorvastatin Calcium; Sertraline; Glyburide
Adverse event in 40 year old male receiving Baclofen
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-03-16
Patient: 40 year old male
Adverse reactions / side effects: Drug Withdrawal Syndrome, Convulsion
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Administration route: Oral
Indication: Back Pain
Start date: 2006-11-27
End date: 2006-11-29
Lyrica
Administration route: Oral
Indication: Back Pain
Start date: 2006-11-27
End date: 2006-11-29
Other drugs received by patient: Amitriptyline HCL; CO-Codamol; Diclofenac Sodium; Erythromycin
Adverse event in 60 year old male receiving Baclofen
Reported by a pharmacist from United States on 2007-03-09
Patient: 60 year old male, weighing 103.0 kg (226.6 pounds)
Adverse reactions / side effects: Drug Effect Decreased, Hallucination, Visual, Drug Withdrawal Syndrome, Disorientation, Hyperhidrosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Adverse event in 40 year old male receiving Baclofen
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-02-07
Patient: 40 year old male
Adverse reactions / side effects: Drug Withdrawal Syndrome, Convulsion
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Administration route: Oral
Indication: Back Pain
Start date: 2006-11-27
End date: 2006-11-29
Lyrica
Administration route: Oral
Indication: Back Pain
Start date: 2006-11-27
End date: 2006-11-29
Other drugs received by patient: Amitriptyline HCL; Acetaminophen and Codeine Phosphate; Diclofenac Sodium; Erythromycin
Adverse event in 40 year old male receiving Baclofen
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-02-01
Patient: 40 year old male
Adverse reactions / side effects: Drug Withdrawal Syndrome, Convulsion
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Administration route: Oral
Indication: Back Pain
Start date: 2006-11-27
End date: 2006-11-29
Lyrica
Administration route: Oral
Indication: Back Pain
Start date: 2006-11-27
End date: 2006-11-29
Other drugs received by patient: Amitriptyline HCL; CO-Codamol; Diclofenac Sodium; Erythromycin
Adverse event in 40 year old male receiving Baclofen
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-01-25
Patient: 40 year old male
Adverse reactions / side effects: Drug Withdrawal Syndrome, Convulsion
Adverse event resulted in: hospitalization
Suspect drug(s):
Baclofen
Administration route: Oral
Indication: Back Pain
Start date: 2006-11-27
End date: 2006-11-29
Lyrica
Administration route: Oral
Indication: Back Pain
Start date: 2006-11-27
End date: 2006-11-29
Other drugs received by patient: Amitriptyline HCL; CO-Codamol; Diclofenac Sodium; Erythromycin
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