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Index of reports
> Cases resulting in other serious reactions (13)
> Cases with Memory Impairment (5)
Below is the selection of adverse event reports related to MS Contin (Morphine) that includes cases resulting in other serious reactions where reactions include memory impairment.
Adverse event in 45 year old male receiving MS Contin (Morphine)
Reported by a physician from United States on 2007-07-09
Patient: 45 year old male, weighing 79.4 kg (174.7 pounds)
Adverse reactions / side effects: Mydriasis, Visual Disturbance, Memory Impairment, Convulsion, Tremor
Suspect drug(s):
MS Contin
Dosage: see image
Administration route: Oral
Indication: Back Pain
Start date: 2004-01-01
End date: 2007-04-01
MS Contin
Dosage: see image
Administration route: Oral
Indication: Back Pain
Start date: 2004-01-01
End date: 2007-04-01
Oxycontin
Dosage: 80 mg, bid, oral
Administration route: Oral
Indication: Back Pain
Start date: 2004-01-01
End date: 2007-04-01
Restoril
Dosage: 60 mg, qd prn, oral
Administration route: Oral
Indication: Insomnia
Start date: 2005-01-01
Roxicodone
Dosage: 30 mg, qid, oral
Administration route: Oral
Indication: Back Pain
Start date: 2004-01-01
End date: 2007-04-01
Adverse event in female receiving MS Contin (Morphine)
Reported by a individual with unspecified qualification on 2007-05-23
Patient: female
Adverse reactions / side effects: Lymphadenopathy, Pruritus, Urticaria, Scleroderma, Pharyngeal Oedema, Connective Tissue Disorder, Abscess Limb, Cutaneous Lupus Erythematosus, Ligament Injury, Pelvic Mass, Pain in Extremity, Osteomyelitis Chronic, Osteitis, Vertebral Injury, Throat Irritation, Dehydration, Lymphoma, Pharmaceutical Product Complaint, Therapeutic Agent Toxicity, Pain, Impaired Work Ability, Constipation, Nasal Oedema, Road Traffic Accident, Adrenal Insufficiency, Myocardial Infarction, Medication Residue, Dyspnoea, Joint Dislocation, Uterine Cancer, Lung Disorder, Alopecia, Memory Impairment, Syncope Vasovagal, Immune System Disorder
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
MS Contin
Dosage: 60 mg, unk
Indication: Systemic Lupus Erythematosus
MS Contin
Dosage: 100 mg, bid prn
Adverse event in female receiving MS Contin (Morphine)
Reported by a individual with unspecified qualification on 2007-05-18
Patient: female
Adverse reactions / side effects: Pruritus, Lymphadenopathy, Urticaria, Scleroderma, Pharyngeal Oedema, Connective Tissue Disorder, Abscess Limb, Cutaneous Lupus Erythematosus, Pelvic Mass, Ligament Injury, Pain in Extremity, Osteomyelitis Chronic, Osteitis, Vertebral Injury, Throat Irritation, Dehydration, Pharmaceutical Product Complaint, Lymphoma, Pain, Impaired Work Ability, Therapeutic Agent Toxicity, Constipation, Nasal Oedema, Road Traffic Accident, Adrenal Insufficiency, Myocardial Infarction, Medication Residue, Dyspnoea, Joint Dislocation, Uterine Cancer, Lung Disorder, Alopecia, Memory Impairment, Immune System Disorder, Syncope Vasovagal
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
MS Contin (Morphine)
Adverse event in 52 year old female receiving MS Contin (Morphine)
Reported by a individual with unspecified qualification on 2007-01-18
Patient: 52 year old female, weighing 63.0 kg (138.6 pounds)
Adverse reactions / side effects: Weight Decreased, Asthma, Abdominal Pain, Pyrexia, Loss of Consciousness, Pneumonia, Drug Abuser, Drug Withdrawal Syndrome, Delirium, Tremor, Paraesthesia, Dehydration, Anorexia, Disturbance in Attention, Vision Blurred, Pain, Disorientation, Somnolence, Speech Disorder, Myalgia, RED Blood Cell Count Decreased, Injection Site Reaction, Dizziness, Depression, Vomiting, Nausea, Dental Caries, Blood Potassium Decreased, Diarrhoea, Alopecia, Bronchitis, Memory Impairment, Asthenia
Adverse event resulted in: hospitalization
Suspect drug(s):
MS Contin
Dosage: unk, unk
Indication: Drug USE FOR Unknown Indication
Start date: 2005-09-25
PEG-Intron
Dosage: unk, unk
Indication: Hepatitis C
Start date: 2005-09-25
Ribasphere
Dosage: unk, unk
Indication: Hepatitis C
Start date: 2005-09-25
Other drugs received by patient: Aspirin; Buspar; Calcium; Glucosamine W / Chondroitin Sulfates; Hydromorphone HCL; Lecithin; Levothyroxine Sodium; Vitamin CAP; Omega-3; Promethazine; Vitamin A+D; Vitamin B Complex CAP; Ascorbic Acid; Vitamin E; Wellbutrin; Albuterol Sulate; Flaxseed OIL; Inderal; Epogen; Iron
Adverse event in 52 year old female receiving MS Contin (Morphine)
Reported by a individual with unspecified qualification from United States on 2007-01-16
Patient: 52 year old female, weighing 63.0 kg (138.6 pounds)
Adverse reactions / side effects: Weight Decreased, Abdominal Pain, Asthma, Pyrexia, Loss of Consciousness, Injection Site Erythema, Pneumonia, Drug Abuser, Injection Site Bruising, Drug Withdrawal Syndrome, Delirium, Tremor, Paraesthesia, Respiratory Tract Congestion, Anorexia, Dehydration, Vision Blurred, Disturbance in Attention, Pain, Injection Site Swelling, Disorientation, Somnolence, Speech Disorder, Myalgia, RED Blood Cell Count Decreased, Injection Site Reaction, Dizziness, Depression, Vomiting, Nausea, Dental Caries, Burning Sensation, Diarrhoea, Blood Potassium Decreased, Alopecia, Bronchitis, Memory Impairment, Asthenia
Adverse event resulted in: hospitalization
Suspect drug(s):
MS Contin
Dosage: unk, unk
Indication: Drug USE FOR Unknown Indication
End date: 2005-10-01
MS Contin
Start date: 2005-01-01
MS Contin
End date: 2005-09-25
PEG-Intron
Dosage: unk, unk
Indication: Hepatitis C
Start date: 2005-09-25
Ribasphere
Administration route: Oral
Indication: Hepatitis C
Start date: 2005-09-25
Other drugs received by patient: Aspirin; Buspar; Calcium; Glucosamine W / Chondroitin Sulfates; Hydromorphone HCL; Inderal; Lecithin; Levothyroxine Sodium; Morphine Sulfate; Vitamin CAP; Omega-3; Promethazine; Vitamin A and D; Vitamin B Complex CAP; Ascorbic Acid; Vitamin E; Wellbutrin; Morphine Sulfate; Flaxseed OIL; Calcium; Albuterol; Epogen; Iron; Inderal; Doxycycline Hydrochloride
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