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MS Contin (Morphine) - Adverse Event Reports - Serious Event - Abnormal Behaviour

 



Index of reports > Cases resulting in a serious event (23) > Cases with Abnormal Behaviour (7)

Below is the selection of adverse event reports related to MS Contin (Morphine) that includes cases resulting in a serious event where reactions include abnormal behaviour.

Adverse event in 42 year old female receiving MS Contin (Morphine)

Reported by a physician from United States on 2007-06-27

Patient: 42 year old female

Adverse reactions / side effects: Confusional State, Dyspnoea, Neuropathy Peripheral, Abnormal Behaviour, Drug Interaction, Mood Swings, Disease Progression

Suspect drug(s):
MS Contin
    Dosage: 15 mg qd po
    Administration route: Oral
    Indication: Complex Regional Pain Syndrome
    Start date: 2006-10-01

Namenda
    Dosage: 10 mg bid po
    Administration route: Oral
    Indication: Neuropathy Peripheral
    Start date: 2006-01-01
    End date: 2006-12-13

Namenda
    Dosage: 5 mg bid po
    Administration route: Oral
    Indication: Neuropathy Peripheral
    Start date: 2006-12-14
    End date: 2006-12-20

Namenda
    Dosage: 5 mg qd po
    Administration route: Oral
    Indication: Neuropathy Peripheral
    Start date: 2006-11-01
    End date: 2006-01-01

Namenda
    Dosage: 5 mg bid po
    Administration route: Oral
    Indication: Neuropathy Peripheral
    Start date: 2006-01-01
    End date: 2006-01-01

Namenda
    Dosage: 15 mg qd po
    Administration route: Oral
    Indication: Neuropathy Peripheral
    Start date: 2006-01-01
    End date: 2006-01-01

Other drugs received by patient: Warfarin Sodium; Crestor; Darvocet; Spiriva; Levoxyl; Oxygen



Adverse event in male receiving MS Contin (Morphine)

Reported by a individual with unspecified qualification on 2007-06-22

Patient: male

Adverse reactions / side effects: Abnormal Behaviour, Disorientation

Adverse event resulted in: hospitalization

Suspect drug(s):
MS Contin
    Dosage: unk mg, see text
    Indication: Procedural Pain

Oxymorphone Hydrochloride
    Dosage: unk, unk
    Indication: Bone Pain



Adverse event in male receiving MS Contin (Morphine)

Reported by a individual with unspecified qualification on 2007-06-22

Patient: male

Adverse reactions / side effects: Abnormal Behaviour, Disorientation

Adverse event resulted in: hospitalization

Suspect drug(s):
MS Contin
    Dosage: unk mg, see text
    Indication: Procedural Pain

Oxymorphone Hydrochloride
    Dosage: unk, unk
    Indication: Bone Pain



Adverse event in female receiving MS Contin (Morphine)

Reported by a individual with unspecified qualification on 2007-06-22

Patient: female

Adverse reactions / side effects: Abnormal Behaviour, Disorientation

Adverse event resulted in: hospitalization

Suspect drug(s):
MS Contin (Morphine)



Adverse event in male receiving MS Contin (Morphine)

Reported by a individual with unspecified qualification on 2007-06-22

Patient: male

Adverse reactions / side effects: Abnormal Behaviour, Disorientation

Adverse event resulted in: hospitalization

Suspect drug(s):
MS Contin (Morphine)



Adverse event in 42 year old female receiving MS Contin (Morphine)

Reported by a physician from United States on 2007-05-09

Patient: 42 year old female

Adverse reactions / side effects: Back Pain, Confusional State, Dyspnoea, Abnormal Behaviour, Condition Aggravated, Drug Interaction, Cognitive Disorder, Amnesia, Complex Regional Pain Syndrome, Neuropathy Peripheral, Mood Swings

Suspect drug(s):
MS Contin
    Dosage: 15 mg qd po
    Administration route: Oral
    Indication: Complex Regional Pain Syndrome
    Start date: 2006-10-01

Namenda
    Dosage: 10 mg bid po
    Administration route: Oral
    Indication: Neuropathy Peripheral
    Start date: 2006-01-01
    End date: 2006-12-13

Namenda
    Dosage: 5 mg bid po
    Administration route: Oral
    Indication: Neuropathy Peripheral
    Start date: 2006-12-14
    End date: 2006-12-20

Namenda
    Dosage: 5 mg qd po
    Administration route: Oral
    Indication: Neuropathy Peripheral
    Start date: 2006-11-01
    End date: 2006-01-01

Namenda
    Dosage: 5 mg bid po
    Administration route: Oral
    Indication: Neuropathy Peripheral
    Start date: 2006-01-01
    End date: 2006-01-01

Namenda
    Dosage: 15 mg qd po
    Administration route: Oral
    Indication: Neuropathy Peripheral
    Start date: 2006-01-01
    End date: 2006-01-01

Other drugs received by patient: Warfarin Sodium; Crestor; Darvocet; Spiriva; Levoxyl; Oxygen



Adverse event in 42 year old female receiving MS Contin (Morphine)

Reported by a physician from United States on 2007-03-13

Patient: 42 year old female

Adverse reactions / side effects: Back Pain, Confusional State, Dyspnoea, Abnormal Behaviour, Drug Interaction, Amnesia, Disease Progression, Hyperaesthesia, Neuropathy Peripheral, Mood Swings

Suspect drug(s):
MS Contin
    Dosage: 15 mg qd po
    Administration route: Oral
    Indication: Complex Regional Pain Syndrome
    Start date: 2006-10-01

Namenda
    Dosage: 10 mg bid po
    Administration route: Oral
    Indication: Neuropathy Peripheral
    Start date: 2006-01-01
    End date: 2006-12-13

Namenda
    Dosage: 5 mg bid po
    Administration route: Oral
    Indication: Neuropathy Peripheral
    Start date: 2006-12-14
    End date: 2006-12-20

Namenda
    Dosage: 5 mg qd po
    Administration route: Oral
    Indication: Neuropathy Peripheral
    Start date: 2006-11-01
    End date: 2006-01-01

Namenda
    Dosage: 5 mg bid po
    Administration route: Oral
    Indication: Neuropathy Peripheral
    Start date: 2006-01-01
    End date: 2006-01-01

Namenda
    Dosage: 15 mg qd po
    Administration route: Oral
    Indication: Neuropathy Peripheral
    Start date: 2006-01-01
    End date: 2006-01-01

Other drugs received by patient: Warfarin Sodium; Crestor; Darvocet (Propoxyphene / Acetaminophen); Spiriva; Levoxyl; Oxygen

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