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MS Contin (Morphine) - Adverse Event Reports - All Cases - Abnormal Behaviour

 



Index of reports > All cases (25) > Cases with Abnormal Behaviour (7)

Below is the selection of adverse event reports related to MS Contin (Morphine) that includes all cases 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 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 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 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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