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MS Contin (Morphine) - Adverse Event Reports - Disability - Nausea

 



Index of reports > Cases resulting in disability (5) > Cases with Nausea (2)

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

Adverse event in 56 year old male receiving MS Contin (Morphine)

Reported by a individual with unspecified qualification on 2007-04-16

Patient: 56 year old male

Adverse reactions / side effects: Confusional State, Nausea, Therapeutic Agent Toxicity, Somnolence, Anticonvulsant Drug Level Increased, Dizziness, Gait Disturbance, Neutropenia, Thrombocytopenia

Adverse event resulted in: disablity

Suspect drug(s):
Dilantin
    Dosage: 300 mg, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

MS Contin
    Dosage: 20 mg, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Sutent
    Dosage: 50 mg, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in 56 year old male receiving MS Contin (Morphine)

Reported by a individual with unspecified qualification on 2007-04-12

Patient: 56 year old male

Adverse reactions / side effects: Confusional State, Nausea, Therapeutic Agent Toxicity, Somnolence, Anticonvulsant Drug Level Increased, Dizziness, Gait Disturbance, Neutropenia, Thrombocytopenia

Adverse event resulted in: disablity

Suspect drug(s):
Dilantin
    Dosage: 300 mg, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

MS Contin
    Dosage: 20 mg, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Sutent
    Dosage: 50 mg, unk
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

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