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Index of reports
> Cases resulting in disability (3)
Below is the selection of adverse event reports related to Marinol (Dronabinol) that includes cases resulting in disability.
Adverse event in female receiving Marinol (Dronabinol)
Reported by a individual with unspecified qualification from Canada on 2007-07-27
Patient: female
Adverse reactions / side effects: Confusional State, Dyspnoea, Palpitations
Adverse event resulted in: life threatening event, disablity
Suspect drug(s):
Marinol (Dronabinol)
Other drugs received by patient: Venlafaxine HCL; Enoxaparin Sodium; Levofloxacin; Metronidazole HCL
Adverse event in 27 year old female receiving Marinol (Dronabinol)
Reported by a physician from United States on 2007-06-15
Patient: 27 year old female, weighing 53.0 kg (116.6 pounds)
Adverse reactions / side effects: Colour Blindness, Visual Field Defect
Adverse event resulted in: disablity
Suspect drug(s):
Marijuana
Dosage: daily dose: as needed
Administration route: Oral
Indication: Porphyria Acute
Start date: 2001-01-01
Marinol
Dosage: daily dose: 30 milligram(s)
Administration route: Oral
Indication: Ill-Defined Disorder
Start date: 2001-11-29
Marinol
Dosage: daily dose: 10 mg as needed
Administration route: Oral
Adverse event in 27 year old female receiving Marinol (Dronabinol)
Reported by a physician from United States on 2007-06-01
Patient: 27 year old female, weighing 53.0 kg (116.6 pounds)
Adverse reactions / side effects: Colour Blindness, Visual Field Defect
Adverse event resulted in: disablity
Suspect drug(s):
Marijuana
Dosage: daily dose: as needed
Administration route: Oral
Indication: Porphyria Acute
Start date: 2001-01-01
Marinol
Dosage: daily dose: 30 milligram(s)
Administration route: Oral
Indication: Ill-Defined Disorder
Marinol
Dosage: daily dose: 10 mg as needed
Administration route: Oral
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