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Index of reports
> Cases resulting in death (4)
> Cases with Blood Pressure Increased (1)
Below is the selection of adverse event reports related to Apokyn (Apomorphine) that includes cases resulting in death where reactions include blood pressure increased.
Adverse event in female receiving Apokyn (Apomorphine)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-01
Patient: female, weighing 61.2 kg (134.7 pounds)
Adverse reactions / side effects: Blood Pressure Increased, Pneumonia, Urinary Tract Infection, Hypotension, Pyrexia
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Apokyn
Dosage: (0.3 ml subcutaneous, (0.4 ml prn subcutaneous), (0.4 ml 1x/8 hours subcutaneous)
Indication: Parkinson's Disease
Start date: 2007-01-01
End date: 2007-07-19
Apokyn
Dosage: (0.3 ml subcutaneous, (0.4 ml prn subcutaneous), (0.4 ml 1x/8 hours subcutaneous)
Indication: Parkinson's Disease
Start date: 2007-05-10
Apokyn
Dosage: (0.3 ml subcutaneous, (0.4 ml prn subcutaneous), (0.4 ml 1x/8 hours subcutaneous)
Indication: Parkinson's Disease
Start date: 2007-07-21
Other drugs received by patient: Sinemet; Tigan; Comtan
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