DUOPA SIDE EFFECTS
The following serious adverse reactions are discussed below and elsewhere in labeling:
- Gastrointestinal and Gastrointestinal Procedure-Related Risks.
- Falling Asleep During Activities of Daily Living and Somnolence.
- Orthostatic Hypotension.
- Impulse Control/Compulsive Behaviors.
- Depression and Suicidality.
- Withdrawal-Emergent Hyperpyrexia and Confusion.
- Cardiovascular Ischemic Events.
- Laboratory Test Abnormalities.
Clinical Trials Experience
Because clinical studies are run under widely varying conditions, the incidence of adverse reactions observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
In clinical studies, 416 patients with advanced Parkinson’s disease received DUOPA. 338 patients were treated with DUOPA for more than 1 year, 233 patients were treated with DUOPA for more than 2 years, and 162 patients were treated with DUOPA for more than 3 years.
In a 12-week, active-controlled clinical trial (Study 1), a total of 71 patients with advanced Parkinson’s disease were enrolled and had a PEG-J procedure. Of these, 37 patients received DUOPA and 34 received oral immediate-release carbidopa-levodopa.
The most common adverse reactions for DUOPA (incidence at least 7% greater than oral immediate-release carbidopa-levodopa) were: complication of device insertion, nausea, depression, peripheral edema, hypertension, upper respiratory tract infection, oropharyngeal pain, atelectasis, and incision site erythema.
Table 1 lists the incidence of adverse reactions occurring in the DUOPA-treated group (requiring at least 2 patients in this group) in Study 1 when the incidence was numerically greater than that for oral immediate-release carbidopa-levodopa.
Table 1: Adverse Reactions in Study 1 for DUOPA in Patients with Advanced Parkinson’s Disease
(n = 37) %
|Oral immediate-release carbidopa-levodopaa
(n = 34) %
|Complication of device insertion||57||44|
|Incision site erythema||19||12|
|Post procedural discharge||11||9|
|Upper respiratory tract infection||8||0|
|Excessive granulation tissue||5||0|
|White blood cells urine positive||5||0|
|aAll patients in the clinical trial regardless of treatment arm received a PEG-J.|
Procedure And Device- Related Adverse Reactions
The most common adverse reactions associated with complications due to naso-jejunal (NJ) insertion were: oropharyngeal pain, abdominal distention, abdominal pain, abdominal discomfort, pain, throat irritation, gastrointestinal injury, esophageal hemorrhage, anxiety, dysphagia, and vomiting.
The most common adverse reactions associated with complications due to PEG-J insertion were: abdominal pain, abdominal discomfort, abdominal distension, flatulence, or pneumoperitoneum.
Additional adverse reactions that were co-reported with complication of naso-jejunal and PEG-J insertion included upper abdominal pain, duodenal ulcer, duodenal ulcer hemorrhage, erosive duodenitis, erosive gastritis, gastrointestinal hemorrhage, intussusception, peritonitis, postoperative abscess, and small intestine ulcer.
SRC: NLM .